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通过高载药量、长效微阵列贴片递送islatravir用于预防或治疗人类免疫缺陷病毒。

Delivery of Islatravir via High Drug-Load, Long-acting Microarray Patches for the Prevention or Treatment of Human Immunodeficiency Virus.

作者信息

Anjani Qonita Kurnia, Johnson Ashley R, Sabri Akmal H, Lutz Ryan, Tignor Steven, Ballard Jeanine, Rudd Nathan, Zhao Li, Vora Lalitkumar K, Barrett Stephanie E, Wagner Angela, Donnelly Ryan F

机构信息

School of Pharmacy, Queen's University Belfast, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, UK.

Sterile and Specialty Products, Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, 07033, USA.

出版信息

Adv Healthc Mater. 2025 Mar;14(7):e2403615. doi: 10.1002/adhm.202403615. Epub 2025 Jan 22.

Abstract

This research focuses on developing and characterizing islatravir-loaded dissolving microarray patches (MAPs) to provide an effective, minimally invasive treatment option for human immunodeficiency virus (HIV-1) prevention and treatment. The research involves manufacturing these MAPs using a double-casting approach, and conducting in vitro and in vivo evaluations. Results show that the MAPs have excellent needle fidelity, structural integrity, and mechanical strength. in vitro studies demonstrate that the MAPs can penetrate skin up to 580 µm and dissolve within 2 hours. Permeation studies reveal that the delivery efficiency of islatravir across the skin is around 40%. In rodent models, these dissolving MAPs sustain islatravir delivery for up to 3 months. Scaling up the MAPs and increasing drug loading produced detectable levels in minipig. Projections from animal data suggest that these dissolving MAPs can achieve effective islatravir levels for a month after a single application in humans. These findings indicate dissolving MAPs as a minimally invasive approach to sustained release of islatravir.

摘要

本研究聚焦于开发和表征负载衣壳组装调节剂(islatravir)的可溶微阵列贴片(MAPs),以为人类免疫缺陷病毒(HIV-1)的预防和治疗提供一种有效、微创的治疗选择。该研究包括采用双铸法制造这些MAPs,并进行体外和体内评估。结果表明,MAPs具有出色的针忠实性、结构完整性和机械强度。体外研究表明,MAPs可穿透皮肤达580微米,并在2小时内溶解。渗透研究显示,islatravir经皮递送效率约为40%。在啮齿动物模型中,这些可溶MAPs可持续递送islatravir长达3个月。扩大MAPs规模并增加药物负载量后,在小型猪体内产生了可检测水平。动物数据预测表明,这些可溶MAPs在人体单次应用后可在一个月内达到有效的islatravir水平。这些发现表明可溶MAPs是一种用于持续释放islatravir的微创方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e39/11912095/18228ac9e721/ADHM-14-0-g002.jpg

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