Emerging Polymeric Mucoadhesive Nanocarriers: A Promising Option for Intravaginal HIV Preexposure Prophylaxis.

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Avichal Kumar, Dhruti Avlani, S Narasimha Murthy, Shivakumar H N, Shammy Jindal
{"title":"Emerging Polymeric Mucoadhesive Nanocarriers: A Promising Option for Intravaginal HIV Preexposure Prophylaxis.","authors":"Avichal Kumar, Dhruti Avlani, S Narasimha Murthy, Shivakumar H N, Shammy Jindal","doi":"10.1080/1061186X.2025.2523991","DOIUrl":null,"url":null,"abstract":"<p><p>The emergence of novel long-acting and antiretroviral (ARV) drug delivery systems has reshaped the landscape of HIV pre-exposure prophylaxis (PrEP). Intravaginal delivery platforms are increasingly recognized for their ability to deliver ARVs directly at the portal of viral entry. These systems are well retained at the portal, ensuring sustained local inhibitory levels, minimizing systemic exposure. Compared to oral PrEP, these systems offer better protection against viral transmission, reduce dosing frequency, and minimize systemic side effects. Among these systems, polymeric nanoparticles (NPs) stand out due to their customizable surface chemistry, mucoadhesive potential, and sustained drug release profiles, ensuring enhanced mucosal retention and minimal systemic absorption. Recent innovations integrate these NPs into versatile platforms such as <i>in-situ</i> gelling systems, bioadhesive films, microneedles, vaginal rings and electrospun nanofibers. These specialized platforms have demonstrated superior user acceptance, stability and pharmacokinetics compared to traditional vaginal formulations. Cell-based HIV challenge models using engineered TZM-bl and PHA-stimulated PBMCs have emerged as reliable in silico tools for evaluation of viral inhibition, cytotoxicity, and mucosal interaction of NPs. This review critically highlights recent advances in intravaginal polymeric NP-based carrier systems for effective and sustained HIV prevention.</p>","PeriodicalId":15573,"journal":{"name":"Journal of Drug Targeting","volume":" ","pages":"1-39"},"PeriodicalIF":4.3000,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Drug Targeting","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/1061186X.2025.2523991","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

The emergence of novel long-acting and antiretroviral (ARV) drug delivery systems has reshaped the landscape of HIV pre-exposure prophylaxis (PrEP). Intravaginal delivery platforms are increasingly recognized for their ability to deliver ARVs directly at the portal of viral entry. These systems are well retained at the portal, ensuring sustained local inhibitory levels, minimizing systemic exposure. Compared to oral PrEP, these systems offer better protection against viral transmission, reduce dosing frequency, and minimize systemic side effects. Among these systems, polymeric nanoparticles (NPs) stand out due to their customizable surface chemistry, mucoadhesive potential, and sustained drug release profiles, ensuring enhanced mucosal retention and minimal systemic absorption. Recent innovations integrate these NPs into versatile platforms such as in-situ gelling systems, bioadhesive films, microneedles, vaginal rings and electrospun nanofibers. These specialized platforms have demonstrated superior user acceptance, stability and pharmacokinetics compared to traditional vaginal formulations. Cell-based HIV challenge models using engineered TZM-bl and PHA-stimulated PBMCs have emerged as reliable in silico tools for evaluation of viral inhibition, cytotoxicity, and mucosal interaction of NPs. This review critically highlights recent advances in intravaginal polymeric NP-based carrier systems for effective and sustained HIV prevention.

新兴的高分子黏附纳米载体:阴道内HIV暴露前预防的一个有希望的选择。
新型长效和抗逆转录病毒(ARV)药物递送系统的出现重塑了艾滋病毒暴露前预防(PrEP)的格局。阴道内给药平台因其在病毒进入门户直接给药的能力而日益得到认可。这些系统很好地保留在门静脉,确保持续的局部抑制水平,最大限度地减少系统暴露。与口服PrEP相比,这些系统可以更好地防止病毒传播,减少给药频率,并最大限度地减少全身副作用。在这些系统中,聚合物纳米颗粒(NPs)因其可定制的表面化学、黏附潜力和持续的药物释放特征而脱颖而出,确保了增强的粘膜保留和最小的全身吸收。最近的创新将这些纳米粒子集成到多功能平台中,如原位胶凝系统、生物胶膜、微针、阴道环和静电纺纳米纤维。与传统的阴道配方相比,这些专门的平台已经证明了优越的用户接受度、稳定性和药代动力学。使用工程化TZM-bl和pha刺激的pbmc的基于细胞的HIV攻击模型已经成为评估NPs病毒抑制、细胞毒性和粘膜相互作用的可靠的计算机工具。本综述重点介绍了阴道内聚合物np载体系统在有效和持续预防艾滋病毒方面的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信