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Characterization of drug metabolites and cytotoxicity assay simultaneously using an integrated microfluidic device

机译:使用集成的微流控设备同时表征药物代谢产物并进行细胞毒性测定

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An integrated microfluidic device was developed for the characterization of drug metabolites and a cytotoxicity assay simultaneously. The multi-layer device was composed of a quartz substrate with embedded separation microchannels and a perforated three-microwell array containing sol-gel bioreactors of human liver microsome (HLM), and two PDMS layers. By aligning the microwell array on the quartz substrate with cell culture chambers on the bottom PDMS layer, drug metabolism studies related to functional units, including metabolite generation, detection and incubation with cultured cells to assess metabolism induced cytotoxicity, were all integrated into the microfluidic device. To validate the feasibility of drug metabolism study on the microfluidic chip, UDP-glucuronosyltransferase (UGT) metabolism of acetaminophen (AP) and its effect on hepG2 cytotoxicity were studied first. Then metabolism based drug-drug interaction between AP and phenytoin (PH), which resulted in increased hepG2 cytotoxicity, was proved on this device. All this demonstrated that the developed microfluidic device could be a potential useful tool for drug metabolism and metabolism based drug-drug interaction research.
机译:开发了一种集成的微流控设备,用于同时表征药物代谢产物和细胞毒性测定。多层设备由具有嵌入式分离微通道的石英基板和包含人肝微粒体(HLM)的溶胶-凝胶生物反应器的穿孔三微孔阵列和两个PDMS层组成。通过将石英基板上的微孔阵列与底部PDMS层上的细胞培养室对准,与功能单元相关的药物代谢研究(包括代谢产物的产生,检测和与培养细胞的孵育以评估代谢诱导的细胞毒性)都整合到了微流体装置中。为了验证在微流控芯片上进行药物代谢研究的可行性,首先研究了对乙酰氨基酚(AP)的UDP-葡萄糖醛酸转移酶(UGT)代谢及其对hepG2细胞毒性的影响。然后在该装置上证明了AP与苯妥英(PH)之间基于代谢的药物相互作用,从而导致hepG2细胞毒性增加。所有这些表明,开发的微流体装置可能是药物代谢和基于代谢的药物-药物相互作用研究的潜在有用工具。

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