Sustainable Primary Cell Banking for Topical Compound Cytotoxicity Assays: Protocol Validation on Novel Biocides and Antifungals for Optimized Burn Wound Care.

IF 1 Q4 CRITICAL CARE MEDICINE
Zhifeng Liao, Nicolas Laurent, Nathalie Hirt-Burri, Corinne Scaletta, Philippe Abdel-Sayed, Wassim Raffoul, Shengkang Luo, Damian J Krysan, Alexis Laurent, Lee Ann Applegate
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Abstract

Thorough biological safety testing of topical therapeutic compounds and antimicrobials is a critical prerequisite for appropriate cutaneous wound care. Increasing pathogen resistance rates to traditional antibiotics and antifungals are driving the development and registration of novel chemical entities. Although they are notably useful for animal testing reduction, the gold standard in vitro cytotoxicity assays in continuous cell lines (HaCaT keratinocytes, 3T3 fibroblasts) may be discussed from a translational relevance standpoint. The aim of this study was thus to establish and validate a sustainable primary cell banking model with a view to performing optimized in vitro cytotoxicity assay development. Primary dermal fibroblasts and adipose-derived stem cell (ASC) types were established from four infant polydactyly sources. A multi-tiered primary cell banking model was then applied to prepare highly sustainable and standardized dermal fibroblast and ASC working cell banks (WCBs), potentially allowing for millions of biological assays to be performed. The obtained cellular materials were then validated for use in cytotoxicity assays through in vitro biosafety testing of topical antiseptics (chlorhexidine, hypochlorous acid) and an antifungal compound (AR-12) of interest for optimized burn wound care. The experimental results confirmed that IC50 values were comparable between cytotoxicity assays, which were performed with cell lines and with primary cells. The results also showed that hypochlorous acid (HOCl) displayed an enhanced toxicological profile as compared to the gold standard chlorhexidine (CLX). Generally, this study demonstrated that highly sustainable primary cell sources may be established and applied for consistent topical compound biological safety assessments with enhanced translational relevance. Overall, the study underscored the safety-oriented interest of functionally benchmarking the products that are applied on burn patient wounds for the global enhancement of burn care quality.

用于局部化合物细胞毒性试验的可持续原代细胞库:新型杀菌剂和抗真菌剂的方案验证,优化烧伤伤口护理。
对局部治疗化合物和抗菌剂进行彻底的生物安全性测试是进行适当的皮肤伤口护理的关键前提。病原体对传统抗生素和抗真菌药物的耐药性不断增加,推动了新型化学实体的开发和注册。尽管体外细胞毒性试验对减少动物试验非常有用,但从转化相关性的角度来看,连续细胞系(HaCaT 角质细胞、3T3 成纤维细胞)体外细胞毒性试验才是金标准。因此,本研究的目的是建立并验证一种可持续的原代细胞库模型,以便进行优化的体外细胞毒性检测开发。原代真皮成纤维细胞和脂肪源性干细胞(ASC)来自四种婴儿多指畸形来源。然后采用多层原代细胞库模式,制备高度可持续和标准化的真皮成纤维细胞和脂肪干细胞工作细胞库(WCB),可进行数百万次生物检测。然后,通过对局部杀菌剂(洗必泰、次氯酸)和一种用于优化烧伤创面护理的抗真菌化合物(AR-12)进行体外生物安全测试,验证了所获得的细胞材料是否可用于细胞毒性试验。实验结果证实,使用细胞系和原代细胞进行的细胞毒性试验的 IC50 值相当。结果还显示,与黄金标准洗必泰(CLX)相比,次氯酸(HOCl)的毒性更强。总体而言,这项研究表明,可以建立高度可持续的原代细胞来源,并将其应用于一致的局部化合物生物安全性评估,从而提高转化相关性。总之,这项研究强调了以安全为导向,对烧伤患者伤口上使用的产品进行功能性基准测试,以全面提高烧伤护理质量的重要性。
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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