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引用本文:吴飞跃,林玳,顾卓珺,郑怀宇,傅军.α-倒捻子素脂质体的药动学研究[J].中国现代应用药学,2017,34(5):703-705.
WU Feiyue,LIN Dai,GU Zhuojun,ZHENG Huaiyu,FU Jun.Study on Pharmacokinetics of α-Mangostin Lipsome[J].Chin J Mod Appl Pharm(中国现代应用药学),2017,34(5):703-705.
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α-倒捻子素脂质体的药动学研究
吴飞跃1, 林玳1, 顾卓珺1, 郑怀宇1, 傅军2
1.舟山医院药剂科, 浙江 舟山 316000;2.同济大学附属第十人民医院药学部, 上海 200072
摘要:
目的 采用LC-MS/MS考察α-倒捻子素脂质体的药动学特征。方法 采用SPF级ICR小鼠,♀,尾静脉注射α-倒捻子素脂质体3 mg·kg-1,用LC-MS/MS测定α-倒捻子素血药浓度,并计算其药动学参数。结果 α-倒捻子素线性范围为5~1 000 ng·mL-1r=0.997 6),定量限为5 ng·mL-1,日内、日间精密度均<11.0%。主要药动学参数:t1/2为(0.99±0.12)h,Cmax为(1 524.60±323.82)ng·mL-1,AUC0-t为(645.84±63.74)ng·h·mL-1,MRT为(0.70±0.11)h,CL为(4.80±0.45)mL·h-1·kg-1,Vd为(6.80±1.00)mL·kg-1结论 该法操作简便、快速、灵敏,可用于测定小鼠血浆中α-倒捻子素浓度。本研究结果可为药物的进一步研究提供依据。
关键词:  α-倒捻子素  脂质体  液相色谱-质谱  药动学
DOI:10.13748/j.cnki.issn1007-7693.2017.05.015
分类号:
基金项目:舟山市医药卫生科技计划(2015G02)
Study on Pharmacokinetics of α-Mangostin Lipsome
WU Feiyue1, LIN Dai1, GU Zhuojun1, ZHENG Huaiyu1, FU Jun2
1.Department of Pharmacy, Zhoushan Hospital, Zhoushan 316000, China;2.Department of Pharmacy, the Tenth People's Hospital Affiliated to Tongji University, Shanghai 200072, China
Abstract:
OBJECTIVE To establish a sensitive and specific LC-MS/MS method for investigating the pharmacokinetics characteristic of α-mangostin liposome in mice. METHODS ICR mice were given in tail vein α-mangostin 3 mg·kg-1. The α-mangostin concentration was determined by LC-MS/MS and pharmacokinetic parameters was calculated. RESULTS The linearity ranged from 5 to 1 000 ng·mL-1 (r=0.997 6). The detectction of α-mangostin was 5 ng·mL-1. The RSDs within day and between days were <11%. The main pharmacokinetic parameters of t1/2, Cmax, AUC0-t, MRT, CL and Vss were (0.99±0.12)h, (1 524.60±323.82)ng·mL-1, (645.84±63.74)ng·h·mL-1, (0.70±0.11)h, (4.80±0.45)mL·h-1·kg-1, and (6.80±1.00)mL·kg-1, respectively. CONCLUSION The precision, accuracy and recovery of the method are found to be adequate for pharmacokinetic studies. The results can provide the basis for future research.
Key words:  α-mangostin  lipsome  LC-MS/MS  pharmacokinetics
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