Ultrasensitive specific stimulant assay based on molecularly imprinted photonic hydrogels

被引:121
作者
Hu, Xiaobin [1 ]
Li, Guangtao [1 ]
Li, Mohan [1 ]
Huang, Jing [1 ]
Li, Yan [1 ]
Gao, Yongbin [1 ]
Zhang, Yihe [2 ]
机构
[1] Tsinghua Univ, Dept Chem, Key Lab Optoelect & Mol Engn, Beijing 100084, Peoples R China
[2] China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
关键词
D O I
10.1002/adfm.200700527
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Taking theophylline and (1R,2S)-(-)-ephedrine as template molecules, two imprinted photonic-hydrogel films are prepared by a combination of colloidal-crystal and molecular-imprinting techniques. This paper shows a new approach for rapid and handy stimulant detection with high sensitivity and specificity. One film is proposed for analogous molecule assay, another one for chiral recognition. The key point of this approach is that the imprinted photonic polymer (IPP) consists of a three-dimensional (313), highly-ordered and interconnected macroporous array with a thin hydrogel wall, where nanocavities complementary to analytes in shape and binding sites are distributed. This special, bicontinuous, hierarchical structure enables this polymer to report quickly, easily, sensitively and directly a molecular recognition event without any transducers and treatments for analytes (label-free). The I inherent affinity of the nanocavities, deriving from molecular imprinting, makes these sensors highly specific to analytes, even if in a competitive environment. Their sensitive and specific responses to stimulants in buffer are determined by Bragg diffractive shifts due to the lattice change of their 3D ordered macroporous arrays resulting from their preferential rebinding to the target molecules. The measurements show that the prepared hydrogel films exhibit high sensitivity in such a 0.1. fM concentration of analytes and specificity even in a competitive urinous buffer. The reported method provides a rapid and handy approach for stimulant assay and drug analysis in athletic sports.
引用
收藏
页码:575 / 583
页数:9
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