Weak Hydrogen Bonding Interactions Influence Slip System Activity and Compaction Behavior of Pharmaceutical Powders

被引:19
|
作者
Khomane, Kailas S. [1 ]
Bansal, Arvind K. [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmaceut, Mohali, Punjab, India
关键词
crystal structure; crystal polymorphism; slip plane system; compaction; mechanical properties; CH center dot center dot center dot O interactions; compression; powder technology; weak hydrogen bonding; RANITIDINE HYDROCHLORIDE POLYMORPHS; CRYSTAL-STRUCTURE; MECHANICAL-PROPERTIES; TABLETING PROPERTIES; EQUATIONS;
D O I
10.1002/jps.23751
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Markedly different mechanical behavior of powders of polymorphs, cocrystals, hydrate/anhydrate pairs, or structurally similar molecules has been attributed to the presence of active slip planes system in their crystal structures. Presence of slip planes in the crystal lattice allows easier slip under the applied compaction pressure. This allows greater plastic deformation of the powder and results into increased interparticulate bonding area and greater tensile strength of the compacts. Thus, based on this crystallographic feature, tableting performance of the active pharmaceutical ingredients can be predicted. Recently, we encountered a case where larger numbers of CH<bold></bold>O type interactions across the proposed slip planes hinder the slip and thus resist plastic deformation of the powder under the applied compaction pressure. Hence, attention must be given to these types of interactions while identifying slip planes by visualization method. Generally, slip planes are visualized as flat layers often strengthened by a two-dimensional hydrogen-bonding network within the layers or planes. No hydrogen bonding should exist between these layers to consider them as slip planes. Moreover, one should also check the presence of CH<bold></bold>O type interactions across these planes. Mercury software provides an option for visualization of these weak hydrogen bonding interactions. Hence, caution must be exercised while selecting appropriate solid form based on this crystallographic feature. (c) 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:4242-4245, 2013
引用
收藏
页码:4242 / 4245
页数:4
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