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Toward the Early Evaluation of Therapeutic Effects: An Electrochemical Platform for Ultrasensitive Detection of Apoptotic Cells

机译:朝着治疗效果的早期评估:凋亡细胞超灵敏检测的电化学平台。

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The ability for early evaluation of therapeutic effects is a significant challenge in leukemia research. To address this challenge, we developed a novel electrochemical platform for ultrasensitive and selective detection of apoptotic cells in response to therapy. In order to construct the platform, a novel three-dimensional (3-D) architecture was initially fabricated after combining nitrogen-doped carbon nanotubes and gold nanoparticles via a layer-by-layer method. The formed architecture provided an effective matrix for annexin V with high stability and bioactivity to enhance sensitivity. On the basis of the specific recognition between annexin V and phosphatidylserine on the apoptotic cell membrane, the annexin V/3-D architecture interface showed a predominant capability for apoptotic cell capture. Moreover, a lectin-based nanoprobe was designed by noncovalent assembly of concanavalin A on CdTe quantum dots (QDs) labeled silica nanospheres with poly(allylamine hydrochloride) as a linker. This nanoprobe incorporated both the specific carbohydrate recognition and the multilabeled QDs-based signal amplification. By coupling with the QDs-based nanoprobe and electrochemical stripping analysis, the proposed sandwich-type cytosensor showed an excellent analytical performance for the ultrasensitive detection of apoptotic cells (as low as 48 cells), revealing great potential toward the early evaluation of therapeutic effects.
机译:早期评估治疗效果的能力是白血病研究中的重大挑战。为了应对这一挑战,我们开发了一种新型电化学平台,用于对治疗反应中的凋亡细胞进行超灵敏和选择性检测。为了构建平台,首先通过逐层方法将掺杂氮的碳纳米管和金纳米颗粒结合在一起,然后首先制造出新颖的三维(3-D)结构。形成的结构为膜联蛋白V提供了有效的基质,具有高稳定性和生物活性以增强敏感性。基于膜联蛋白V和磷脂酰丝氨酸在凋亡细胞膜上的特异性识别,膜联蛋白V / 3-D结构界面显示出凋亡细胞捕获的主要能力。此外,基于凝集素A的纳米探针是通过将伴刀豆球蛋白A非共价组装在以聚烯丙胺盐酸盐为连接基的CdTe量子点(QDs)标记的二氧化硅纳米球上而设计的。该纳米探针结合了特定的碳水化合物识别和基于多标记QDs的信号放大。通过与基于QDs的纳米探针和电化学剥离分析相结合,所提出的夹心型细胞传感器对凋亡细胞(低至48个细胞)的超灵敏检测显示出出色的分析性能,为早期评估治疗效果显示了巨大的潜力。

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