Effect of Processing Route on the Surface Properties of Amorphous Indomethacin Measured by Inverse Gas Chromatography

被引:21
作者
Burnett, D. J. [1 ]
Khoo, J. [2 ]
Naderi, M. [2 ]
Heng, J. Y. Y. [3 ]
Wang, G. D. [3 ]
Thielmann, F. [4 ]
机构
[1] Surface Measurement Syst Ltd, Allentown, PA 18103 USA
[2] Surface Measurement Syst Ltd, Alperton, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Chem Engn, London SW7 2AZ, England
[4] Novartis PharmaAG, Basel, Switzerland
关键词
heterogeneity; indomethacin; inverse gas chromatography; surface disorder; surface energy; SALBUTAMOL SULFATE; CONTACT-ANGLE; FREE-ENERGY; HETEROGENEITY; POLYMORPHISM; CRYSTALLINE; ENERGETICS; CHEMISTRY;
D O I
10.1208/s12249-012-9881-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to investigate the effect of processing route (i.e., quench cooling and ball milling) on the surface energy heterogeneity and surface chemistry of indomethacin (IMC). Recently developed inverse gas chromatography (IGC) methodology at finite concentrations was employed to determine the surface energy distributions of crystalline, quench cooled and milled IMC samples. Surface properties of crystalline and processed IMC were measurably different as determined by the IGC and other conventional characterization techniques: differential scanning calorimetry and powder X-ray diffraction. Quench cooled IMC was in fully amorphous form. Milled IMC showed no amorphous character by calorimetric or X-ray diffraction studies. It was demonstrated that both processed IMC samples were energetically more active than the crystalline IMC. In particular, milled IMC exhibited a relatively higher dispersive surface energy and higher surface basicity (electron donor capability). This may be attributed to the creation of surface defect sites or exposure of higher energy crystal facets during the milling process. This study confirms that processing route has notable influence on the surface energy distribution and surface acid-base character. IGC was demonstrated as a powerful technique for investigating surface properties of real-world, heterogeneous pharmaceutical materials.
引用
收藏
页码:1511 / 1517
页数:7
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