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聚维酮碘治疗腺病毒性结膜炎的体外研究

[Povidone-iodine for treatment of adenoviral conjunctivitis: an in vitro study].

作者信息

Monnerat N, Bossart W, Thiel M A

机构信息

Augenklinik, Universitätsspital Zürich.

出版信息

Klin Monbl Augenheilkd. 2006 May;223(5):349-52. doi: 10.1055/s-2006-926633.

Abstract

BACKGROUND

Adenoviral conjunctivitis causes high socioeconomic costs due to high contagiousness and therefore the need for extended quarantine. To date the only potentially active, topical antiviral agent is povidone-iodine (PVI). The aim of this study was to investigate the effect of diluted PVI on free adenovirus and adenoviral infected cells as well as to evaluate the cellular toxicity of PVI on non-infected cells.

MATERIAL AND METHODS

PVI was diluted to a final concentration of 0.0008 %. Virucidal activity was measured IN VITRO using adenovirus 8 and A549 human epithelial cell cultures. Cytotoxicity effects on healthy cells after short- and long-term exposure to diluted PVI were measured in A549 cell cultures.

RESULTS

Exposure to PVI at a concentration of 1:10 (0.8 %) completely extinguishes infectivity of free adenovirus after an exposure time of 10 minutes. PVI is less effective against intracellular adenovirus resulting in a decreased infectivity and viral activity for approximately one day with a narrow spectrum between toxicity and virucidal activity. Healthy epithelial cells can be exposed to PVI for up to 6 hours without a cytotoxic effect.

CONCLUSIONS

PVI is highly effective against free adenovirus but less effective against intracellular adenoviral particles in already infected cell. Short- and long-term exposure of PVI causes little cytotoxicity for healthy cells. Therefore, administration of diluted PVI at a concentration of 1:10 is a potential option to reduce contagiousness in cases of adenoviral infections.

摘要

背景

腺病毒性结膜炎具有高度传染性,会导致高昂的社会经济成本,因此需要延长隔离期。迄今为止,唯一具有潜在活性的局部抗病毒药物是聚维酮碘(PVI)。本研究的目的是研究稀释后的PVI对游离腺病毒和腺病毒感染细胞的作用,并评估PVI对未感染细胞的细胞毒性。

材料与方法

将PVI稀释至终浓度为0.0008%。使用腺病毒8和A549人上皮细胞培养物在体外测量杀病毒活性。在A549细胞培养物中测量短期和长期暴露于稀释后的PVI后对健康细胞的细胞毒性作用。

结果

在暴露10分钟后,以1:10(0.8%)的浓度暴露于PVI可完全消除游离腺病毒的感染性。PVI对细胞内腺病毒的效果较差,导致感染性和病毒活性降低约一天,在毒性和杀病毒活性之间的范围较窄。健康的上皮细胞可以暴露于PVI长达6小时而无细胞毒性作用。

结论

PVI对游离腺病毒高度有效,但对已感染细胞内的腺病毒颗粒效果较差。PVI的短期和长期暴露对健康细胞几乎没有细胞毒性。因此,以1:10的浓度施用稀释后的PVI是降低腺病毒感染病例传染性的一种潜在选择。

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