Extracellular vesicle microRNA quantification from plasma using an integrated microfluidic device

被引:112
作者
Ramshani, Zeinab [1 ,2 ,3 ]
Zhang, Chenguang [1 ,2 ]
Richards, Katherine [3 ,4 ]
Chen, Lulu [5 ]
Xu, Geyang [6 ]
Stiles, Bangyan L. [5 ]
Hill, Reginald [7 ,8 ]
Senapati, Satyajyoti [1 ,2 ,3 ]
Go, David B. [1 ,9 ]
Chang, Hsueh-Chia [1 ,2 ,3 ,9 ]
机构
[1] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Ctr Microfluid & Med Diagnost, Notre Dame, IN 46556 USA
[3] Univ Notre Dame, Harper Canc Res Inst, Notre Dame, IN 46556 USA
[4] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA
[5] Univ Southern Calif, Sch Pharm, Pharmacol & Pharmaceut Sci, Los Angeles, CA 90211 USA
[6] Jinan Univ, Sch Med, Dept Physiol, Guangzhou 510632, Guangdong, Peoples R China
[7] Univ Southern Calif, Lawrence J Ellison Inst Transformat Med, Beverly Hills, CA 90211 USA
[8] Univ Southern Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[9] Univ Notre Dame, Dept Aerosp & Mech Engn, Notre Dame, IN 46556 USA
关键词
CIRCULATING MICRORNAS; PANCREATIC-CANCER; EXOSOMES; EXCHANGE; MIR-21; BIOMARKERS;
D O I
10.1038/s42003-019-0435-1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extracellular vesicles (EV) containing microRNAs (miRNAs) have tremendous potential as biomarkers for the early detection of disease. Here, we present a simple and rapid PCR-free integrated microfluidics platform capable of absolute quantification (<10% uncertainty) of both free-floating miRNAs and EV-miRNAs in plasma with 1 pM detection sensitivity. The assay time is only 30 minutes as opposed to 13 h and requires only similar to 20 mu L of sample as oppose to 1 mL for conventional RT-qPCR techniques. The platform integrates a surface acoustic wave (SAW) EV lysing microfluidic chip with a concentration and sensing microfluidic chip incorporating an electrokinetic membrane sensor that is based on non-equilibrium ionic currents. Unlike conventional RT-qPCR methods, this technology does not require EV extraction, RNA purification, reverse transcription, or amplification. This platform can be easily extended for other RNA and DNA targets of interest, thus providing a viable screening tool for early disease diagnosis, prognosis, and monitoring of therapeutic response.
引用
收藏
页数:9
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