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Evaluation of Effects of Pharmaceutical Processing on Structural Disorders of Active Pharmaceutical Ingredient Crystals Using Nanoindentation and High-Resolution Total Scattering Pair Distribution Function Analysis

机译:纳米压痕和高分辨率总散射对分布函数分析评价药物加工对药物活性成分晶体结构失序的影响

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摘要

Pharmaceutical unit operations such as milling and compaction can often generate disordered regions in crystals of active pharmaceutical ingredients (APIs). This may lead to changes in a number of important pharmaceutical properties including dissolution, stability, hygroscopicity, and so on. It is therefore important for pharmaceutical industry to evaluate the effects of pharmaceutical processing on API structural orders, and to investigate and develop analytical tools that are capable of accurately detecting and assessing subtle process-induced structural disorders in pharmaceutical crystals. In this study, nanoindentation was first used to determine the intrinsic mechanical properties including hardness and Young's modulus of two API crystals, compounds 1 and 2. These crystals of different mechanical properties were then milled and compacted under various conditions. The resulting structural disorders in these crystals were subsequently evaluated using synchrotron-based high-resolution total scattering pair distribution function (TS-PDF) analysis. Furthermore, principal component analysis was applied to the PDF data to assess the relative extents of disorders in the API crystals, which showed a good correlation with the process conditions. The study demonstrates that high-resolution TS-PDF analysis coupled with nanoindentation measurement is a valuable and effective tool for detecting and assessing process-induced subtle structural disorders in API crystals. (c) 2014 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 103:3879-3890, 2014
机译:诸如研磨和压实之类的药物单元操作通常会在活性药物成分(API)的晶体中产生无序区域。这可能导致许多重要的药物特性发生变化,包括溶解,稳定性,吸湿性等。因此,对于制药行业而言,评估药物加工对API结构顺序的影响以及研究和开发能够准确地检测和评估药物晶体中由过程引起的细微结构异常的分析工具非常重要。在这项研究中,首先使用纳米压痕确定两种API晶体(化合物1和2)的固有机械性能,包括硬度和杨氏模量。然后将这些具有不同机械性能的晶体在各种条件下进行研磨和压实。随后使用基于同步加速器的高分辨率总散射对分布函数(TS-PDF)分析,评估了这些晶体中产生的结构紊乱。此外,将主成分分析应用于PDF数据以评估API晶体中无序的相对程度,这显示出与工艺条件的良好相关性。这项研究表明,高分辨率的TS-PDF分析与纳米压痕测量相结合,是检测和评估API晶体中由过程引起的细微结构失调的有价值且有效的工具。 (c)2014年Wiley Periodicals,Inc.和美国药剂师协会J Pharm Sci 103:3879-3890,2014年

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