Suppr超能文献

儿科迷你片剂:预测填充错误的潜在风险。

Pediatric Mini-Tablets: Predicting the Hidden Risk of Fill Errors.

作者信息

Gerberich Brandon G, Okoh Grace A, DiNunzio James C, Lowinger Michael B

机构信息

Oral Formulation Sciences, Merck & Co., Inc., Kenilworth, NJ 07065, USA.

出版信息

Pharmaceutics. 2023 Feb 10;15(2):594. doi: 10.3390/pharmaceutics15020594.

Abstract

Compressed mini-tablets in sachets or capsules are an increasingly prevalent oral solid dosage form for pediatric products. While resembling adult tablets, additional care is required to control weight and potency (blend uniformity) variation due to their small size (≤2.5 mm average diameter). Additionally, sachet fill count errors complicate dose accuracy as they are difficult to resolve with weight-checking equipment. This study quantified the probability of failing content uniformity (CU) specifications (which results in the inability to release a batch) defined in USP <905> using a Monte Carlo computational model. Failure risk was modeled as a function of sachet fill count, mini-tablet weight, potency distribution, and fill error frequency. The model allows product developers to (1) determine appropriate fill counts based on anticipated product weight and potency relative standard deviation (RSD), (2) set fill error probability tolerances for sachet filling processes, (3) identify CU improvement opportunities, and (4) quantify the probability of CU failure informing risk management activities and risk disclosure for regulatory agencies. A representative product with weight and potency RSD no greater than 5%, fill count of 1-4 mini-tablets per sachet, and fill error probability per mini-tablet filled of 0.1% may experience CU batch failure probabilities as high as 8.23%, but only 0.283% if the fill count is increased to 5-10 mini-tablets per sachet. Generally, fill counts of less than five mini-tablets per sachet should be avoided where possible.

摘要

袋装或胶囊装的压缩微型片剂是儿科产品中越来越普遍的口服固体剂型。虽然它们与成人片剂相似,但由于尺寸较小(平均直径≤2.5毫米),需要格外注意控制重量和效价(混合均匀度)的变化。此外,袋装填充计数错误会使剂量准确性复杂化,因为难以用重量检查设备解决这些问题。本研究使用蒙特卡洛计算模型量化了美国药典<905>中定义的含量均匀度(CU)规格不符合(导致批次无法放行)的概率。将失败风险建模为袋装填充计数、微型片剂重量、效价分布和填充错误频率的函数。该模型使产品开发人员能够:(1)根据预期产品重量和效价相对标准偏差(RSD)确定合适的填充计数;(2)为袋装填充过程设定填充错误概率公差;(3)识别CU改进机会;(4)量化CU失败的概率,为风险管理活动和向监管机构披露风险提供依据。一种代表性产品,其重量和效价RSD不超过5%,每袋填充1-4片微型片剂,每片微型片剂的填充错误概率为0.1%,可能会有高达8.23%的CU批次失败概率,但如果每袋填充计数增加到5-10片微型片剂,失败概率仅为0.283%。一般来说,应尽可能避免每袋填充少于五片微型片剂的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ce5/9961976/221d0125b96a/pharmaceutics-15-00594-g003.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验