首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Red light-driven photoelectrochemical biosensing for ultrasensitive and scatheless assay of tumor cells based on hypotoxic AgInS2 nanoparticles
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Red light-driven photoelectrochemical biosensing for ultrasensitive and scatheless assay of tumor cells based on hypotoxic AgInS2 nanoparticles

机译:基于低毒性agins2纳米颗粒的肿瘤细胞超细胞瘤和无耻测定的红色光触发光电化学生物诱导

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摘要

A novel red light-driven photoelectrochemical (PEC) biosensing platform based on hypotoxic ternary mercaptopropionic acid (MPA)-capped AgInS2 nanoparticles (NPs) with excellent hydrophily and biocompatibility was proposed. AgInS2 NPs as a PEC sensing substrate exhibited high photon-to-current conversion efficiency under red light excitation, generating an intensive photocurrent for enhancing the sensitivity of PEC determination. After the introduction of the amino-terminated sgc8c aptamer onto the interface of AgInS2 NPs, the over-expressed protein tyrosine kinase-7 on the surface of lymphoblast CCRF-CEM cells could be efficiently captured. Using CCRF-CEM cell as a model analyte, an ultrasensitive PEC biosensor for scatheless assay of cells at the applied potential of 0.15 V under a red light excitation of 630 nm was designed based on the significant decline of photocurrent intensity after capturing CCRF-CEM cells. The developed PEC cytosensor demonstrated an excellent cell-capture ability, as well as a wide linear range from 1.5 x 10(2) to 3.0 x 10(5) cells/mL and a low detection limit of 16 cells/mL for CCRF-CEM cells. In addition, the resulting assay method verified high selectivity and negligible cytotoxicity for cells assay. This work provided an alternative method for scatheless assay of tumor cells, which would have promising prospect in clinical diagnoses of cancer.
机译:提出了一种基于低毒三元巯基丙酮酸(MPA)的新型红光光电电化学(PEC)生物传感平台,其具有优异的亲水性和生物相容性的agins2纳米蛋白2纳米颗粒(NPS)。作为PEC检测基板的Agins2NPS在红色光激发下表现出高的光子 - 电流转化效率,产生密集的光电流以提高PEC测定的灵敏度。在将氨基终止的SGC8C适体进入agins2NPS的界面之后,可以有效地捕获淋巴细胞CCRF-CEM细胞表面上的过表达的蛋白酪氨酸激酶-7。使用CCRF-CEM单元作为模型分析物,在捕获CCRF-CEM细胞后的显着下降630nm的红色光激发下,设计了用于在0.15V的施加电位的细胞的微观测定的超敏性PEC生物传感器。 。发育的PEC胞子传感器证明了优异的电池捕获能力,以及宽的线性范围为1.5×10(2)至3.0×10(5)个细胞/ mL,以及CCRF-CEM的16个细胞/ mL的低检测限。细胞。此外,所得的测定方法验证了细胞测定的高选择性和可忽略的细胞毒性。这项工作提供了一种替代方法,用于对肿瘤细胞进行恶意的测定,这将在临床诊断中具有很有希望的癌症前景。

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