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本文引用的文献

1
Film forming systems for topical and transdermal drug delivery.用于局部和透皮给药的成膜系统。
Asian J Pharm Sci. 2017 Nov;12(6):487-497. doi: 10.1016/j.ajps.2017.07.004. Epub 2017 Jul 5.
2
Controlled Release Film Forming Systems in Drug Delivery: The Potential for Efficient Drug Delivery.药物递送中的控释成膜系统:高效药物递送的潜力
Pharmaceutics. 2019 Jun 20;11(6):290. doi: 10.3390/pharmaceutics11060290.
3
Chloroacetamide derivatives as a promising topical treatment for fungal skin infections.氯乙酰胺衍生物有望成为治疗真菌感染性皮肤病的局部治疗药物。
Mycologia. 2019 Jul-Aug;111(4):612-623. doi: 10.1080/00275514.2019.1620550. Epub 2019 Jun 17.
4
Clioquinol is a promising preventive morphological switching compound in the treatment of Candida infections linked to the use of intrauterine devices.弹性蛋白醇是一种有前途的预防形态转换化合物,可用于治疗与宫内节育器使用相关的念珠菌感染。
J Med Microbiol. 2018 Nov;67(11):1655-1663. doi: 10.1099/jmm.0.000850. Epub 2018 Sep 26.
5
Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties.壳聚糖-聚乙烯醇纳米级液膜形成系统通过增强抗菌和抗生物膜特性促进耐甲氧西林金黄色葡萄球菌感染伤口的愈合。
Int J Nanomedicine. 2018 Sep 3;13:4987-5002. doi: 10.2147/IJN.S161680. eCollection 2018.
6
Efficacy of liposomal amphotericin B against four species of Candida biofilms in an experimental mouse model of intravascular catheter infection.脂质体两性霉素B在血管内导管感染实验小鼠模型中对四种念珠菌生物膜的疗效。
J Infect Chemother. 2018 Dec;24(12):958-964. doi: 10.1016/j.jiac.2018.08.011. Epub 2018 Sep 9.
7
Grafting antibiofilm polymer hydrogel film onto catheter by SARA SI-ATRP.通过 SARA SI-ATRP 将抗生物膜聚合物水凝胶膜接枝到导管上。
J Biomater Sci Polym Ed. 2018 Dec;29(17):2106-2123. doi: 10.1080/09205063.2018.1507268. Epub 2018 Dec 20.
8
activities of antifungals alone and in combination with tigecycline against biofilms.抗真菌药物单独及与替加环素联合对生物被膜的活性。
PeerJ. 2018 Jul 25;6:e5263. doi: 10.7717/peerj.5263. eCollection 2018.
9
Invasive candidiasis.侵袭性念珠菌病。
Nat Rev Dis Primers. 2018 May 11;4:18026. doi: 10.1038/nrdp.2018.26.
10
Biofilms: Threats, Challenges, and Promising Strategies.生物膜:威胁、挑战与前景策略
Front Med (Lausanne). 2018 Feb 13;5:28. doi: 10.3389/fmed.2018.00028. eCollection 2018.

合理选择抗真菌药物,提出一种新的制剂策略来控制静脉导管上念珠菌生物膜的形成。

Rational selection of antifungal drugs to propose a new formulation strategy to control Candida biofilm formation on venous catheters.

机构信息

Programa de Pós-Graduação em Microbiologia Agrícola e do Ambiente, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Laboratório de Micologia Aplicada, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

出版信息

Braz J Microbiol. 2020 Sep;51(3):1037-1049. doi: 10.1007/s42770-020-00242-z. Epub 2020 Feb 19.

DOI:10.1007/s42770-020-00242-z
PMID:32077074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7455648/
Abstract

INTRODUCTION

Infections associated with medical devices are often related to colonization by Candida spp. biofilm; in this way, numerous strategies have been developed and studied, mainly in order to prevent this type of fungal growth.

AIM

Considering the above, the main objective of the present study is to make a rational choice of the best antifungal therapy for the in vitro treatment of the biofilm on venous catheters, proposing an innovative formulation of a film-forming system to coat the surface in order to prevent the formation of biofilms.

METHODOLOGY

Anidulafungin, fluconazole, voriconazole, ketoconazole, amphotericin B, and the association of anidulafungin and amphotericin B were tested against biofilms of C. albicans, C. tropicalis, and C. parapsilosis strains in microtiter plates and in a polyurethane catheter. Besides, anidulafungin, amphotericin B, and the combination of both were incorporated in a film-forming system and were evaluated against biofilm.

RESULTS

The superior activity of anidulafungin was demonstrated in relation to the other antifungal agents. Although amphotericin B showed good activity, high concentrations were required. The combination showed a synergistic action, in solution and in the formulation, showing excellent results, with activity above 90%.

CONCLUSION

Due to the superiority of anidulafungin and the synergistic activity of the combination, these alternatives were the most promising options for use in a formulation proposal as a new strategy to combat the Candida spp. biofilm. These formulations demonstrated high in vitro performance in the prevention of biofilms, indicating that they are candidates with great potential for in vivo tests.

摘要

简介

与医疗器械相关的感染通常与念珠菌属生物膜的定植有关;为此,已经开发和研究了许多策略,主要是为了预防这种真菌生长。

目的

鉴于上述情况,本研究的主要目的是为体外治疗静脉导管生物膜选择最佳抗真菌治疗方法,提出一种创新的成膜系统配方,以涂覆表面,从而防止生物膜的形成。

方法

在微量滴定板和聚氨酯导管中,对白色念珠菌、热带念珠菌和近平滑念珠菌的生物膜进行了安尼拉fungin、氟康唑、伏立康唑、酮康唑、两性霉素 B 以及安尼拉fungin 和两性霉素 B 联合治疗的测试。此外,将安尼拉fungin、两性霉素 B 和两者的组合纳入成膜系统,并对生物膜进行了评估。

结果

与其他抗真菌药物相比,安尼拉fungin 的活性更高。尽管两性霉素 B 表现出良好的活性,但需要高浓度。联合用药显示出协同作用,无论是在溶液中还是在配方中,都取得了极好的效果,活性超过 90%。

结论

由于安尼拉fungin 的优越性和联合用药的协同作用,这些替代方案是作为对抗念珠菌属生物膜的新策略在配方建议中最有前途的选择。这些配方在预防生物膜方面表现出了很高的体外性能,表明它们是具有很大体内测试潜力的候选药物。