{"title":"用梯形惯性微流控芯片临床分离乳腺癌循环肿瘤细胞","authors":"Zahra Sadeghi , Mohsen Nasr Esfahany , Hossein Salehi , Azar Baradaran","doi":"10.1016/j.bej.2025.109788","DOIUrl":null,"url":null,"abstract":"<div><div>In recent years, various detection and isolation methods for breast cancer have emerged. However, the lack of simple, unbiased separation techniques limits clinical applications of Circulating Tumor Cells (CTCs). This study introduces an inertial microfluidic chip with a trapezoidal cross-section for rapid, simple separation of MCF-7 CTCs from patient blood using an optimized SLA 3D printing technique. Simulations and experiments showed that increasing the slant angle enhances Dean vortices, with 1.2 mL/min as the optimal flow rate. Spiking MCF-7 cells into Phosphate-Buffered Saline (PBS) yielded a recovery rate of 88 ± 3.5 % and a purity of 99.99 %. When spiked into 7.5 mL lysed blood, the recovery was 86 ± 2.9 % and purity 94 ± 2.3 %, with over 90 % of cells remaining viable. Clinically, the chip detected MCF-7 cells in 8 out of 10 breast cancer patients (80 %), with cell counts ranging from 2 to 21 cells/mL and purities between 89 ± 1.6 % and 92 ± 5.8 %. These results confirm the chip’s high sensitivity and viability preservation. This straightforward inertial microfluidic method offers a promising alternative to traditional affinity-based CTC separation, supporting fundamental research and aiding patient treatment strategies.</div></div>","PeriodicalId":8766,"journal":{"name":"Biochemical Engineering Journal","volume":"221 ","pages":"Article 109788"},"PeriodicalIF":3.7000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical isolation of breast cancer Circulating Tumor Cells with an inertial microfluidic chip with a trapezoidal cross-section\",\"authors\":\"Zahra Sadeghi , Mohsen Nasr Esfahany , Hossein Salehi , Azar Baradaran\",\"doi\":\"10.1016/j.bej.2025.109788\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In recent years, various detection and isolation methods for breast cancer have emerged. However, the lack of simple, unbiased separation techniques limits clinical applications of Circulating Tumor Cells (CTCs). This study introduces an inertial microfluidic chip with a trapezoidal cross-section for rapid, simple separation of MCF-7 CTCs from patient blood using an optimized SLA 3D printing technique. Simulations and experiments showed that increasing the slant angle enhances Dean vortices, with 1.2 mL/min as the optimal flow rate. Spiking MCF-7 cells into Phosphate-Buffered Saline (PBS) yielded a recovery rate of 88 ± 3.5 % and a purity of 99.99 %. When spiked into 7.5 mL lysed blood, the recovery was 86 ± 2.9 % and purity 94 ± 2.3 %, with over 90 % of cells remaining viable. Clinically, the chip detected MCF-7 cells in 8 out of 10 breast cancer patients (80 %), with cell counts ranging from 2 to 21 cells/mL and purities between 89 ± 1.6 % and 92 ± 5.8 %. These results confirm the chip’s high sensitivity and viability preservation. This straightforward inertial microfluidic method offers a promising alternative to traditional affinity-based CTC separation, supporting fundamental research and aiding patient treatment strategies.</div></div>\",\"PeriodicalId\":8766,\"journal\":{\"name\":\"Biochemical Engineering Journal\",\"volume\":\"221 \",\"pages\":\"Article 109788\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-05-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochemical Engineering Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1369703X25001627\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369703X25001627","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Clinical isolation of breast cancer Circulating Tumor Cells with an inertial microfluidic chip with a trapezoidal cross-section
In recent years, various detection and isolation methods for breast cancer have emerged. However, the lack of simple, unbiased separation techniques limits clinical applications of Circulating Tumor Cells (CTCs). This study introduces an inertial microfluidic chip with a trapezoidal cross-section for rapid, simple separation of MCF-7 CTCs from patient blood using an optimized SLA 3D printing technique. Simulations and experiments showed that increasing the slant angle enhances Dean vortices, with 1.2 mL/min as the optimal flow rate. Spiking MCF-7 cells into Phosphate-Buffered Saline (PBS) yielded a recovery rate of 88 ± 3.5 % and a purity of 99.99 %. When spiked into 7.5 mL lysed blood, the recovery was 86 ± 2.9 % and purity 94 ± 2.3 %, with over 90 % of cells remaining viable. Clinically, the chip detected MCF-7 cells in 8 out of 10 breast cancer patients (80 %), with cell counts ranging from 2 to 21 cells/mL and purities between 89 ± 1.6 % and 92 ± 5.8 %. These results confirm the chip’s high sensitivity and viability preservation. This straightforward inertial microfluidic method offers a promising alternative to traditional affinity-based CTC separation, supporting fundamental research and aiding patient treatment strategies.
期刊介绍:
The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology.
The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields:
Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics
Biosensors and Biodevices including biofabrication and novel fuel cell development
Bioseparations including scale-up and protein refolding/renaturation
Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells
Bioreactor Systems including characterization, optimization and scale-up
Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization
Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals
Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release
Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites
Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation
Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis
Protein Engineering including enzyme engineering and directed evolution.