| 引用本文: | 保敏敏,吕蓓蓓,魏文芝,张敏娟.奥卡西平半片制剂的往复筒溶出方法研究及分剂量评价[J].中国现代应用药学,2023,40(15):2117-2123. |
| BAO Minmin,LYU Beibei,WEI Wenzhi,ZHANG Minjuan.Study on Oxcarbazepine Half-tablet Preparation by Reciprocating Cylinder Method and Partial Dose Evaluation[J].Chin J Mod Appl Pharm(中国现代应用药学),2023,40(15):2117-2123. |
|
| |
|
|
| 本文已被：浏览 949次 下载 764次 |
码上扫一扫！ |
|
|
| 奥卡西平半片制剂的往复筒溶出方法研究及分剂量评价 |
|
保敏敏1,2,3,4, 吕蓓蓓2,3,4, 魏文芝2,3,4, 张敏娟2,3,4
|
|
1.青海大学医学院药学系, 西宁 810016;2.青海省药品检验检测院, 西宁 810016;3.青海省中藏药现代化研究重点实验室, 西宁 810016;4.国家药品监督管理局中药(藏药)质量控制重点实验室, 西宁 810016
|
|
| 摘要: |
| 目的 建立往复筒溶出方法考察奥卡西平刻痕片仿制药与原研药分割后半片制剂的体外溶出行为相似性，评价原研药和仿制药的分剂量药学特性差异。方法 以pH 1.2盐酸溶液、pH 4.5醋酸盐缓冲液、pH 6.8磷酸盐缓冲液和水(均含0.5%十二烷基硫酸钠250 mL)为溶出介质，往复频率为10 dip·min-1，采用往复筒溶出装置测定仿制药和原研药的溶出曲线，结合相似因子(f2)法评价仿制药和原研药的溶出行为相似性，并与桨法进行比较。采用脆碎度检测仪及电子天平，通过人工掰分法和切药器法测定各厂家半片制剂的脆碎度、分割后质量差异及质量损失。结果 仿制药A在4种溶出介质中的f2均>50，与原研药的溶出行为相似；仿制药B在4种溶出介质中f2均<50，和原研药的溶出行为不相似。仿制药A、B分割后质量差异、质量损失和脆碎度均高于原研药。结论 采用往复筒法测定奥卡西平半片制剂的溶出曲线相较于桨法具有良好的区分力，且仿制药的分剂量质量控制相较于原研药仍有一定差距。 |
| 关键词: 奥卡西平 刻痕片 往复筒法 溶出曲线 分剂量 |
| DOI：10.13748/j.cnki.issn1007-7693.20222109 |
| 分类号:R943 |
| 基金项目:国家药品抽检计划项目(国药监药管〔2019〕2号) |
|
| Study on Oxcarbazepine Half-tablet Preparation by Reciprocating Cylinder Method and Partial Dose Evaluation |
|
BAO Minmin1,2,3,4, LYU Beibei2,3,4, WEI Wenzhi2,3,4, ZHANG Minjuan2,3,4
|
|
1.Department of Pharmacy, College of Medical, Qinghai University, Xining 810016, China;2.Qinghai Provincial Drug Inspection and Testing Institute, Xining 810016, China;3.Qinghai Provincial Key Laboratory of Modernization of Traditional Chinese and Tibetan Medicine, Xining 810016, China;4.NMPA Key Laboratory for Quality Control of Traditional Chinese Medicine(Tibetan Medicine), Xining 810016, China
|
| Abstract: |
| OBJECTIVE To establish a reciprocating tube dissolution method to investigate the similarity of in vitro dissolution behavior of oxcarbazepine scored tablet preparations between the original and generic drugs, and to evaluate the differences in dose-specific pharmaceutical properties between the original and generic drugs. METHODS Using 250 mL of pH 1.2 hydrochloric acid solution, pH 4.5 acetate buffer, pH 6.8 phosphate buffer, and water(all 0.5% sodium dodecyl sulfate) as the dissolution medium, and reciprocating frequency of 10 dip min-1, using a reciprocating tube dissolution device to determine the dissolution curves of generic drugs and original research drugs, and combining the similarity factor(f2) method to evaluate the similarity of dissolution behavior between generic drugs and original research drugs, and compared the result with paddle method. The friability, weight variation and loss of mass of half-tablets were determined by friability tester and electronic balance through splitting by hand and by the cutting device respectively. RESULTS The f2 of generic drug A in 4 dissolution medium were higher than 50 and showed its similarity to original drug. While the generic drug B was not consistent with the dissolution behavior of original drug as its f2 factorswere all less than 50 in 4 dissolution. The post-segmentation weight variation, loss of mass and fragility of generic drug A and B were higher than those of the original drug. CONCLUSION The dissolution curve of oxcarbazepine half tablet preparation measured by the reciprocating cylinder method has good discrimination compared to the paddle method, and there is still a certain gap in the quality control of the generic drug in different doses compared to the original research drug. |
| Key words: oxcarbazepine scored tablet reciprocating cylinder method dissolution curve dosage segmentation |
|
|
|
|
