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Assessment of in vitro and in vivo recovery of sinomenine using microdialysis.

机译:使用微透析评估青藤碱的体外和体内恢复。

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BACKGROUND/PURPOSE: For microdialysis studies in the skin, laboratory-made linear probes are often used. The application of the microdialysis technique to the investigation of pharmacokinetics and pharmacodynamics of drugs requires careful assessment of the linear probes' performance to ensure validity of the data obtained using this technique. The aim of this study was to establish and validate the microdialysis technique for investigation of the pharmacokinetics and pharmacodynamics of sinomenine. METHODS: Using different lengths of the dialysis membrance and different perfusion flow rates, a flow rate of 2 microL/min with 20-min sampling intervals was selected for the subsequent studies, based on the analysis of sinomenine from the microdialysis probe. In vitro recovery of sinomenine from the microdialysis probe was independent of concentration, stable over an 8-h period. Comparable in vitro recoveries were obtained by different established approaches including recovery estimation by gain, loss and the zero-net flux (ZNF) method. Recovery by loss was used to study the in vivo recovery of sinomenine from rat subcutaneous tissue. RESULTS: The performance of the microdialysis system was stable over an 8-h study, resulting in a mean in vitro recovery of 51.91+/-1.29%. Recovery obtained using the ZNF plot was 52.43%. In vivo recovery of sinomenine was 34.46+/-0.76% and was stable over the 7-h study period. CONCLUSION: The in vitro and in vivo performance of the microdialysis technique was established for the study of sinomenine. It would prove to be a useful and reliable tool to study the pharmacokinetics and pharmacodynamics of sinomenine. The data obtained in our study highlight the importance of a systematic examination of microdialysis linear probe validation.
机译:背景/目的:对于皮肤的微透析研究,经常使用实验室制造的线性探针。将微透析技术应用于药物的药代动力学和药效学研究,需要仔细评估线性探针的性能,以确保使用此技术获得的数据的有效性。这项研究的目的是建立和验证微透析技术,以研究青藤碱的药代动力学和药效学。方法:使用不同长度的透析膜和不同的灌注流速,基于微透析探针对青藤碱的分析,选择流速为2 microL / min,采样间隔为20分钟的样品进行后续研究。从微透析探针的青藤碱的体外回收率与浓度无关,在8小时内稳定。可通过不同的既定方法获得可比的体外回收率,包括通过增益,损耗和零净通量(ZNF)方法估算回收率。通过损失恢复来研究青藤碱从大鼠皮下组织的体内恢复。结果:微透析系统的性能在8小时的研究中保持稳定,体外平均回收率为51.91 +/- 1.29%。使用ZNF图获得的回收率为52.43%。青藤碱的体内回收率为34.46 +/- 0.76%,并且在7小时的研究期内保持稳定。结论:建立了微透析技术的体外和体内性能用于青藤碱的研究。研究青藤碱的药代动力学和药效学将被证明是一种有用且可靠的工具。在我们的研究中获得的数据突出了对微透析线性探针验证进行系统检查的重要性。

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