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Sensitive Hyaluronidase Biosensor Based on Target-Responsive Hydrogel Using Electronic Balance as Readout

化学 聚乙烯亚胺 透明质酸酶 色谱法 水解 生物传感器 自愈水凝胶 酶 生物化学 高分子化学 转染 基因
作者
Zhixin Li,Caixi Tang,Da Huang,Wenjuan Qin,Fang Luo,Jian Wang,Longhua Guo,Bin Qiu,Zhenyu Lin
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:91 (18): 11821-11826 被引量:43
标识
DOI:10.1021/acs.analchem.9b02487
摘要

The development of simple but sensitive methods for hyaluronidase (HAase) detection has been paid a great deal of attention because HAase is a potential cancer marker. In this work, a novel system coupled with a controlled release system has been designed for HAase determination without complex analytical instruments and skilled technicians. Pt@SiO2 nanoparticles (NPs), which can catalyze the breakdown of H2O2 into O2 and H2O, was embedded in the hydrogel constructed by polyethylenimine (PEI) and hyaluronic acid (HA). In the presence of HAase, the hydrogel was broken down as HAase can catalyze the degradation of HA and hence the Pt@SiO2 NPs in the hydrogel was released. The released Pt@SiO2 NPs mixed with H2O2 solution in a drainage device, and then O2 was generated due to the decomposition of H2O2, resulting in an enhancement of pressure in the drainage device because of the low solubility of O2. A certain amount of H2O overflowed from the drainage device because the difference of the pressure between the inner and outer of the drainage device. The overflowed H2O was collected by a tube, and its amount was easily measured by an electronic balance. The weight of the H2O has a linear relationship with the HAase concentration in the range of 1–60 U/mL (120 min enzymatic hydrolysis time) and 0.2–10 U/mL (240 min enzymatic hydrolysis time). The developed system has been applied to detect the activity of HAase in urine samples with satisfied results.
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