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Photoresponsive hollow molecularly imprinted polymer for trace triamterene in biological samples.
Gong, Cheng-Bin; Wei, Yu-Bo; Liu, Lan-Tao; Zheng, An-Xun; Yang, Yue-Hong; Chow, Cheuk-Fai; Tang, Qian.
Afiliación
  • Gong CB; The Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
  • Wei YB; The Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
  • Liu LT; The Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
  • Zheng AX; The Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
  • Yang YH; The Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
  • Chow CF; Department of Science and Environmental Studies, The Education University of Hong Kong, Hong Kong. Electronic address: cfchow@eduhk.hk.
  • Tang Q; The Key Laboratory of Applied Chemistry of Chongqing Municipality, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China. Electronic address: qiantang@swu.edu.cn.
Mater Sci Eng C Mater Biol Appl ; 76: 568-578, 2017 Jul 01.
Article en En | MEDLINE | ID: mdl-28482565
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 1.25vol.% 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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polímeros Límite: Humans Idioma: En Revista: Mater Sci Eng C Mater Biol Appl Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polímeros Límite: Humans Idioma: En Revista: Mater Sci Eng C Mater Biol Appl Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos