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作 者:亓蕖[1] 郝琨[1] 李飞燕[1] 曹丽娟[1] 王广基[1] 郝海平[1]
机构地区:[1]中国药科大学天然药物活性组分与药效国家重点实验室,药物代谢动力学重点实验室,南京210009
出 处:《中国天然药物》2013年第5期560-565,共6页
基 金:supported by the Natural Science Foundation of Jiangsu Province(Nos.BK2011065,BK2012026);Jiangsu Province Key Lab of Drug Metabolism and Pharmacokinetics(No.BM2012012)~~
摘 要:目的:鉴定丹酚酸B静注后在大鼠体内的代谢产物并对主要代谢物进行定量。方法:应用LC-IT/TOF-MS对大鼠胆汁、血浆和尿液中的代谢产物进行分析鉴定;应用LC-MS/MS对两个主要代谢产物进行定量,得到血浆药时曲线。结果:在大鼠胆汁、血浆和尿液中,共发现了九种代谢产物,包括丹酚酸B的甲基化产物,紫草酸及紫草酸的脱羧和甲基化产物,丹酚酸S及其脱水产物;药动学研究表明紫草酸和单甲基-丹酚酸B的t1/2都较小,单甲基-丹酚酸B与紫草酸相比有较大的AUC。结论:丹酚酸B静注后,在大鼠体内共发现了9种代谢产物,绘制了代谢通路图并对紫草酸和单甲基-丹酚酸B的药物代谢动力学进行了研究,阐明了丹酚酸B在大鼠体内主要的代谢方式是甲基化。AIM: To identify and quantify the major metabolites of salvianolic acid B (SAB) after intravenous injection in rats. METHODS: LC-IT/TOF-MS was used to identify the metabolites in rat bile, plasma, and urine; LC-MS/MS was used to quantify the two major metabolites. RESULTS: In rat bile, plasma, and urine, nine metabolites were identified, including methylated metabolites of SAB, lithospermic acid (LSA), the decarboxylation and methylation metabolites of LSA, salvianolic acid S (SAS), and dehy- drated-SAS. The t1/2 of monomethyl-SAB and LSA were both very short, and monomethyl-SAB had a larger AUC than LSA in rats. CONCLUSION: Nine metabolites were found, the metabolic pathway was described, and the pharmacokinetic profiles of LSA and monomethyl-SAB were studied, thereby clarifying that methylation was the dominant metabolic pathway for SAB in rats.
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