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用于提高抗癌药物测试可重复性的一式三份动态细胞培养平台。

Triplicate Dynamic Cell Culture Platform for Enhanced Reproducibility in Anti-Cancer Drug Testing.

作者信息

Lu Yu-Lun, Lin Chiao-Min, Huang Jen-Huang

机构信息

Department of Chemical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

ACS Biomater Sci Eng. 2025 Feb 10;11(2):1222-1231. doi: 10.1021/acsbiomaterials.4c02142. Epub 2025 Jan 14.

DOI:10.1021/acsbiomaterials.4c02142
PMID:39809465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11815626/
Abstract

The development of stable and standardized in vitro cytotoxicity testing models is essential for drug discovery and personalized medicine. Microfluidic technologies, recognized for their small size, reduced reagent consumption, and control over experimental variables, have gained considerable attention. However, challenges associated with external pumps, particularly inconsistencies between individual pumping systems, have limited the real-world application of cancer-on-a-chip technology. This study introduces a novel triplicate cell culture system (Tri-CS) that simultaneously supports dynamic cultures in three independent units using a single peristaltic pump, ensuring consistent flow conditions. Our findings demonstrate that the Tri-CS significantly reduces variability compared to individual pump systems, enhancing the reliability of anticancer drug cytotoxicity testing. Furthermore, we evaluated gemcitabine cytotoxicity, which shows enhanced drug efficacy in dynamic conditions. Fluorescein diffusion tests revealed greater diffusion efficiency in dynamic cultures, which contributed to the higher observed drug efficacy. The potential for broader application of the Tri-CS, including its compatibility with commercially available transwells and the opportunity for use in more complex cancer-on-chip models, positions this system as a valuable tool for advancing microphysiological systems in preclinical research.

摘要

开发稳定且标准化的体外细胞毒性测试模型对于药物发现和个性化医疗至关重要。微流控技术因其体积小、试剂消耗少以及对实验变量的控制能力而备受关注。然而,与外部泵相关的挑战,尤其是各个泵系统之间的不一致性,限制了芯片上癌症技术在实际中的应用。本研究引入了一种新型的三联细胞培养系统(Tri-CS),该系统使用单个蠕动泵同时在三个独立单元中支持动态培养,确保流动条件一致。我们的研究结果表明,与单个泵系统相比,Tri-CS显著降低了变异性,提高了抗癌药物细胞毒性测试的可靠性。此外,我们评估了吉西他滨的细胞毒性,结果显示在动态条件下药物疗效增强。荧光素扩散测试表明,动态培养中的扩散效率更高,这导致观察到的药物疗效更高。Tri-CS更广泛应用的潜力,包括其与市售Transwell的兼容性以及用于更复杂的芯片上癌症模型的机会,使该系统成为临床前研究中推进微生理系统的有价值工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/aa189030e5f9/ab4c02142_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/68c5b68434c5/ab4c02142_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/efe92d8c23be/ab4c02142_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/04c791d9e4af/ab4c02142_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/57dc8324c2d9/ab4c02142_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/aa189030e5f9/ab4c02142_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/68c5b68434c5/ab4c02142_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/efe92d8c23be/ab4c02142_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/04c791d9e4af/ab4c02142_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/57dc8324c2d9/ab4c02142_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6385/11815626/aa189030e5f9/ab4c02142_0005.jpg

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本文引用的文献

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Mucosa-like differentiation of head and neck cancer cells is inducible and drives the epigenetic loss of cell malignancy.头颈癌细胞的黏膜样分化是可诱导的,并导致细胞恶性程度的表观遗传丧失。
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