Lozenski Karissa, Kish-Catalone Tina, Pirrone Vanessa, Rando Robert F, Labib Mohamed, Wigdahl Brian, Krebs Fred C
Department of Microbiology and Immunology, Center for Sexually Transmitted Disease, Institute for Molecular Medicine and Infectious Disease, Drexel University College of Medicine, 245 N. 15th Street, Philadelphia, PA 19102, USA.
J Biomed Biotechnol. 2011;2011:941061. doi: 10.1155/2011/941061. Epub 2011 Oct 24.
Vaginal microbicides that reduce or eliminate the risk of HIV-1 sexual transmission must do so safely without adversely affecting the integrity of the cervicovaginal epithelium. The present studies were performed to assess the safety of the biguanide-based antiviral compound NB325 in a formulation suitable for topical application. Experiments were performed using a mouse model of cervicovaginal microbicide application, which was previously shown to be predictive of topical agent toxicity revealed in microbicide clinical trials. Mice were exposed vaginally to unformulated NB325 or NB325 formulated in the hydroxyethyl cellulose "universal placebo." Following exposures to formulated 1% NB325 for 10 min to 24 h, the vaginal and cervical epithelia were generally intact, although some areas of minimal vaginal epithelial damage were noted. Although formulated NB325 appeared generally safe for application in these studies, the low but observable level of toxicity suggests the need for improvements in the compound and/or formulation.
能够降低或消除HIV-1性传播风险的阴道杀微生物剂必须在不影响宫颈阴道上皮完整性的前提下安全发挥作用。开展本研究以评估基于双胍的抗病毒化合物NB325在适合局部应用的制剂中的安全性。实验采用了宫颈阴道杀微生物剂应用的小鼠模型,该模型先前已被证明可预测杀微生物剂临床试验中揭示的局部用药毒性。将小鼠阴道暴露于未配制的NB325或用羟乙基纤维素“通用安慰剂”配制的NB325。在暴露于配制的1%NB325 10分钟至24小时后,阴道和宫颈上皮通常完整,尽管注意到有一些轻微的阴道上皮损伤区域。尽管在这些研究中配制的NB325总体上似乎应用安全,但低水平但可观察到的毒性表明需要对该化合物和/或制剂进行改进。