Chitosan, chondroitin sulfate, and hyaluronic acid based in-situ forming scaffold for efficient cell grafting

被引:8
作者
Kirwale, Shrikant Sitaram [1 ]
Sharma, Swati [1 ]
Roy, Aniruddha [1 ]
机构
[1] Birla Inst Technol & Sci, Dept Pharm, Vidya Vihar 333031, Rajasthan, India
关键词
Chitosan; Chondroitin sulfate; Hyaluronic acid; In-situ scaffold; Cell-grafting; Wound healing; HUMAN SKIN FIBROBLASTS; EXTRACELLULAR-MATRIX; MYOFIBROBLAST DIFFERENTIATION; ALGINATE; HYDROGELS; PROLIFERATION; ENCAPSULATION; REGENERATION; FIBRONECTIN; MORPHOLOGY;
D O I
10.1016/j.ijbiomac.2022.11.157
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current cell grafting techniques are majorly dependent on seeding cells on a pre-formed scaffold. However, cells grow in a 2-dimensional (2D) space in such constructs, not mimicking the tissue's 3-dimensional (3D) architecture. The present study evaluated a unique poly-electrolyte complexation (PEC) based strategy for the 3D engraftment of cells in a porous polymeric scaffold. The scaffold was synthesized using a positively charged polysaccharide chitosan (CH) and negatively charged glycosaminoglycans chondroitin sulfate (CS) and hyaluronic acid (HA). Two different scaffolds were synthesized, one using CH and CS [CH-CS] and another using CH and CS + HA [CH-(CS-HA)]. The physicochemical characterization of both the PECs confirmed electrostatic interactions, leading to a porous and viscoelastic PEC formation. Fibroblast cells were grafted and seeded in both scaffolds to evaluate the effect of different scaffold compositions and the difference between seeded and grafted cells. Imaging studies confirmed that grafting of the fibroblast cells supports cellular proliferation. The qPCR studies demonstrated increased expression of functional markers TGF-ss, alpha-SMA, collagen-I, and fibronectin in the CH-(CS-HA) grafted cells. In summary, it was demonstrated that an in-situ forming PEC of CH, CS, and HA had good physicochemical properties for cell grafting and supported grafted cells with improved function.
引用
收藏
页码:938 / 951
页数:14
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