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采用"化学、药效与毒理"三结合方法筛选优化抗关节炎中药复方青附蠲痹汤的最佳制备工艺

张婷 陈聪 蔡雄 余黄合 林也 李鑫 唐琳 宋厚盼 彭清华 王炜 刘良

数字中医药(英文)2018,Vol.1Issue(4):289-301,13.
数字中医药(英文)2018,Vol.1Issue(4):289-301,13.

采用"化学、药效与毒理"三结合方法筛选优化抗关节炎中药复方青附蠲痹汤的最佳制备工艺

Combinative Approaches of Chemistry, Pharmacology and Toxicology for the Optimal Pharmaceutical Preparation of an Anti-arthritic Chinese Medicine Formulation QFJBT

张婷 1陈聪 2蔡雄 2余黄合 1林也 1李鑫 3唐琳 1宋厚盼 2彭清华 2王炜 4刘良2

作者信息

  • 1. 湖南中医药大学中药粉体与创新药物省部共建国家重点实验室(培育基地),湖南长沙 410208,中国
  • 2. 湖南中医药大学中医学院,湖南长沙 410208,中国
  • 3. 湖南中医药大学药学院,湖南长沙 410208,中国
  • 4. 广东药科大学中药学院,广东广州 510224,中国
  • 折叠

摘要

Abstract

Objective Qing Fu Juan Bi Tang (QFJBT) is an anti-arthritic Chinese medicine formula consisting of five herbs: Aconiti Lateralis Radix Praeparata (Fu Zi, 附子), Sinomenii Caulis (Qing Feng Teng, 青风藤), Astragali Radix (Huang Qi, 黄芪), Paeoniae Radix Alba (Bai Shao, 白芍) and Moutan Cortex (Mu Dan Pi, 牡丹皮), which have well-established histories of use for treatment of rheumatic and arthritic diseases. We intended to establish the optimized and standardized pharmaceutical procedures and manufacturing processes for the pilot production of QFJBT to develop it as a novel botanical drug product for treatment of rheumatoid arthritis (RA). Methods The combinative approaches of chemical assessment, toxicological and pharmacological evaluation were explored to define the pharmaceutical preparation of QFJBT. Results The optimized and standardized pharmaceutical procedures and manufacturing processes for the pilot production of QFJBT were established in terms of greatest chemical contents of bioactive constituents, potent anti-inflammatory and antinociceptive activities, and favorable safety profile. Quality analysis of the pilot product of QFJBT by high-performance liquid chromatography (HPLC) demonstrated that the chromatographic fingerprint profiles of three batches of QFJBT were basically identical and the contents of four characteristic and bioactive markers were relatively consistent. General toxicological studies showed a favorable safety profile of QFJBT. The maximum tolerated single dose of QFJBT was determined in both sexes of rats to be 33.63 g/kg body weight which is equivalent to 346 times of clinical dose. In the chronic oral toxicity study, the results of laboratory investigation showed that QFJBT at doses of 3.89, 6.80 and 9.72 g/kg body weight (equivalent to 40, 70 and 100-fold clinical doses, respectively) caused no changes in all hematological parameters and blood biochemical parameters of rats. No mortality or specific toxic responses were observed in animals after three months of repeated dosing with QFJBT. Conclusion The optimized and standardized pharmaceutical and manufacturing processes for the production of QFJBT have been successfully screened and identified through established rigorous in-process controls.

关键词

青附蠲痹汤/类风湿关节炎/制备工艺/质量控制/安全性/抗炎镇痛

Key words

QFJBT/Rheumatoid arthritis/Pharmaceutical preparation/Quality control/Safety profile/Anti-inflammatory and antinociceptive effects

引用本文复制引用

张婷,陈聪,蔡雄,余黄合,林也,李鑫,唐琳,宋厚盼,彭清华,王炜,刘良..采用"化学、药效与毒理"三结合方法筛选优化抗关节炎中药复方青附蠲痹汤的最佳制备工艺[J].数字中医药(英文),2018,1(4):289-301,13.

基金项目

We thank for the funding support from the National Natural Science Foundation of China (No. 81704065), China Postdoctoral Science Foundation (No. 2016M600632 and No. 2017T100604),Hunan Provincial Natural Science Foundation (No. 2017JJ3239 andNo.2018JJ2293),Hunan Education Department's Science & Research Project (No. 17K069), Hunan Provincial Science& Research Project of Chinese Medicine (No. 201790), and National First-class Disciple Construction Project of Chinese Medicine of Hunan University of Chinese Medicine. (No. 81704065)

数字中医药(英文)

2096-479X

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