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Rapid Prototyping of Thermoplastic Microfluidic 3D Cell Culture Devices by Creating Regional Hydrophilicity Discrepancy.
Bai, Haiqing; Olson, Kristen N Peters; Pan, Ming; Marshall, Thomas; Singh, Hardeep; Ma, Jingzhe; Gilbride, Paige; Yuan, Yu-Chieh; McCormack, Jenna; Si, Longlong; Maharjan, Sushila; Huang, Di; Qian, Xiaohua; Livermore, Carol; Zhang, Yu Shrike; Xie, Xin.
Afiliação
  • Bai H; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Olson KNP; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Pan M; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Marshall T; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Singh H; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Ma J; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Gilbride P; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Yuan YC; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • McCormack J; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Si L; CAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, P. R. China.
  • Maharjan S; University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
  • Huang D; Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA, 02142, USA.
  • Qian X; Research Center for Nano-biomaterials & Regenerative Medicine, College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan, 030024, P. R. China.
  • Livermore C; Xellar Biosystems, Cambridge, MA, 02458, USA.
  • Zhang YS; Department of Mechanical and Industrial Engineering, Northeastern University, Boston, MA, 02115, USA.
  • Xie X; Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA, 02142, USA.
Adv Sci (Weinh) ; 11(7): e2304332, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38032118
Microfluidic 3D cell culture devices that enable the recapitulation of key aspects of organ structures and functions in vivo represent a promising preclinical platform to improve translational success during drug discovery. Essential to these engineered devices is the spatial patterning of cells from different tissue types within a confined microenvironment. Traditional fabrication strategies lack the scalability, cost-effectiveness, and rapid prototyping capabilities required for industrial applications, especially for processes involving thermoplastic materials. Here, an approach to pattern fluid guides inside microchannels is introduced by establishing differential hydrophilicity using pressure-sensitive adhesives as masks and a subsequent selective coating with a biocompatible polymer. Optimal coating conditions are identified using polyvinylpyrrolidone, which resulted in rapid and consistent hydrogel flow in both the open-chip prototype and the fully bonded device containing additional features for medium perfusion. The suitability of the device for dynamic 3D cell culture is tested by growing human hepatocytes in the device under controlled fluid flow for a 14-day period. Additionally, the study demonstrated the potential of using the device for pharmaceutical high-throughput screening applications, such as predicting drug-induced liver injury. The approach offers a facile strategy of rapid prototyping thermoplastic microfluidic organ chips with varying geometries, microstructures, and substrate materials.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatócitos / Microfluídica Limite: Humans Idioma: En Revista: Adv Sci (Weinh) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatócitos / Microfluídica Limite: Humans Idioma: En Revista: Adv Sci (Weinh) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Alemanha