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Quantitative assessment of microbicide-induced injury in the ovine vaginal epithelium using confocal microendoscopy

DOI: 10.1186/1471-2334-12-48

Keywords: Benzalkonium chloride, Confocal endomicroscopy, Epithelial disruption, Imaging, Microbicides, Nonoxynol-9

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Abstract:

A quantitative approach using confocal fluorescence microendoscopy (CFM) for assessment of microbicide-induced injury to the vaginal epithelium was developed. Sheep were treated intravaginally with one of five agents in solution (PBS; 0.02% benzalkonium chloride (BZK); 0.2% BZK) or gel formulation (hydroxyethyl cellulose (HEC); Gynol II nonoxynol-9 gel (N-9)). After 24 hours the vaginal tract was removed, labeled with propidium iodide (PI), imaged, then fixed for histology. An automated image scoring algorithm was developed for quantitative assessment of injury and applied to the data set. Image-based findings were validated with histological visual gradings that describe degree of injury and measurement of epithelial thickness.Distinct differences in PI staining were detected following BZK and N-9 treatment. Images from controls had uniformly distributed nuclei with defined borders, while those after BZK or N-9 showed heavily stained and disrupted nuclei, which increased in proportion to injury detected on histology. The confocal scoring system revealed statistically significant scores for each agent versus PBS controls with the exception of HEC and were consistent with histology scores of injury.Confocal microendoscopy provides a sensitive, objective, and quantitative approach for non-invasive assessment of vaginal epithelial integrity and could serve as a tool for real-time safety evaluation of emerging intravaginal topical agents.Effective preclinical microbicide safety testing is of great importance to insure that only the most promising candidates are advanced to clinical trials. This is particularly important in light of the fact that several clinical trials of emerging microbicides have been terminated due to safety concerns [1-3]. Several early microbicide candidates were shown to increase susceptibility to infection in vivo [4,5] and were associated with surface epithelial disruption and inflammation [4-6]. Additionally, undetected changes in the epithelia

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