An innovative electrically conductive biopolymer based on poly (β-cyclodextrin) towards recognition of ascorbic acid in real sample: Utilization of biocompatible advanced materials in biomedical analysis

被引:15
作者
Behyar, Milad Baghal [1 ,2 ]
Kholafazad-Kordasht, Houman [3 ]
Hassanpour, Soodabeh [4 ]
Hasanzadeh, Mohammad [1 ,5 ]
机构
[1] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[4] Palacky Univ Olomouc, Fac Sci, Dept Analyt Chem, Olomouc, Czech Republic
[5] Tabriz Univ Med Sci, Nutr Res Ctr, Tabriz, Iran
关键词
advanced biopolymer; biocompatible materials; electrochemical oxidation; electropolymerization; sensor technology; beta-cyclodextrin; URIC-ACID; ELECTROCHEMICAL SENSOR; LIQUID-CHROMATOGRAPHY; DOPAMINE; IDENTIFICATION; ANTIOXIDANT; ELECTRODE; FRUIT; FOOD; DNA;
D O I
10.1002/jmr.2953
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a sensitive platform was designed for the electrocatalytical oxidation and recognition of ascorbic acid (AA) based on poly(beta-cyclodextrin) modified glassy carbon electrode (p(beta-CD-GCE). Electropolymerization of beta-CD on the surface of GCE was performed on the potential range of -1 to 1.5 V. So, a novel biopolymer was prepared on the surface of GCE towards sensitive recognition of AA in human plasma samples. The developed platform has good sensitivity and accuracy for electrooxidation and detection of AA with lower limit of quantification (LLOQ) of 1 nM and linear range of 1 nM to 100 mM. Moreover, the designed electrochemical sensor was employed for the analysis of AA on human plasma samples with high sensitivity. Based on advantages of p(beta-CD) prepared by electropolymerization procedure (green, fast, homogeny, and efficient eletrocatalytical behaviour), this conductive biopolymer showed excellent analytical behaviour towards electrooxidation of AA. It is expected that the prepared polymeric interface is able to use in the analysis of biological species in clinical samples.
引用
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页数:10
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