Issue 36, 2024, Issue in Progress

Convenient two-step method constructed silicon-based microfluidic chip for fast CYP2C19 SNPs detection

Abstract

The rapid detection of single nucleotide polymorphisms (SNPs) in the CYP2C19 gene is crucial for precise clopidogrel usage. Quantitative real-time polymerase chain reaction (qPCR), as a powerful amplification tool, has been widely employed for CYP2C19 SNPs detection. However, traditional qPCR suffers from long amplification times and high reagent consumption. To address these challenges, this work presents a microfluidic SNPs detection device based on on-chip qPCR. The device includes a rapid thermal cycling system, an optical detection system, a control system, and a complementary silicon-glass chip for CYP2C19 SNPs detection. Compared to commercial qPCR instruments that take 1 hour for testing, this device completes the test in just 15 minutes (40 PCR cycles). The resulting linearity is similar to that found using commercial qPCR instruments but with higher amplification efficiency. Additionally, compared with other silicon-based qPCR chips, this chip is constructed by using a convenient two-step method and offers low manufacturing costs, which potentially reduces single-test costs to an acceptable level. This makes our chip promising for point-of-care testing (POCT).

Graphical abstract: Convenient two-step method constructed silicon-based microfluidic chip for fast CYP2C19 SNPs detection

Supplementary files

Article information

Article type
Paper
Submitted
28 May 2024
Accepted
11 Aug 2024
First published
19 Aug 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 26007-26015

Convenient two-step method constructed silicon-based microfluidic chip for fast CYP2C19 SNPs detection

H. Wang, C. Yan, H. Tong, X. Ye, X. Yuan, C. Liu and H. Li, RSC Adv., 2024, 14, 26007 DOI: 10.1039/D4RA03913K

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