D'Cruz Osmond J, Samuel Peter, Uckun Fatih M
Drug Discovery Program, Parker Hughes Institute, St Paul, MN 55113, USA.
AAPS PharmSciTech. 2005 Sep 20;6(1):E56-64. doi: 10.1208/pt060111.
The objective of this study was to develop a nontoxic and noncontraceptive vaginal drug delivery vehicle for lipophilic anti-human immunodeficiency virus (HIV) microbicides. Three representative poorly water-soluble novel broad-spectrum anti-HIV microbicides, PHI-113, PHI-346, and PHI-443, were evaluated in 11 different solvent systems. Based on their solubility profiles, a novel nonspermicidal self-emulsifying gel (viz Conceival) composed of pharmaceutical excipients, sorbitol, polyethylene glycol 400, polysorbate 80, microcrystalline cellulose, xanthan gum, and water was optimized. Conceival enhanced the solubility of these poorly water-soluble (<0.001 mg/mL) anti-HIV drugs by at least 150- to 270-fold. Conceival was evaluated in vivo in the New Zealand white rabbit model for the preservation of sperm function based on pregnancy outcome and the potential for vaginal irritation following single and multiple intravaginal applications, respectively. Conceival administered intravaginally immediately prior to artificial insemination with semen had no adverse effects on subsequent reproductive performance, neonatal survival, or pup development when compared with untreated control group. Histologic evaluation of vaginal tissues of rabbits exposed intravaginally to Conceival for 14 consecutive days revealed lack of epithelial, submucosal, and vascular changes at the gel application site (total irritation score <3 out of a possible 16). These findings indicate that Conceival has potential to become a clinically useful, safe noncontraceptive vaginal vehicle for lipophilic microbicides.
本研究的目的是开发一种用于亲脂性抗人类免疫缺陷病毒(HIV)杀微生物剂的无毒且非避孕的阴道给药载体。在11种不同的溶剂体系中对三种具有代表性的水溶性差的新型广谱抗HIV杀微生物剂PHI - 113、PHI - 346和PHI - 443进行了评估。根据它们的溶解度曲线,优化了一种由药用辅料、山梨醇、聚乙二醇400、聚山梨酯80、微晶纤维素、黄原胶和水组成的新型无杀精作用的自乳化凝胶(即Conceival)。Conceival使这些水溶性差(<0.001 mg/mL)的抗HIV药物的溶解度提高了至少150至270倍。分别基于妊娠结局以及单次和多次阴道内给药后阴道刺激的可能性,在新西兰白兔模型中对Conceival进行了体内精子功能保存评估。与未处理的对照组相比,在人工授精前立即经阴道给予Conceival对随后的生殖性能、新生儿存活或幼崽发育没有不良影响。对连续14天经阴道暴露于Conceival的兔子阴道组织进行组织学评估,结果显示凝胶应用部位缺乏上皮、黏膜下层和血管变化(总刺激评分在可能的16分中<3分)。这些发现表明,Conceival有潜力成为一种临床上有用的、安全的非避孕亲脂性杀微生物剂阴道给药载体。