Visualizing the conversion of carbamazepine in aqueous suspension with and without the presence of excipients: A single crystal study using SEM and Raman microscopy

被引:44
作者
Tian, F.
Sandler, N.
Gordon, K. C.
McGoverin, C. M.
Reay, A.
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 Otago, Dept Geol, Dunedin, New Zealand
[4] Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, Helsinki, Finland
基金
芬兰科学院;
关键词
hydration; carbamazepine; single crystal; dihydrate; scanning electron microscopy; Raman microscopy; excipient;
D O I
10.1016/j.ejpb.2006.05.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Visual observations of the hydration process of single carbamazepine (CBZ) crystals in water and in various excipient solutions [(1% w/v) - hydroxypropyl cellulose (HPC), poly(vinyl pyrrolidone) (PVP), sodium carboxymethyleellulose (CMC) at pH 7.5 and 3.0, and polyethylene glycol (PEG)] using scanning electron microscopy (SEM) are reported in this paper. Raman microscopy was used to confirm the chemical structures of the unconverted CBZ and the CBZ dihydrate (DH) needles. It was found that defect structures were a more important driving force than the nature of crystal faces for the initiation of the hydration, but face differences became obvious after 6 It immersion. The biggest crystal face grown from methanol, (100), was the slowest one to be covered with DH needles. A comparison of the molecular arrangements along the three crystal faces [(100), (010) and (001)] was carried out using crystal structure visualization software, and fewer polar groups exposed on the (100) face than on the (001) and (010) faces were found, explaining the comparatively weak interaction of the (100) face with water during hydration. Furthermore, investigation of the influence of excipients on the hydration of CBZ showed that both HPC and PVP strongly inhibited conversion, and no conversion of CBZ to DH was found after 18 It immersion in water. PEG and CMC (pH 7.5) were less potent inhibitors than HPC and PVP, and DH needles were observed on all the faces except the (100) face after 18 It immersion. No conversion was detected for the crystal immersed in CMC solution at pH 3.0. This is likely to be caused by the decreased polarity of CMC in water at pH 3.0 (pK(a),cmc = 4.3), and thus a higher surface adsorption of CMC to the CBZ crystals in dispersion. The influence of excipients on the conversion of CBZ observed in this study agreed well with our previous quantitative studies using Raman spectroscopy. In this study, visual observation using electron microscopy has been demonstrated to be a unique and powerful tool to improve our understanding of polymorphic conversions of CBZ in aqueous suspension. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:326 / 335
页数:10
相关论文
共 31 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]   Fluorescence studies of the transformation of carbamazepine anhydrate form III to its dihydrate phase [J].
Brittain, HG .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (02) :375-383
[3]   The relationship between crystal growth and defect structure: a study of potassium hydrogen phthalate using x-ray topography and atomic force microscopy [J].
Ester, GR ;
Price, R ;
Halfpenny, PJ .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 1999, 32 (10A) :A128-A132
[4]  
Han J, 1998, Pharm Dev Technol, V3, P587, DOI 10.3109/10837459809028643
[5]   STRUCTURE OF CARBAMAZEPINE - "5H-DIBENZ[B.F]AZEPINE-5-CARBOXAMIDE [J].
HIMES, VL ;
MIGHELL, AD ;
DECAMP, WH .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE, 1981, 37 (DEC) :2242-2245
[6]   Investigating the structure and properties of hydrated hydroxypropyl methylcellulose and egg albumin matrices containing carbamazepine:: EPR and NMR study [J].
Katzhendler, I ;
Mäder, K ;
Azoury, R ;
Friedman, M .
PHARMACEUTICAL RESEARCH, 2000, 17 (10) :1299-1308
[7]   The effect of egg albumin on the crystalline properties of carbamazepine in sustained release hydrophilic matrix tablets and in aqueous solutions [J].
Katzhendler, I ;
Azoury, R ;
Friedman, M .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (03) :331-343
[8]   Physicochemical properties and bioavailability of carbamazepine polymorphs and dihydrate [J].
Kobayashi, Y ;
Ito, S ;
Itai, S ;
Yamamoto, K .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 193 (02) :137-146
[9]   FORMATION OF DIHYDRATE FROM CARBAMAZEPINE ANHYDRATE IN AQUEOUS CONDITIONS [J].
LAINE, E ;
TUOMINEN, V ;
ILVESSALO, P ;
KAHELA, P .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1984, 20 (03) :307-314
[10]  
LUHTALA S, 1992, ACTA PHARM NORDICA, V4, P85