Rapid Isolation and Multiplexed Detection of Exosome Tumor Markers Via Queued Beads Combined with Quantum Dots in a Microarray

التفاصيل البيبلوغرافية
العنوان: Rapid Isolation and Multiplexed Detection of Exosome Tumor Markers Via Queued Beads Combined with Quantum Dots in a Microarray
المؤلفون: Huiying Liu, Jianlong Zhao, Hongju Mao, Zule Cheng, Kun Wang, Yunxing Lu, Shihui Qiu, Youlan Qu, Yanan Bai, Zhenhua Wu, Lin Zhou
المصدر: Nano-Micro Letters
Nano-Micro Letters, Vol 11, Iss 1, Pp 1-11 (2019)
سنة النشر: 2019
مصطلحات موضوعية: Materials science, Microarray, 02 engineering and technology, lcsh:Technology, Exosome, Article, Metastasis, 03 medical and health sciences, medicine, Electrical and Electronic Engineering, Liquid biopsy, Lung cancer, 030304 developmental biology, Tumor marker, 0303 health sciences, lcsh:T, Quantum dot, Cancer, Cancer diagnosis, 021001 nanoscience & nanotechnology, medicine.disease, Microvesicles, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, Cell biology, Multiplexed detection, 0210 nano-technology
الوصف: Highlights A bead-based microarray for exosome isolation and multiplexed tumor marker detection was developed.The beads are uniformly trapped and queued among the micropillars in the chip, which can avoid optical interference and enable more accurate test results.The results with different types of lung cancer exosome samples showed distinctive marker expression levels. Electronic supplementary material The online version of this article (10.1007/s40820-019-0285-x) contains supplementary material, which is available to authorized users.
Tumor-derived exosomes are actively involved in cancer progression and metastasis and have emerged as a promising marker for cancer diagnosis in liquid biopsy. Because of their nanoscale size, complex biogenesis, and methodological limitations related to exosome isolation and detection, advancements in their analysis remain slow. Microfluidic technology offers a better analytic approach compared with conventional methods. Here, we developed a bead-based microarray for exosome isolation and multiplexed tumor marker detection. Using this method, exosomes are isolated by binding to antibodies on the bead surface, and tumor markers on the exosomes are detected through quantum dot (QD) probes. The beads are then uniformly trapped and queued among micropillars in the chip. This design benefits fluorescence observation by dispersing the signals into every single bead, thereby avoiding optical interference and enabling more accurate test results. We analyzed exosomes in the cell culture supernatant of lung cancer and endothelial cell lines, and different lung cancer markers labeled with three QD probes were used to conduct multiplexed detection of exosome surface protein markers. Lung cancer-derived samples showed much higher (~ sixfold–tenfold) fluorescence intensity than endothelial cell samples, and different types of lung cancer samples showed distinctive marker expression levels. Additionally, using the chip to detect clinical plasma samples from cancer patients showed good diagnostic power and revealed a well consistency with conventional tests for serological markers. These results provide insight into a promising method for exosome tumor marker detection and early-stage cancer diagnosis. Electronic supplementary material The online version of this article (10.1007/s40820-019-0285-x) contains supplementary material, which is available to authorized users.
تدمد: 2150-5551
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::266ab483576aaf5d4045aecbabc3ccc4
https://pubmed.ncbi.nlm.nih.gov/34137993
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....266ab483576aaf5d4045aecbabc3ccc4
قاعدة البيانات: OpenAIRE