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表面工程量子点/静电纺纳米纤维作为网络化荧光适体传感平台用于生物标志物检测。

Surface-engineered quantum dots/electrospun nanofibers as a networked fluorescence aptasensing platform toward biomarkers.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, P. R. China.

出版信息

Nanoscale. 2017 Nov 9;9(43):17020-17028. doi: 10.1039/c7nr04817c.

DOI:10.1039/c7nr04817c
PMID:29082397
Abstract

A membrane-based fluorescent sensing platform is a facile, point-of-care and promising technique in chemo/bio-analytical fields. However, the existing fluorescence sensing films for cancer biomarkers have several problems, with dissatisfactory sensitivity and selectivity, low utilization of probes encapsulated in films as well as the tedious design of membrane structures. In this work, a novel fluorescence sensing platform is fabricated by bio-grafting quantum dots (QDs) onto the surface of electrospun nanofibers (NFs). The aptamer integrated into the QDs/NFs can result in high specificity for recognizing and capturing biomarkers. Partially complementary DNA-attached gold nanoparticles (AuNPs) are employed to efficiently hybridize with the remaining aptamer to quench the fluorescence of QDs by nanometal surface energy transfer (NSET) between them both, which are constructed for prostate specific antigen (PSA) assay. Taking advantage of the networked nanostructure of aptamer-QDs/NFs, the fluorescent film can detect PSA with high sensitivity and a detection limit of 0.46 pg mL, which was further applied in real clinical serum samples. Coupling the surface grafted techniques to the advanced network nanostructure of electrospun NFs, the proposed aptasensing platform can be easily extended to achieve sensitive and selective assays for other biomarkers.

摘要

基于膜的荧光传感平台在化学/生物分析领域中是一种简便、即时和有前途的技术。然而,现有的用于癌症生物标志物的荧光传感膜存在一些问题,例如灵敏度和选择性差、膜结构设计繁琐以及封装在膜中的探针利用率低等。在这项工作中,通过将量子点(QDs)生物接枝到静电纺纳米纤维(NFs)的表面,制备了一种新型荧光传感平台。整合到 QDs/NFs 中的适体可以实现对生物标志物的高特异性识别和捕获。部分互补的 DNA 连接的金纳米粒子(AuNPs)被用于有效地与剩余的适体杂交,通过它们之间的纳米金属表面能量转移(NSET)来猝灭 QDs 的荧光,这是为前列腺特异性抗原(PSA)测定而构建的。利用适体-QDs/NFs 的网络状纳米结构,该荧光膜可以高灵敏度检测 PSA,检测限为 0.46pg/mL,进一步应用于真实的临床血清样本。通过将表面接枝技术与静电纺纳米纤维的先进网络纳米结构相结合,所提出的适体传感平台可以很容易地扩展到实现其他生物标志物的灵敏和选择性测定。

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