Processing and preservation of amniotic membranes as biological wound dressings

P. Karawak, R. Chiangnoon, P. Uttayarat, M. Kitporntheranunt, T. Yooyen, K. Chahorm, N. Thamrongsiripak, N. Jangsawang, N. Neramitmansook
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Abstract

Amniotic membrane derived from the human placenta is a collagen-based extracellular matrix that contains various growth factors, which offers an excellent source of biological materials for tissue engineering applications. The aim of this study was to investigate different pretreatment conditions combined with gamma irradiation to establish the processing condition for long-term preservation of amniotic membranes as biological wound dressings. Human amniotic membranes (hAMs) were first isolated from donated placentas obtained by caseation, cleaned off blood remnants, and cut into 10 cm $\times 10 cm$ sheets. During the pretreatment step, 0.05 - 0.5% (w/v) hypochlorite solution or a combination of penicillin-streptomycin, neomycin, and amphotericin (PNA) solution at 50, 100, and 2.5 $\mu$ g/mL, respectively, was first performed to reduce bacterial contamination. After air drying under sterile environment, the amniotic sheets were individually packed and tightly sealed in double-layered polyethylene bags before exposed to gamma irradiation at 25 kGy under cold condition. Plate count methods were performed on as-received hAMs and after pretreatment and gamma irradiation steps to check the bacterial contamination on the samples. Results showed that pretreating the amniotic membranes in 0.5% (w/v) hypochlorite for 2 h or PNA for 18 h could sufficiently reduce the bacterial contamination below 103 colony-forming unit, and gamma irradiation under cold condition could maintain the membranes’ transparency as well as ensure the sterility of samples up to 6 months. Therefore, this combined pretreatment and irradiation steps could be applied to preserve dried hAMs for long-term use as wound dressings.
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羊膜生物创面敷料的加工与保存
来源于人胎盘的羊膜是一种以胶原蛋白为基础的细胞外基质,含有多种生长因子,为组织工程应用提供了良好的生物材料来源。本研究的目的是研究不同的预处理条件,并结合γ辐照,建立羊膜作为生物伤口敷料长期保存的工艺条件。首先从捐赠胎盘中分离出人羊膜(hAMs),清洗掉血液残留物,切成10 cm × 10 cm的薄片。在预处理步骤中,首先使用0.05 - 0.5% (w/v)次氯酸盐溶液或青霉素-链霉素、新霉素和两性霉素(PNA)溶液的组合,浓度分别为50、100和2.5 $\mu$ g/mL,以减少细菌污染。在无菌环境下风干后,将羊膜片单独包装并密封在双层聚乙烯袋中,然后在低温条件下暴露于25 kGy的伽马辐射下。对收到的火腿进行板计数,并在预处理和γ辐照步骤后检查样品上的细菌污染。结果表明,0.5% (w/v)次氯酸盐预处理羊膜2 h或PNA预处理羊膜18 h,可充分降低细菌污染,使其菌落形成单位低于103,冷条件下γ辐照可保持膜的透明度,并保证样品的无菌性长达6个月。因此,这种预处理和辐照相结合的方法可以长期保存干火腿作为伤口敷料。
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