A novel method for deriving true density of pharmaceutical solids including hydrates and water-containing powders

被引:99
作者
Sun, CQ [1 ]
机构
[1] Pfizer Global Res & Dev, Kalamazoo, MI 49001 USA
关键词
true density; porosity; tableting; modified Heckel equation; nonlinear regression;
D O I
10.1002/jps.10595
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
True density is commonly measured using helium pyenometry. However, most water-containing powders, for example, hydrates, amorphous drugs and excipients, and most tablet formulations, release water when exposed to a dry helium atmosphere. Because released water brings significant errors to the measured true density and drying alters the nature of water-containing solids, the helium pycnometry is not suitable for those substances. To overcome this problem, a novel method has been developed to accurately calculate powder true density from compaction data. No drying treatment of powder samples is required. Consequently, the true density thus obtained is relevant to tableting characterization studies because no alteration to the solid is induced by drying. This method involves nonlinear regression of compaction pressure-tablet density data based on a modified Heckel equation. When true density values of water-free powders derived by this novel method were plotted against values measured using pycnometry, a regression line with slope close to unity and intercept close to zero was obtained. Thus, the validity of this method was supported. Using this new method, it was further demonstrated that helium pycnometry always overestimates true densities of water containing powders, for example, hydrates, microcrystalline cellulose (MCC), and tablet formulations. The calculated true densities of powders were the same for different particle shapes and sizes of each material. This further suggests that true density values calculated using this novel method are characteristic of given materials and independent of particulate properties. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:646 / 653
页数:8
相关论文
共 18 条
[11]  
Sun C, 2001, J PHARM SCI, V90, P569, DOI 10.1002/1520-6017(200105)90:5<569::AID-JPS1013>3.0.CO
[12]  
2-4
[13]  
SUN C, 2004, IN PRESS PHARM RES
[14]  
SUN C, 2002, AAPS PHARMSCI, V4, pW4299
[15]   Effects of initial particle size on the tableting properties of L-lysine monohydrochloride dihydrate powder [J].
Sun, CQ ;
Grant, DJW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 215 (1-2) :221-228
[16]   Influence of crystal structure on the tableting properties of sulfamerazine polymorphs [J].
Sun, CQ ;
Grant, DJW .
PHARMACEUTICAL RESEARCH, 2001, 18 (03) :274-280
[18]   CRYSTAL STRUCTURE OF L-LYSINE MONOHYDROCHLORIDE DIHYDRATE [J].
WRIGHT, DA ;
MARSH, RE .
ACTA CRYSTALLOGRAPHICA, 1962, 15 (JAN10) :54-&