药物输送
伤口愈合
血管生成
微粒
材料科学
生物医学工程
化学
纳米技术
化学工程
免疫学
工程类
医学
生物
内科学
作者
Canwen Chen,Yuetong Wang,Dagan Zhang,Xiuwen Wu,Yun Zhao,Luoran Shang,Jianan Ren,Yuanjin Zhao
标识
DOI:10.1016/j.apmt.2021.101000
摘要
Natural polysaccharides have a demonstrated value in drug encapsulation and delivery. Efforts in this area are focused on improving the performances of these biomaterials. In this study, we present a multicompartment polysaccharide core-shell microparticle to construct a sustainable dual-release system of active molecules for enhancing wound healing. These microparticles were generated utilizing a microfluidic electrospray approach, in which a mixture of cellulose nanocrystals (CNC) and vascular endothelial growth factor (VEGF) were employed as the cores, with doxycycline hydrochloride (DH) mixed alginate as the shells. The resultant multicompartment particles exhibited wonderful antibacterial properties inherited from the alginate shell, and angiogenesis properties from the CNC core after the shell disintegrated. It was demonstrated that these core-shell microparticles performed their outstanding capabilities in inhibiting inflammation, promoting granulation tissue formation, collagen deposition, and angiogenesis, thereby accelerating rodents' wound healing. These findings support the great potential value of CNC/alginate core-shell microparticles based on the synergistic drug delivery strategy for orchestrating wound healing.
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