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Integrated sensor arrays for bioluminescence and fluorescence bio-chemical analysis

机译:用于生物发光和荧光生物化学分析的集成传感器阵列

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We present on-chip luminescence and fluorescence bio-chemical analysis, using integrated photodiodes. The detectors and the read-out electronics are implemented on a silicon substrate using standard CMOS processing. The photosensitive structures result from two-stacked PN junctions and an (optional) optical filter. The bioluminescent analyses are based on a light producing reaction - the conversion of ATP (adenosine triphosphate) molecules to AMP - catalyzed by the enzyme luciferase. The obtained results for three different initial concentrations of ATP molecules, in ATP consuming reactions, are presented. Initial fluorescent measurements have been conducted, based on the enzyme protein tyrosine phosphatase (PTP1B) using molecular probes DiFMUP (UV excitable). An enzyme solution (500 pg//spl mu/l) was mixed with DiFMUP. The reaction product DiFMU exhibits excitation/emission maxima of /spl sim/358/455 nm. The undesired excitation (UV) light was filtered out with. an integrated on-chip high pass filter with wavelength cut-off at 400 nm.
机译:我们使用集成光电二极管呈现片上发光和荧光生物化学分析。使用标准CMOS处理在硅衬底上在硅衬底上实现探测器和读出电子器件。光敏结构由两堆叠的PN结和(可选)光学滤波器产生。生物发光分析基于光产生反应 - 由酶荧光素酶催化ATP(腺苷三磷酸三磷酸盐)分子转化为AMP的助剂。提出了在ATP消耗反应中获得三种不同初始浓度的ATP分子的结果。使用分子探针Difmup(UV激发)基于酶蛋白酪氨酸磷酸酶(PTP1B)进行初始荧光测量。将酶溶液(500pg // Spl mu / L)与DIFMUP混合。反应产物DIFMU表现出/ SPL SIM / 358 / 455nm的激发/发射最大值。过滤不希望的激发(UV)光。一个集成的片上高通滤波器,波长截止为400nm。

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