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Microarray Platforms Based on 3D Printing.
Qin, Jinglin; Qian, Zhenwei; Lai, Yiwen; Zhang, Chen; Zhang, Xiannian.
Afiliación
  • Qin J; Department of Neurobiology, School of Basic Medical Sciences, Beijing Key Laboratory of Neural Regeneration and Repair, Capital Medical University, Beijing 100069, China.
  • Qian Z; Peking University 302 Clinical Medical School, Beijing 100039, China.
  • Lai Y; Department of Neurobiology, School of Basic Medical Sciences, Beijing Key Laboratory of Neural Regeneration and Repair, Capital Medical University, Beijing 100069, China.
  • Zhang C; Department of Neurobiology, School of Basic Medical Sciences, Beijing Key Laboratory of Neural Regeneration and Repair, Capital Medical University, Beijing 100069, China.
  • Zhang X; Chinese Institute for Brain Research, Beijing 102206, China.
Anal Chem ; 96(15): 6001-6011, 2024 04 16.
Article en En | MEDLINE | ID: mdl-38566481
ABSTRACT
This paper introduces an innovative method for the fabrication and infusion of microwell arrays based on digital light processing (DLP) 3D printing. A low-cost DLP 3D printer is employed to fabricate microstructures rapidly with a broad dynamic range while maintaining high precision and fidelity. We constructed microwell arrays with varying diameters, from 200 to 2000 µm and multiple aspect ratios, in addition to microchannels with widths ranging from 45 to 1000 µm, proving the potential and flexibility of this fabrication method. The superimposition of parallel microchannels onto the microwell array, facilitated by positive or negative pressure, enabled the transfer of liquid to the microwells. Upon removal of the microchannel chip, a dispensed microdroplet array was obtained. This array can be modulated by adjusting the volume of the microwells and the inflow fluid. The filled microwell array allows chip-to-chip dispensing to the microreactor array through binding and centrifugation, facilitating multistep and multireagent assays. The 3D printing approach also enables the fabrication of intricate cavity designs, such as micropyramid arrays, which can be integrated with parallel microchannels to generate spheroid flowcells. This device demonstrated the ability to generate spheroids and manipulate their environment. We have successfully utilized precise modulation of spheroids size and performed parallel drug dose-response assays to evaluate its effectiveness. Furthermore, we managed to execute dynamic drug combinations based on a compact spheroids array, utilizing two orthogonal parallel microchannels. Our findings suggest that both the combination and temporal sequence of drug administration have a significant impact on therapeutic outcomes.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esferoides Celulares / Técnicas de Cultivo de Célula Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Esferoides Celulares / Técnicas de Cultivo de Célula Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: China