Mucoadhesive, thermosensitive, prolonged-release vaginal gel for clotrimazole:: β-cyclodextrin complex

被引:107
作者
Bilensoy, Erem [1 ]
Rouf, M. Abdur
Vural, Imran
Sen, Murat
Hincal, A. Atilla
机构
[1] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Dept Chem, TR-06532 Ankara, Turkey
关键词
clotrimazole; thermosensitive; mucoadhesive; prolonged release; cyclodextrin; vaginal;
D O I
10.1208/pt070238
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to achieve a better therapeutic efficacy and patient compliance in the treatment for vaginitis. Clotrimazole ( 1%) has been formulated in a vaginal gel using the thermosensitive polymer Pluronic F127 ( 20%) together with mucoadhesive polymers such as Carbopol 934 and hydroxypropylmethylcellulose ( 0.2% for both). To increase its aqueous solubility, clotrimazole was incorporated as its inclusion complex with 1: 1 molar ratio with beta-cyclodextrin. The inclusion complex was thoroughly characterized using various techniques, including H-1 NMR spectroscopy, FT IR spectrophotometry, differential scanning calorimetry, scanning electron microscopy, phase solubility studies, and determination of stability constant ( k(1:1)). The gelation temperature and rheological behavior of different formulations at varying temperatures were measured. In vitro release profiles of the gels were determined in pH 5.5 citrate buffer. It was observed that complexation with cyclodextrin slowed down the release of clotrimazole considerably. Carbopol 934, on the other hand, was found to interact with beta-cyclodextrin, inducing precipitation. As far as rheological properties are concerned, thermosensitive in situ gelling was obtained with formulations containing drug: cyclodextrin complex rather than with free drug. Thus, the optimum formulation for a controlled-release thermosensitive and mucoadhesive vaginal gel was determined to be clotrimazole: beta-cyclodextrin 1% with 0.2% hydroxypropylmethylcellulose in Pluronic F127 gel ( 20%) providing continuous and prolonged release of active material above MIC values.
引用
收藏
页数:7
相关论文
共 30 条
  • [21] Direct formation of nanospheres from amphiphilic β-cyclodextrin inclusion complexes
    Memisoglu, E
    Bochot, A
    Özalp, M
    Sen, M
    Duchêne, D
    Hincal, AA
    [J]. PHARMACEUTICAL RESEARCH, 2003, 20 (01) : 117 - 125
  • [22] MIYAZAKI S, 1991, Yakuzaigaku, V51, P36
  • [23] PARK H, 1985, Journal of Controlled Release, V2, P47, DOI 10.1016/0168-3659(85)90032-X
  • [24] PHARMACOKINETIC FUNDAMENTALS OF VAGINAL TREATMENT WITH CLOTRIMAZOLE
    RITTER, W
    PATZSCHKE, K
    KRAUSE, U
    STETTENDORF, S
    [J]. CHEMOTHERAPY, 1982, 28 : 37 - 42
  • [25] SAWYER PR, 1975, DRUGS, V9, P424, DOI 10.2165/00003495-197509060-00003
  • [26] NMR studies of cyclodextrins and cyclodextrin complexes
    Schneider, HJ
    Hacket, F
    Rudiger, V
    Ikeda, H
    [J]. CHEMICAL REVIEWS, 1998, 98 (05) : 1755 - 1785
  • [27] Mechanisms of drug release from cyclodextrin complexes
    Stella, VJ
    Rao, VM
    Zannou, EA
    Zia, V
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 1999, 36 (01) : 3 - 16
  • [28] FORMATION AND ANTIMICROBIAL ACTIVITY OF COMPLEXES OF BETA-CYCLODEXTRIN AND SOME ANTIMYCOTIC IMIDAZOLE DERIVATIVES
    VANDOORNE, H
    BOSCH, EH
    LERK, CF
    [J]. PHARMACEUTISCH WEEKBLAD-SCIENTIFIC EDITION, 1988, 10 (02) : 80 - 85
  • [29] Controlled release of vancomycin from Poloxamer 407 gels
    Veyries, ML
    Couarraze, G
    Geiger, S
    Agnely, F
    Massias, L
    Kunzli, B
    Faurisson, F
    Rouveix, B
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 192 (02) : 183 - 193
  • [30] WOLFSSON AD, 2002, MODIFIED RELEASE DRU, P759