磷酸钙增强壳聚糖-卡拉胶支架:伤口愈合的表征和体外评估

Vinita Patole, Gaurav Kavitkar, Ganesh Ingavle, Isha Behere, Ravindra Wavhale, Abhishek Jha, Sanjeevani Deshkar, Avinash Sanap and Pramod Sakpal
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引用次数: 0

摘要

伤口愈合是一个多方面和动态的生物过程,传统的伤口敷料往往不能充分支持,导致愈合时间延长。开发具有支持细胞增殖和血管生成等生物过程能力的伤口敷料,并提供恢复细胞内活动所需的活性物质,以促进伤口愈合,将是非常有益的。目前的工作旨在开发一种壳聚糖(CH)和阴离子聚合物的聚电解质复合物,与磷酸钙(CaP)粉末凝聚,以达到抗菌和血管生成的潜力,细胞增殖,适当的肿胀指数,并促进伤口愈合。以壳聚糖(CH)为阳离子聚合物,以果胶(PE)、海藻酸钠(SA)和卡拉胶(CA)为阴离子聚合物,经冻干法制备聚电解质配合物(PECs)。通过观察其振动频率、结构和热性能的变化,通过FTIR、XRD和DSC证实了PEC的形成。扫描电镜显示了支架的多孔结构。从制备的PEC支架中,根据膨胀指数、孔隙率和降解研究选择壳聚糖-卡拉胶(CH-CA)进行进一步的研究。采用微波辅助合成法制备CaP粉末后,用FTIR、SEM、XRD和能量色散x射线(EDX)技术对粉末进行表征,然后将粉末加载到CH-CA支架上。原子吸收光谱(AAS)分析结果表明,CH-CA支架在pH 5.5的PBS溶液中,24 h内钙离子(Ca++)释放量约为60.75%,支架具有较高的溶胀指数,对大肠杆菌和金黄色葡萄球菌具有抗菌活性。在鸡卵黄囊膜实验中,发现支架具有血液相容性和血管生成潜力,刺激新血管发育。细胞增殖研究证明了支架的细胞相容性,并且在活/死实验中观察到L929小鼠成纤维细胞系细胞密度的改善。总之,载钙CH-CA支架具有抗菌性能,增加血管生成,血液相容性和细胞增殖,表明其作为合适的伤口敷料材料的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Calcium phosphate reinforced chitosan–carrageenan scaffolds: characterization and in vitro assessment for wound healing†

Calcium phosphate reinforced chitosan–carrageenan scaffolds: characterization and in vitro assessment for wound healing†

Wound healing is a multifaceted and dynamic biological process, which traditional wound dressings often fail to adequately support, leading to prolonged healing times. It would be highly beneficial to develop wound dressings with the ability to support biological processes such as cell proliferation and angiogenesis and deliver the active agents required to restore intracellular activities to promote wound healing. The current work aimed at developing a polyelectrolyte complex of chitosan (CH) and an anionic polymer, condensed with calcium phosphate (CaP) powder to attain antibacterial and angiogenic potential, cell proliferation, appropriate swelling index, and enhanced wound healing. Polyelectrolyte complexes (PECs) were formulated using chitosan (CH), as a cationic polymer and pectin (PE), sodium alginate (SA), and carrageenan (CA), respectively, as an anionic polymer through a lyophilization process. PEC formation was confirmed by FTIR, XRD, and DSC by observing the changes in their vibrational frequencies, structures, and thermal properties. SEM revealed the porous structure of the scaffolds. From the prepared PEC scaffolds, chitosan–carrageenan (CH-CA) was selected for further studies based on the swelling index, porosity, and degradation studies. Following the production of CaP powder using a microwave-assisted synthesis method, the powder was characterized by FTIR, SEM, XRD, and energy dispersive X-ray (EDX) techniques before being loaded onto CH-CA scaffolds. The results demonstrated approximately 60.75% release of calcium ions (Ca++) from the CH-CA scaffolds in PBS, pH 5.5, as analysed by atomic absorption spectroscopy (AAS) over 24 h. The scaffolds demonstrated a higher swelling index and exhibited antimicrobial activity against E. coli and S. aureus. The scaffolds were found to be hemocompatible and demonstrated angiogenic potential, evidenced by stimulating new blood vessel development in a chick yolk sac membrane assay. Cell proliferation studies demonstrated the cytocompatibility of the scaffolds, and improvement in the cell density of the L929 mouse fibroblast cell line was observed in a live/dead assay. In conclusion, the calcium-loaded CH-CA scaffolds demonstrated antimicrobial properties, increased angiogenesis, blood compatibility, and cell proliferation, indicating their potential as an appropriate wound dressing material.

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