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Photoresponsive hollow molecularly imprinted polymer for trace triamterene in biological samples.

Authors :
Gong, Cheng-Bin
Wei, Yu-Bo
Liu, Lan-Tao
Zheng, An-Xun
Yang, Yue-Hong
Chow, Cheuk-Fai
Tang, Qian
Source :
Materials Science & Engineering: C. Jul2017, Vol. 76, p568-578. 11p.
Publication Year :
2017

Abstract

This paper reports a photoresponsive hollow molecularly imprinted polymer for the determination of trace triamterene in biological sample. The photoresponsive hollow molecularly imprinted polymer was prepared on sacrificial silica microspheres via surface imprinting technique through atom transfer radical polymerization using a novel water-soluble azobenzene derivative, 4-[(4-methacryloyloxy)phenylazo]-3,5-dimethyl benzenesulfonic acid, as the functional monomer, and the sacrificial silica core was subsequently removed using HF etching method with 1.25 vol.% HF ethanolic solution. The morphologies and properties of the photoresponsive hollow molecularly imprinted polymer were further characterized and compared systematically with the corresponding photoresponsive surface molecularly imprinted polymer. Compared with surface imprinted polymer, the hollow material displayed higher binding capacity, better recognition ability, faster mass-transfer rate, and larger isomerization rate constants toward triamterene. The static binding properties of the imprinted materials were investigated under three irradiation conditions. The photoresponsive hollow molecularly imprinted polymer showed better specificity toward triamterene than its structural analogues (folic acid and caffeine) as examined by UV–vis and HPLC. The photoresponsive hollow molecularly imprinted polymer was utilized for the determination of trace triamterene in biological samples (human urine and serum) with advantages of simple sample pre-treatment, good recovery and good sensitivity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09284931
Volume :
76
Database :
Academic Search Index
Journal :
Materials Science & Engineering: C
Publication Type :
Academic Journal
Accession number :
122880718
Full Text :
https://doi.org/10.1016/j.msec.2017.03.135