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Cancer drug screening with an on-chip multi-drug dispenser in digital microfluidics.
Zhai, Jiao; Li, Caiwei; Li, Haoran; Yi, Shuhong; Yang, Ning; Miao, Kai; Deng, Chuxia; Jia, Yanwei; Mak, Pui-In; Martins, Rui P.
Affiliation
  • Zhai J; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau, China. yanweijia@um.edu.mo.
  • Li C; Department of Biomedical Sciences/Tung Biomedical Sciences Centre, City University of Hong Kong, Hong Kong, China.
  • Li H; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau, China. yanweijia@um.edu.mo.
  • Yi S; Faculty of Science and Technology - DECE, University of Macau, Macau, China.
  • Yang N; State Key Laboratory of Analog and Mixed-Signal VLSI, Institute of Microelectronics, University of Macau, Macau, China. yanweijia@um.edu.mo.
  • Miao K; Faculty of Science and Technology - DECE, University of Macau, Macau, China.
  • Deng C; Liver Transplantation Center, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Jia Y; Department of Electronic Information Engineering, Jiangsu University, Zhenjiang, China.
  • Mak PI; Faculty of Health Sciences, University of Macau, Macau, China.
  • Martins RP; MoE Frontiers Science Center for Precision Oncology, University of Macau, Macau, China.
Lab Chip ; 21(24): 4749-4759, 2021 12 07.
Article in En | MEDLINE | ID: mdl-34761772
ABSTRACT
Microfluidics has been the most promising platform for drug screening with a limited number of cells. However, convenient on-chip preparation of a wide range of drug concentrations remains a large challenge and has restricted wide acceptance of microfluidics in precision medicine. In this paper, we report a digital microfluidic system with an innovative control structure and chip design for on-chip drug dispensing to generate concentrations that span three to four orders of magnitude, enabling single drug or combinatorial multi-drug screening with simple electronic control. Specifically, we utilize droplet ejection from a drug drop sitting on a special electrode, named a drug dispenser, under high-voltage pulse actuation to deliver the desired amount of drugs to be picked up by a cell suspension drop driven by low-voltage sine wave actuation. Our proof-of-principle validation for this technique as a convenient single and multi-drug screening involved testing of the drug toxicity of two chemotherapeutics, cisplatin (Cis) and epirubicin (EP), towards MDA-MB-231 breast cancer cells and MCF-10A normal breast cells. The results are consistent with those screened based on traditional 96-well plates. These findings demonstrate the reliability of the drug screening system with an on-chip drug dispenser. This system with fewer cancer cells, less drug consumption, a small footprint, and high scalability with regard to concentration could pave the way for drug screening on biopsied primary tumor cells for precision medicine or any concentration-related research.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Pharmaceutical Preparations / Neoplasms Type of study: Diagnostic_studies / Screening_studies Language: En Journal: Lab Chip Year: 2021 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Pharmaceutical Preparations / Neoplasms Type of study: Diagnostic_studies / Screening_studies Language: En Journal: Lab Chip Year: 2021 Type: Article Affiliation country: China