Lyophilization of dehydrated human amniotic membrane: a proactive approach to preserve growth factors for enhanced wound healing.

IF 1.4 4区 医学 Q4 CELL BIOLOGY
Gayathri Anoop, M Kamaraj, T G Nithya, Pothireddy Raghu Babu, Seetha S Babu
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Abstract

The preservation of key growth factors in the human amniotic membrane (hAM) that are involved in tissue regeneration and wound healing is the primary focus of this research work. Here, we quantified the total protein content and the major growth factors present in different sample preparations of hAM. The membrane is initially processed, dehydrated, and gamma-irradiated and subsequently subjected to histological staining, cytotoxicity assays, and total protein estimation. The ELISA method was used to quantify TGF b1, bFGF, PDGF-BB, VEGF-A, and EGF in three distinct preservation samples: tissue homogenate (AC-H), ball milled powder (AC-P), and lyophilized powder (AC-L). An in-vitro scratch assay was performed to analyse cell migration and wound healing. Higher TGF-b1 and FGF-b concentrations indicate the potential impact of HAM on re-epithelialization and granular tissue formation. For major growth factors, the quantification shows no significant differences between the samples. On treating the wound area with concentrations of 0.4 mg/ml and 0.6 mg/ml, the remaining wound area for AC-H, AC-L, and AC-P are 39.71%, 40.31%, 55.99% and 25.48%, 62.8%, and 29.65%, respectively. This indicates the presence of growth factors in the membrane promotes wound healing and facilitates cell migration and proliferation. This study provides insights into the quantity of key growth factors within the human amniotic membrane, thereby presenting the approach as a viable option for treating chronic wounds. Additionally, as lyophilization preserves more growth factors and offers greater stability and shelf life than other preservation techniques, it may be an appropriate substitute for ball milling.

脱水人羊膜的冻干:一种积极的方法来保存生长因子,以增强伤口愈合。
人羊膜(hAM)中参与组织再生和伤口愈合的关键生长因子的保存是本研究的主要重点。在这里,我们量化了总蛋白含量和主要生长因子存在于不同的样品制备火腿。膜最初经过处理、脱水和γ辐照,随后进行组织学染色、细胞毒性测定和总蛋白估计。采用ELISA法定量组织匀浆(AC-H)、球磨粉(AC-P)和冻干粉(AC-L)三种不同保存样品中的TGF b1、bFGF、PDGF-BB、VEGF-A和EGF。采用体外划痕实验分析细胞迁移和伤口愈合情况。较高的TGF-b1和FGF-b浓度表明HAM对再上皮化和颗粒组织形成的潜在影响。对于主要生长因子,样品间的定量结果无显著差异。在浓度为0.4 mg/ml和0.6 mg/ml时,AC-H、AC-L和AC-P的剩余创面面积分别为39.71%、40.31%、55.99%和25.48%、62.8%和29.65%。这表明膜中生长因子的存在促进了伤口愈合,促进了细胞的迁移和增殖。这项研究提供了对人羊膜内关键生长因子数量的见解,从而提出了该方法作为治疗慢性伤口的可行选择。此外,由于冻干保存了更多的生长因子,比其他保存技术提供了更大的稳定性和保质期,它可能是球磨的合适替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell and Tissue Banking
Cell and Tissue Banking CELL BIOLOGY-ENGINEERING, BIOMEDICAL
CiteScore
3.10
自引率
13.30%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Cell and Tissue Banking provides a forum for disseminating information to scientists and clinicians involved in the banking and transplantation of cells and tissues. Cell and Tissue Banking is an international, peer-reviewed journal that publishes original papers in the following areas: basic research concerning general aspects of tissue banking such as quality assurance and control of banked cells/tissues, effects of preservation and sterilisation methods on cells/tissues, biotechnology, etc.; clinical applications of banked cells/tissues; standards of practice in procurement, processing, storage and distribution of cells/tissues; ethical issues; medico-legal issues.
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