Functionally modified gelatin microspheres impregnated collagen scaffold as novel wound dressing to attenuate the proteases and bacterial growth

被引:47
作者
Adhirajan, N. [1 ]
Shanmugasundaram, N. [1 ]
Shanmuganathan, S. [2 ]
Babu, Mary [1 ]
机构
[1] TICEL Biopk, Cent Leather Res Inst, Biomat Div, Madras 600113, Tamil Nadu, India
[2] Sri Ramachandra Univ, Coll Pharm, Madras, Tamil Nadu, India
关键词
Gelatin microspheres; Matrix metalloproteinase; Collagen; Wound dressing; Wound healing; IN-VITRO RELEASE; SILVER SULFADIAZINE; AMINATED GELATIN; DELIVERY-SYSTEM; DESIGN; MATRIX; METALLOPROTEINASES; METHOTREXATE; PEPTIDE; FLUID;
D O I
10.1016/j.ejps.2008.09.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An attempt was made to develop a new therapeutic delivery system which would play a dual role of attenuating MMP activity in the wounds and also prevent infection by controlled delivery of antimicrobials. A catechol type MMP inhibitor 2,3-dihydroxybenzoic acid (DHBA) was conjugated to gelatin microspheres using EDC/NHS as coupling agents. The potential of the modified gelatin microspheres (DHB-MS) to attenuate the proteases such as MMP 2 and MMP 9 in the diabetic wound tissues was investigated by gelatin zymography. Further the modified microspheres were loaded with doxycycline and impregnated in a reconstituted collagen scaffold as novel wound dressing. The in vitro release behavior of doxycycline from both DHB-MS and DHB-MS impregnated Collagen scaffold was investigated. DHB-MS when incubated with the tissue lysate for 6 h displayed the complete inhibition of the MMPs in the tissue lysate. The in vitro drug release studies from the collagen scaffold exhibited the burst release of 44%, exerted immediate chemo prophylaxis and sustained delivery for 72h. The MTT assay and fluorescent labeling with calcein AM indicated that the DHB-MS is biocompatible to human foreskin fibroblasts, Thus the system developed provides wider scope to control the pathogens involved in infection and also the excess matrix degradation. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:235 / 245
页数:11
相关论文
共 32 条
[1]   Gelatin microspheres cross-linked with EDC as a drug delivery system for doxycyline: Development and characterization [J].
Adhirajan, N. ;
Shanmugasundaram, N. ;
Babu, Mary .
JOURNAL OF MICROENCAPSULATION, 2007, 24 (07) :659-671
[2]   Chemically modified chitosans as enzyme inhibitors [J].
Bernkop-Schnürch, A ;
Kast, CE .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 52 (02) :127-137
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   THE DETERMINATION OF EPSILON-AMINO GROUPS IN SOLUBLE AND POORLY SOLUBLE PROTEINACEOUS MATERIALS BY A SPECTROPHOTOMETRIC METHOD USING TRINITROBENZENESULFONIC ACID [J].
BUBNIS, WA ;
OFNER, CM .
ANALYTICAL BIOCHEMISTRY, 1992, 207 (01) :129-133
[5]   Mechanism of action of PROMOGRAN, a protease modulating matrix, for the treatment of diabetic foot ulcers [J].
Cullen, B ;
Smith, R ;
McCulloch, E ;
Silcock, D ;
Morrison, L .
WOUND REPAIR AND REGENERATION, 2002, 10 (01) :16-25
[6]   Cross-linking of dermal sheep collagen using a water-soluble carbodiimide [J].
Damink, LHHO ;
Dijkstra, PJ ;
vanLuyn, MJA ;
vanWachem, PB ;
Nieuwenhuis, P ;
Feijen, J .
BIOMATERIALS, 1996, 17 (08) :765-773
[7]   Gelatin microspheres: Influence of preparation parameters and thermal treatment on chemico-physical and biopharmaceutical properties [J].
Esposito, E ;
Cortesi, R ;
Nastruzzi, C .
BIOMATERIALS, 1996, 17 (20) :2009-2020
[8]   MINIMAL INHIBITORY CONCENTRATIONS OF 34 ANTI-MICROBIAL AGENTS FOR CONTROL STRAINS ESCHERICHIA-COLI ATCC 25922 AND PSEUDOMONAS-AERUGINOSA ATCC 27853 [J].
FASS, RJ ;
BARNISHAN, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1979, 16 (05) :622-624
[9]  
Franz T J, 1978, Curr Probl Dermatol, V7, P58
[10]   Effect of microbial siderophores on matrix metalloproteinase-2 activity [J].
Gendron, R ;
Grenier, D ;
Sorsa, T ;
Uitto, VJ ;
Mayrand, D .
JOURNAL OF PERIODONTAL RESEARCH, 1999, 34 (01) :50-53