详细信息
Pharmacokinetics,bioavailability and tissue distribution of chitobiose and chitotriose in rats
文献类型:期刊文献
中文题名:Pharmacokinetics,bioavailability and tissue distribution of chitobiose and chitotriose in rats
作者:Mai Chen[1];Jiayang Jin[1];Xiaoguo Ji[1];Kunlin Chang[1];Juan Li[2];Liming Zhao[1,3]
机构:[1]School of Biotechnology,State Key Laboratory of Bioreactor Engineering,R&D Center of Separation and Extraction Technology in Fermentation Industry,East China University of Science and Technology,Shanghai 200237,China;[2]Department of Nutrition,Chang-Zheng Hospital,Naval Medical University,Shanghai 200003,China;[3]Shanghai Collaborative Innovation Center for Biomanufacturing Technology(SCICBT),Shanghai 200237,China
年份:2022
卷号:9
期号:1
起止页码:1551
中文期刊名:Bioresources and Bioprocessing
外文期刊名:生物资源与生物加工(英文)
基金:financially supported by the National Key R&D Program of China(2019YFD0901805);the 111 Project(B18022);the Fundamental Research Funds for the Central Universities,and the Open Project Funding of the State Key Laboratory of Bioreactor Engineering,ECUST(ZDXM2019).
语种:英文
中文关键词:Chitobiose;Chitotriose;UPLC–MS;Pharmacokinetics;Tissue distribution
摘要:Chitooligosaccharides(COSs)have various physiological activities and broad application prospects;however,their pharmacokinetics and tissue distribution remain unclear.In this study,a sensitive and selective ultra-performance liquid chromatography-mass spectrometry(UPLC-MS)method for determining chitobiose(COS 2)and chitotriose(COS 3)in rat serum and tissues was developed.This method was successfully validated based on FDA guidelines in terms of selectivity,calibration curves(lower limit of quantification was 0.002μg/mL for COS 2 and 0.02μg/mL for COS 3),precision(intra-day relative standard deviation of 0.04%-3.55%and inter-day relative standard deviation of 1.94%-11.63%),accuracy(intra-day relative error of?1.81%-11.06%and inter-day relative error of?9.41%-8.63%),matrix effects,recovery(97.10%-101.29%),stability,dilution integrity,and carry-over effects.Then,the method was successfully applied to the pharmacokinetics and tissue distribution study of COS 2 and COS 3 after intragastric and intravenous administration.After intragastric administration,COS 2 and COS 3 were rapidly absorbed,reached peak concentrations in the serum after approximately 0.45 h,and showed rapid elimination with clearances greater than 18.82 L/h/kg and half-lives lower than 6 h.The absolute oral bioavailability of COS 2 and COS 3 was 0.32%-0.52%.COS 2 and COS 3 were widely distributed in Wistar rat tissues and could penetrated the blood-brain barrier without tissue accumulation.
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