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用于同时检测胆碱、葡萄糖、谷氨酸、乳酸、赖氨酸和尿酸盐的电化学发光生物传感器阵列。

Electrochemiluminescent biosensors array for the concomitant detection of choline, glucose, glutamate, lactate, lysine and urate.

作者信息

Marquette Christophe A, Degiuli Agnès, Blum Loïc J

机构信息

Laboratoire de Génie Enzymatique et Biomoléculaire UMR 5013 CNRS Université Claude Bernard Lyon 1 Bât. CPE-43 Bd. 11 Nov. 1918, 69622 Villeurbanne Cedex, France.

出版信息

Biosens Bioelectron. 2003 Dec 30;19(5):433-9. doi: 10.1016/s0956-5663(03)00225-2.

Abstract

A multifunctional bio-sensing chip was designed based on the electrochemiluminescent (ECL) detection of enzymatically produced hydrogen peroxide. Six different oxidases specific for choline, glucose, glutamate, lactate, lysine and urate were non-covalently immobilised on imidodiacetic acid chelating beads (glucose oxidase only) or on diethylaminoethyl (DEAE) anion exchanger beads, and spotted on the surface of a glassy carbon foil (25 mm(2) square), entrapped in PVA-SbQ photopolymer. The chip measurement was achieved by applying during 3 min a +850 mV potential between the glassy carbon electrode and a platinum pseudo-reference, while capturing a numeric image of the multifunctional bio-sensing chip with a CCD camera. The use of luminol supporting beads (DEAE-Sepharose) included in the sensing layer was shown to enable the achievement of spatially well defined signals, and to solve the hydrogen peroxide parasite signal which appeared between contiguous spots using luminol free in solution. The detection limits of the different biosensor were found to be 1 microM for glutamate, lysine and uric acid, 20 microM for glucose and 2 microM for choline and lactate. The detection ranges were 1-25 microM (uric acid), 1 microM-0.5 mM (glutamate and lysine), 20 microM-2 mM (glucose) and 2 microM-0.2 mM (choline and lactate). The ECL chip was used for the detection of glucose, lactate and uric acid in human serum matrix. Good correlations between measured and expected values were found without the need of internal calibration of the sample, demonstrating the potentiality of the ECL multifunctional bio-sensing chip.

摘要

基于对酶促产生的过氧化氢的电化学发光(ECL)检测,设计了一种多功能生物传感芯片。六种分别对胆碱、葡萄糖、谷氨酸、乳酸、赖氨酸和尿酸具有特异性的不同氧化酶被非共价固定在亚氨基二乙酸螯合珠(仅葡萄糖氧化酶)或二乙氨基乙基(DEAE)阴离子交换珠上,并点样在玻碳箔(25平方毫米)表面,包埋于聚乙烯醇 - 苯醌光聚合物中。通过在玻碳电极和铂伪参比电极之间施加 +850 mV 电位 3 分钟来实现芯片测量,同时用 CCD 相机捕获多功能生物传感芯片的数字图像。结果表明,传感层中包含的鲁米诺支撑珠(DEAE - 琼脂糖)的使用能够实现空间上清晰定义的信号,并解决了使用溶液中游离鲁米诺时相邻斑点之间出现的过氧化氢寄生信号。发现不同生物传感器的检测限分别为:谷氨酸、赖氨酸和尿酸为 1 μM,葡萄糖为 20 μM,胆碱和乳酸为 2 μM。检测范围分别为:尿酸 1 - 25 μM,谷氨酸和赖氨酸 1 μM - 0.5 mM,葡萄糖 20 μM - 2 mM,胆碱和乳酸 2 μM - 0.2 mM。该 ECL 芯片用于检测人血清基质中的葡萄糖、乳酸和尿酸。在无需对样品进行内部校准的情况下,测量值与预期值之间具有良好的相关性,证明了 ECL 多功能生物传感芯片的潜力。

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