Peet M Melissa, Agrahari Vivek, Anderson Sharon M, Hanif Homaira, Singh Onkar N, Thurman Andrea R, Doncel Gustavo F, Clark Meredith R
CONRAD, Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Arlington, VA 22209, USA.
Pharmaceutics. 2019 Aug 1;11(8):374. doi: 10.3390/pharmaceutics11080374.
The development of topical inserts for the prevention of sexually transmitted infections (STIs), particularly human immunodeficiency virus (HIV), represents a promising alternative to oral and parenteral pre-exposure prophylaxis (PrEP) dosage forms. They may be used for vaginal and/or rectal administration of a variety of agents with antiviral activity. Topical inserts deliver drugs to the portal of viral entry, i.e., the genital or rectal mucosa, with low systemic exposure, and therefore are safer and have fewer side effects than systemic PrEP agents. They may dissolve fast, releasing the active drugs within minutes of insertion, or slowly for long-acting drug delivery. Furthermore, they are user-friendly being easy to administer, discreet and highly portable. They are also economical and easy to manufacture at scale and to distribute, with excellent stability and shelf-life. Altogether, topical inserts represent a particularly promising form of drug delivery for HIV and STI prevention. Highlighted within this review are end-user acceptability research dedicated to understanding preferred attributes for this form of drug delivery, advantages and disadvantages of the formulation platform options, considerations for their development, clinical assessment of select placebo prototypes, future directions, and the potential impact of this dosage form on the HIV prevention landscape.
用于预防性传播感染(STIs),特别是人类免疫缺陷病毒(HIV)的局部插入剂的开发,是口服和肠胃外暴露前预防(PrEP)剂型的一种有前景的替代方案。它们可用于阴道和/或直肠给药多种具有抗病毒活性的药物。局部插入剂将药物递送至病毒进入门户,即生殖器或直肠粘膜,全身暴露量低,因此比全身性PrEP药物更安全且副作用更少。它们可能快速溶解,在插入后几分钟内释放活性药物,或缓慢溶解以实现长效给药。此外,它们使用方便,易于给药,隐蔽且高度便携。它们还经济实惠,易于大规模生产和分发,具有出色的稳定性和保质期。总之,局部插入剂是预防HIV和性传播感染的一种特别有前景的药物递送形式。本综述重点介绍了终端用户可接受性研究,致力于了解这种药物递送形式的首选属性、制剂平台选项的优缺点、其开发的考虑因素、选定安慰剂原型的临床评估、未来方向以及这种剂型对HIV预防格局的潜在影响。