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探究晶体尺寸和形状对冲压堵塞影响的分子机理。

Toward a Molecular Understanding of the Impact of Crystal Size and Shape on Punch Sticking.

机构信息

Pharmaceutical Materials Science and Engineering Laboratory, Department of Pharmaceutics, College of Pharmacy, University of Minnesota, 9-127B Weaver-Densford Hall, 308 Harvard Street S.E., Minneapolis, Minnesota 55455, United States.

Pfizer Worldwide Research and Development, Sandwich CT13 9ND, U.K.

出版信息

Mol Pharm. 2020 Apr 6;17(4):1148-1158. doi: 10.1021/acs.molpharmaceut.9b01185. Epub 2020 Mar 5.

Abstract

Punch sticking during tablet manufacturing is a common problem facing the pharmaceutical industry. Using several model compounds, effects of crystal size and shape of active pharmaceutical ingredients (API) on punch sticking propensity were systematically investigated in this work to provide molecular insights into the punch-sticking phenomenon. In contrast to the common belief that smaller API particles aggravate punch sticking, results show that particle size reduction can either reduce or enhance API punch sticking, depending on the complex interplay among the particle surface area, plasticity, cohesive strength, and specific surface functional groups. Therefore, other factors, such as crystal mechanical properties, surface chemistry of crystal facets exposed to the punch face, and choice of excipients in a formulation, should be considered for a more reliable prediction of the initiation and progression of punch sticking. The exposure of strong electronegative groups to the punch face facilitates the onset of sticking, while higher plasticity and cohesive strength aggravate sticking.

摘要

压片过程中出现粘冲是制药行业面临的一个常见问题。本工作中使用了几种模型化合物,系统地研究了原料药(API)的晶体尺寸和形状对粘冲倾向的影响,以期深入了解粘冲现象。与普遍认为的小粒径 API 颗粒会加剧粘冲的观点相反,结果表明,颗粒粒径减小会减轻或加剧 API 粘冲,这取决于颗粒表面积、塑性、内聚强度和比表面积官能团之间的复杂相互作用。因此,在更可靠地预测粘冲的起始和发展时,还应考虑其他因素,如晶体力学性能、暴露于冲头表面的晶面的表面化学性质以及配方中赋形剂的选择。暴露于冲头表面的强电负性基团有利于粘冲的发生,而较高的塑性和内聚强度会加剧粘冲。

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