Mohammad Hossein Pourghasemian , Ali Kheirkhah Barzoki , Mahdi Dizani , Amir Hossein Kazemipour Ashkezari , Amir Shamloo
{"title":"基于新型微流控装置的快速低成本液滴pcr及微混合器效应的数值研究","authors":"Mohammad Hossein Pourghasemian , Ali Kheirkhah Barzoki , Mahdi Dizani , Amir Hossein Kazemipour Ashkezari , Amir Shamloo","doi":"10.1016/j.snr.2025.100327","DOIUrl":null,"url":null,"abstract":"<div><div>Droplet microfluidics, recognized for its precise dispensing and sample handling capabilities at microliter and lower volumes, has emerged as a popular method for miniaturizing polymerase chain reaction (PCR) platforms. This technology enables the accurate detection of low-abundance biological variations through droplet PCR (dPCR). In this study, we introduce a low-cost PCR thermal cycler setup, an optical system for DNA detection, and a 3D-printed droplet-based microfluidic device engineered to produce hundreds of nanoliter water-in-oil droplets. The microfluidic chip incorporates 21 cycles, each equipped with a micromixer. For the first time, we investigate the impact of integrating micromixers into the PCR chip cycles and demonstrate that this integration enhances the efficiency and specificity of the PCR process. Following the completion of the PCR cycles, the droplets are gathered in a chamber located at the end of the chip for amplification detection. A simple fluorescent optical setup is developed for fluorescence detection and accurate measurement of DNA concentration in the sample. This setup comprises a cost-effective high-resolution camera, a dichroic mirror, and an LED light source. Subsequently, the fluorescent images captured are processed using Python (OpenCV library) and analyzed for fluorescent emission intensity and droplet size distribution. The outcomes of the dPCR conducted with the microfluidic chip are subsequently assessed through a gel electrophoresis test and compared to the identical results from a commercial quantitative PCR (qPCR) device. Our study demonstrates the ability to perform rapid dPCR analysis via endpoint imaging utilizing a cost-effective and easy-to-fabricate setup.</div></div>","PeriodicalId":426,"journal":{"name":"Sensors and Actuators Reports","volume":"9 ","pages":"Article 100327"},"PeriodicalIF":6.5000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid and low-cost droplet pcr using a novel microfluidic setup with a numerical study on micromixer effects\",\"authors\":\"Mohammad Hossein Pourghasemian , Ali Kheirkhah Barzoki , Mahdi Dizani , Amir Hossein Kazemipour Ashkezari , Amir Shamloo\",\"doi\":\"10.1016/j.snr.2025.100327\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Droplet microfluidics, recognized for its precise dispensing and sample handling capabilities at microliter and lower volumes, has emerged as a popular method for miniaturizing polymerase chain reaction (PCR) platforms. This technology enables the accurate detection of low-abundance biological variations through droplet PCR (dPCR). In this study, we introduce a low-cost PCR thermal cycler setup, an optical system for DNA detection, and a 3D-printed droplet-based microfluidic device engineered to produce hundreds of nanoliter water-in-oil droplets. The microfluidic chip incorporates 21 cycles, each equipped with a micromixer. For the first time, we investigate the impact of integrating micromixers into the PCR chip cycles and demonstrate that this integration enhances the efficiency and specificity of the PCR process. Following the completion of the PCR cycles, the droplets are gathered in a chamber located at the end of the chip for amplification detection. A simple fluorescent optical setup is developed for fluorescence detection and accurate measurement of DNA concentration in the sample. This setup comprises a cost-effective high-resolution camera, a dichroic mirror, and an LED light source. Subsequently, the fluorescent images captured are processed using Python (OpenCV library) and analyzed for fluorescent emission intensity and droplet size distribution. The outcomes of the dPCR conducted with the microfluidic chip are subsequently assessed through a gel electrophoresis test and compared to the identical results from a commercial quantitative PCR (qPCR) device. Our study demonstrates the ability to perform rapid dPCR analysis via endpoint imaging utilizing a cost-effective and easy-to-fabricate setup.</div></div>\",\"PeriodicalId\":426,\"journal\":{\"name\":\"Sensors and Actuators Reports\",\"volume\":\"9 \",\"pages\":\"Article 100327\"},\"PeriodicalIF\":6.5000,\"publicationDate\":\"2025-04-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sensors and Actuators Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666053925000451\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sensors and Actuators Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666053925000451","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Rapid and low-cost droplet pcr using a novel microfluidic setup with a numerical study on micromixer effects
Droplet microfluidics, recognized for its precise dispensing and sample handling capabilities at microliter and lower volumes, has emerged as a popular method for miniaturizing polymerase chain reaction (PCR) platforms. This technology enables the accurate detection of low-abundance biological variations through droplet PCR (dPCR). In this study, we introduce a low-cost PCR thermal cycler setup, an optical system for DNA detection, and a 3D-printed droplet-based microfluidic device engineered to produce hundreds of nanoliter water-in-oil droplets. The microfluidic chip incorporates 21 cycles, each equipped with a micromixer. For the first time, we investigate the impact of integrating micromixers into the PCR chip cycles and demonstrate that this integration enhances the efficiency and specificity of the PCR process. Following the completion of the PCR cycles, the droplets are gathered in a chamber located at the end of the chip for amplification detection. A simple fluorescent optical setup is developed for fluorescence detection and accurate measurement of DNA concentration in the sample. This setup comprises a cost-effective high-resolution camera, a dichroic mirror, and an LED light source. Subsequently, the fluorescent images captured are processed using Python (OpenCV library) and analyzed for fluorescent emission intensity and droplet size distribution. The outcomes of the dPCR conducted with the microfluidic chip are subsequently assessed through a gel electrophoresis test and compared to the identical results from a commercial quantitative PCR (qPCR) device. Our study demonstrates the ability to perform rapid dPCR analysis via endpoint imaging utilizing a cost-effective and easy-to-fabricate setup.
期刊介绍:
Sensors and Actuators Reports is a peer-reviewed open access journal launched out from the Sensors and Actuators journal family. Sensors and Actuators Reports is dedicated to publishing new and original works in the field of all type of sensors and actuators, including bio-, chemical-, physical-, and nano- sensors and actuators, which demonstrates significant progress beyond the current state of the art. The journal regularly publishes original research papers, reviews, and short communications.
For research papers and short communications, the journal aims to publish the new and original work supported by experimental results and as such purely theoretical works are not accepted.