Accelerated wound healing and anti-inflammatory effects of physically cross linked polyvinyl alcohol-chitosan hydrogel containing honey bee venom in diabetic rats

被引:66
作者
Amin, Mohamed A. [1 ]
Abdel-Raheem, Ihab T. [2 ]
机构
[1] Al Azhar Univ, Fac Pharm, Dept Pharmaceut, Assiut, Egypt
[2] Damanhour Univ, Dept Pharmacol & Toxicol, Fac Pharm, Damanhour, Egypt
关键词
Chitosan; Bee venom; Wound healing; PVA; Anti-inflammatory; Hydroxyproline; IN-VIVO EVALUATION; CONTROLLED-RELEASE; STEREOCOMPLEX FORMATION; OXIDIZED ALGINATE; DEXTRAN HYDROGELS; OXIDATIVE STRESS; PROTEIN RELEASE; DRUG-RELEASE; LACTIC-ACID; FIBROBLASTS;
D O I
10.1007/s12272-013-0308-y
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Diabetes is one of the leading causes of impaired wound healing. The objective of this study was to develop a bee venom-loaded wound dressing with an enhanced healing and anti-inflammatory effects to be examined in diabetic rats. Different preparations of polyvinyl alcohol (PVA), chitosan (Chit) hydrogel matrix-based wound dressing containing bee venom (BV) were developed using freeze-thawing method. The mechanical properties such as gel fraction, swelling ratio, tensile strength, percentage of elongation and surface pH were determined. The pharmacological activities including wound healing and anti-inflammatory effects in addition to primary skin irritation and microbial penetration tests were evaluated. Moreover, hydroxyproline, glutathione and IL-6 levels were measured in the wound tissues of diabetic rats. The bee venom-loaded wound dressing composed of 10 % PVA, 0.6 % Chit and 4 % BV was more swellable, flexible and elastic than other formulations. Pharmacologically, the bee venom-loaded wound dressing that has the same pervious composition showed accelerated healing of wounds made in diabetic rats compared to the control. Moreover, this bee venom-loaded wound dressing exhibited anti-inflammatory effect that is comparable to that of diclofenac gel, the standard anti-inflammatory drug. Simultaneously, wound tissues covered with this preparation displayed higher hydroxyproline and glutathione levels and lower IL-6 levels compared to control. Thus, the bee venom-loaded hydrogel composed of 10 % PVA, 0.6 % Chit and 4 % BV is a promising wound dressing with excellent forming and enhanced wound healing as well as anti-inflammatory activities.
引用
收藏
页码:1016 / 1031
页数:16
相关论文
共 82 条
[1]
Wound Healing Activities of Rafflesia Hasseltii Extract in Rats [J].
Abdulla, Mahmood A. ;
Ahmed, Khaled A. ;
Ali, Hapipah M. ;
Noor, Suzita M. ;
Ismail, Salmah .
JOURNAL OF CLINICAL BIOCHEMISTRY AND NUTRITION, 2009, 45 (03) :304-308
[2]
Production of hydrogel wound dressings using gamma radiation [J].
Ajji, Z ;
Othman, I ;
Rosiak, JM .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 2005, 229 (3-4) :375-380
[3]
Alnahdi HS., 2012, J HEALTH SCI, V2, P33, DOI DOI 10.5923/J.HEALTH.20120204.03
[4]
Wound healing and anti-inflammatory activities of bee venom-chitosan blend films [J].
Amin, M. A. ;
Abdel-Raheem, I. T. ;
Madkor, H. R. .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2008, 18 (06) :424-430
[5]
Anilkumar J. S., 2011, IJARP, V2, P271
[6]
Topical Simvastatin Accelerates Wound Healing in Diabetes by Enhancing Angiogenesis and Lymphangiogenesis [J].
Asai, Jun ;
Takenaka, Hideya ;
Hirakawa, Satoshi ;
Sakabe, Jun-ichi ;
Hagura, Asami ;
Kishimoto, Saburo ;
Maruyama, Kazuichi ;
Kajiya, Kentaro ;
Kinoshita, Shigeru ;
Tokura, Yoshiki ;
Katoh, Norito .
AMERICAN JOURNAL OF PATHOLOGY, 2012, 181 (06) :2217-2224
[7]
Evaluation of an in situ forming hydrogel wound dressing based on oxidized alginate and gelatin [J].
Balakrishnan, B ;
Mohanty, M ;
Umashankar, PR ;
Jayakrishnan, A .
BIOMATERIALS, 2005, 26 (32) :6335-6342
[8]
Belhekar SN, 2013, INDIAN J PHARM SCI, V75, P217
[9]
Structure and interactions in chitosan hydrogels formed by complexation or aggregation for biomedical applications [J].
Berger, J ;
Reist, M ;
Mayer, JM ;
Felt, O ;
Gurny, R .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 57 (01) :35-52
[10]
Bonferoni MC, 2006, AAPS PHARMSCITECH, V7