Bioengineered mannan sulphate capped silver nanoparticles for accelerated and targeted wound healing: Physicochemical and biological investigations

被引:20
|
作者
Mugade, Megha [1 ]
Patole, Milind [2 ]
Pokharkar, Varsha [1 ]
机构
[1] Bharati Vidyapeeth Univ, Poona Coll Pharm, Dept Pharmaceut, Pune 411038, Maharashtra, India
[2] Natl Ctr Cell Sci, NCCS Complex,Pune Univ Campus, Pune 411007, Maharashtra, India
关键词
Mannose receptor; Mannan sulphate; Silver nanoparticles; Biocompatibility; Targeting; Wound model; MACROPHAGE MANNOSE RECEPTOR; GREEN SYNTHESIS; IN-VITRO; GOLD NANOPARTICLES; LEAF EXTRACT; ANTIBACTERIAL; DELIVERY; CYTOTOXICITY; STABILITY; LECTIN;
D O I
10.1016/j.biopha.2017.04.017
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In the present study, surface functionalized mannan sulphate silver nanoparticles (MS-AgNPs) were prepared and assessed for their wound healing potential. 20 nm sized, spherical MS-AgNPs were prepared by one pot synthesis approach wherein the sulphated polysaccharide mannan sulphate (MS) played dual role of reducing as well as capping agent. The crystalline MS-AgNPs exhibited surface plasmon resonance centered at 400 nm along with -32.40 mV zeta potential. These stable MS-AgNPs showed enhanced cytocompatibility, targeting potential and cellular uptake in murine macrophages, human skin fibroblasts and human keratinocytes as compared to citrate reduced silver nanoparticles (CAgNPs). In the in vivo excision and incision wound models, MS-AgNPs as hydrogel formulations indicated better efficacy than the conventional and marketed silver formulations. Thus, the synthesized MS-AgNPs depicted a promising potential for site-specific topical delivery in accelerated wound therapy. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:95 / 110
页数:16
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