Jilie Kong

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Name: 孔继烈; JiLie Kong; Jilie Kong
Organization: Fudan University , China
Department: Department of Chemistry and Institutes of Biomedical Sciences
Title: Professor(PhD)

TOPICS

Co-reporter:Wei Zhao, Ji-Shi Wei, Peng Zhang, Jie Chen, Ji-Lie Kong, Lian-Hua Sun, Huan-Ming Xiong, and Helmuth Möhwald
ACS Applied Materials & Interfaces June 7, 2017 Volume 9(Issue 22) pp:18474-18474
Publication Date(Web):May 25, 2017
DOI:10.1021/acsami.7b02542
ZnO@polymer core–shell nanoparticles are assembled into novel capsule shells with diameters of about 100 nm to load isotretinoin (ISO) with a capacity as high as 34.6 wt %. Although ISO, a widely used drug for acne treatment, by itself is not suitable for treating cancer because of its hydrophobicity, our ZnO–ISO composite showed much stronger anticancer activity. The improved cytotoxicity is ascribed to the synergistic effects of the ZnO@polymer and ISO, where the ZnO@polymer helps in the accumulation of ISO in cancer cells on the one hand, and on the other hand, ISO is released completely through ZnO decomposition under acidic conditions of cancer cells. Such a pH-triggered drug-delivery system exhibits a much improved killing of cancer cells in vitro in comparison with the benchmarks, Nintedanib and Crizotinib, two commercial drugs clinically applied against lung cancer.Keywords: cancer cell; core−shell; drug delivery; isotretinoin; ZnO nanoparticle;
Co-reporter:Weiwei Chen, Xueen Fang, Hua Li, Hongmei Cao, Jilie Kong
Biosensors and Bioelectronics 2017 Volume 94(Volume 94) pp:
Publication Date(Web):15 August 2017
DOI:10.1016/j.bios.2017.02.025
•In the present study, a nanoassembly of DNA and Pt nanoparticles was prepared.•The DNA-Pt hybrid nanoparticles would induce a rapid colorimetric response for efficient and quick detection of target DNA.•A rapid and simple paper-based ananlytical device (PAD) was designed for quantitative analysis of DNA.•We further employed the magnetic beads-based strategy for the specific target DNA assay.In this research, we found that the peroxidase-like activities of noncovalent DNA-Pt hybrid nanoparticles could be obviously blocked, when Pt nanoparticles (PtNPs) were synthesized in situ using DNA as a template. Moreover, this self-assembled synthetic process was very convenient and rapid (within few mintues), and the inhibition mediated by DNA was also very effective. First, by the paper-based analytical device (PAD) we found the catalytic activities of DNA-Pt hybrid nanoparticles exhibited a linear response to the concentration of DNA in the range from 0.0075 to 0.25 µM. Then, with the magnetic bead isolated system and target DNA-induced hybridization chain reaction (HCR), we realized the specific target DNA analysis with a low detection of 0.228 nM, and demonstrated its effectivity in distinguishing the target DNA from other interferences. To our knowledge, this is the first report that used the nanoassembly between DNA and PtNPs for colorimetric detection of nucleic acids, which was based on DNA-mediated inhibition of catalytic activities of platinum nanoparticles. The results may be useful for understanding the interactions between DNA and metal nanoparticles, and for development of other convenient and effective analytical strategies.
Co-reporter:Qianqian Zhao, Ren Zhang, Daixin Ye, Song Zhang, Hui ChenJilie Kong
ACS Applied Materials & Interfaces 2017 Volume 9(Issue 3) pp:
Publication Date(Web):December 27, 2016
DOI:10.1021/acsami.6b12047
The monitoring of reactive oxygen species (ROS) in living cells remains challenging because of the complexity, short half-life, and autofluorescence of biological samples. In this work, we designed a ratiometric fluorescent probe for the detection and imaging of ROS, which was constructed from silicon quantum dots (Si QDs) with chlorin e6 (Ce6) through electrostatic attraction and showed well-resolved dual fluorescence emission signals (490 and 660 nm). Sensitive and selective biosensing of hydroxyl radical (•OH) was demonstrated on the basis of fluorescence quenching of the Si QDs and Ce6 as an internal reference to avoid environmental interference, with a detection limit of ∼0.97 μM. The endogenous release of •OH was also monitored and imaged in living cells.Keywords: cell imaging; chlorin e6 (Ce6); highly reactive oxygen species; hydroxyl radical (•OH); ratiometric fluorescence probe; silicon quantum dots;
Co-reporter:Hongmei Cao, Xueen Fang, Haipeng Li, Hua Li, Jilie Kong
Talanta 2017 Volume 164() pp:588-592
Publication Date(Web):1 March 2017
DOI:10.1016/j.talanta.2016.07.018
•The mucin 1 protein, as a tumor marker, is present in a variety of malignant tumors. Therefore, the sensitive and specific detection of mucin 1 has great significance for early cancer diagnoses.•Report a novel technique of Immuno-Loop-Mediated Isothermal Amplification for the rapid quantitative detection of MUC-1 with high sensitivity (120 MUC-1 molecules by calculation) and specificity.•Finally, this approach is also successfully applied in the analysis of human blood serum samples. It also lays the foundation for the early diagnosis of different types of low-abundance cancer biomarkers.Mucin 1 (MUC-1), a glycoprotein over-expressed on most malignant epithelial cell surfaces, such as colorectal, lung, prostate, pancreatic, ovarian, and bladder carcinomas, has been confirmed as a useful biomarker for the diagnosis of early cancers. Therefore, it is very important for early cancer diagnoses to develop the sensitive and specific detection approach of MUC-1. In this paper, we report a novel technique of aptamer-based Immuno-Loop-Mediated Isothermal Amplification (Im-LAMP) for the quantitative detection of MUC-1 by MUC-1 aptamer with high affinity for MUC-1. The cycle time is linearly dependent on the logarithm (log) of the concentration of mucin 1 ranging from 1.0 pM to 1.0 aM. We call this technique Im-LAMP, which is a novel method for the detection of low-abundance proteins with high sensitivity (a low detection limit of 120 MUC-1 molecules by calculation)and specificity. Finally, this approach is also successfully applied in the analysis of human blood serum samples. It also lays the foundation for the early diagnosis of different types of low-abundance cancer biomarkers.
Co-reporter:Weiwei Chen;Xueen Fang;Xin Ye;Hua Li;Hongmei Cao
Microchimica Acta 2017 Volume 184( Issue 12) pp:4869-4877
Publication Date(Web):31 October 2017
DOI:10.1007/s00604-017-2511-x
The authors describe a protein-triggered self-assembling DNA nanomachine for the detection of interferon-γ (IFN-γ), an important cytokine associated with immuno response. The DNA nanoprobe exhibits good specificity and sensitivity for interferon-γ (IFN-γ) detection. In the presence of the target (IFN-γ), four functional DNA probes are assembled to form a DNA nanocomplex. It promotes the release of the target for recycling. The captured DNA probe (biotinylated-C1) is then brought into contact with streptavidin-functionalized magnetic beads (sa-MB). These cause the dissociation of the B3 primer signal probe (S1) from the reaction solution which then is available for loop-mediated isothermal amplification (LAMP) analysis. As the deficiency of the B3 primer inhibits the LAMP reaction, the resulting point of inflexion (POI) value (the starting point of LAMP) is increased. In the absence of IFN-γ, the operation of the DNA nanomachine is not triggered, and the LAMP reaction remains unaffected. In this way, the POI values indirectly report the concentration of IFN-γ. The feasibility of the protein-driven DNA nanomachine was first demonstrated by the gel electrophoresis and real-time fluorescence analysis. Then, under optimal conditions, IFN-γ in concentrations as low as 5 ng·mL−1 can be quantified, and the detection limit is 2.3 ng·mL−1. Besides, this strategy can effectively discriminate IFN-γ from other proteins and displayed acceptable recoveries even in serum samples. In our perception, this approach holds great promise as it may be adapted to detect numerous other proteins.
Co-reporter:Dai-Xin Ye, Ying-Ying Ma, Wei Zhao, Hong-Mei Cao, Ji-Lie Kong, Huan-Ming Xiong, and Helmuth Möhwald
ACS Nano 2016 Volume 10(Issue 4) pp:4294
Publication Date(Web):March 28, 2016
DOI:10.1021/acsnano.5b07846
ZnO quantum dots (QDs) were synthesized with polymer shells, coordinated with Gd3+ ions and adsorbed doxorubicin (DOX) together to form a new kind of multifunctional ZnO-Gd-DOX nanoplatform. Such pH sensitive nanoplatforms were shown to release DOX to cancer cells in vitro and to mouse tumors in vivo, and reveal better specificity and lower toxicity than free DOX, and even better therapeutic efficacy than an FDA approved commercial DOX-loading drug DOX-Liposome Injection (DOXIL, NDA#050718). The ZnO-Gd-DOX nanoplatforms exhibited strong red fluorescence, which benefited the fluorescent imaging on live mice. Due to the special structure of ZnO-Gd-DOX nanoparticles, such nanoplatforms possessed a high longitudinal relaxivity r1 of 52.5 mM–1 s–1 at 0.55 T, which was superior to many other Gd3+ based nanoparticles. Thus, both fluorescence labeling and magnetic resonance imaging could be applied simultaneously on the tumor bearing mice along with drug delivery. After 36 days of treatment on these mice, ZnO-Gd-DOX nanoparticles greatly inhibited the tumor growth without causing any appreciable abnormality in major organs. The most important merit of ZnO-Gd-DOX was that such a nanoplatform was biodegraded completely and showed no toxic side effects after H&E (hematoxylin and eosin) staining of tumor slices and ICP-AES (inductively coupled plasma atomic emission spectrometry) bioanalyses.Keywords: anticancer; drug delivery; fluorescent imaging; magnetic resonance imaging; ZnO
Co-reporter:Daixin Ye, Li Wang, Ren Zhang, Baohong Liu, Yi Wang and Jilie Kong  
Journal of Materials Chemistry A 2015 vol. 3(Issue 29) pp:15171-15176
Publication Date(Web):11 Jun 2015
DOI:10.1039/C5TA03060A
The use of environmental waste products as materials for the production of energy is an extremely attractive prospect for both economic and social development. Sludge flocs (SFs) are environmental waste products that are difficult to handle. We used these SFs as a source of carbon and nitrogen for the preparation of N-doped mesocellular graphene foam (SF-NMGF) via a simple one-step pyrolysis method. The particular composition and structure of the SFs meant that the resultant SF-NMGF had a large Brunauer–Emmett–Teller surface area and consisted of a graphitic framework surrounded by ultrathin nanosheets. The material contained foam-like mesopores with a size centred at about 15 nm and the N was incorporated homogeneously with a high percentage (40.5 at%) of graphitic-N. As a result of these unique properties, the SF-NMGF had an excellent electrocatalytic activity with 4e when used as a metal-free catalyst for the oxygen reduction reaction (ORR). Specifically, the prepared SF-NMGF catalyst exhibited a high diffusion-limited current, superior durability and better immunity towards methanol crossover for the ORR in alkaline solution than a commercial 20 wt% Pt/C catalyst. The synthesis of the SF-NMGF can be scaled up at low cost, which will be beneficial for both sludge handling and the development of materials for the ORR.
Co-reporter:Xueen Fang, Qianqian Zhao, Hongmei Cao, Juan Liu, Ming Guan and Jilie Kong  
Analyst 2015 vol. 140(Issue 22) pp:7823-7826
Publication Date(Web):28 Sep 2015
DOI:10.1039/C5AN01016K
In this work, bovine serum albumin (BSA)–Au nanoclusters were used to coat a paper-based microfluidic device. This device acted as a Cu2+ biosensor that showed fluorescence quenching on detection of copper ions. The detection limit of this sensor could be adjusted by altering the water absorbing capacity of the device. Qualitative and semi-quantitative results could be obtained visually without the aid of any advanced instruments. This sensor could test Cu2+ rapidly with high specificity and sensitivity, which would be useful for point-of-care testing (POCT).
Co-reporter:Xueen Fang, Qianqian Zhao, Hongmei Cao, Juan Liu, Ming Guan and Jilie Kong  
Analyst 2015 vol. 140(Issue 24) pp:8217-8217
Publication Date(Web):13 Nov 2015
DOI:10.1039/C5AN90091C
Correction for ‘Rapid detection of Cu2+ by a paper-based microfluidic device coated with bovine serum albumin (BSA)–Au nanoclusters’ by Xueen Fang, et al., Analyst, 2015, 140, 7823–7826.
Co-reporter:Xueen Fang, Ming Guan and Jilie Kong  
RSC Advances 2015 vol. 5(Issue 79) pp:64614-64616
Publication Date(Web):14 Jul 2015
DOI:10.1039/C5RA09430E
We described a novel system of paper fluidics, in which isothermal nucleic acid amplification and detection are performed. This paper system made the nucleic acid test simpler, easier to operate, cheap, and provided the performance of point-of-care testing. This system was used to detect the ebolavirus rapidly with high specificity and sensitivity.
Co-reporter:Daixin Ye, Tong Wu, Hongmei Cao, Yi Wang, Baohong Liu, Song Zhang and Jilie Kong  
RSC Advances 2015 vol. 5(Issue 34) pp:26710-26715
Publication Date(Web):13 Jan 2015
DOI:10.1039/C4RA14452J
The electrochemical oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER) are of great interest since they are involved in energy conversion between fuel and electricity. Here, we developed a bifunctional MnO2/graphene/carbon nanotube that is free of noble metals and that could be a promising candidate electrocatalyst for these oxygen reduction and evolution reactions. It was shown to be able to act as an efficient cathode catalyst for the ORR, having a positive half-wave potential that differs by only ∼55 mV from that of commercial Pt/C, and a high cathodic current density that is comparable to that of the Pt/C catalyst. Moreover, the hybrid exhibited superior durability with nearly no decay in ORR activity even after 10000 s of continuous operation in 0.1 M KOH, while Pt/C shows a 20% decrease in the activity. Most importantly, the hybrid was also shown to be highly active for the OER. These observations show this hybrid to be a high-performance non-precious metal-based bi-catalyst for both the ORR and OER.
Co-reporter:Daixin Ye, Ren Zhang, Yiming Fu, Juan Bu, Yi Wang, Baohong Liu, Jilie Kong
Electrochimica Acta 2015 160() pp: 306-312
Publication Date(Web):
DOI:10.1016/j.electacta.2015.01.157
Co-reporter:Hongmei Cao, Ailing Yang, Hua Li, Lele Wang, Shunpin Li, Jilie Kong, Xichang Bao, Renqiang Yang
Sensors and Actuators B: Chemical 2015 214() pp: 169-173
Publication Date(Web):
DOI:10.1016/j.snb.2015.03.026
Co-reporter:Peng Zhang, Jilie Kong
Talanta 2015 Volume 134() pp:501-507
Publication Date(Web):1 March 2015
DOI:10.1016/j.talanta.2014.09.041
•A nanocomposite-based pH controlled drug delivery and release system was successfully developed.•Hydrazine@FSiNPs showed little cytotoxicity even at high concentrations.•The intracellular localization of the DOX-Hyd@FSiNPs nanocomposites can be visualized by means of confocal laser scanning microscopy (CLSM).The therapeutic potential of doxorubicin hydrochloride (DOX), an anticancer drug, is limited by its dose-related side effects and non-selective delivery to healthy and cancerous cells. Here we show a drug delivery system based on doxorubicin-tethered fluorescent silica nanoparticles (DOX-Hyd@FSiNPs). The DOX was conjugated to the FSiNPs through a hydrazone linkage. After uptake into the acidic environment of cancer cells, DOX was released from the FSiNPs’ surfaces because of the breakage of the pH-sensitive hydrazine bond. The decreased viability of cells in the HeLa cancer cell line indicates that DOX-Hyd@FSiNPs are potential candidates for cancer therapy. Nuclear staining and Z-axis scanning with confocal laser scanning microscopy demonstrated that DOX-Hyd@FSiNPs were effectively delivered into the cytoplasm of HeLa cells; the released DOX accumulating in the nucleus. The fluorescence of the FSiNPs also allowed the live-tracking of the nanoparticles in the cell.
Co-reporter:Jing Wang, Dai-Xin Ye, Guo-Hai Liang, Jian Chang, Ji-Lie Kong and Ji-Yao Chen  
Journal of Materials Chemistry A 2014 vol. 2(Issue 27) pp:4338-4345
Publication Date(Web):02 May 2014
DOI:10.1039/C4TB00366G
We report a novel method for synthesizing water-dispersible silicon nanoparticles (Si NPs) with a simple one-step procedure using mild reagents (3-aminopropyl) trimethoxysilane (APTES) and ascorbate sodium (AS). This is the first report of “green” synthesis of Si NPs on a large scale and at low cost. The method involves a quick reaction in a commonly used round bottom flask at room temperature and pressure without additional treatment and any special equipment. The as-prepared Si NPs have an average diameter of 2 nm and an emission band at 530 nm with a full width at half maximum height (FWHM) of 70 nm and a quantum yield (QY) of 0.21. Moreover, the fluorescence lifetime of these Si NPs is much longer than that of native fluorophores in living cells. Therefore, these Si NPs allow effective imaging of living cells with a fluorescence lifetime imaging microscope (FLIM). Using the time gating model in FLIM, an excellent image was obtained in which the auto-fluorescence interference of cellular fluorophores was suppressed demonstrating that the Si NPs are promising probes for cell imaging particularly using the FLIM technique.
Co-reporter:Peng Zhang, Tong Wu, and Ji-Lie Kong
ACS Applied Materials & Interfaces 2014 Volume 6(Issue 20) pp:17446
Publication Date(Web):September 18, 2014
DOI:10.1021/am5059519
Therapeutic platforms such as chemotherapy that respond to physical and biological stimuli are highly desirable for effective cancer therapy. In this study, pH-responsive charge-reversal, polymer-coated mesoporous silica nanoparticles [PAH-cit/APTES-MSNs; PAH-cit refers to poly(allylamine)–citraconic anhydride; APTES refers to (3-aminopropyl)triethoxysilane] were synthesized for application as drug-delivery systems for the treatment of malignant cells. Confocal laser scanning microscopy (CLSM) revealed that the PAH-cit/APTES-MSNs nanocomposite effectively delivered and released doxorubicin hydrochloride to the nucleus of HeLa (human cervical carcinoma) cells. Additionally, the real-time dynamic drug-release process was monitored by CLSM. The current pH-controlled-smart-release platform holds promise in drug-delivery and cancer therapy-related applications.Keywords: doxorubicin hydrochloride; drug delivery; mesoporous silica nanoparticles; pH-controlled release; pH-responsive charge-reversal polymer
Co-reporter:Xueen Fang, Shasha Wei and Jilie Kong  
Lab on a Chip 2014 vol. 14(Issue 5) pp:911-915
Publication Date(Web):08 Jan 2014
DOI:10.1039/C3LC51246K
In this report, we describe a simple, low-cost, straight forward and highly reproducible fabrication method of microfluidic systems. This system was cut on a glass fiber membrane by a common cutter without using any other sophisticated equipment or organic solvents. This format represents a novel type of paper-based microfluidics with high resolution of the microchannel down to ~137 μm, comparable to those made by conventional photolithography. We successfully applied this method to microfluidics to create a star micro-array format of multiplexed urine tests in this study.
Co-reporter:Xianxia Zhang, Kunyi Xiao, Liwei Cheng, Hui Chen, Baohong Liu, Song Zhang, and Jilie Kong
Analytical Chemistry 2014 Volume 86(Issue 11) pp:5567
Publication Date(Web):May 12, 2014
DOI:10.1021/ac501068k
Rapid and efficient detection of cancer cells at their earliest stages is one of the central challenges in cancer diagnostics. We developed a simple, cost-effective, and highly sensitive colorimetric method for visually detecting rare cancer cells based on cell-triggered cyclic enzymatic signal amplification (CTCESA). In the absence of target cells, hairpin aptamer probes (HAPs) and linker DNAs stably coexist in solution, and the linker DNA assembles DNA-AuNPs, producing a purple solution. In the presence of target cells, the specific binding of HAPs to the target cells triggers a conformational switch that results in linker DNA hybridization and cleavage by nicking endonuclease-strand scission cycles. Consequently, the cleaved fragments of linker DNA can no longer assemble into DNA-AuNPs, resulting in a red color. UV–vis spectrometry and photograph analyses demonstrated that this CTCESA-based method exhibited selective and sensitive colorimetric responses to the presence of target CCRF-CEM cells, which could be detected by the naked eye. The linear response for CCRF-CEM cells in a concentration range from 102 to 104 cells was obtained with a detection limit of 40 cells, which is approximately 20 times lower than the detection limit of normal AuNP-based methods without amplification. Given the high specificity and sensitivity of CTCESA, this colorimetric method provides a sensitive, label-free, and cost-effective approach for early cancer diagnosis and point-to-care applications.
Co-reporter:Hongmei Cao, Daixin Ye, Qianqian Zhao, Juan Luo, Song Zhang and Jilie Kong  
Analyst 2014 vol. 139(Issue 19) pp:4917-4923
Publication Date(Web):08 Jul 2014
DOI:10.1039/C4AN00844H
A novel strategy for the quantitative determination of human colon cancer DLD-1 cells utilizing an electrochemical aptasensor was developed by effective surface recognition between Mucin 1 glycoprotein over-expressed on the cell membrane and MUC-1 aptamer (MUC-1) bound on carbon nanospheres (CNSs). An MTT assay revealed that the as-prepared CNSs by green route exhibited satisfactory biocompatibility for cell viability, providing a suitable platform for the cell adhesion study. Furthermore, using CNSs as a sensing layer accelerated electron transfer and provided a highly stable matrix for the convenient conjugation of target MUC-1 aptamer, considerably amplifying the electrochemical signals. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) were applied to assess the optimal conditions and detection performance of the as-fabricated aptasensor. The attachment of colon cancer DLD-1 cells onto the MUC-1 aptamer immobilized CNSs led to increased EIS responses, which changed linearly in cell concentration ranging from 1.25 × 102 to 1.25 × 106 cells per mL with a lower detection limit of 40 cells per mL. With this method, colon cancer DLD-1 cells can be easily distinguished from normal cells, Human astrocytes 1800. The novel aptasensor revealed high specificity to DLD-1 cells. Furthermore, the aptasensor described here showed good reproducibility and high stability because of the CNSs of high stability and biocompatibility. The proposed protocols are a promising technique for the early monitoring of human colon cancer, and might have potential clinical applications such as cancer diagnosis, drug screening.
Co-reporter:Yi Wang, Huixiang Li, Jilie Kong
Sensors and Actuators B: Chemical 2014 193() pp: 708-714
Publication Date(Web):
DOI:10.1016/j.snb.2013.11.105
Co-reporter:Juan Luo, Xueen Fang, Daixing Ye, Huixiang Li, Hui Chen, Song Zhang, Jilie Kong
Biosensors and Bioelectronics 2014 60() pp: 84-91
Publication Date(Web):
DOI:10.1016/j.bios.2014.03.073
Co-reporter:Huixiang Li, Yi Wang, Daixin Ye, Juan Luo, Biquan Su, Song Zhang, Jilie Kong
Talanta 2014 Volume 127() pp:255-261
Publication Date(Web):1 September 2014
DOI:10.1016/j.talanta.2014.03.034
•MWNTs bridged mesocellular graphene foam (MWNTs/MGF) was obtained by a simple method.•MWNTs/MGF possessed large surface areas and excellent electrical conductivity.•AA, DA, UA and TRP could be simultaneously detected.A multi-walled carbon nanotubes (MWNTs) bridged mesocellular graphene foam (MGF) nanocomposite (MWNTs/MGF) modified glassy carbon electrode was fabricated and successfully used for simultaneous determination of ascorbic acid (AA), dopamine (DA), uric acid (UA) and tryptophan (TRP). Comparing with pure MGF, MWNTs or MWNTs/GS (graphene sheets), MWNTs/MGF displayed higher catalytic activity and selectivity toward the oxidation of AA, DA, UA and TRP. Under the optimal conditions, MWCNs/MGF/GCE can simultaneously detect AA, DA, UA and TRP with high selectivity and sensitivity. The detection limits were 18.28 µmol L−1, 0.06 µmol L−1, 0.93 µmol L−1 and 0.87 µmol L−1, respectively. Moreover, the modified electrode exhibited excellent stability and reproducibility.
Co-reporter:Peng Zhang, Tian-Yi Wang, Huan-Ming Xiong, Ji-Lie Kong
Talanta 2014 Volume 127() pp:43-50
Publication Date(Web):1 September 2014
DOI:10.1016/j.talanta.2014.03.045
•A nanocomposite-based Antisense oligonucleotides (ASOs) delivery system was successfully developed.•PEI/FSNPs show little cytotoxicity even at high concentrations.•The perinuclear region was the location where ASOs regulation process took place.•The intracellular localization of the ASOs/PEI/FSNPs composites can be visualized in situ by means of confocal laser scanning microscopy (CLSM).Antisense oligonucleotides (ASOs) are often utilized to interfere with gene expression at mRNA level for cancer treatment. Here, we synthesized fluorescein doped silica nanoparticles (FSNPs) and coated them by polyethyleneimine (PEI) for carrying ASOs. Agarose gel electrophoresis proved that PEI/FSNPs could load ASOs by a weight ratio as high as 30:1. We tracked the delivery process of ASOs from the ASOs/PEI/FSNPs composites to HeLa cells in situ by the confocal laser scanning microscopy (CLSM) techniques, including nuclear staining and Z-axis scanning. We found the ASOs/PEI/FSNPs composites exhibited their biological effects at specific intracellular localization, and the fluorescence of the FSNPs showed the dynamic delivery process in the cells.
Co-reporter:Guohai Liang, Daixin Ye, Xianxia Zhang, Fang Dong, Hui Chen, Song Zhang, Jianqi Li, Xianrong Shen and Jilie Kong  
Journal of Materials Chemistry A 2013 vol. 1(Issue 29) pp:3545-3552
Publication Date(Web):03 Jun 2013
DOI:10.1039/C3TB20440E
Multimodal imaging that aims to advance imaging by strategically combining existing technologies with uniquely designed probes has attracted great interest in recent years. Here, Gd3+-functionalized gold nanoclusters (Gd-AuNCs) were synthesized for dual model (fluorescence/magnetic resonance) imaging. We designed a cyclodecapeptide that contained one tyrosine and two cysteines for the synthesis, and it biomineralized gold nanoclusters and chelated Gd3+ ions at the same time. The Gd-AuNC probes emit an intense red fluorescence under UV light, while exhibiting a high longitudinal relaxivity of 41.5 ± 2.5 mM−1 s−1 and a low r2/r1 ratio of 1.2 at 0.55 T. The versatility of the probes for dual model imaging has been demonstrated by means of cellular imaging and in vivo T1-weighted MRI. Thanks to the optimal size of the nanocluster, it can freely circulate in the blood pool without significant accumulation in the liver and spleen, but with a long circulation half-life (t1/2) of ∼128 min. Moreover, the nanoclusters can be noticeably excreted from the body within a period of 24 h through renal clearance, making it attractive for in vivo multimodal imaging.
Co-reporter:Guohai Liang, Lili Cao, Hui Chen, Zhengyong Zhang, Song Zhang, Shaoning Yu, Xianrong Shen and Jilie Kong  
Journal of Materials Chemistry A 2013 vol. 1(Issue 5) pp:629-638
Publication Date(Web):28 Nov 2012
DOI:10.1039/C2TB00243D
Inorganic nanoparticle-based T1 contrast agents with high longitudinal relaxivity (r1) and low r2/r1 ratio have attracted great interest in recent years. However, the r1 relaxivity of inorganic nanoparticles reported to date is relatively low. In this work, 2.3 ± 0.1 nm paramagnetic gadolinium hydrated carbonate nanoparticles (GHC-1) with a high r1 relaxivity of 34.8 mM−1 s−1 and low r2/r1 ratio of 1.17 are synthesized using a one-pot hydrothermal process. The r1 of GHC-1 is 9.4 times higher than that of Gd-DTPA at 0.55 T. The synthetic procedure is simple, cost effective, and easy to scale up. The nanoparticles have a small core size, an amorphous phase, and are well-coated by poly(acrylic acid). Due to the hydrophilic polymer coating, the particles are highly dispersible and stable in aqueous solution. No significant cellular or in vivo toxicity are observed for the nanoparticles, which guarantees the in vivo application of this material. Finally, we apply the nanoparticles to in vivo magnetic resonance imaging and study the biodistribution in organs. This study reveals GHC-1 as a potential candidate for a T1 contrast agent with extraordinary ability to enhance MR images.
Co-reporter:Yi Wang, Hong Sun, Ren Zhang, Shaoning Yu, Jilie Kong
Carbon 2013 Volume 53() pp:245-251
Publication Date(Web):March 2013
DOI:10.1016/j.carbon.2012.10.055
We demonstrate that single graphene sheets can be easily synthesized in large amounts by using zeolite Ni-MCM-22 as a catalyst and template. The graphene has a large surface area, high conductivity, and controllable two-dimensional sizes. Its use in supercapacitor electrode materials reveals excellent electrochemical double layer capacitance and galvanostatic charge/discharge properties with specific capacitances of 233 F/g in aqueous KOH.
Co-reporter:Daixin Ye, Huixiang Li, Guohai Liang, Juan Luo, Xianxia Zhang, Song Zhang, Hui Chen, Jilie Kong
Electrochimica Acta 2013 Volume 109() pp:195-200
Publication Date(Web):30 October 2013
DOI:10.1016/j.electacta.2013.06.119
A nonenzymatic hydrogen-peroxide (H2O2) sensor was fabricated using the graphene, carbon nanotube and MnO2 hybrid as the sensing material. The hybrid was synthesized in a one-pot reaction process by chemical method. The sensor exhibited extremely high electrocatalytic activity toward the oxidation of H2O2. Under optimum conditions, the proposed biosensor can be applied to the quantification analysis of H2O2 with a wide linear range covering 1–1030 μM (R = 0.9998) and a low detection limit of 0.1 μM.
Co-reporter:Zhengyong Zhang, Lingjia Xu, Huixiang Li and Jilie Kong  
RSC Advances 2013 vol. 3(Issue 1) pp:59-63
Publication Date(Web):30 Oct 2012
DOI:10.1039/C2RA21785F
This work reports a simple and novel method for the synthesis of wavelength-tunable luminescent gold nanoparticles (NPs) based on a cooperation ligand exchange using 11-mercaptoundecanoic acid (11-MUA) and D-penicillamine (DPA). Next, the obtained luminescent gold NPs were used for cellular imaging, and the observations indicated that the wavelength-tunable luminescent gold NPs have potential applications in cellular luminescence labeling and imaging.
Co-reporter:Daixin Ye, Guohai Liang, Huixiang Li, Juan Luo, Song Zhang, Hui Chen, Jilie Kong
Talanta 2013 Volume 116() pp:223-230
Publication Date(Web):15 November 2013
DOI:10.1016/j.talanta.2013.04.008
•The sensor has wide liner range and low detection limit.•The sensor can detect glucose in real saliva samples with good results.Here, we report on a novel nonenzymatic amperometric glucose sensor based on CuO nanoneedle/graphene/carbon nanofiber modified electrode. The results of the scanning electron microscopy indicate that electronic network was formed through their direct binding with the graphene/carbon nanofiber, which leads to larger active surface areas and faster electron transfer for the glucose sensor. High electrocatalytic activity toward the oxidation of glucose was observed with a rapid response (<2 s), a low detection limit (0.1 µM), a wide and useful linear range (1–5.3 mM) as well as good stability and repeatability. Moreover, the common interfering species, such as ascorbic acid, uric acid, dopamine and so forth did not cause obvious interference. The sensor can also be used for quantification of glucose concentration in real saliva samples. Therefore, this work has demonstrated a simple and effective sensing platform for nonenzymatic detection of glucose.
Co-reporter:Dr. Zheng-Yong Zhang;Yu-Dong Xu;Ying-Ying Ma;Li-Li Qiu;Dr. Yi Wang; Ji-Lie Kong; Huan-Ming Xiong
Angewandte Chemie International Edition 2013 Volume 52( Issue 15) pp:4127-4131
Publication Date(Web):
DOI:10.1002/anie.201300431
Co-reporter:Dr. Zheng-Yong Zhang;Yu-Dong Xu;Ying-Ying Ma;Li-Li Qiu;Dr. Yi Wang; Ji-Lie Kong; Huan-Ming Xiong
Angewandte Chemie 2013 Volume 125( Issue 15) pp:4221-4225
Publication Date(Web):
DOI:10.1002/ange.201300431
Co-reporter:Lingjia Xu;Wenyan Wang;Zhengyong Zhang;Pengyuan Yang;Huizhi Fan
Microchimica Acta 2013 Volume 180( Issue 7-8) pp:613-618
Publication Date(Web):2013 June
DOI:10.1007/s00604-013-0950-6
We have developed a simple microchip-based method for the separation and enrichment of acetylated proteins and peptides using a microchip technique. Poly (dimethylsiloxane) (PDMS) microfluidic channels were modified by passing an acidic solution of hydrogen peroxide through them. This resulted in hydrophilic silanol-covered surfaces onto which poly (diallyldimethylammonium chloride) (PDDA) can be coated. Protein A/G beads were then captured by the PDDA layer and antibodies can then be immobilized via the protein A/G. This technique enables efficient capture of antigens due to the optimal spacing and orientation of surface molecules. Two solutions, one containing 72.5 fmol μL−1 of acetylated bovine serum albumin (BSA-Ac), the other 72.5 fmol μL−1 of tryptic BSA-Ac digest were then enriched. High selectivities were obtained, and a 82.4 % recovery of the acetylated proteins was attained. This on-chip platform was then coupled to MALDI-MS to provide information on the acetylation sites of proteins and peptides. Additional peaks were observed in the mass spectra after enrichment and were assigned to acetylated peptides. This is significant with respect to understanding the mechanism and function of acetylation. In our opinion, this microchip-based technique has a large potential for detecting acetylated proteins and peptides in complex biological mixtures, and in acetylomics in general.
Co-reporter:Jiaqin Wang, Hui Chen, Peng Zhang, Zhengyong Zhang, Song Zhang, Jilie Kong
Talanta 2013 Volume 114() pp:204-210
Publication Date(Web):30 September 2013
DOI:10.1016/j.talanta.2013.03.079
Co-reporter:Guohai Liang, Lifu Xiao, Hui Chen, Qian Liu, Song Zhang, Fuyou Li, Jilie Kong
Biosensors and Bioelectronics 2013 Volume 41() pp:78-83
Publication Date(Web):15 March 2013
DOI:10.1016/j.bios.2012.07.025
In the present work, we demonstrate that nucleotide can adsorb efficiently on the surface of carboxylic acid-functionalized nanoparticles and stabilize the particles against aggregation. In the present study we take magnetic nanoparticles (MNPs), manganese oxide nanoparticles (MnO), and upconversion nanophosphors (UCNPs) as models. The result shows that not only MNPs, but also other kinds of nanoparticles that have similar surface properties can be dispersed and stabilized by nucleotides. Interestingly, adenosine bearing different numbers of phosphate groups has distinct stabilizing effect. On the basis of this observation, we developed a magnetic relaxation-based enzyme assay for quantitative analysis of alkaline phosphatase. A detection limit of 0.002 U/μL for calf intestine alkaline phosphatase (CIAP) could be obtained, which is lower than the gold nanoparticle-based colorimetric method. In contrast to the conventional magnetic relaxation switches (MRSw), this assay was achieved without covalent modification and separation steps, sandwich type binding was not required as well, which would potentially expand the application of magnetic relaxation-based analysis.Highlights► Nucleotide can efficiently adsorb on carboxylic acid-functionalized nanoparticles, such as magnetic nanoparticles (Fe3O4), manganese oxide nanoparticles (MnO), and upconverting nanophosphors, and stabilize the nanoparticles against aggregation. ► Adenosine bearing different numbers of phosphate groups has distinct stabilizing effect. ► A non-sandwich type magnetic relaxation-based detection system for quantitatively probing enzyme was developed.
Co-reporter:Hui Chen, Jiaqin Wang, Guohai Liang, Peng Zhang and Jilie Kong  
Chemical Communications 2012 vol. 48(Issue 2) pp:269-271
Publication Date(Web):22 Nov 2011
DOI:10.1039/C1CC16127J
We describe herein a novel exonuclease III aided amplification method based on single walled carbon nanotube quenching (EASQ) for sensitive and convenient nucleic acid detection, which enabled 80-fold decrease of detection limit for HIV1 DNA assay compared with no target recycling.
Co-reporter:Xueen Fang, Hui Chen, Lingjia Xu, Xingyu Jiang, Wenjuan Wu and Jilie Kong  
Lab on a Chip 2012 vol. 12(Issue 8) pp:1495-1499
Publication Date(Web):13 Feb 2012
DOI:10.1039/C2LC40055C
In this work, we developed a portable integrated microchip of loop-mediated isothermal nucleic acid amplification (LAMP). This chip, with sample-to-answer capability, could perform rapid DNA release, exponential signal amplification and naked-eye result read-out in single or multiplex format. We call it iμLAMP, namely integrated micro-LAMP, which was successfully used for point-of-care identification of bacteria.
Co-reporter:Lili Cao, Liwei Cheng, Zhengyong Zhang, Yi Wang, Xianxia Zhang, Hui Chen, Baohong Liu, Song Zhang and Jilie Kong  
Lab on a Chip 2012 vol. 12(Issue 22) pp:4864-4869
Publication Date(Web):06 Sep 2012
DOI:10.1039/C2LC40564D
Rapid and efficient measurement of cancer cells is a major challenge in early cancer diagnosis. In the present study, a miniature multiplex chip was created for in situ detection of cancer cells by implementing a novel graphene oxide (GO)-based Förster resonance energy transfer (FRET) biosensor strategy, i.e. assaying the cell-induced fluorescence recovery from the dye-labeled aptamer/graphene oxide complex. Fluorescence intensity measurement and image analyses demonstrated that this microfluidic biosensing method exhibited rapid, selective and sensitive fluorescence responses to the quantities of the target cancer cells, CCRF-CEM cells. Seven different cancer cell samples can be measured at the same time in such a microfluidic chip. The linear response for target CCRF-CEM cells in a concentration range from 2.5 × 101 to 2.5 × 104 cells mL−1 was obtained, with a detection limit about 25 cells mL−1, which is about ten times lower than those of normal biosensors. The novel fluorescence biosensing microfluidic chip supplies a rapid, visible and high-throughput approach for early cancer diagnosis with high sensitivity and specificity.
Co-reporter:Yi Wang, Song Zhang, Hui Chen, Huixiang Li, Peng Zhang, Zhengyong Zhang, Guohai Liang, Jilie Kong
Electrochemistry Communications 2012 Volume 17() pp:63-66
Publication Date(Web):April 2012
DOI:10.1016/j.elecom.2012.01.027
Hybrid nanomaterials (GAg) of graphene nanosheets and Ag nanoparticles (Ag NPs) were prepared by a one-pot reduction of both Ag+ and graphene oxide (GO), and studied for electrochemical oxidation of methanol in alkaline solution. From TEM, XRD and other measurements, the crystalline Ag NPs with a typical diameter of 5–15 nm were homogeneously decorated on graphene nanosheets without aggregation, while their densities (25.6%–61.0%) could be easily controlled by changing the synthesis ratio of graphene oxide nanosheets to Ag+. Cyclic voltammograms results reveal that the GAg materials had the increased electrocatalytic activity (reversed catalytic peak current: 0.22 × 10− 5 A–1.01 × 10− 5 A) with the increase of Ag NPs loading for methanol oxidation in alkaline solution, and the catalytic current was linear to the concentration of CH3OH. At last, the stability of GAg catalysts-modified electrodes and the influence of catalytic reaction temperature towards methanol oxidation were also investigated. The facile synthesis, low cost and high activity of the GAg materials make them have great potential applications in the direct methanol alkaline fuel cells (DMAFCs).Highlights► Developing a cost-saving method to synthesize GAg nanomaterials with different loading amount of Ag NPs. ► The GAg was used as a stable catalyst for methanol oxidation in alkaline solution at a much lower potential. ► The GAg showed the increased electrocatalytic activity with the increase of Ag NPs loading. ► The catalytic current was linear to the concentration of CH3OH in solution. ► The GAg is a promising nanomaterial in the application of DMAFCs.
Co-reporter:Guohai Liang, Peng Zhang, Huixiang Li, Zhengyong Zhang, Hui Chen, Song Zhang, Jilie Kong
Analytica Chimica Acta 2012 Volume 726() pp:73-78
Publication Date(Web):13 May 2012
DOI:10.1016/j.aca.2012.03.024
It is highly attractive to develop a detection system that is not only sensitive and selective but also simple, rapid, practical and cost-effective in operation. Here, we report an interesting observation that single-stranded oligonucleotide (ssDNA) can adsorb efficiently on carboxylic acid-functionalized magnetic nanoparticles (CAMNPs) and stabilize the nanoparticles against aggregation in weakly acidic solution. The adsorbing rate closely correlates with the pH of the solution, the temperature and the sequence length of ssDNA. On the basis of this observation, we have designed a highly sensitive, non-sandwich type magnetic relaxation-based detection system for quantitatively probing mercury ion. The assay is independent of the sample's optical properties, requires no covalent modification of the ssDNA or the CAMNPs surfaces, and can be used for high-throughput analysis. By varying the concentration of CAMNPs, four orders of dynamic response range and a detection limit of 0.3 nM for Hg2+ are achieved. Moreover, we developed a multi-sample assay to detect Hg2+ in real environmental samples with high sensitivity, selectivity and efficiency.Graphical abstractHighlights► Single-stranded oligonucleotide (ssDNA) can adsorb efficiently on carboxylic acid-functionalized magnetic nanoparticles (CAMNPs). ► We use ssDNA to stabilize the CAMNPs against aggregation in weakly acidic solution. ► We develop a non-sandwich type magnetic relaxation-based detection system for quantitatively probing mercury ion (Hg2+). ► We use the MRI-based high-throughput screening method to detect Hg2+ in 40 samples at the same time.
Co-reporter:Guohai Liang, Hui Chen, Song Zhang, Wenjuan Wu and Jilie Kong  
Analyst 2012 vol. 137(Issue 3) pp:675-679
Publication Date(Web):07 Dec 2011
DOI:10.1039/C1AN15897J
With current concerns of the global threat from tuberculosis, it has become important to rapidly identify the bacteria. Traditional technologies involving isolation and amplification of the pathogenic bacteria are complicated and time-consuming. In this work, we describe a sensitive NMR-based detection method to identify bacteria via bacteria-induced self-assembly of magnetic nanoparticles. Bacillus Calmette-Guérin (BCG) was used as a surrogate for Mycobacterium tuberculosis. We prepared the probes by covalent immobilization of the anti-BCG monoclonal antibody onto carboxylic acid-functionalized magnetic nanoparticles. Once a solution containing BCG was introduced, the probes switched from a well dispersed state to an aggregated one, leading to a distinct and dose-dependent change in the spin–spin relaxation time (T2) of the solution. Thus the qualitative and quantitative detection method for BCG was established. The method provides specific detection of as few as 8 bacterial cells per millilitre in experimental samples within 1 hour, which will be promising for rapid detection ofM. tuberculosis in clinical samples.
Co-reporter:Hui-Xiang LI, Xiao-Li XU, Hui CHEN, Song ZHANG, Ji-Lie KONG
Chinese Journal of Analytical Chemistry 2012 Volume 40(Issue 6) pp:817-822
Publication Date(Web):June 2012
DOI:10.1016/S1872-2040(11)60550-1
A sensitive molecularly imprinted electrochemical sensor was fabricated for selective detection of propranolol hydrochloride by electropolymerization of dopamine on glassy carbon electrode (GCE) modified with multi-walled carbon nanotubes (MWNTs). The electrochemical performance and morphology of the imprinted sensor were characterized by scanning electron microscope (SEM), cyclic voltammetry (CV), differential pulse voltammetry (DPV). The test conditions were optimized and the selective response to the structurally similar compounds of propranolol hydrochloride was studied. The results showed that the sensor had the advantage of good selectivity and the sensitivity increased greatly due to the introduction of MWNTs. A linear relationship was obtained between the current and the concentration of propranolol hydrochloride over a range from 0.20 μM to 100 μM with a detection limit of 2.53 × 10−8 M (S/N = 3). Moreover, the sensor exhibited excellent stability and reproducibility.
Co-reporter:Xueen Fang, Hui Chen, Shaoning Yu, Xingyu Jiang, and Jilie Kong
Analytical Chemistry 2011 Volume 83(Issue 3) pp:690
Publication Date(Web):December 10, 2010
DOI:10.1021/ac102858j
Multiplex gene assay is a valuable molecular tool not only in academic science but also in clinical diagnostics. Multiplex PCR assays, DNA microarrays, and various nanotechnology-based methods are examples of major techniques developed for analyzing multiple genes; none of these, however, are suitable for point-of-care diagnostics, especially in resource-limited settings. In this report, we describe an octopus-like multiplex microfluidic loop-mediated isothermal amplification (mμLAMP) assay for the rapid analysis of multiple genes in the point-of-care format and provide a robust approach for predicting viruses. This assay with the ability of analyzing multiple genes qualitatively and quantitatively is highly specific, operationally simple, and cost/time-effective with the detection limit of less than 10 copies/μL in 2 μL quantities of sample within 0.5 h. We successfully developed a mμLAMP chip for differentiating three human influenza A substrains and identifying eight important swine viruses.
Co-reporter:Xueen Fang, Hui Chen, Xingyu Jiang, and Jilie Kong
Analytical Chemistry 2011 Volume 83(Issue 9) pp:3596
Publication Date(Web):March 21, 2011
DOI:10.1021/ac200024a
In this report, we describe a simple-to-fabricate microfluidic device constructed on a silica gel plate by a waterproof marker pen. We call it pen-based assay on silica, which was successfully applied to simultaneously analyze multiple targets qualitatively and quantitatively based on colorimetric assays for protein, glucose, and pH value.
Co-reporter:Song Zhang, Guoliang Zhou, Xiaoli Xu, Lili Cao, Guohai Liang, Hui Chen, Baohong Liu, Jilie Kong
Electrochemistry Communications 2011 Volume 13(Issue 9) pp:928-931
Publication Date(Web):September 2011
DOI:10.1016/j.elecom.2011.06.002
A sensitive and reagentless electrochemical aptamer-based (E-AB) sensor for specific recognition of thrombin was developed based on the Fe3O4-nanoparticle(FNP)-tagged technique. The FNP-tagged aptasensor was fabricated with a bifunctional aptamer covalently linked by a FNP tag at 3′-terminus and self-assembled on the gold electrode at 5′-terminus, which were characterized by TEM, AFM, UV–Vis and electrochemical impedance spectra. Specific binding of thrombin with the aptamer on this aptasensor produced a redox signal and detected by differential pulse voltammetry, where FNP-tag could gain signal-amplification due to its containing more redox centers. The aptasensor showed a linear response for thrombin in the range of 1.0–75 nM, and a lower detection limit of 0.1 nM (at S/N = 3). The E-AB sensor was high sensitive and stable, and could be used to detect target protein at a clinic level in biological samples.Research highlights► A reagentless aptasensor for specific recognition of thrombin was developed. ► Specific binding of thrombin with the aptamer on this aptasensor produced a redox signal. ► The Fe3O4-nanoparticle tag is sensitive and can gain signal-amplification. ► A detection limit of 0.1 nM for thrombin with desirable specificity, stability and sensitivity. ► The aptasensor can selectively detect the target protein in complex samples.
Co-reporter:Guohai Liang, Shaoyu Cai, Peng Zhang, Youyuan Peng, Hui Chen, Song Zhang, Jilie Kong
Analytica Chimica Acta 2011 Volume 689(Issue 2) pp:243-249
Publication Date(Web):18 March 2011
DOI:10.1016/j.aca.2011.01.046
We describe a sensitive biosensing system combining magnetic relaxation switch diagnosis and colorimetric detection of human α-thrombin, based on the aptamer–protein interaction induced aggregation of Fe3O4@Au nanoparticles. To demonstrate the concept, gold-coated iron oxide nanoparticle was synthesized by iterative reduction of HAuCl4 onto the dextran-coated Fe3O4 nanoparticles. The resulting core–shell structure had a flowerlike shape with pretty narrow size distribution (referred to as “nanorose”). The two aptamers corresponding to human α-thrombin were conjugated separately to two distinct nanorose populations. Once a solution containing human α-thrombin was introduced, the nanoroses switched from a well dispersed state to an aggregated one, leading to a change in the spin–spin relaxation time (T2) as well as the UV–Vis absorption spectra of the solution. Thus the qualitative and quantitative detection method for human α-thrombin was established. The dual-mode detection is clearly advantageous in obtaining a more reliable result; the detection range is widened as well. By using the dual-mode detection method, a detectable T2 change is observed with 1.0 nM human α-thrombin, and the detection range is from 1.6 nM to 30.4 nM.
Co-reporter:Shaoyu Cai, Guohai Liang, Peng Zhang, Hui Chen, Song Zhang, Baohong Liu and Jilie Kong  
Analyst 2011 vol. 136(Issue 1) pp:201-204
Publication Date(Web):14 Oct 2010
DOI:10.1039/C0AN00362J
A rational strategy of magnetic relaxation switches was proposed here to detect a1-acid glycoprotein (AGP), an acute phase a-globulin plasma glycoprotein. The assay was based on the relaxation time change between the aggregation of magnetic nanoparticles with concanavalin A and the redispersion with AGP, which can avoid the prozone effect and improve the detection accuracy. The assay was an easy and efficient method with two mixing steps and one measurement step, showing a detection limit of 0.66 nM in 0∼0.3 μg mL−1AGP, which was far lower than its normal level in human plasma.
Co-reporter:Zhengyong Zhang, Peng Zhang, Kai Guo, Guohai Liang, Hui Chen, Baohong Liu, Jilie Kong
Talanta 2011 Volume 85(Issue 5) pp:2695-2699
Publication Date(Web):15 October 2011
DOI:10.1016/j.talanta.2011.06.032
A novel fluorescent Au@SiO2 nanocomposite, with average size of ca. 30 nm in the diameter, was prepared via a simple microemulsion method. Additionally, transmission electron microscopy (TEM), UV–Vis absorption spectra, Fourier transform infrared (FT-IR) spectra and fluorescence spectra were used to characterize this nanocomposite. This newly synthesized, silica-wrapped, gold nanocluster has the following advantages: good water solubility, exceptional biocompatibility, favorable surface properties and excellent fluorescence properties. Because of these advantages, a Au@SiO2 nanocomposite is exceptionally suitable for biological applications. In this study, cellular imaging, as a form of biological application, has been fully investigated, and it was discovered, after covalent conjugation of folic acid (FA), that the nanocomposite effectively recognized over expressed folic acid receptors (FARs) on the HeLa cell's surface. Therefore, this fluorescent Au@SiO2 nanocomposite could be used as a new fluorescent probe for selective biological imaging.
Co-reporter:Shaoyu Cai, Guohai Liang, Peng Zhang, Hui Chen, Song Zhang, Baohong Liu, Jilie Kong
Biosensors and Bioelectronics 2011 Volume 26(Issue 5) pp:2258-2263
Publication Date(Web):15 January 2011
DOI:10.1016/j.bios.2010.09.045
A miniature multi-sample chip for protein detection with a bench-top magnetic resonance imager was created on the basis of magnetic relaxation switches. The chip was assessed with two protein systems. Both qualitative and quantitative results for the target proteins were obtained by image analysis and relaxation time measurement, respectively. The detection of prostate specific antigen, the serum marker of human prostate cancer, showed a linear concentration range of 17.3–43.2 ng mL−1 and a detection limit of 13.7 ng mL−1. As proof of concept, the analysis of 18 samples with a volume of 6.37 μL each was completed in 26 min by this chip. This technique may become an easy and efficient approach for rapid and high-throughput protein assay and protein–protein interaction screening.
Co-reporter:Xueen Fang, Yingyi Liu, Jilie Kong and Xingyu Jiang
Analytical Chemistry 2010 Volume 82(Issue 7) pp:3002
Publication Date(Web):March 10, 2010
DOI:10.1021/ac1000652
This work shows that loop-mediated isothermal amplification (LAMP) of nucleic acid can be integrated in an eight-channel microfluidic chip for readout either by the naked eye (as a result of the insoluble byproduct pyrophosphate generating during LAMP amplification) or via absorbance measured by an optic sensor; we call this system microLAMP (μLAMP). It is capable of analyzing target nucleic acids quantitatively with high sensitivity and specificity. The assay is straightforward in manipulation. It requires a sample volume of 0.4 μL and is complete within 1 h. The sensitivity of the assay is comparable to standard methods, where 10 fg of DNA sample could be detected under isothermal conditions (63 °C). A real time quantitative μLAMP assay using absorbance detection is possible by integration of optical fibers within the chip.
Co-reporter:Meiyan Wang, Shaoning Yu, Chuan Wang, and Jilie Kong
ACS Nano 2010 Volume 4(Issue 11) pp:6483
Publication Date(Web):October 26, 2010
DOI:10.1021/nn101445y
The endocytic pathway of a recombinant protein toxin, ricin A-chain (RTA), delivered by multiwalled carbon nanotubes (MWCNTs) was tracked in HeLa cells by tagging RTA with enhanced green fluorescent protein (EGFP). EGFP−RTA was found to accumulate in the endosome and to be retrogradely transported to the endoplasmic reticulum, from which it translocated into the cytosol. Nuclear staining, Z-axis scanning with a laser scanning confocal microscope (LSCM), and transmission electron microscopy (TEM) indicated that the RTA exerted its toxic effects. Endocytosis-inhibiting tests with LSCM and flow cytometry showed that MWCNT−EGFP−RTA conjugates penetrated cells principally via clathrin-mediated endocytosis. These studies are beneficial to understanding the MWCNT-based intracellular drug delivery mechanism and provide guidelines for designing promising MWCNT-based vectors for targeting diagnostic or therapeutic compounds, not only to specific cells, but even to specific cellular compartments.Keywords: cancer cells; endocytic pathway; endoplasmic reticulum; nanotubes; protein toxin
Co-reporter:Hui Chen, Cheng Yu, Chunming Jiang, Song Zhang, Baohong Liu and Jilie Kong  
Chemical Communications 2009 (Issue 33) pp:5006-5008
Publication Date(Web):14 Jul 2009
DOI:10.1039/B910457G
We describe herein a novel, selective and sensitive biosensing system based on the dissolution and aggregation of single-walled carbon nanotubes directed by the aptamer–protein interaction for the clinical assays of proteins.
Co-reporter:Chunming Jiang, Hui Chen, Cheng Yu, Song Zhang, Baohong Liu, Jilie Kong
Electrochimica Acta 2009 Volume 54(Issue 3) pp:1134-1140
Publication Date(Web):1 January 2009
DOI:10.1016/j.electacta.2008.08.071
In this work, a novel 3D nanocomposite is presented, which is consisted of poly(N-acetylaniline) (PAANI)/multi-walled carbon nanotubes (MWNTs) nanorods (in which the inner layer was comprised of MWNTs and the outer layer was PAANI, forming a core-shell structure) and the decorated Pt nanoparticles. Electrochemical techniques (such as electrochemical impedance spectroscopy (EIS)), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM) are used to characterize the nanocomposite. The resulting Pt/PAANI/MWNTs nanocomposite can be served as a higher efficient catalyst for the electrochemical oxidation of formaldehyde at 0.41 V with the catalytic current of 0.73 mA, which was accompanied with about 45 mV potential negative shifts and two-fold increase in peak current comparison to the Pt/PAANI. These results reveal that the Pt/PAANI/MWNTs nanocomposite film is quite promising in the fuel cell applications.
Co-reporter:Chunming Jiang, Hui Chen, Jilie Kong
Electrochimica Acta 2009 Volume 55(Issue 1) pp:142-147
Publication Date(Web):15 December 2009
DOI:10.1016/j.electacta.2009.08.023
A novel containing sulfonic acid group aniline monomer, N-(3-sulfonicpropion) anilide, was synthesized in three steps and subsequently to be electropolymerized on a glassy carbon electrode (GCE). The resulting self-doped poly(N-(3-sulfonicpropion) anilide) (SPAN/GCE) held 79.5% electrochemical activity when transferred from 0.1 M pH 7.0 PBS to 0.1 M pH 10.0 PBS, indicating its remarkable extension of the redox activity. The SPAN/GCE was characterized by X-ray photoelectron spectroscopy (XPS) and found that 30% of the nitrogen atoms are sulfonated. Preliminary experimental results show that after the immobilization of alcohol dehydrogenase (ADH) on the SPAN/GCE (ADH/SPAN/GCE), the ADH/SPAN/GCE showed good electrocatalytic activity toward the oxidation of ethanol. These reveal that the SPAN/GCE is quite promising in the fields of biosensors, biofuel cells and other bioelectrochemical devices.
Co-reporter:Xiaoli Xu, Song Zhang, Hui Chen, Jilie Kong
Talanta 2009 Volume 80(Issue 1) pp:8-18
Publication Date(Web):15 November 2009
DOI:10.1016/j.talanta.2009.06.039
Micro-total analysis systems (μTAS) integrate different analytical operations like sample preparation, separation and detection into a single microfabricated device. With the outstanding advantages of low cost, satisfactory analytical efficiency and flexibility in design, highly integrated and miniaturized devices from the concept of μTAS have gained widespread applications, especially in biochemical assays. Electrochemistry is shown to be quite compatible with microanalytical systems for biochemical assays, because of its attractive merits such as simplicity, rapidity, high sensitivity, reduced power consumption, and sample/reagent economy. This review presents recent developments in the integration of electrochemistry in microdevices for biochemical assays. Ingenious microelectrode design and fabrication methods, and versatility of electrochemical techniques are involved. Practical applications of such integrated microsystem in biochemical assays are focused on in situ analysis, point-of-care testing and portable devices. Electrochemical techniques are apparently suited to microsystems, since easy microfabrication of electrochemical elements and a high degree of integration with multi-analytical functions can be achieved at low cost. Such integrated microsystems will play an increasingly important role for analysis of small volume biochemical samples. Work is in progress toward new microdevice design and applications.
Co-reporter:Xiaoli Xu, Guoliang Zhou, Huixiang Li, Qian Liu, Song Zhang, Jilie Kong
Talanta 2009 Volume 78(Issue 1) pp:26-32
Publication Date(Web):15 April 2009
DOI:10.1016/j.talanta.2008.10.041
A sensitive molecularly imprinted electrochemical sensor was created for selective detection of a tricyclic antidepressant imipramine by combination of Au nanoparticles (Au-NPs) with a thin molecularly imprinted film. The sensor was fabricated onto the indium tin oxide (ITO) electrode via stepwise modification of Au-NPs by self-assembly and a thin film of molecularly imprinted polymers (MIPs) via sol–gel technology. It was observed that the molecularly imprinted film displayed excellent selectivity towards the target molecule imipramine. Meanwhile, the introduced Au-NPs exhibited noticeable catalytic activities towards imipramine oxidation, which remarkably enhanced the sensitivity of the imprinted film. Due to such combination, the as-prepared sensor responded quickly to imipramine, within only 1 min of incubation. The differential voltammetric anodic peak current was linear to the logarithm of imipramine concentration in the range from 5.0 × 10−6 to 1.0 × 10−3 mol L−1, and the detection limits obtained was 1.0 × 10−9 mol L−1. This method proposed was successfully applied to the determination of imipramine in drug tablets, and proven to be reliable compared with conventional UV method. These results reveal that such a sensor fulfills the selectivity, sensitivity, speed and simplicity requirements for imipramine detection, and provides possibilities of clinical application in physiological fluids.
Co-reporter:Wei Li, Guiying Jin, Hui Chen, Jilie Kong
Talanta 2009 Volume 78(Issue 3) pp:717-722
Publication Date(Web):15 May 2009
DOI:10.1016/j.talanta.2008.12.030
A highly sensitive and reproducible lead sensor based on a cyclodextrin-modified gold electrode was created. A self-assembled monolayer (SAM) of thiolated β-cyclodextrin (6-(2-mercapto-ethylamino)-6-deoxy-β-cyclodextrin (MEA-β-CD)) was prepared and modified on a gold electrode (MCGE) for specific Pb2+-sensing. Thus the mercury-free sensors for Pb2+ assay based on MCGE were established. A linear calibration response for Pb2+ was found in the range of 1.7 × 10−8 M to 9.3 × 10−7 M. The detection limit was 7.1 × 10−9 M (with S/N > 3), which was 10 times lower than other reported methods of detection Pb2+ with CD. The measurement results via this method for real blood samples were well agree with those obtained by ICP-AES, and thus presented a novel strategy in design of specific lead sensors with high sensitivity and stability for analysis of trace Pb2+ in real blood samples.
Co-reporter:Hui Chen, Chunming Jiang, Cheng Yu, Song Zhang, Baohong Liu, Jilie Kong
Biosensors and Bioelectronics 2009 Volume 24(Issue 12) pp:3399-3411
Publication Date(Web):15 August 2009
DOI:10.1016/j.bios.2009.03.020
Recent advances in molecular biology elucidate that tumor markers play an important role in diagnosis, prognosis and providing insights into the etiology of cancer. Widespread use of tumor markers in healthcare will ultimately depend upon the detection of many tumor markers with high selectivity and sensitivity. This goal has not been obtained with conventional methods which are time-consuming, have poor precision, or experience difficulty in realizing automation. Recently, much attention has been paid to the use of electrochemical immunosensors for the detection of tumor markers due to their high sensitivity, easy miniaturization and automation. This brief review focuses on the current developments, challenges, and trends of electrochemical immunosensors for tumor markers based on protein chips. Whereafter, the recent applications of nanomaterials in tumor marker immunoassays are reviewed. We also introduce some of our group's research works of novel electrochemical immunosensors for the determination of tumor markers.
Co-reporter:Guiying Jin, Wei Li, Shaoning Yu, Youyuan Peng and Jilie Kong  
Analyst 2008 vol. 133(Issue 10) pp:1367-1372
Publication Date(Web):10 Jul 2008
DOI:10.1039/B802120A
Novel superparamagnetic core-shell imprinting microspheres (MCSIMs) were synthesized using magnetite microspheres with 350 nm diameter and 70 nm thickness silica gel to form core-shell Fe3O4/SiO2 composite for template phenylephrine (Phen) recognition and high efficiency separation. Compared to the previous imprinting recognition, the main advantage of this strategy lies in two aspects: one is the high stability and monodispersity of the MCSIMs structure, the other is the use of superparamagnetic Fe3O4/SiO2 microspheres as an immobilization matrix and separation tool, thus greatly simplifying time-consuming washing steps. The affinity and selectivity of the MCSIMs were monitored by QCM and electrochemistry measurements. Imprinting microspheres have a remarkable affinity to Phen over that of structurally related molecules, including DA, EP, Phe and Tyr. The relative binding selectivity for different analytes estimated from amperometric signals was Phen : DA : EP = 40 : 5 : 1. The MCSIMs sensor showed a high sensitivity (400 μA mM−1), short response time (reaching 98% within 10 s), and broad linear response range from 1 μM to 0.1 mM and low detection limit (0.1 μM). Additionally, the results of control experiments showed that only negligible signal was obtained for non-imprinting microspheres. This could be reasonably attributed to the unique surface pores, charges and especially the nature of the functional groups inside MCSIMs cavities.
Co-reporter:Guiying Jin, Fei Huang, Wei Li, Shaoning Yu, Song Zhang, Jilie Kong
Talanta 2008 Volume 74(Issue 4) pp:815-820
Publication Date(Web):15 January 2008
DOI:10.1016/j.talanta.2007.07.023
A poly-ABSA/SWNTs composite-modified electrode was fabricated by electropolymerizing aminobenzene sulphonic acid (ABSA) on the surface of glassy carbon electrode (GCE) modified with single-wall carbon nanotubes (SWNTs). SWNTs provide a 3D porous and conductive network for the polymer immobilization. The nanocomposite film was characterized by scanning electron microscope (SEM) and electrochemical impedance spectroscopy (EIS). The results indicated that this composite-modified electrode had strong electrocatalytic activity toward the oxidation of trifluoperazine (TFP). TFP could effectively accumulate on the modified electrode and generate a sensitive anodic peak at 0.72 V (versus SCE) in pH 6.1 phosphate buffer solution. Under the selected conditions, the anodic peak current of TFP was linear with its concentration within the range from 1.0 × 10−7 to 1.0 × 10−5 mol L−1 and 1.0 × 10−5 to 1.0 × 10−4 mol L−1, and the detection limit was 1.0 × 10−9 mol L−1 (S/N = 3). This method was successfully applied to the detection of trifluoperazine in drug samples and the recovery was satisfactory. In comparison with the SWNTs/GCE or poly-ABSA/GCE prepared in the similar way, this composite-modified electrode exhibited better catalytic activity.
Co-reporter:Fei Huang, Guiying Jin, Yang Liu, Jilie Kong
Talanta 2008 Volume 74(Issue 5) pp:1435-1441
Publication Date(Web):15 February 2008
DOI:10.1016/j.talanta.2007.09.018
Co-reporter:Ying Liu, Sheng Meng, Li Mu, Guiying Jin, Wei Zhong, Jilie Kong
Biosensors and Bioelectronics 2008 Volume 24(Issue 4) pp:710-715
Publication Date(Web):1 December 2008
DOI:10.1016/j.bios.2008.06.041
A novel renewable immunosensor was created comprising a temperature-controlled surface composed of poly(n-isopropylacrylamide) (PNIPAAm)–antibody conjugates that could reversibly bind the antigen. Bovine serum albumin (BSA) and the corresponding antibody (anti-BSA) were chosen as a model antibody–antigen system to demonstrate the concept. The thermally responsive PNIPAAm conjugated to anti-BSA displayed a controllable conformation change between an expanded and a collapsed form, below and above its characteristic phase transition temperature, i.e. low critical solution temperature (LCST). This showed a remarkable change in the bioaffinity of the conjugate for BSA. Thus, a renewable anti-BSA surface was generated for re-binding of the target antigen at the thermally controllable PNIPAAm–anti-BSA conjugated surface. The temperature-controlling strategy resulted in the regeneration of immunosensors on which immobilized anti-BSA antibodies retained their activity and specificity for more than 30 reproducible assays. The level of dissociation reached 89%, which is comparable with established recovery methods, while offering easer handing. The controlled binding and dissociation were monitored by quartz crystal microbalance (QCM), confocal fluorescence, native electrophoresis, laser-induced fluorescence, and electrochemical impedance methods.
Co-reporter:Fei Huang;Song Qu;Song Zhang;Baohong Liu
Microchimica Acta 2008 Volume 161( Issue 1-2) pp:149-155
Publication Date(Web):2008 April
DOI:10.1007/s00604-007-0781-4
Clomipramine, an effective and important antipsychotic drug with low redox activity and poor hydrophilicity, was found to effectively accumulate on hydrophobic 16-mercaptohexadecanoic acid (i.e. MHA) self-assembled monolayer (SAM) modified gold electrode (i.e. MHA/Au) and generating a sensitive anodic peak at about 0.86 V (vs. SCE) in 0.05 M Tris–HCl (pH = 8.1) buffer solution. Thus, quantitative measurement of clomipramine was established with high sensitivity under optimum conditions. The anodic peak current was linear to clomipramine concentration in the range from 1 × 10−6 to 5 × 10−5 M, with a detection limit of 6 × 10−9 M. This method was successfully applied to the detection of clomipramine in drug tablets and proved to be reliable compared to UV. The spectral features, electrochemical characteristics and wettability of MHA-SAM were also studied.
Co-reporter:Mianhong Shi, Youyuan Peng, Jia Zhou, Baohong Liu, Yipin Huang, Jilie Kong
Biosensors and Bioelectronics 2007 Volume 22(Issue 12) pp:2841-2847
Publication Date(Web):15 June 2007
DOI:10.1016/j.bios.2006.11.023
A novel, simple and label-free multianalyte immunoassay system is presented here by integrating arrayed electrodes on a silicon chip via MEMS. The chip is consisted of six Au disk electrodes, an Au counter electrode and an Ag/AgCl reference electrode. Semi-insulating poly(o-phenylenediamine) (PoPD) was utilized to co-polymerize and immobilize antibodies at the arrayed Au electrodes, and wider linear detection range was obtained than those prepared with completely insulating PoPD. Electrochemical cyclic voltammogram (CV), AC impedance spectroscopy, AFM and fluorescence microscopy were employed to characterize the system. The arrayed electrodes offered exact control of deposition position via electrochemical operation, allowing selectively immobilization of different antibodies at desired positions on a single chip. Specific recognition of antibody (Ab) to corresponding antigen (An) was quantitatively monitored by cyclic voltammograms in the presence of electrochemical redox probe, ferrocene methanol. The proposed immunoassay chips showed sensitive response to three liver fibrosis markers, hyaluronic acid (HA), collagen type IV (IV-C) and lamin (LN) at ng/mL level simultaneously and specifically in a tiny amount of volume, usually 50 μL. The results obtained via chips were well consistent with those obtained by commercial radio immunoassays (RIA).
Co-reporter:Yunxia Wang, Fang Zhang, Jing Liang, Hua Li, Jilie Kong
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2007 Volume 68(Issue 2) pp:279-283
Publication Date(Web):October 2007
DOI:10.1016/j.saa.2006.11.031
In this work, a novel strategy was constructed to determine the enantiomeric composition of chiral substances discriminated by bovine serum albumin (BSA) based on the UV–vis spectra of the receptor–ligand mixtures coupled with partial least squares (PLS-1) analysis. Taking tryptophan (Trp) enantiomer as an example, when 20 μM BSA was used, the enantiomeric composition was accurately determined with concentration of only 100 nM and the corresponding enantiomeric excess as high as 98% (or −98%), which is relatively more sensitive than in literature. Furthermore, the BSA-based approach was also used to predict the enantiomeric composition of other chiral compounds, such as phenylalanine (Phe), tyrosine (Tyr), alanine (Ala), cysteine (Cys), DOPA and propranolol (Prop). The results fully demonstrate that BSA is effective in determination of enantiomeric composition of some chiral compounds.
Co-reporter:Li Mu Dr.;Ying Liu Dr.;Shaoyu Cai Dr.  Dr.
Chemistry - A European Journal 2007 Volume 13(Issue 18) pp:
Publication Date(Web):3 APR 2007
DOI:10.1002/chem.200601624

The smart surface created in a microfluidic chip has shown the capability of adsorbing and releasing proteins under electrical control. The inner surface of the chip channel was first coated by a thin layer of Au through sputtering and was subsequently modified with loosely packed self-assembled monolayers (SAMs) of thiols with terminal carboxylic or amino groups. Upon application of an external electric potential to the gold substrate, reversible conformational transformation between “bent” and “straight” states for the anchored mercapto chains could be modulated, through the electrostatic effect between the ionized terminal groups and the charged gold substrate. Thus, a hydrophobic or hydrophilic channel surface was established and could be reversibly switched electrochemically. Accordingly, the microchips prepared in this way can reversibly and selectively adsorb and release differently charged proteins under electrical control. Two model proteins, avidin and streptavidin, were demonstrated to be readily adsorbed by the smart chips under negative and positive potential, respectively. Also, more than 90 % of the adsorbed proteins could be released upon an electrical command. Furthermore, these chips were applied to the controlled separation of avidin and streptavidin mixtures with 1:1 and 1:1000 molar ratios. Under specific applied potentials, the chips adsorbed a certain protein from the mixture whereas the other protein was allowed to flow out, after which the adsorbed protein could be released by switching the applied potential. Thus, two eluted protein fractions were obtained and the separation of the two proteins was achieved. For the former mixture, each eluted fraction contained up to ≈80–90 % avidin or streptavidin. For the latter mixture, the resulting separation efficiency indicated that the molar ratio of avidin and streptavidin could be increased from 1:1000 to about 32:1 after five run separations.

Co-reporter:Jingjing Xu;Yidong Lu;Baohong Liu;Chunhe Xu
Journal of Solid State Electrochemistry 2007 Volume 11( Issue 12) pp:1689-1695
Publication Date(Web):2007 December
DOI:10.1007/s10008-007-0330-4
An ultrathin, ordered, and packed protein film, consisting of the 2-mercaptoacetic acid (MAA), polydimethyldiallylammonium chloride (PDDA), and wild-type (WT) photosynthetic reaction center (RC; termed as WT-RC) or its pheophytin (Phe)-replaced counterpart (termed as Phe-RC), was fabricated by self-assembling technique onto gold electrode for facilitating the electron transfer (ET) between RC and the electrode surface. Near-infrared (NIR)-visible (Vis) absorption and fluorescence (FL) emission spectra revealed the influence of pigment substitution on the cofactors arrangement and excitation relaxation of the proteins, respectively. Square wave voltammetry (SWV) and photoelectric tests were employed to systematically address the differences between the WT-RC films and mutant ones on the direct and photo-induced ET. The electrochemical results demonstrated that ET initiated by the oxidation of the primary donor (P) was obviously slowed down, and the formed P+ had more population as well as more positive redox potential in the Phe-RC films compared with those in the WT ones. The photoelectrochemical results displayed the dramatically enhanced photoelectric performances of the mutant ones, further suggesting the slow-down formation of final charge-separated state in Phe-RC. The functionalized protein films introduced in this paper provided an efficient approach to sensitively probe the redox cofactors and ET differences resulting from only minor changes in pigment arrangement in the pigment–protein complex. The favored ET process observed for the membrane proteins RC was potentially valuable for a deep understanding of the multi-step biological ET process and development of versatile bioelectronic devices.
Co-reporter:Fei Huang, Song Qu, Song Zhang, Baohong Liu, Jilie Kong
Talanta 2007 Volume 72(Issue 2) pp:457-462
Publication Date(Web):30 April 2007
DOI:10.1016/j.talanta.2006.11.004
Clozapine, an effective antipsychotic drug, was found generating a pair of redox peaks at about 0.33–0.4 V (versus SCE) at 16-mercaptohexadecanoic acid (i.e. MHA) self-assembled monolayer (SAM) modified gold electrode (i.e. MHA/Au) in 0.05 mol L−1 Tris–HCl (pH 8.1) buffer solution. Sensitive and quantitative measurement of clozapine based on anodic peak was established under optimum conditions. The anodic peak current was linear to clozapine concentration in the range from 1 × 10−6 to 5 × 10−5 mol L−1 with the detection limit of 7 × 10−9 mol L−1. This method was successfully applied to the detection of clozapine in drug tablets and proved to be reliable compared with ultraviolet spectrophotometry (UV). The MHA SAM was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), contact angle goniometry, electrochemical impedance spectroscopy (EIS) and electrochemical probe.
Co-reporter:Mianhong Shi, Youyuan Peng, Jia Zhou, Baohong Liu, Yipin Huang, Jilie Kong
Biosensors and Bioelectronics 2006 Volume 21(Issue 12) pp:2210-2216
Publication Date(Web):15 June 2006
DOI:10.1016/j.bios.2005.11.011
A novel immunoassays for screening of disease markers in human serum are presented by miniaturizing interdigitated array (IDA) of microelectrodes via micro electro-mechanical system (MEMS) on a silicon chip for multi-channel electrochemical measurement. Different selected antibodies (Abs) are incorporated site-specifically into the electrochemically deposited polypyrrole (PPy) formed on the IDA of the silicon chip, which was characterized by fluorescence microscope photo and the electrochemical quartz crystal microbalance (EQCM) measurements. The selective recognition of Ab to the corresponding antigen (Ag) is monitored through the measurable conductivity change, which is directly visualized by cyclic voltammograms (CVs) in presence of the redox probe, Fe (CN)63−/4−. By using the strategy presented here, three liver fibrosis markers, hyaluronic acid (HA), lamin (LN) and collagen type IV (IV-C), are detected simultaneously and specifically at the surface of the chip with calibration curves, y = 21.75 + 0.84x (R = 0.995), y = 57.54 + 0.47x (R = 0.999) and y = 37.92 + 0.28x (R = 0.999), separately. Either the standard or the serum samples can be detected at ng/mL concentration level in a tiny amount of volume, ∼50 μL. The chip-based immunoassay shows the advantages of high sensitivity, good specificity, high throughput, low sample consumption, and the stability offered via batch production by MEMS as well, which is expected to benefit the multi-target screening of desired clinical analytes.
Co-reporter:Xianrong Shen;Bin Chen
Journal of Separation Science 2005 Volume 28(Issue 3) pp:286-290
Publication Date(Web):15 FEB 2005
DOI:10.1002/jssc.200401815

Isolation and identification of natural products is a very important and active research field. However, establishing the purity of the samples during the isolation process is quite difficult, especially when the retention times are similar for two desired components in HPLC. Although some technologies, e. g. MS and NMR, offer effective ways of obtaining purity information about the samples, the expensive instrumentation required or the off-line nature of coupling (generally speaking) make purity analysis somewhat inconvenient. In this paper, an on-line analytical system coupling HPLC and a CCD spectrometer for determination of purity for each eluate was developed in a thin layer spectrometric cell. The effectiveness of the system was demonstrated by differentiating Tanshinone I, Tanshinone IIA, and their mixture. The time-resolved UV-Vis spectra promptly revealed significant differences between the three samples while conventional single wavelength detection (CSWLD) could not. The system was then used to distinguish two steroid compounds which behaved as a single component in CSWLD. The compounds were isolated from a Chinese marine invertebrate animal, a marine annelid, Arenicola cristata, referred to here as Stimpson. The method reported here provided an efficient, convenient, fast, and inexpensive approach holding promise for on-line determination of the purity of samples isolated from natural products.

Co-reporter:Li Mu, Ying Liu, Song Zhang, Baohong Liu and Jilie Kong  
New Journal of Chemistry 2005 vol. 29(Issue 6) pp:847-852
Publication Date(Web):05 May 2005
DOI:10.1039/B410610E
A low-density self-assembled monolayer (LD-SAM) surface was generated via covalent bonding between Au and the inclusion complex, cyclodextrin (CD) encapsulated 16-mercaptohexadecanoic acid, followed by the dissociation of CD. The resulted LD-SAM was characterized by cyclic voltammetry, QCM and MALDI-TOF-MS measurements. Electric potential triggered reversible switching property of the LD-SAM was observed by contact angle measurements. The selective assembly of charged proteins, avidin and streptavidin, on the LD-SAM surface, which was carried out under different applied potentials, was investigated by QCM measurements and fluorescence spectrometry.
Co-reporter:Chen Bin;Shen Xian-Rong;Kong Ji-Lie
Chinese Journal of Chemistry 2005 Volume 23(Issue 5) pp:
Publication Date(Web):14 JUN 2005
DOI:10.1002/cjoc.200590599

Marine organisms are the important source of the bioactive metabolites. A novel enolic sulfated sterol, arenicolsterol A, has been isolated from a marine annelid Arenicola cristata collected in the coast of Mainland of China. The structure was elucidated using all sorts of spectroscopic data including ESIMS, 1D and 2D NMR etc. The cytotoxic bioactivity of this sterol was evaluated by MTT assay. It could inhibit the growth of human cervix cancer cell line (Hela) and human non-small cell lung cancer cell line (NCI-h6) with IC50 of (3.1±0.6) µg/mL and (7.6±0.8) µg/mL.

Co-reporter:Ying Liu;Li Mu;Baohong Liu
Chemistry - A European Journal 2005 Volume 11(Issue 9) pp:
Publication Date(Web):3 JAN 2005
DOI:10.1002/chem.200400931

The macroscopic properties of a surface can be intelligently controlled by alternating the states of the modified molecules, such as polymers, metallic oxide, or self-assembled monolayers (SAMs). This article reviews various approaches to create a switchable surface and different types of external stimuli used to switch the surface properties. This area is of potential benefit for biomaterials, biosensors, information storage, microfluidic systems, adhesive materials, nanolithography, and so on.

Co-reporter:Hui Chen, Jiaqin Wang, Guohai Liang, Peng Zhang and Jilie Kong
Chemical Communications 2012 - vol. 48(Issue 2) pp:NaN271-271
Publication Date(Web):2011/11/22
DOI:10.1039/C1CC16127J
We describe herein a novel exonuclease III aided amplification method based on single walled carbon nanotube quenching (EASQ) for sensitive and convenient nucleic acid detection, which enabled 80-fold decrease of detection limit for HIV1 DNA assay compared with no target recycling.
Co-reporter:Hui Chen, Cheng Yu, Chunming Jiang, Song Zhang, Baohong Liu and Jilie Kong
Chemical Communications 2009(Issue 33) pp:
Publication Date(Web):
DOI:10.1039/B910457G
Co-reporter:Daixin Ye, Li Wang, Ren Zhang, Baohong Liu, Yi Wang and Jilie Kong
Journal of Materials Chemistry A 2015 - vol. 3(Issue 29) pp:NaN15176-15176
Publication Date(Web):2015/06/11
DOI:10.1039/C5TA03060A
The use of environmental waste products as materials for the production of energy is an extremely attractive prospect for both economic and social development. Sludge flocs (SFs) are environmental waste products that are difficult to handle. We used these SFs as a source of carbon and nitrogen for the preparation of N-doped mesocellular graphene foam (SF-NMGF) via a simple one-step pyrolysis method. The particular composition and structure of the SFs meant that the resultant SF-NMGF had a large Brunauer–Emmett–Teller surface area and consisted of a graphitic framework surrounded by ultrathin nanosheets. The material contained foam-like mesopores with a size centred at about 15 nm and the N was incorporated homogeneously with a high percentage (40.5 at%) of graphitic-N. As a result of these unique properties, the SF-NMGF had an excellent electrocatalytic activity with 4e when used as a metal-free catalyst for the oxygen reduction reaction (ORR). Specifically, the prepared SF-NMGF catalyst exhibited a high diffusion-limited current, superior durability and better immunity towards methanol crossover for the ORR in alkaline solution than a commercial 20 wt% Pt/C catalyst. The synthesis of the SF-NMGF can be scaled up at low cost, which will be beneficial for both sludge handling and the development of materials for the ORR.
Co-reporter:Jing Wang, Dai-Xin Ye, Guo-Hai Liang, Jian Chang, Ji-Lie Kong and Ji-Yao Chen
Journal of Materials Chemistry A 2014 - vol. 2(Issue 27) pp:NaN4345-4345
Publication Date(Web):2014/05/02
DOI:10.1039/C4TB00366G
We report a novel method for synthesizing water-dispersible silicon nanoparticles (Si NPs) with a simple one-step procedure using mild reagents (3-aminopropyl) trimethoxysilane (APTES) and ascorbate sodium (AS). This is the first report of “green” synthesis of Si NPs on a large scale and at low cost. The method involves a quick reaction in a commonly used round bottom flask at room temperature and pressure without additional treatment and any special equipment. The as-prepared Si NPs have an average diameter of 2 nm and an emission band at 530 nm with a full width at half maximum height (FWHM) of 70 nm and a quantum yield (QY) of 0.21. Moreover, the fluorescence lifetime of these Si NPs is much longer than that of native fluorophores in living cells. Therefore, these Si NPs allow effective imaging of living cells with a fluorescence lifetime imaging microscope (FLIM). Using the time gating model in FLIM, an excellent image was obtained in which the auto-fluorescence interference of cellular fluorophores was suppressed demonstrating that the Si NPs are promising probes for cell imaging particularly using the FLIM technique.
Co-reporter:Guohai Liang, Daixin Ye, Xianxia Zhang, Fang Dong, Hui Chen, Song Zhang, Jianqi Li, Xianrong Shen and Jilie Kong
Journal of Materials Chemistry A 2013 - vol. 1(Issue 29) pp:NaN3552-3552
Publication Date(Web):2013/06/03
DOI:10.1039/C3TB20440E
Multimodal imaging that aims to advance imaging by strategically combining existing technologies with uniquely designed probes has attracted great interest in recent years. Here, Gd3+-functionalized gold nanoclusters (Gd-AuNCs) were synthesized for dual model (fluorescence/magnetic resonance) imaging. We designed a cyclodecapeptide that contained one tyrosine and two cysteines for the synthesis, and it biomineralized gold nanoclusters and chelated Gd3+ ions at the same time. The Gd-AuNC probes emit an intense red fluorescence under UV light, while exhibiting a high longitudinal relaxivity of 41.5 ± 2.5 mM−1 s−1 and a low r2/r1 ratio of 1.2 at 0.55 T. The versatility of the probes for dual model imaging has been demonstrated by means of cellular imaging and in vivo T1-weighted MRI. Thanks to the optimal size of the nanocluster, it can freely circulate in the blood pool without significant accumulation in the liver and spleen, but with a long circulation half-life (t1/2) of ∼128 min. Moreover, the nanoclusters can be noticeably excreted from the body within a period of 24 h through renal clearance, making it attractive for in vivo multimodal imaging.
Co-reporter:Guohai Liang, Lili Cao, Hui Chen, Zhengyong Zhang, Song Zhang, Shaoning Yu, Xianrong Shen and Jilie Kong
Journal of Materials Chemistry A 2013 - vol. 1(Issue 5) pp:NaN638-638
Publication Date(Web):2012/11/28
DOI:10.1039/C2TB00243D
Inorganic nanoparticle-based T1 contrast agents with high longitudinal relaxivity (r1) and low r2/r1 ratio have attracted great interest in recent years. However, the r1 relaxivity of inorganic nanoparticles reported to date is relatively low. In this work, 2.3 ± 0.1 nm paramagnetic gadolinium hydrated carbonate nanoparticles (GHC-1) with a high r1 relaxivity of 34.8 mM−1 s−1 and low r2/r1 ratio of 1.17 are synthesized using a one-pot hydrothermal process. The r1 of GHC-1 is 9.4 times higher than that of Gd-DTPA at 0.55 T. The synthetic procedure is simple, cost effective, and easy to scale up. The nanoparticles have a small core size, an amorphous phase, and are well-coated by poly(acrylic acid). Due to the hydrophilic polymer coating, the particles are highly dispersible and stable in aqueous solution. No significant cellular or in vivo toxicity are observed for the nanoparticles, which guarantees the in vivo application of this material. Finally, we apply the nanoparticles to in vivo magnetic resonance imaging and study the biodistribution in organs. This study reveals GHC-1 as a potential candidate for a T1 contrast agent with extraordinary ability to enhance MR images.
(2S-trans)-18-carboxy-20-(carboxymethyl)-13-ethyl-2,3-dihydro-3,7,12,17-tetramethyl-8-vinyl-21H,23H-porphine-2-propionic acid
Streptavidin
b-D-Galactopyranoside,4-aminophenyl
Hydroxyl
5-FITC (ultra pure)