Evaluation of Antiseptic Drug Candidate Pyridosept in Preclinical in Vitro Studies.

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Renata Kazakova, Alfiya Iksanova, Mariya Agafonova, Anna Lubina, Elena Bulatova, Elena Nikitina, Svetlana Lisovskaya, Airat Kayumov, Oxana Bondar, Albina Malanyeva, Olga Vasileva, Marina Zeldi, Alina Gatina, Sergei Koshkin, Natalia Komcharova, Yulia Konyakhina, Kseniia Titova, Aleksandr Sergeev, Sergey Sapozhnikov, Nikita Shtyrlin, Yurii Shtyrlin
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引用次数: 0

Abstract

Introduction: This work provides preclinical in vitro studies of an innovative antimicrobial agent named pyridosept, belonging to the quaternary bis-ammonium salts and synthesized on the base of pyridoxine. Since the wide spread of pathogens with tolerance to both antibiotics and antiseptics challenges the development of new antimicrobials providing high efficiency against fungi and microorganisms with multiple resistance.

Method: This work presents in vitro studies of pyridosept, such as antibacterial and anti-fungal activities (determination of minimal inhibitory concentration and quantitative suspension test method), as well as antibacterial activity of metal surface test, sporicidal and spermicidal activities, formation of resistance (to bacteria and fungi), Skin-PAMPA (study of membrane transdermal permeability), mutagenicity assays (in Ames test and OS-chromotest), cytotoxicity (MTT-assay) and comet assay in human skin fibroblasts.

Results: Pyridosept demonstrates advantageous antibacterial and antifungal activity in both suspension and metal surface tests; it has anti-SARS-CoV-2, spermicidal and sporicidal activities (comparable to chlorhexidine digluconate). On the other hand, it demonstrates a low frequency of bacterial resistance development (no more than 2-4-fold in- crease of the MIC in 30 passages, with MIC values fluctuating within 1-8 μg/ml for Gram-positive bacteria and 4-32 μg/ml for Gram-negative bacteria) and membrane transdermal permeability (Skin-PAMPA, 500-fold less compared to progesterone). While cytotoxicity (in MTT- and comet assay) of pyridosept is comparable with those for bezalkonium chloride and chlorhexidine, our results suggest that pyridosept represents an advantageous structure for the design of new antiseptics.

Conclusion: The information obtained during the studies demonstrated that pyridosept has a good efficacy and safety profile, which allows us to consider it as a potential anti-septic and disinfectant, for which it is necessary to conduct additional in vivo studies.

抗菌候选药物Pyridosept的临床前体外研究评价。
摘要:本研究以吡哆醇为基料合成了一种新型抗菌药物pyridosept,属季双铵盐。由于对抗生素和防腐剂都具有耐药性的病原体的广泛传播,开发新的抗微生物药物对具有多重耐药性的真菌和微生物具有高效率。方法:本工作介绍了吡哆酮的体外研究,如抗菌和抗真菌活性(最小抑菌浓度测定和定量悬浮试验方法),以及金属表面抗菌活性试验,杀孢和杀精活性,形成耐药性(对细菌和真菌),皮肤pampa(研究膜透皮性),致突变性试验(在Ames试验和sos显色试验中),人皮肤成纤维细胞的细胞毒性(mtt试验)和彗星试验。结果:Pyridosept在悬浮液和金属表面试验中均表现出良好的抗菌和抗真菌活性;具有抗sars - cov -2、杀精和杀孢活性(与二光酸氯己定相当)。另一方面,细菌耐药发生频率较低(30传代MIC升高不超过2-4倍,革兰氏阳性菌MIC值波动在1-8 μg/ml,革兰氏阴性菌MIC值波动在4-32 μg/ml),膜透皮性(Skin-PAMPA,比黄体酮低500倍)。虽然pyridosept的细胞毒性(在MTT-和彗星试验中)与bezalkonium chloride和chlorhexidine相当,但我们的研究结果表明pyridosept代表了一种设计新型防腐剂的有利结构。结论:研究结果表明,pyridosept具有良好的有效性和安全性,可以考虑将其作为一种潜在的防腐剂和消毒剂,有必要进行进一步的体内研究。
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
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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