Shutao Wang

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Co-reporter:Qing Bian;Minmin Jin;Shuo Chen;Liping Xu;Guojie Wang
Polymer Chemistry (2010-Present) 2017 vol. 8(Issue 36) pp:5525-5532
Publication Date(Web):2017/09/19
DOI:10.1039/C7PY00946A
A novel visible light responsive polymeric multilayer was constructed by layer-by-layer (LbL) electrostatic self-assembly, from which the trapping/release of cargoes via azobenzene/cyclodextrin-based host–guest interactions could be realized upon light stimulation. Visible light responsive poly{6-[(2,6-dimethoxyphenyl)azo-4-(2′,6′ dimethoxy)phenoxy]propyl dimethylaminoethyl methacrylate-random-poly(2-(N,N-dimethylaminoethyl) methacrylate)} (Azo-PDMAEMA) was synthesized, which was used as a polycation to combine with polyacrylic acid (PAA) for the construction of multilayers through the LbL electrostatic self-assembly technique. The cargo molecules, cyclodextrins modified with rhodamine B, could be loaded into the multilayers via the interaction between the trans azobenzene and cyclodextrin. Green light would induce isomerization of azobenzene from the trans-configuration to the cis, which disassembled the host–guest complex and resulted in the release of cargoes from the multilayers. Upon blue light irradiation, the cis azobenzene could recover to the trans form, thus a stable inclusion complex would be formed and the cargoes could be reloaded into the multilayers again. It is noted that the visible-light-controlled trapping/release of cargoes from the multilayers could be reconstructed reliably and conveniently. The electrostatically self-assembled multilayers of the prepared azobenzene-functionalized polymers combined with cyclodextrin show great potential in reversible trapping and release of cargoes controlled by visible light.
Co-reporter:Qing Bian, Wenshuo Wang, Shutao Wang, and Guojie Wang
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 40) pp:27360
Publication Date(Web):September 20, 2016
DOI:10.1021/acsami.6b09734
Cell adhesion behaviors of stimuli-responsive surfaces have attracted significant attention for their potential biomedical applications. Distinct from temperature and pH stimuli, photoswitching avoids the extra input of thermal energy or chemicals. Herein, we designed a novel reusable cyclodextrin (CD)-modified surface to realize photoswitched specific cell release utilizing host–guest interactions between CD and azobenzene. The azobenzene-grafted specific cell capture agent was assembled onto the CD-modified surface to form a smart surface controlling cell adhesion by light radiation. After UV light irradiation, the azobenzene switched from trans- to cis-isomers, and the cis-azobenzene was not recognized by CD due to the unmatched host–guest pairs; thus, the captured MCF-7 cells could be released. Light-triggered specific cancer cell release with high efficiency may afford a smart surface with significant potential applications for the isolation and analysis of circulating tumor cells.Keywords: aptamer; azobenzene; cell adhesion; host−guest; photoswitch
Co-reporter:Qing Bian;Wenshuo Wang;Guoxiang Han;Yupeng Chen;Dr. Shutao Wang;Dr. Guojie Wang
ChemPhysChem 2016 Volume 17( Issue 16) pp:2503-2508
Publication Date(Web):
DOI:10.1002/cphc.201600362

Abstract

Stimuli-responsive surfaces that can regulate and control cell adhesion have attracted much attention for their great potential in diverse biomedical applications. Unlike for pH- and temperature-responsive surfaces, the process of photoswitching requires no additional input of chemicals or thermal energy. In this work, two different photoresponsive azobenzene films are synthesized by chemisorption and electrostatic layer-by-layer (LbL) assembly techniques. The LbL film exhibits a relatively loose packing of azobenzene chromophores compared with the chemisorbed film. The changes in trans/cis isomer ratio of the azobenzene moiety and the corresponding wettability of the LbL films are larger than those of the chemisorbed films under UV light irradiation. The tendency for cell adhesion on the LbL films decreases markedly after UV light irradiation, whereas adhesion on the chemisorbed films decreases only slightly, because the azobenzene chromophores stay densely packed. Interestingly, the tendency for cell adhesion can be considerably increased on rough substrates, the roughness being introduced by use of photolithography and inductively coupled plasma deep etching techniques. For the chemisorbed films on rough substrates, the amount of cells that adhere also changes slightly after UV light irradiation, whereas, the amount of cells that adhere to LbL films on rough substrates decreases significantly.

Co-reporter:Jiantao Feng, Ling Lin, Peipei Chen, Wenda Hua, Quanmei Sun, Zhuo Ao, Dongsheng Liu, Lei Jiang, Shutao Wang, and Dong Han
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 17) pp:8961
Publication Date(Web):May 12, 2014
DOI:10.1021/am5016827
Mucoadhesives have been perceived as an effective approach for targeting the mucosa-associated diseases, which relied on the adhesive molecules to enhance the specificity. Here, topographical binding is proposed based on the fabrication of surface pore size tunable pollen-mimetic microspheres with phase separation and electrospray technology. We proved that microspheres with large-pores (pore size of 1005 ± 448 nm) were the excellent potential candidate for the mucoadhesives, as they not only possessed better adhesion ability, but also could topographically bind cervical cancer cells. Our methods of topographical binding offered a new way of designing the mucoadhesives for treating the mucosa-associated diseases.Keywords: adhesive; cancer cell; microsphere; mucosa; topographical binding;
Co-reporter:Xueli Liu and Shutao Wang  
Chemical Society Reviews 2014 vol. 43(Issue 8) pp:2385-2401
Publication Date(Web):06 Feb 2014
DOI:10.1039/C3CS60419E
Three-dimensional nano-biointerface has been emerging as an important topic for chemistry, nanotechnology, and life sciences in recent years. Understanding the exchanges of materials, signals, and energy at biological interfaces has inspired and helped the serial design of three-dimensional nano-biointerfaces. The intimate interactions between cells and nanostructures bring many novel properties, making three-dimensional nano-biointerfaces a powerful platform to guide cell fate in a controllable and accurate way. These advantages and capabilities endow three-dimensional nano-biointerfaces with an indispensable role in developing advanced biological science and technology. This tutorial review is mainly focused on the recent progress of three-dimensional nano-biointerfaces and highlights the new explorations and unique phenomena of three-dimensional nano-biointerfaces for cell-related fundamental studies and biomedical applications. Some basic bio-inspired principles for the design and creation of three-dimensional nano-biointerfaces are also delivered in this review. Current and further challenges of three-dimensional nano-biointerfaces are finally addressed and proposed.
Co-reporter:Xuefei Gao;Li-Ping Xu;Zhongxin Xue;Lin Feng;Jitao Peng;Yongqiang Wen;Xueji Zhang
Advanced Materials 2014 Volume 26( Issue 11) pp:1771-1775
Publication Date(Web):
DOI:10.1002/adma.201304487
Co-reporter:Pengchao Zhang;Hongliang Liu;Jingxin Meng;Gao Yang;Xueli Liu;Lei Jiang
Advanced Materials 2014 Volume 26( Issue 19) pp:3131-3135
Publication Date(Web):
DOI:10.1002/adma.201305914
Co-reporter:Yue Cai;Ling Lin;Zhongxin Xue;Mingjie Liu;Lei Jiang
Advanced Functional Materials 2014 Volume 24( Issue 6) pp:809-816
Publication Date(Web):
DOI:10.1002/adfm.201302034

Surfaces with anisotropic wettability, widely found in nature, have inspired the development of one-dimensional water control on surfaces relying on the well-arranged surface features. Controlling the wetting behavior of organic liquids, especially the motion of oil fluid on surfaces, is of great importance for a broad range of applications including oil transportation, oil-repellent coatings, and water/oil separation. However, anisotropic oil-wetting surfaces remain unexplored. Here, the unique skin of a filefish Navodon septentrionalis shows anisotropic oleophobicity under water. On the rough skin of N. septentrionalis, oil droplets tend to roll off in a head-to-tail direction, but pin in the opposite direction. This pronounced wetting anisotropy results from the oriented hook-like spines arrayed on the fish skin. It inspires further exploration of the artificial anisotropic underwater oleophobic surfaces: By mimicking the oriented hook-like microstructure on a polydimethylsiloxane layer via soft lithography and subsequent oxygen-plasma treatment to make the PDMS hydrophilic, artificial fish skin is fabricated which has similar anisotropic underwater oleophobicity. Drawn from the processing of artificial fish skin, a simple principle is proposed to achieve anisotropic underwater oleophobicity by adjusting the hydrophilicity of surface composition and the anisotropic microtextures. This principle can guide the simple mass manufacturing of various inexpensive high surface-energy materials, and the principle is demonstrated on commercial cloth corduroy. This study will profit broad applications involving low-energy, low-expense oil transportation, underwater oil collection, and oil-repellant coatings on ship hulls and oil pipelines.

Co-reporter:Qing Ha, Gao Yang, Zhuo Ao, Dong Han, Fenglan Niu and Shutao Wang  
Nanoscale 2014 vol. 6(Issue 14) pp:8318-8325
Publication Date(Web):06 May 2014
DOI:10.1039/C4NR01415D
Activated tumor-associated fibroblasts (TAFs) with abundant fibroblast activation protein (FAP) expression attract tremendous attention in tumor progression studies. In this work, we report a rapid 24 h FAP activation method for fibroblasts using silicon nanowires (SiNWs) as culture substrates instead of growth factors or chemokines. In contrast with cells cultured on flat silicon which rarely express FAP, SiNW cultivated cells exhibit FAP levels similar to those found in cancerous tissue. We demonstrated that activated cells grown on SiNWs maintain their viability and proliferation in a time-dependent manner. Moreover, environmental scanning electron microscopy (ESEM) and focused ion beam and scanning electron microscopy (FIB-SEM) analysis clearly revealed that activated cells on SiNWs adapt to the structure of their substrates by filling inter-wire cavities via filopodia in contrast to cells cultured on flat silicon which spread freely. We further illustrated that the expression of FAP was rarely detected in activated cells after being re-cultured in Petri dishes, suggesting that the unique structure of SiNWs may have a certain influence on FAP activation.
Co-reporter:Xiuling Li, Hongliang Liu, Guangyan Qing, Shutao Wang and Xinmiao Liang  
Journal of Materials Chemistry A 2014 vol. 2(Issue 16) pp:2276-2281
Publication Date(Web):07 Feb 2014
DOI:10.1039/C4TB00130C
For the development of rapid glycopeptide enrichment materials, conventional monolayer phenylboronic acid (PBA) based materials inevitably encounter many problems, such as low loading efficiency, long incubation time, and unsatisfactory selectivity. Extending the materials from a 1D monolayer to a 3D polymeric matrix will be one of the best candidates tackling these problems. In this work, a PBA-based polymer material (denoted as polyPBA@SiO2) was developed, in which flexible PBA polymer brushes were immobilized on the surface of silica microspheres, constructing an ideal platform for the efficient enrichment of glycopeptides. This material exhibits stronger interaction with glycopeptides in a higher concentration of organic solvent than in aqueous solution, resulting in the high binding capacity of 60 mg g−1. Moreover, higher selectivity for glycopeptides can be achieved with polyPBA@SiO2 than with both monolayer PBA modified silica and commercial PBA-agarose. These unique features of polyPBA@SiO2 could be attributed to the synergistic effect of polyvalent interactions provided by the polymer brush, specific interaction between PBA and glycopeptides and suppression of the non-specific binding of non-glycopeptides under high ACN concentration.
Co-reporter:Gao Yang;Hongliang Liu;Xueli Liu;Pengchao Zhang;Chao Huang;Tailin Xu;Lei Jiang
Advanced Healthcare Materials 2014 Volume 3( Issue 3) pp:332-337
Publication Date(Web):
DOI:10.1002/adhm.201300233
Co-reporter:Dr. Pengchao Zhang; Shutao Wang
ChemPhysChem 2014 Volume 15( Issue 8) pp:1550-1561
Publication Date(Web):
DOI:10.1002/cphc.201301230

Abstract

Fractal structures in nature offer a unique “fractal contact mode” that guarantees the efficient working of an organism with an optimized style. Fractal nanostructured biointerfaces have shown great potential for the ultrasensitive detection of disease-relevant biomarkers from small biomolecules on the nanoscale to cancer cells on the microscale. This review will present the advantages of fractal nanostructures, the basic concept of designing fractal nanostructured biointerfaces, and their biomedical applications for the ultrasensitive detection of various disease-relevant biomarkers, such microRNA, cancer antigen 125, and breast cancer cells, from unpurified cell lysates and the blood of patients.

Co-reporter:Dr. Gao Yang;MSc. Yanhua Cao;Dr. Junbing Fan;Dr. Hongliang Liu;Dr. Feilong Zhang;Dr. Pengchao Zhang;Dr. Chao Huang; Lei Jiang; Shutao Wang
Angewandte Chemie International Edition 2014 Volume 53( Issue 11) pp:2915-2918
Publication Date(Web):
DOI:10.1002/anie.201309974

Abstract

The control of cell gradients is critical for understanding many biological systems and realizing the unique functionality of biomimetic implants. Herein, we report a nanotopographic gradient strategy that can rapidly generate cell gradients on a nanodendritic silica substrate without any chemical modification. We can achieve controllable cell gradients within only half an hour of cell incubation solely induced by the topographic effect of the gradient nanodendrites. We also demonstrate that cell gradients can be modulated by the combination of nanotopographic and chemical gradients. The results reveal that the enhanced topographic interactions between the nanodentritic structure and nanoscaled filopodia of the cells mainly contribute to the generation of cell gradients.

Co-reporter:HongLiang Liu
Science China Chemistry 2014 Volume 57( Issue 4) pp:552-557
Publication Date(Web):2014 April
DOI:10.1007/s11426-013-5051-1
Poly(N-isopropylacrylamide) (PNIPAAm)-based thermo-responsive surfaces can switch their wettability (from wettable to non-wettable) and adhesion (from sticky to non-sticky) according to external temperature changes. These smart surfaces with switchable interfacial properties are playing increasingly important roles in a diverse range of biomedical applications; these controlling cell-adhesion behavior has shown great potential for tissue engineering and disease diagnostics. Herein we reviewed the recent progress of research on PNIPAAm-based thermo-responsive surfaces that can dynamically control cell adhesion behavior. The underlying response mechanisms and influencing factors for PNIPAAm-based surfaces to control cell adhesion are described first. Then, PNIPAAm-modified two-dimensional flat surfaces for cell-sheet engineering and PNIPAAm-modified three-dimensional nanostructured surfaces for diagnostics are summarized. We also provide a future perspective for the development of stimuli-responsive surfaces.
Co-reporter:Dr. Gao Yang;MSc. Yanhua Cao;Dr. Junbing Fan;Dr. Hongliang Liu;Dr. Feilong Zhang;Dr. Pengchao Zhang;Dr. Chao Huang; Lei Jiang; Shutao Wang
Angewandte Chemie 2014 Volume 126( Issue 11) pp:2959-2962
Publication Date(Web):
DOI:10.1002/ange.201309974

Abstract

The control of cell gradients is critical for understanding many biological systems and realizing the unique functionality of biomimetic implants. Herein, we report a nanotopographic gradient strategy that can rapidly generate cell gradients on a nanodendritic silica substrate without any chemical modification. We can achieve controllable cell gradients within only half an hour of cell incubation solely induced by the topographic effect of the gradient nanodendrites. We also demonstrate that cell gradients can be modulated by the combination of nanotopographic and chemical gradients. The results reveal that the enhanced topographic interactions between the nanodentritic structure and nanoscaled filopodia of the cells mainly contribute to the generation of cell gradients.

Co-reporter:Li-Ping Xu;Jing Zhao;Bin Su;Xueli Liu;Jitao Peng;Yibiao Liu;Hongliang Liu;Gao Yang;Lei Jiang;Yongqiang Wen;Xueji Zhang
Advanced Materials 2013 Volume 25( Issue 4) pp:606-611
Publication Date(Web):
DOI:10.1002/adma.201203461
Co-reporter:Hongliang Liu;Xueli Liu;Jingxin Meng;Pengchao Zhang;Gao Yang;Bin Su;Kang Sun;Li Chen;Dong Han;Lei Jiang
Advanced Materials 2013 Volume 25( Issue 6) pp:922-927
Publication Date(Web):
DOI:10.1002/adma.201203826
Co-reporter:Pengchao Zhang;Li Chen;Tailin Xu;Hongliang Liu;Xueli Liu;Jingxin Meng;Gao Yang;Lei Jiang
Advanced Materials 2013 Volume 25( Issue 26) pp:3566-3570
Publication Date(Web):
DOI:10.1002/adma.201300888
Co-reporter:Juan Jin;Yongzheng Xing;Yanli Xi;Xueli Liu;Tao Zhou;Xinxin Ma;Zhongqiang Yang;Dongsheng Liu
Advanced Materials 2013 Volume 25( Issue 34) pp:4714-4717
Publication Date(Web):
DOI:10.1002/adma.201301175
Co-reporter:Hongliang Liu ; Yingying Li ; Kang Sun ; Junbing Fan ; Pengchao Zhang ; Jingxin Meng ; Shutao Wang ;Lei Jiang
Journal of the American Chemical Society 2013 Volume 135(Issue 20) pp:7603-7609
Publication Date(Web):April 19, 2013
DOI:10.1021/ja401000m
Artificial stimuli-responsive surfaces that can mimic the dynamic function of living systems have attracted much attention. However, there exist few artificial systems capable of responding to dual- or multistimulation as the natural system does. Herein, we synthesize a pH and glucose dual-responsive surface by grafting poly(acrylamidophenylboronic acid) (polyAAPBA) brush from aligned silicon nanowire (SiNW) array. The as-prepared surface can reversibly capture and release targeted cancer cells by precisely controlling pH and glucose concentration, exhibiting dual-responsive AND logic. In the presence of 70 mM glucose, the surface is pH responsive, which can vary from a cell-adhesive state to a cell-repulsive state by changing the pH from 6.8 to 7.8. While keeping the pH at 7.8, the surface becomes glucose responsive—capturing cells in the absence of glucose and releasing cells by adding 70 mM glucose. Through simultaneously changing the pH and glucose concentration from pH 6.8/0 mM glucose to pH 7.8/70 mM glucose, the surface is dual responsive with the capability to switch between cell capture and release for at least 5 cycles. The cell capture and release process on this dual-responsive surface is noninvasive with cell viability higher than 95%. Moreover, topographical interaction between the aligned SiNW array and cell protrusions greatly amplifies the responsiveness and accelerates the response rate of the dual-responsive surface between cell capture and release. The responsive mechanism of the dual-responsive surface is systematically studied using a quartz crystal microbalance, which shows that the competitive binding between polyAAPBA/sialic acid and polyAAPBA/glucose contributes to the dual response. Such dual-responsive surface can significantly impact biomedical and biological applications including cell-based diagnostics, in vivo drug delivery, etc.
Co-reporter:Xueli Liu, Li Chen, Hongliang Liu, Gao Yang, Pengchao Zhang, Dong Han, Shutao Wang and Lei Jiang
NPG Asia Materials 2013 5(9) pp:e63
Publication Date(Web):2013-09-01
DOI:10.1038/am.2013.43
The softness of materials is very important in cellular processes, such as cell adhesion, spread, proliferation and differentiation. Using soft materials benefits many biological studies and applications, such as wound healing, tissue engineering and clinical surgery. However, in other areas, such as rare cancer-cell capture and isolation, the importance of the softness of materials has not yet been studied. Extracellular matrix suitable for cell contact and survival is formed from soft materials with specific molecules and nanostructures. Herein, we report a soft polystyrene nanotube substrate inspired by the cell microenvironment that achieves rapid and highly efficient breast cancer-cell capture from whole-blood samples with high cell viability by integrating the soft nature of polystyrene polymer with specific capture agents and surface structures. This study provides a potentially optimal candidate for a high-quality breast cancer-cell detection platform and will provide new prospects for designing cell-material interfaces for advanced cell-based biological studies and clinical applications in the future.
Co-reporter:Jun-Bing Fan, Chao Huang, Lei Jiang and Shutao Wang  
Journal of Materials Chemistry A 2013 vol. 1(Issue 17) pp:2222-2235
Publication Date(Web):28 Feb 2013
DOI:10.1039/C3TB00021D
Multiscale nanoporous microspheres have attracted great research interest in multiple fields, such as separation, catalysis, sensors, energy storage, tissues engineering and drug release, due to their excellent permeability, high surface area, low density and stable mechanical properties. In this review, well-defined nanoporous microspheres ranging from inorganic to organic nanoporous microspheres are presented and categorized. First, we classify nanoporous microspheres into three main structural categories that include an “opened” nanoporous microsphere, a “closed” nanoporous microsphere and surface nanoporous microspheres. The corresponding approaches to fabricating these nanoporous microspheres are further presented, which mainly include hydrothermal/solvothermal synthesis, thermal decomposition, suspension polymerization, dispersion polymerization, precipitation polymerization, emulsion polymerization, multiple emulsion–solvent evaporation, template and microfluidic methods. In addition, our discussions focus on the healthcare applications of nanoporous microspheres, such as bioseparation, drug control and release and tissue engineering. This review will be expected to provide a comprehensive guide to the design and synthesis of functional nanoporous microspheres that closely relate to healthcare applications.
Co-reporter:Li-Ping Xu, Xiuwen Wu, Jingxin Meng, Jitao Peng, Yongqiang Wen, Xueji Zhang and Shutao Wang  
Chemical Communications 2013 vol. 49(Issue 78) pp:8752-8754
Publication Date(Web):05 Jul 2013
DOI:10.1039/C3CC44003F
Inspired by selective wettability and hierarchical structure of papillae on lotus seeds, papilla-like magnetic particles were fabricated by thermal treatment of Fe microparticles. The papilla-like magnetic particles modified by lauric acid exhibited superhydrophobicity, superoleophilicity and great oil removing capability from water.
Co-reporter:Yanli Xi, Hua Dong, Kang Sun, Hongliang Liu, Ruiming Liu, Yuansen Qin, Zuojun Hu, Yong Zhao, Fuqiang Nie, and Shutao Wang
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 11) pp:4821
Publication Date(Web):April 29, 2013
DOI:10.1021/am4004683
This work investigates the influence of cytophilic and anisotropic nanomaterials on accelerated cell attachment and directional migration toward rapid wound healing. Inspired by the anisotropic protein nanofibers in scab, a polyurethane (PU) nanofibrous membrane with an aligned structure was fabricated. The membrane showed good affinity for wound-healing-related cells and could guide cell migration in the direction of PU nanofibers. Also, the morphology and distribution of F-actin and paxillin of attached cells were influenced by the underlying nanofibers. The randomly distributed PU nanofibers and planar PU membrane did not show a distinct impact on cell migration. This scab-inspired cytophilic membrane is promising in applications as functional interfacial biomaterials for rapid wound healing, bone repair, and construction of neural networks.Keywords: anisotropic nanofibrous membranes; cell attachment; cell migration; cytophilic; wound healing;
Co-reporter:Li-Ping Xu, Jitao Peng, Yibiao Liu, Yongqiang Wen, Xueji Zhang, Lei Jiang, and Shutao Wang
ACS Nano 2013 Volume 7(Issue 6) pp:5077
Publication Date(Web):May 17, 2013
DOI:10.1021/nn400650f
Because of the frequent oil spill accidents in marine environment, stable superoleophobic coatings under seawater are highly desired. Current underwater superoleophobic surfaces often suffer from mechanical damages and lose their superoleophobicity gradually. It remains a challenge to fabricate a stable and robust underwater superoleophobic film which can endure harsh conditions in practical application. Nacre is one of most extensively studied rigid biological materials. Inspired by the outstanding mechanical property of seashell nacre and those underwater superoleophobic surfaces from nature, we fabricated a polyelectrolyte/clay hybrid film via typical layer-by-layer (LBL) method based on building blocks with high surface energy. ‘Bricks-and-mortar’ structure of seashell nacre was conceptually replicated into the prepared film, which endows the obtained film with excellent mechanical property and great abrasion resistance. In addtion, the prepared film also exhibits stable underwater superoleophobicity, low oil adhesion, and outstanding environment durability in artificial seawater. We anticipate that this work will provide a new method to design underwater low-oil-adhesion film with excellent mechanical property and improved stability, which may advance the practical applications in marine antifouling and microfluidic devices.Keywords: interfaces; layer-by-layer; nacre; oil-adhesion; superoleophobicity; underwater
Co-reporter:Xueli Liu;Jie Zhou;Zhongxin Xue;Jun Gao;Jingxin Meng;Lei Jiang
Advanced Materials 2012 Volume 24( Issue 25) pp:3401-3405
Publication Date(Web):
DOI:10.1002/adma.201200797
Co-reporter:Meihua Jin, Shasha Li, Jing Wang, Zhongxin Xue, Mingyi Liao and Shutao Wang  
Chemical Communications 2012 vol. 48(Issue 96) pp:11745-11747
Publication Date(Web):18 Oct 2012
DOI:10.1039/C2CC34805E
The interesting oil-wetting behavior to a superamphiphobic surface in water has been investigated. We demonstrated that the trapped air can tune the underwater wettability of the surface, changing from superoleophilic to superoleophobic. The trapped air in the grooves of the superamphiphobic surface can cause the significant change of the three-phase contact line (TCL).
Co-reporter:Qunfeng Cheng, Mingzhu Li, Fu Yang, Mingjie Liu, Lin Li, Shutao Wang and Lei Jiang  
Soft Matter 2012 vol. 8(Issue 25) pp:6740-6743
Publication Date(Web):21 May 2012
DOI:10.1039/C2SM25421B
An underwater pH-responsive superoleophobic surface successfully demonstrated a reversible switch of oil-adhesion on a nanostructured poly(acrylic acid) (PAA) surface by changing the environmental pH values. At low pH, intramolecular hydrogen bonding of PAA is formed, and results in high oil-adhesion. As for high pH, the oil droplets can easily roll off due to the intermolecular hydrogen bonding between PAA and surrounding water.
Co-reporter:Xueli Liu, Jun Gao, Zhongxin Xue, Li Chen, Ling Lin, Lei Jiang, and Shutao Wang
ACS Nano 2012 Volume 6(Issue 6) pp:5614
Publication Date(Web):May 19, 2012
DOI:10.1021/nn301550v
Oil pollution to aquatic devices, especially to those oil-cleaning devices and equipment-repairing robots during oil spill accidents, has drawn great attention and remains an urgent problem to be resolved. Developing devices that can move freely in an oil/water system without contamination from oil has both scientific and practical importance. In nature, the insect water strider can float on water by utilizing the superhydrophobic supporting force received by its legs. Inspired by this unique floating phenomenon, in this article, we designed a model device named “oil strider” that could float stably at the oil/water interface without contamination by oil. The floating capability of the oil strider originated from the huge underwater superoleophobic supporting force its “legs” received. We prepared the micro/nanohierarchical structured copper-oxide-coated copper wires, acting as the artificial legs of oil strider, by a simple base-corrosion process. The surface structures and hydrophilic chemical components of the coatings on copper wires induced the huge superoleophobic force at the oil/water interface, to support the oil strider from sinking into the oil. Experimental results and theoretical analysis demonstrate that this supporting force is mainly composed of three parts: the buoyancy force, the curvature force, and the deformation force. We anticipate that this artificial oil strider will provide a guide for the design of smart aquatic devices that can move freely in an oil/water system with excellent oil repellent capability, and be helpful in practical situations such as oil handling and oil spill cleanup.Keywords: aquatic devices; copper materials; interfaces; micro/nanostructures; oil-repellent surfaces; superoleophobic force; underwater superoleophobicity
Co-reporter:Tong Zhang, Mingzhu Li, Bin Su, Changqing Ye, Kan Li, Weizhi Shen, Li Chen, Zhongxin Xue, Shutao Wang and Lei Jiang  
Soft Matter 2011 vol. 7(Issue 18) pp:7973-7975
Publication Date(Web):21 Jul 2011
DOI:10.1039/C1SM05366C
Bio-inspired micro/nano-surfaces with novel anisotropic functionalities were obtained by utilizing the outward wings of grasshopper as a natural stamp. The two-step replica exhibited anisotropic high hydrophobicity and light reflection.
Co-reporter:Qunfeng Cheng, Mingzhu Li, Yongmei Zheng, Bin Su, Shutao Wang and Lei Jiang  
Soft Matter 2011 vol. 7(Issue 13) pp:5948-5951
Publication Date(Web):19 Apr 2011
DOI:10.1039/C1SM05452J
We discovered underwater superoleophobicity on the lower side of a lotus leaf, and fabricated Janus interface materials with in-air superhydrophobicity on one side and underwater superoleophobicity on the other side inspired by the Janus feature of the lotus leaf. The ingenious design on lotus leaf surfaces, superhydrophobicity on its upper side and underwater superoleophobicity on its lower side, not only helps us thoroughly understand the special surface wettability of the lotus leaf, but also gives a typical example of multi-functionality in biological systems. This study supplies us with an intelligent strategy to design and create bionic multi-functional interface materials.
Co-reporter:Dr. Li Chen;Dr. Haifeng Meng; Lei Jiang; Shutao Wang
Chemistry – An Asian Journal 2011 Volume 6( Issue 7) pp:1757-1760
Publication Date(Web):
DOI:10.1002/asia.201100010
Co-reporter:Li-Ping Xu, Xiuwen Wu, Jingxin Meng, Jitao Peng, Yongqiang Wen, Xueji Zhang and Shutao Wang
Chemical Communications 2013 - vol. 49(Issue 78) pp:NaN8754-8754
Publication Date(Web):2013/07/05
DOI:10.1039/C3CC44003F
Inspired by selective wettability and hierarchical structure of papillae on lotus seeds, papilla-like magnetic particles were fabricated by thermal treatment of Fe microparticles. The papilla-like magnetic particles modified by lauric acid exhibited superhydrophobicity, superoleophilicity and great oil removing capability from water.
Co-reporter:Xiuling Li, Hongliang Liu, Guangyan Qing, Shutao Wang and Xinmiao Liang
Journal of Materials Chemistry A 2014 - vol. 2(Issue 16) pp:NaN2281-2281
Publication Date(Web):2014/02/07
DOI:10.1039/C4TB00130C
For the development of rapid glycopeptide enrichment materials, conventional monolayer phenylboronic acid (PBA) based materials inevitably encounter many problems, such as low loading efficiency, long incubation time, and unsatisfactory selectivity. Extending the materials from a 1D monolayer to a 3D polymeric matrix will be one of the best candidates tackling these problems. In this work, a PBA-based polymer material (denoted as polyPBA@SiO2) was developed, in which flexible PBA polymer brushes were immobilized on the surface of silica microspheres, constructing an ideal platform for the efficient enrichment of glycopeptides. This material exhibits stronger interaction with glycopeptides in a higher concentration of organic solvent than in aqueous solution, resulting in the high binding capacity of 60 mg g−1. Moreover, higher selectivity for glycopeptides can be achieved with polyPBA@SiO2 than with both monolayer PBA modified silica and commercial PBA-agarose. These unique features of polyPBA@SiO2 could be attributed to the synergistic effect of polyvalent interactions provided by the polymer brush, specific interaction between PBA and glycopeptides and suppression of the non-specific binding of non-glycopeptides under high ACN concentration.
Co-reporter:Jun-Bing Fan, Chao Huang, Lei Jiang and Shutao Wang
Journal of Materials Chemistry A 2013 - vol. 1(Issue 17) pp:NaN2235-2235
Publication Date(Web):2013/02/28
DOI:10.1039/C3TB00021D
Multiscale nanoporous microspheres have attracted great research interest in multiple fields, such as separation, catalysis, sensors, energy storage, tissues engineering and drug release, due to their excellent permeability, high surface area, low density and stable mechanical properties. In this review, well-defined nanoporous microspheres ranging from inorganic to organic nanoporous microspheres are presented and categorized. First, we classify nanoporous microspheres into three main structural categories that include an “opened” nanoporous microsphere, a “closed” nanoporous microsphere and surface nanoporous microspheres. The corresponding approaches to fabricating these nanoporous microspheres are further presented, which mainly include hydrothermal/solvothermal synthesis, thermal decomposition, suspension polymerization, dispersion polymerization, precipitation polymerization, emulsion polymerization, multiple emulsion–solvent evaporation, template and microfluidic methods. In addition, our discussions focus on the healthcare applications of nanoporous microspheres, such as bioseparation, drug control and release and tissue engineering. This review will be expected to provide a comprehensive guide to the design and synthesis of functional nanoporous microspheres that closely relate to healthcare applications.
Co-reporter:Xueli Liu and Shutao Wang
Chemical Society Reviews 2014 - vol. 43(Issue 8) pp:NaN2401-2401
Publication Date(Web):2014/02/06
DOI:10.1039/C3CS60419E
Three-dimensional nano-biointerface has been emerging as an important topic for chemistry, nanotechnology, and life sciences in recent years. Understanding the exchanges of materials, signals, and energy at biological interfaces has inspired and helped the serial design of three-dimensional nano-biointerfaces. The intimate interactions between cells and nanostructures bring many novel properties, making three-dimensional nano-biointerfaces a powerful platform to guide cell fate in a controllable and accurate way. These advantages and capabilities endow three-dimensional nano-biointerfaces with an indispensable role in developing advanced biological science and technology. This tutorial review is mainly focused on the recent progress of three-dimensional nano-biointerfaces and highlights the new explorations and unique phenomena of three-dimensional nano-biointerfaces for cell-related fundamental studies and biomedical applications. Some basic bio-inspired principles for the design and creation of three-dimensional nano-biointerfaces are also delivered in this review. Current and further challenges of three-dimensional nano-biointerfaces are finally addressed and proposed.
Co-reporter:Meihua Jin, Shasha Li, Jing Wang, Zhongxin Xue, Mingyi Liao and Shutao Wang
Chemical Communications 2012 - vol. 48(Issue 96) pp:NaN11747-11747
Publication Date(Web):2012/10/18
DOI:10.1039/C2CC34805E
The interesting oil-wetting behavior to a superamphiphobic surface in water has been investigated. We demonstrated that the trapped air can tune the underwater wettability of the surface, changing from superoleophilic to superoleophobic. The trapped air in the grooves of the superamphiphobic surface can cause the significant change of the three-phase contact line (TCL).
Benzamide, 2,6-bis(4-aminophenoxy)-N-[4-[[4-[[4-(phenylamino)phenyl]amino]phenyl]amino]phenyl]-
Disodium 3,3'-carbonylbis(6-fluorobenzenesulfonate)
Silanamine,1,1,1-trimethyl-N-(trimethylsilyl)-, germanium(2+) salt (2:1)
POLY(N,N-DIMETHYL ACRYLAMIDE)
2-Propenoic acid,2-methyl-, sodium salt (1:1), homopolymer