LAPSE:2024.0786v1
Published Article

LAPSE:2024.0786v1
An Injection-Mold Based Method with a Nested Device for Microdroplet Generation by Centrifugation
June 7, 2024
Abstract
Microdroplets have been widely used in different fields due to their unique properties, such as compartmentalization, single-molecule sensitivity, chemical and biological compatibility, and high throughput. Compared to intricate and labor-intensive microfluidic techniques, the centrifuge-based method is more convenient and cost-effective for generating droplets. In this study, we developed a handy injection molding based method to readily produce monodisperse droplets by centrifugation. Briefly, we used two three-dimensional (3D) printed master molds with internal cavities to forge two coupled sub-molds by injecting polydimethylsiloxane (PDMS) and casted these two PDMS sub-molds into a nested structure that clamps the micro-channel array (MiCA) by injecting polyurethane resin. This method enables the generation of various sizes of monodispersed microdroplets by centrifugation with proper parameters within 10 min. To assess the performance of this method, homogeneous fluorescent hydrogel microspheres were generated and droplet digital polymerase chain reaction (ddPCR) was carried out. Overall, this method offers high-throughput droplet generation, reduces costs compared to other methods, and is user-friendly.
Microdroplets have been widely used in different fields due to their unique properties, such as compartmentalization, single-molecule sensitivity, chemical and biological compatibility, and high throughput. Compared to intricate and labor-intensive microfluidic techniques, the centrifuge-based method is more convenient and cost-effective for generating droplets. In this study, we developed a handy injection molding based method to readily produce monodisperse droplets by centrifugation. Briefly, we used two three-dimensional (3D) printed master molds with internal cavities to forge two coupled sub-molds by injecting polydimethylsiloxane (PDMS) and casted these two PDMS sub-molds into a nested structure that clamps the micro-channel array (MiCA) by injecting polyurethane resin. This method enables the generation of various sizes of monodispersed microdroplets by centrifugation with proper parameters within 10 min. To assess the performance of this method, homogeneous fluorescent hydrogel microspheres were generated and droplet digital polymerase chain reaction (ddPCR) was carried out. Overall, this method offers high-throughput droplet generation, reduces costs compared to other methods, and is user-friendly.
Record ID
Keywords
centrifuge-based, fluorescent hydrogel microspheres, injection molding, microdroplet generation
Subject
Suggested Citation
Li J, Li W, Wu B, Bu W, Li M, Ou J, Xiong Y, Wu S, Huang Y, Fan Y, Men Y. An Injection-Mold Based Method with a Nested Device for Microdroplet Generation by Centrifugation. (2024). LAPSE:2024.0786v1
Author Affiliations
Li J: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China; Nano Science and Technology Institute, University of Science and Technology of China, Hefei 230052, China
Li W: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China [ORCID]
Wu B: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Bu W: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Li M: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Ou J: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Xiong Y: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Wu S: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Huang Y: Biomedical Pioneering Innovation Center (BIOPIC), Peking-Tsinghua Center for Life Sciences, Beijing Advanced Innovation Center for Genomics (ICG), College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China [ORCID]
Fan Y: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China [ORCID]
Men Y: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China [ORCID]
Li W: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China [ORCID]
Wu B: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Bu W: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Li M: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Ou J: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Xiong Y: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Wu S: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China
Huang Y: Biomedical Pioneering Innovation Center (BIOPIC), Peking-Tsinghua Center for Life Sciences, Beijing Advanced Innovation Center for Genomics (ICG), College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China [ORCID]
Fan Y: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China [ORCID]
Men Y: Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China [ORCID]
Journal Name
Processes
Volume
12
Issue
3
First Page
483
Year
2024
Publication Date
2024-02-27
ISSN
2227-9717
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PII: pr12030483, Publication Type: Journal Article
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LAPSE:2024.0786v1
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https://doi.org/10.3390/pr12030483
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Jun 7, 2024
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