Characterization of amorphous solids with weak glass transitions using high ramp rate differential scanning calorimetry

被引:26
作者
Katayama, Derrick S. [3 ]
Carpenter, John F. [3 ]
Manning, Mark Cornell [4 ]
Randolph, Theodore W. [5 ]
Setlow, Peter [6 ]
Menard, Kevin P. [1 ,2 ]
机构
[1] Univ N Texas, Dept Mat Sci & Engn, Denton, TX 76203 USA
[2] Perkin Elmer Instruments, Shelton, CT USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Pharmaceut Sci, Ctr Pharmaceut Biotechnol, Denver, CO USA
[4] Legacy Biodesign LLC, Loveland, CO USA
[5] Univ Colorado, Dept Chem & Biol Engn, Ctr Pharmaceut Biotechnol, Boulder, CO 80503 USA
[6] Univ Connecticut, Ctr Hlth, Dept Mol Microbial & Struct Biol, Farmington, CT 06032 USA
关键词
amorphous; solid state; freeze drying/lyophilization; calorimetry (DSC); biotechnology;
D O I
10.1002/jps.20991
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Measurement of the glass transition temperature (T-g) of proteins and other high molecular weight polymers in the amorphous state is often difficult, since the transition is extremely weak, that is, the Delta C-p at the glass transition temperature is small. For example, little is known about the solid-state properties of hydroxyethyl starch (HES), which is beginning to become more commonly evaluated as a bulking agent in pharmaceutical products. For weak thermal events, such as the change in heat capacity at the T-g of a pure protein or large synthetic polymer, increased heating rate should produce greater sensitivity in terms of heat flow. Recent innovations in rapid scanning technology for differential scanning calorimetry (DSC) allow measurements on materials where the thermal events are difficult to detect by conventional DSC. In the current study, measurements of the T-g of proteins in the solid state, amorphous pharmaceutical excipients which have small Delta C-p at the glass transition temperature, and bacterial spores, have all been made using high ramp rate DSC, providing information on materials that was inaccessible using conventional DSC methods. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1013 / 1024
页数:12
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