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口服固本解毒胶囊后正常和糖尿病肾病大鼠样本中六种主要生物活性成分的 UPLC-MS/MS 比较药代动力学分析。

Comparative pharmacokinetic analysis of six major bioactive constituents using UPLC-MS/MS in samples isolated from normal and diabetic nephropathy rats after oral administration of Gushen Jiedu capsule.

机构信息

Department of Pharmacy, Beijing Shijitan Hospital, Capital Medical University, Beijing, China; Beijing Key Laboratory of Bio-characteristic Profiling for Evaluation of Rational Drug Use, Beijing, China.

Department of Pharmacy, Fuwai Central China Cardiovascular Hospital, Zhengzhou, China.

出版信息

J Pharm Biomed Anal. 2023 Oct 25;235:115638. doi: 10.1016/j.jpba.2023.115638. Epub 2023 Aug 11.

Abstract

Berberine, palmatine, physcion, rhein, calycosin-7-O-glucoside, and ferulic acid are six major active consituents that are present in Gushen Jiedu capsule (GSJD) extracts. The aim of this study was to determine the pharmacokinetics of the six active consituents in vivo by a rapid, sensitive, and precise UPLC-MS/MS method, which were compared between normal and diabetic nephropathy (DN) rats. Good separation of the target analytes and internal standards (ketoprofen and puerarin) was obtained on a Waters BEH C UPLC column with a mobile phase of 0.1 % formic acid acetonitrile-0.1 % formic acid water. All the calibration curves showed good linearity with a regression coefficient (r) of ≥ 0.9908. The lower limits of quantification (LLOQ) for berberine, palmatine, physcion, rhein, calycosin-7-O-glucoside, and ferulic acid were 20, 2.5, 20, 20, 2.5, and 2.5 ng/mL, respectively. The relative standard deviations (RSDs) of intra-day and inter-day precision were all within 12.66 %, and the relative errors of intra-day and inter-day accuracy ranged from - 15.00 to 14.93 %. Good extraction recovery and matrix effects were obtained. The stability study confirmed the stability of the six analytes (RSD < 15 %). Finally, the data showed that the pharmacokinetic parameters (especially CLz/F, AUC and T) of the six target analytes in DN rats were significantly different from those in normal rats. PK studies under pathological conditions could provide new thoughts to elucidate the underlying mechanism of GSJD and promote the clinical development of GSJD to treat DN.

摘要

小檗碱、黄连碱、小檗红碱、大黄酸、毛蕊异黄酮-7-O-葡萄糖苷和阿魏酸是苦参解毒胶囊(GSJD)提取物中存在的六种主要活性成分。本研究旨在建立一种快速、灵敏、准确的 UPLC-MS/MS 法测定这六种活性成分在正常和糖尿病肾病(DN)大鼠体内的药代动力学,并对其进行比较。在 Waters BEH C UPLC 柱上,采用 0.1%甲酸乙腈-0.1%甲酸水作为流动相,可实现目标分析物和内标(酮洛芬和葛根素)的良好分离。所有校准曲线的线性良好,相关系数(r)均≥0.9908。小檗碱、黄连碱、小檗红碱、大黄酸、毛蕊异黄酮-7-O-葡萄糖苷和阿魏酸的定量下限(LLOQ)分别为 20、2.5、20、20、2.5 和 2.5ng/mL。日内和日间精密度的相对标准偏差(RSD)均在 12.66%以内,日内和日间准确度的相对误差范围在-15.00%至 14.93%之间。提取回收率和基质效应良好。稳定性研究证实了六种分析物的稳定性(RSD<15%)。最后,数据表明,DN 大鼠六种目标分析物的药代动力学参数(尤其是 CLz/F、AUC 和 T)与正常大鼠有显著差异。在病理条件下进行的 PK 研究可以为阐明 GSJD 的潜在机制提供新的思路,并促进 GSJD 治疗 DN 的临床开发。

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