Influence of sample characteristics on quantification of carbamazepine hydrate formation by X-ray powder diffraction and Raman spectroscopy

被引:39
作者
Tian, F.
Zhang, F.
Sandler, N.
Gordon, K. C.
McGoverin, C. M.
Strachan, C. J.
Saville, D. J.
Rades, T.
机构
[1] Univ Otago, Sch Pharm, Dunedin, New Zealand
[2] Univ Otago, Dept Chem, Dunedin, New Zealand
[3] Univ Helsinki, DDTC, FIN-00014 Helsinki, Finland
关键词
Raman spectroscopy; X-ray powder diffraction; carbamazepine; carbamazepine dihydrate; quantification;
D O I
10.1016/j.ejpb.2006.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to assess the suitability of two widely utilized solid state characterization techniques namely powder X-ray diffraction (XRPD) and Raman spectroscopy, in polymorph detection and quantification for carbamazepine anhydrate and dihydrate mixtures. The influences of particle size, particle morphology, mixing, and in particular, surface bias on quantitation were investigated. Binary mixtures of carbarnazepine anhydrate (form III) and dihydrate were prepared and analyzed using both XRPD and Raman spectroscopy in combination with partial least squares analysis. lt was found that in principle both XRPD and Raman spectroscopy could be used to build calibration models for quantitative analysis, and a satisfactory correlation between the two techniques could be achieved. However, Raman spectroscopy appeared to be a more reliable quantification method because problems such as different particle size, morphology, and special distribution of the two solid state forms of the drug seemed to have no significant influence on Raman scattering in this study. The robust nature of Raman analysis greatly facilitates the whole quantification process from the preparation of calibration models to the quantification of in situ CBZ-DH conversion. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:466 / 474
页数:9
相关论文
共 40 条
[1]   Laser Raman spectroscopic analysis of polymorphic forms in microliter fluid volumes [J].
Anquetil, PA ;
Brenan, CJH ;
Marcolli, C ;
Hunter, IW .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (01) :149-160
[2]   Development of sampling methods for Raman analysis of solid dosage forms of therapeutic and illicit drugs [J].
Bell, SEJ ;
Beattie, JR ;
McGarvey, JJ ;
Peters, KL ;
Sirimuthu, NMS ;
Speers, SJ .
JOURNAL OF RAMAN SPECTROSCOPY, 2004, 35 (05) :409-417
[3]   Micro X-ray diffraction on capillary powder samples: a novel and effective technique for overcoming preferred orientation [J].
Bergese, P ;
Bontempi, E ;
Colombo, I ;
Depero, LE .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2001, 34 :663-665
[4]  
Brittain H.G., 1995, PHYS CHARACTERIZATIO, P1
[5]   Characterization of the solid-state: spectroscopic techniques [J].
Bugay, DE .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 48 (01) :43-65
[6]   PHARMACEUTICAL SOLIDS - A STRATEGIC APPROACH TO REGULATORY CONSIDERATIONS [J].
BYRN, S ;
PFEIFFER, R ;
GANEY, M ;
HOIBERG, C ;
POOCHIKIAN, G .
PHARMACEUTICAL RESEARCH, 1995, 12 (07) :945-954
[7]   Full phase analysis of portland clinker by penetrating synchrotron powder diffraction [J].
de la Torre, AG ;
Cabeza, A ;
Calvente, A ;
Bruque, S ;
Aranda, MAG .
ANALYTICAL CHEMISTRY, 2001, 73 (02) :151-156
[8]   A COMPARISON OF FOURIER-TRANSFORM INFRARED AND NEAR-INFRARED FOURIER-TRANSFORM RAMAN-SPECTROSCOPY FOR QUANTITATIVE MEASUREMENTS - AN APPLICATION IN POLYMORPHISM [J].
DEELEY, CM ;
SPRAGG, RA ;
THRELFALL, TL .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1991, 47 (9-10) :1217-1223
[9]   Comparison of the four anhydrous polymorphs of carbamazepine and the crystal structure of form I [J].
Grzesiak, AL ;
Lang, MD ;
Kim, K ;
Matzger, AJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (11) :2260-2271
[10]  
Han J, 1998, Pharm Dev Technol, V3, P587, DOI 10.3109/10837459809028643