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Methods for the measurement of cell and tissue compatibility including tissue regeneration processes

机译:测量细胞和组织相容性的方法包括组织再生过程

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摘要

Biocompatibility is one of the main requirements for the safe use of medical devices. Determination of cytotoxicity is part of the initial evaluation stipulated by ISO standards for the biological evaluation of medical devices. The use of cell cultures to test the biocompatibility of drugs, biomaterials or treatment techniques used in various disciplines is gaining in importance. A wide variety of self-initiated and commercially available cell lines has been evaluated and used: cultured fibroblasts from human skin, buccal mucosa, periodontal membrane, embryonic lung, epithelial and HeLa cells; cultures of human keratinocytes and HaCaT cells; different murine cell lines (C3H-L, Balb/c 3T3, L929 and others) as well as murine cells cultured from liver and spleen; T-lymphocytes from lymph nodes and macrophages obtained by lavage.All of the above cells are suitable for use in biocompatibility tests. Nevertheless, the general opinion is that toxicity tests in vitro will be more convincing when performed with cells that are homologous with the human tissue concerned. In accordance, appropriate cell lines for use in cytotoxicity and tolerance tests concerning the skin would be human dermal fibroblasts and human epidermal keratinocytes, as they take an active part in the immune response, inflammatory processes, and wound healing.The evaluation of the in vitro cytotoxicity of a biomaterial is often a qualitative analysis based on the morphological examination of cell damage and growth after direct or indirect contact with the material. Different commercial assays based on the determination of nucleic acids, metabolic activity, protein content or membrane integrity are available to measure cell proliferation and cell viability. A small selection – Pico Green® DNA Cell Proliferation Assay, ATPLite™ Luminescence ATP Detection Assay, BC Assay: protein quantitation kit, AlamarBlue™ Proliferation Assay and Live/Dead Staining with SYTO-13 and EthD-2 – are discussed concerning sensitivity, reliability and applicability.
机译:生物相容性是安全使用医疗器械的主要要求之一。细胞毒性的测定是ISO标准规定的用于医疗器械生物学评估的初始评估的一部分。使用细胞培养物来测试各种学科中使用的药物,生物材料或治疗技术的生物相容性变得越来越重要。已经评估并使用了多种自启动的和可商购的细胞系:来自人皮肤,颊粘膜,牙周膜,胚胎肺,上皮和HeLa细胞的培养成纤维细胞;人角质形成细胞和HaCaT细胞的培养;不同的鼠细胞系(C3H-L,Balb / c 3T3,L929等),以及从肝脏和脾脏培养的鼠细胞;来自淋巴结的T淋巴细胞和通过灌洗获得的巨噬细胞。上述所有细胞均适用于生物相容性测试。然而,普遍的看法是,当使用与有关人体组织同源的细胞进行体外毒性试验时,其毒性将更具说服力。因此,用于皮肤细胞毒性和耐受性测试的合适细胞系将是人真皮成纤维细胞和人表皮角质形成细胞,因为它们积极参与免疫反应,炎症过程和伤口愈合。生物材料的细胞毒性通常是基于直接或间接接触该材料后细胞损伤和生长的形态学检查进行的定性分析。基于核酸,代谢活性,蛋白质含量或膜完整性的测定的不同商业化测定可用于测量细胞增殖和细胞活力。一小部分选择– Pico Green ® DNA细胞增殖测定,ATPLite™发光ATP检测测定,BC测定:蛋白质定量试剂盒,AlamarBlue™增殖测定以及用SYTO-13和EthD-2进行活/死染色–讨论了敏感性,可靠性和适用性。

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