Natural polysaccharide based complex drug delivery system from microfluidic electrospray for wound healing

被引:44
|
作者
Chen, Canwen [1 ]
Wang, Yuetong [2 ,3 ]
Zhang, Dagan [3 ]
Wu, Xiuwen [1 ]
Zhao, Yun [1 ,4 ]
Shang, Luoran [2 ]
Ren, Jianan [1 ,4 ]
Zhao, Yuanjin [1 ,3 ]
机构
[1] Nanjing Univ, Jinling Hosp, Med Sch, Res Inst Gen Surg, Nanjing 210002, Peoples R China
[2] Fudan Univ, Inst Biomed Sci, Zhongshan Xuhui Hosp, Shanghai Key Lab Med Epigenet, Shanghai 200, Peoples R China
[3] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Peoples R China
[4] Nanjing Med Univ, Affiliated BenQ Hosp, BenQ Med Ctr, Dept Gen Surg, Nanjing 2100, Peoples R China
基金
中国国家自然科学基金;
关键词
Cellulose nanocrystal; Microfluidic electrospray; Core-shell particle; Drug delivery; Wound healing; CELLULOSE NANOCRYSTALS; HYDROGELS;
D O I
10.1016/j.apmt.2021.101000
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Natural polysaccharides have a demonstrated value in drug encapsulation and delivery. Effort s 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. (c) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页数:9
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