期刊
JOURNAL OF MICROBIOLOGICAL METHODS
卷 88, 期 2, 页码 292-296出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.mimet.2011.12.013
关键词
HIV; Microbicide; Lactobacillus; Vortex mixing; Bacterial quantitation
资金
- International Partnership for Microbicides
- CONRAD
- Pendleton Charitable Trust
- NIH NIAID [U01 AI068633]
- NIAID [AI39061]
The development of topical microbicides for intravaginal use to prevent HIV infection requires that the drugs and formulated products be nontoxic to the endogenous vaginal Lactobacillus. In 30 min exposure tests we found dapivirine, tenofovir and UC781 (reverse transcriptase inhibitor anti-HIV drugs) as pure drugs or formulated as film or gel products were not deleterious to Lactobacillus species; however, PSC-RANTES (a synthetic CCR5 antagonist) killed 2 strains of Lactobacillus jensenii. To demonstrate the toxicity of formulated products a new assay was developed for use with viscous and non-viscous samples that we have termed the Lactobacillus toxicity test. We found that the vortex mixing of vaginal Lactobacillus species can lead to reductions in bacterial viability. Lactobacillus can survive briefly, about 2 s, but viability declines with increased vortex mixing. The addition of heat inactivated serum or bovine serum albumin, but not glycerol, prevented the decrease in bacterial viability. Bacillus atrophaeus spores also demonstrated loss of viability upon extended mixing. We observed that many of the excipients used in film formulation and the films themselves also afford protection from the killing during vortex mixing. This method is of relevance for toxicity for cidal activities of viscous products. (C) 2011 Elsevier B.V. All rights reserved.
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