首页> 美国卫生研究院文献>Biomedicines >Efficient Portable Urea Biosensor Based on Urease Immobilized Membrane for Monitoring of Physiological Fluids
【2h】

Efficient Portable Urea Biosensor Based on Urease Immobilized Membrane for Monitoring of Physiological Fluids

机译:基于尿素固定的膜的高效便携式尿素生物传感器用于监测生理流体

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Numerous studies have addressed the utilization of glutaraldehyde (GA) as a homobifunctional cross-linker. However, its applicability has been impeded due to several issues, including the tendency of GA molecules to undergo polymerization. Herein, a portable urea biosensor was developed for the real-time monitoring of the flow of physiological fluids; this was achieved by using disuccinimidyl cross-linker-based urease immobilization. Urease was immobilized on a porous polytetrafluoroethylene (PTFE) solid support using different disuccinimidyl cross-linkers, namely disuccinimidyl glutarate (DSG), disuccinimidyl suberate (DSS) and bis-N-succinimidyl-(pentaethylene glycol) ester (BS(PEG)5). A urease activity test revealed that DSS exhibited the highest urease immobilizing efficiency, whereas FT-IR analysis confirmed that urease was immobilized on the PTFE membrane via DSS cross-linking. The membrane was inserted in a polydimethylsiloxane (PDMS) fluidic chamber that generated an electrochemical signal in the presence of a flowing fluid containing urea. Urea samples were allowed to flow into the urea biosensor (1.0 mL/min) and the signal was measured using chronoamperometry. The sensitivity of the DSS urea biosensor was the highest of all the trialed biosensors and was found to be superior to the more commonly used GA cross-linker. To simulate real-time monitoring in a human patient, flowing urea-spiked human serum was measured and the effective urease immobilization of the DSS urea biosensor was confirmed. The repeatability and interference of the urea biosensor were suitable for monitoring urea concentrations typically found in human patients.
机译:许多研究已经解决了利用戊二醛(Ga)作为同型交联剂。然而,由于几个问题,其适用性已经受阻,包括Ga分子经历聚合的趋势。在此,开发了一种便携式尿素生物传感器,用于实时监测生理流体流动;这是通过使用硫氨酰基交联剂的脲酶固定来实现的。使用不同的四琥氨酸交联剂,即戊二醇铟(DSG),大琥珀酰亚胺(DSS)和双-N-琥珀酰亚胺基(五甲基二醇)酯(BS(PEG)5),将脲酶固定在多孔聚四氟乙烯(PTFE)固体载体上固定在多孔聚四氟乙烯。脲酶活性试验显示DSS表现出最高的脲酶固定效率,而FT-IR分析证实,通过DSS交联将脲酶固定在PTFE膜上。将膜插入聚二甲基硅氧烷(PDMS)流体室中,在含有尿素的流动流体存在下产生电化学信号。允许尿素样品流入尿素生物传感器(1.0mL / min),并使用慢荧光测量测量信号。 DSS尿素生物传感器的敏感性是所有试验生物传感器中最高的,发现优于更常用的GA交联剂。为了模拟人类患者的实时监测,测量流动的尿素尖刺的人血清,证实了DSS尿素生物传感器的有效脲酶固定化。尿素生物传感器的可重复性和干扰适用于监测通常在人类患者中发现的尿素浓度。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号