Pluronic F127 复合水凝胶用于兔模型收缩抑制性全厚皮肤伤口的修复。

IF 3.2 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Current Research in Translational Medicine Pub Date : 2024-06-19 DOI:10.1016/j.retram.2024.103458
Khan Sharun , S. Amitha Banu , Merlin Mamachan , Athira Subash , Mathesh Karikalan , Obli Rajendran Vinodhkumar , K.M. Manjusha , Rohit Kumar , A.G. Telang , Kuldeep Dhama , A.M. Pawde , Swapan Kumar Maiti , Amarpal
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引用次数: 0

摘要

由于与细胞外基质相似,水凝胶通常被用作细胞递送的载体。本研究采用收缩抑制全厚伤口模型来评估负载有脂肪源性基质血管组分(AdSVF)、间充质干细胞(AdMSC)和条件培养基(AdMSC-CM)的Pluronic F127(PF127)水凝胶对兔子伤口修复的治疗潜力。实验研究以48只健康的成年新西兰白兔为对象,随机分为8组,每组6只,分别使用AdSVF、AdMSC和AdMSC-CM作为注射或局部制剂。通过与阳性对照组和阴性对照组比较,根据伤口愈合百分比、上皮化时间、表皮厚度、疤痕评估、组织病理学分析、组织化学评估、免疫组织化学(I 型胶原)和羟脯氨酸检测,评估了不同脂肪源性细胞疗法和无细胞疗法的愈合潜力。使用不同染色方法、免疫组织化学和羟脯氨酸测定进行的胶原蛋白密度分析一致表明,在 PF127 水凝胶中输送 AdMSC 和 AdMSC-CM 可增强上皮化、胶原蛋白生成和组织,有助于提高组织强度和质量。尽管异体 AdSVF 可促进兔子的伤口愈合,但其潜力低于 AdMSC 和 AdMSC-CM。当将 AdMSC 和 AdMSC-CM 装入 PF127 水凝胶并局部使用时,它们的伤口愈合潜力得到了增强。尽管使用 AdMSC 治疗的伤口优于 AdMSC-CM,但在大多数情况下并未观察到伤口愈合质量的显著差异,这表明两者的治疗潜力几乎相似。研究结果表明,当 AdMSC 和 AdMSC-CM 装入 PF127 水凝胶并局部使用时,其伤口愈合潜力得到了增强。这些治疗方法促进了胶原蛋白的生成、组织结构和表皮再生,最终改善了整体愈合效果。
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Pluronic F127 composite hydrogel for the repair of contraction suppressed full-thickness skin wounds in a rabbit model

Hydrogels are commonly used as carriers for cell delivery due to their similarities to the extracellular matrix. A contraction-suppressed full-thickness wound model was used to evaluate the therapeutic potential of Pluronic F127 (PF127) hydrogel loaded with adipose-derived stromal vascular fraction (AdSVF), mesenchymal stem cells (AdMSC), and conditioned media (AdMSC-CM) for the repair of wounds in a rabbit model. The experimental study was conducted on forty-eight healthy adult New Zealand white rabbits randomly divided into eight groups with six animals each and treated with AdSVF, AdMSC, and AdMSC-CM as an injectable or topical preparation. The healing potential of different adipose-derived cell-based and cell-free therapeutics was evaluated based on percentage wound healing, period of epithelialization, epidermal thickness, scar evaluation, histopathology analysis, histochemical evaluation, immunohistochemistry (collagen type I), and hydroxyproline assay by comparing with the positive and negative control. Collagen density analysis using different staining methods, immunohistochemistry, and hydroxyproline assay consistently showed that delivering AdMSC and AdMSC-CM in PF127 hydrogel enhanced epithelialization, collagen production, and organization, contributing to improved tissue strength and quality. Even though allogeneic AdSVF was found to promote wound healing in rabbits, it has a lower potential than AdMSC and AdMSC-CM. The wound healing potential of AdMSC and AdMSC-CM was enhanced when loaded in PF127 hydrogel and applied topically. Even though wounds treated with AdMSC outperformed AdMSC-CM, a significant difference in the healing quality was not observed in most instances, indicating almost similar therapeutic potential. The findings indicate that the wound healing potential of AdMSC and AdMSC-CM was enhanced when loaded in PF127 hydrogel and applied topically. These treatments promoted collagen production, tissue organization, and epidermal regeneration, ultimately improving overall healing outcomes.

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来源期刊
Current Research in Translational Medicine
Current Research in Translational Medicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
7.00
自引率
4.90%
发文量
51
审稿时长
45 days
期刊介绍: Current Research in Translational Medicine is a peer-reviewed journal, publishing worldwide clinical and basic research in the field of hematology, immunology, infectiology, hematopoietic cell transplantation, and cellular and gene therapy. The journal considers for publication English-language editorials, original articles, reviews, and short reports including case-reports. Contributions are intended to draw attention to experimental medicine and translational research. Current Research in Translational Medicine periodically publishes thematic issues and is indexed in all major international databases (2017 Impact Factor is 1.9). Core areas covered in Current Research in Translational Medicine are: Hematology, Immunology, Infectiology, Hematopoietic, Cell Transplantation, Cellular and Gene Therapy.
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