Evaluation of Mucoadhesive Hydrogels Loaded with Diclofenac Sodium-Chitosan Microspheres for Rectal Administration

被引:60
作者
El-Leithy, Eman S. [1 ]
Shaker, Dalia S. [1 ]
Ghorab, Mohamed K. [1 ]
Abdel-Rashid, Rania S. [1 ]
机构
[1] Helwan Univ, Coll Pharm, Dept Pharmaceut, Cairo, Egypt
来源
AAPS PHARMSCITECH | 2010年 / 11卷 / 04期
关键词
carbopol; 934; diclofenac sodium-chitosan microspheres; histopathological study; HPMC; rectal mucoadhesive hydrogel; CONTROLLED-RELEASE; LIQUID SUPPOSITORY; DRUG-RELEASE; IN-VIVO; BIOAVAILABILITY; ABSORPTION; RATS; FORMULATIONS; DELIVERY; INVITRO;
D O I
10.1208/s12249-010-9544-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Considering the advantageous for the rectal administration of non-steroidal anti-inflammatory drugs, the objective of this study was to formulate and evaluate rectal mucoadhesive hydrogels loaded with diclofenac-sodium chitosan (DFS-CS) microspheres. Hydroxypropyl methylcellulose (HPMC; 5%, 6%, and 7% w/w) and Carbopol 934 (1% w/w) hydrogels containing DFS-CS microspheres equivalent to 1% w/w active drug were prepared. The physicochemical characterization revealed that all hydrogels had a suitable pH for rectal application (6.5-7.4). The consistency of HPMC hydrogels showed direct proportionality to the concentration of the gelling agent, while carbopol 934 gel showed its difficulty for rectal administration. Farrow's constant for all hydrogels were greater than one indicating pseudoplastic flow. In vitro drug release from the mucoadhesive hydrogel formulations showed a controlled drug release pattern, reaching 34.6-39.7% after 6 h. The kinetic analysis of the release data revealed that zero-order was the prominent release mechanism. The mucoadhesion time of 7% w/w HPMC hydrogel was 330 min, allowing the loaded microspheres to be attached to the surface of rectal mucosa. Histopathological examination demonstrated the lowest irritant response to the hydrogel loaded with DFS-CS microspheres in response to other forms of the drug.
引用
收藏
页码:1695 / 1702
页数:8
相关论文
共 30 条
  • [1] Sustained release of diclofenac from polymer-containing suppository and the mechanism involved
    Azechi, Y
    Ishikawa, K
    Mizuno, N
    Takahashi, K
    [J]. DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (11) : 1177 - 1183
  • [2] Preparation and characterization of chitosan microspheres as drug carrier for prednisolone sodium phosphate as model for antiinflammatory drugs
    Berthold, A
    Cremer, K
    Kreuter, J
    [J]. JOURNAL OF CONTROLLED RELEASE, 1996, 39 (01) : 17 - 25
  • [3] Bravo SA, 2002, J PHARM PHARM SCI, V5, P213
  • [4] Dodov Marija Glavas, 2005, Acta Pharmaceutica (Zagreb), V55, P251
  • [5] El-Leithy ES, 2010, DRUG DISCOV THER, V4, P208
  • [6] Formulation and evaluation of diclofenac sodium buccoadhesive discs
    El-Samaligy, MS
    Yahia, SA
    Basalious, EB
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 286 (1-2) : 27 - 39
  • [7] ElHady S.S., 2003, Saudi Pharm. J, V11, P159
  • [8] Comparative in vitro-in vivo study of two quinine rectal gel formulations
    Fawaz, F
    Koffi, A
    Guyot, M
    Millet, P
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 280 (1-2) : 151 - 162
  • [9] CONTROLLED-RELEASE OF SUBSTITUTED BENZOIC AND NAPHTHOIC ACIDS USING CARBOPOL(R) GELS - MEASUREMENT OF DRUG CONCENTRATION PROFILES AND CORRELATION TO RELEASE RATE KINETICS
    FRENCH, DL
    HAGLUND, BO
    HIMMELSTEIN, KJ
    MAUGER, JW
    [J]. PHARMACEUTICAL RESEARCH, 1995, 12 (10) : 1513 - 1520
  • [10] GONCALVES VL, 2005, CIENC TECNOL, V15, P6