XiaoYan Liu

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Name: 刘晓燕; Liu, XiaoYan
Organization: Lanzhou University , China
Department: Metals Chemistry and Resources Utilization of Gansu Province and College of Chemistry and Chemical Engineering
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Jiaojiao Wang, Jingfeng Lan, Huihui Li, Xiaoyan Liu, Haixia Zhang
Talanta 2017 Volume 162() pp:380-389
Publication Date(Web):1 January 2017
DOI:10.1016/j.talanta.2016.10.003
•A series of pH sensitive groups grafted SBA-15 were synthesized via ATRP.•The proposed materials had selective adsorption for some proteins at a certain pH.•The selective removal of the target protein from protein mixtures can be achieved.•The complexity of real biological samples can be reduced by the proposed process.In proteomic studies, poor detection of low abundant proteins is a major problem due to the presence of highly abundant proteins. Therefore, the specific removal or depletion of highly abundant proteins prior to analysis is necessary. In response to this problem, a series of pH-sensitive functional mesoporous silica materials composed of 2–(diethylamino)ethyl methacrylate and methacrylic acid units were designed and synthesized via atom transfer radical polymerization. These functional mesoporous silica materials were characterized and their ability for adsorption and separation of proteins was evaluated. Possessing a pH-sensitive feature, the synthesized functional materials showed selective adsorption of some proteins in aqueous or buffer solutions at certain pH values. The specific removal of a particular protein from a mixed protein solution was subsequently studied. The analytical results confirmed that all the target proteins (bovine serum albumin, ovalbumin, and lysozyme) can be removed by the proposed materials from a five–protein mixture in a single operation. Finally, the practical application of this approach was also evaluated by the selective removal of certain proteins from real biological samples. The results revealed that the maximum removal efficiencies of ovalbumin and lysozyme from egg white sample were obtained as 99% and 92%, respectively, while the maximum removal efficiency of human serum albumin from human serum sample was about 80% by the proposed method. It suggested that this treatment process reduced the complexity of real biological samples and facilitated the identification of hidden proteins in chromatograms.
Co-reporter:Xiaoyan Liu, Xuezhao Shi, Hongmei Wang, Haixia Zhang
Microporous and Mesoporous Materials 2014 200() pp: 165-173
Publication Date(Web):
DOI:10.1016/j.micromeso.2014.08.027
Co-reporter:Xiaoyan Liu, Huihui Li, Zhigang Xu, Jialin Peng, Shuqiang Zhu, Haixia Zhang
Analytica Chimica Acta 2013 Volume 797() pp:40-49
Publication Date(Web):3 October 2013
DOI:10.1016/j.aca.2013.08.020
•A series of novel polymers were prepared. Its synthesis was simple and cheap.•These polymers can interact with aflatoxins through non-covalent interactions.•The polymer I can be used as SPE sorbent to enrich the trace aflatoxins.A novel approach for assembling homogeneous hyperbranched polymers based on non-covalent interactions with aflatoxins was developed; the polymers were used to evaluate the extraction of aflatoxins B1, B2, G1 and G2 (AFB1, AFB2, AFG1 and AFG2) in simulant solutions. The results showed that the extraction efficiencies of three kinds of synthesized polymers for the investigated analytes were not statistically different; as a consequence, one of the representative polymers (polymer I) was used as the solid-phase extraction (SPE) sorbent to evaluate the influences of various parameters, such as desorption conditions, pH, ionic strength, concentration of methanol in sample solutions, and the mass of the sorbent on the extraction efficiency. In addition, the extraction efficiencies for these aflatoxins were compared between the investigated polymer and the traditional sorbent C18. The results showed that the investigated polymer had superior extraction efficiencies. Subsequently, the proposed polymer for the SPE packing material was employed to enrich and analyze four aflatoxins in the cereal powder samples. The limits of detection (LODs) at a signal-to-noise (S/N) ratio of 3 were in the range of 0.012–0.120 ng g−1 for four aflatoxins, and the limits of quantification (LOQs) calculated at S/N = 10 were from 0.04 to 0.40 ng g−1 for four aflatoxins. The recoveries of four aflatoxins from cereal powder samples were in the range of 82.7–103% with relative standard deviations (RSDs) lower than 10%. The results demonstrate the suitability of the SPE approach for the analysis of trace aflatoxins in cereal powder samples.
1H,3H-NAPHTHO[1,8-CD]PYRAN-1,3-DIONE, 6-(DIMETHYLAMINO)-
5-CARBOXYFLUORESCEIN
Spiro[1H-isoindole-1,9'-[9H]xanthen]-3(2H)-one, 2-amino-3',6'-bis(diethylamino)-
1-Cyclohexene-1-carboxaldehyde, 2-chloro-3-(hydroxymethylene)-
Ethanaminium,N,N,N-trimethyl-2-[(1-oxo-2-propen-1-yl)oxy]-, chloride (1:1), homopolymer
Poly(oxy-1,4-phenylenesulfonyl-1,4-phenylene)
2-ETHYL-4,6-DIMETHYLANILINE
POLYMETHACRYLATE
LYSOZYME