Nanoparticle-mediated interplay of chitosan and melatonin for improved wound epithelialisation

被引:61
作者
Blazevic, Filip [1 ]
Milekic, Tamara [1 ]
Romic, Marieta Duvnjak [2 ]
Juretic, Marina [1 ]
Pepic, Ivan [1 ]
Filipovic-Grcic, Jelena [1 ]
Lovric, Jasmina [1 ]
Hafner, Anita [1 ]
机构
[1] Univ Zagreb, Fac Pharm & Biochem, Dept Pharmaceut, Zagreb 41000, Croatia
[2] PLIVA Croatia Ltd, R&D, Zagreb, Croatia
关键词
Melatonin; Chitosan; Nanoparticles; Wound healing; Scratch test; Keratinocytes; MOLECULAR-WEIGHT; IN-VITRO; DRUG-RELEASE; SKIN; FIBROBLASTS; FORMULATION; DIALYSIS; REPAIR; ASSAY;
D O I
10.1016/j.carbpol.2016.03.074
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Herein, we propose an innovative approach to improving wound healing. Our strategy is to deliver melatonin locally at the wound site by means of lecithin/chitosan nanoparticles. We used four types of chitosan that differed in terms of molecular weight and/or deacetylation degree. Melatonin encapsulation efficiency, nanoparticle size, zeta potential, biocompatibility and in vitro drug release were studied as a function of the type of chitosan used in preparation. The nanoparticles were evaluated in terms of their potential to promote wound epithelialisation via an in vitro scratch assay using a human keratinocyte (HaCaT) monolayer. The model wounds were treated with nanoparticle suspensions at a chitosan concentration of 5 mu g ml(-1), which was based on preceding cell biocompatibility studies. Nanoparticles prepared with different types of chitosan showed similar effect on the keratinocyte proliferation/migration. Nanoparticle-mediated interplay of chitosan and melatonin was shown to be crucial for improved wound epithelialisation. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:445 / 454
页数:10
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