Composite alginate and gelatin based bio-polymeric wafers containing silver sulfadiazine for wound healing

被引:89
作者
Boateng, Joshua [1 ]
Burgos-Amador, Rocio [1 ]
Okeke, Obinna [1 ]
Pawar, Harshavardhan [1 ]
机构
[1] Univ Greenwich Medway, Fac Engn & Sci, Dept Pharmaceut Chem & Environm Sci, Chatham ME4 4TB, Kent, England
关键词
Bio-polymeric; Wafers; Wound healing; DRUG-DELIVERY-SYSTEMS; MUCOADHESIVE POLYMERS; DRESSINGS; FILMS; MEMBRANES;
D O I
10.1016/j.ijbiomac.2015.04.048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Lyophilized wafers comprising sodium alginate (SA) and gelatin (GE) (0/100, 75/25, 50/50, 25/75,0/100 SA/GE, respectively) with silver sulfadiazine (SSD, 0.1% w/w) have been developed for potential application on infected chronic wounds. Polymer-drug interactions and physical form were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD), respectively, while morphological structure was examined using scanning electron microscopy (SEM). Functional characteristics [(mechanical hardness and adhesion using texture analyzer, and swelling capacity)] of blank wafers were determined in order to select the optimal formulations for drug loading. Finally, the in vitro drug dissolution properties of two selected drug loaded wafers were investigated. There was an increase in hardness and a decrease in mucoadhesion with increasing GE content. FTIR showed hydrogen bonding and electrostatic interaction between carboxyl of SA and amide of GE but no interaction between the polymers and drug was observed, with XRD showing that SSD remained crystalline during gel formulation and freeze-drying. The results suggest that 75/25 SA/GE formulations are the ideal formulations due to their uniformity and optimal mucoadhesivity and hydration. The drug loaded wafers showed controlled release of SSD over a 7 h period which is expected to reduce bacterial load within infected wounds. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 71
页数:9
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