Development of L-lactate dehydrogenase biosensor based on porous silicon resonant microcavities as fluorescence enhancers

被引:33
|
作者
Jenie, S. N. Aisyiyah [1 ]
Prieto-Simon, Beatriz [1 ]
Voelcker, Nicolas H. [1 ]
机构
[1] Univ S Australia, Mawson Inst, ARC Ctr Excellence Convergent Bionano Sci & Techn, Mawson Lakes, SA 5095, Australia
来源
基金
澳大利亚研究理事会;
关键词
Lactate dehydrogenase; Porous silicon; Microcavity; Fluorescence enhancement; Biosensor; OPTICAL-PROPERTIES; SURFACE; ISOENZYMES; CANCER; DEATH; SERUM;
D O I
10.1016/j.bios.2015.07.025
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The up-regulation of L-lactate dehydrogenase (LDH), an intracellular enzyme present in most of all body tissues, is indicative of several pathological conditions and cellular death. Herein, we demonstrate LDH detection using porous silicon (psi) microcavities as a luminescence-enhancing optical biosensing platform. Non-fluorescent resazurin was covalently attached onto the pSi surface via thermal hydrocarbonisation, thermal hydrosylilation and acylation. Each surface modification step was confirmed by means of FTIR and the optical shifts of the resonance wavelength of the microcavity. Thermal hydrocarbonisation also afforded excellent surface stability, ensuring that the resazurin was not reduced on the pSi surface. Using a pSi microcavity biosensor, the fluorescence signal upon detection of LDH was amplified by 10 and 5-fold compared to that of a single layer and a detuned microcavity, respectively, giving a limit of detection of 0.08 U/ml. The biosensor showed a linear response between 0.16 and 6.5 U/ml, covering the concentration range of LDH in normal as well as damaged tissues. The biosensor was selective for LDH and did not produce a signal upon incubation with another NAD-dependant enzyme L-glutamic dehydrogenase. The use of the pSi microcavity as a sensing platform reduced reagent usage by 30% and analysis time threefold compared to the standard LDH assay in solution. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:637 / 643
页数:7
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