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设计、制剂与评价含有利匹韦林的新型溶解微阵列贴片用于阴道给药。

Design, Formulation, and Evaluation of Novel Dissolving Microarray Patches Containing Rilpivirine for Intravaginal Delivery.

机构信息

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

PATH, 2201 Westlake Avenue, Seattle, WA, 98121, USA.

出版信息

Adv Healthc Mater. 2019 May;8(9):e1801510. doi: 10.1002/adhm.201801510. Epub 2019 Mar 6.

Abstract

Antiretroviral (ARV) drugs have, for many years, been studied and administered in the prevention and treatment of human immunodeficiency virus (HIV). Intramuscular (IM) injection of long acting (LA) ARVs are in clinical development, but injectable formulations require regular access to healthcare facilities and disposal facilities for sharps. The development of a discrete, self-administered, and self-disabling vehicle to deliver ARVs could obviate these issues. This study describes the formulation, mechanical characterization, and in vivo evaluation of dissolving microarray patches (MAPs) containing a LA nanosuspension of the ARV, rilpivirine (RPV, RPV LA), for vaginal delivery. This is the first study to apply MAPs into vaginal tissue. The RPV LA MAPs penetrate ex vivo skin and a synthetic vaginal skin model and withstand the effects of potential dragging motion across synthetic vaginal epithelium. In in vivo studies, the mean plasma concentration of RPV in rats at the 56 day endpoint (116.5 ng mL ) is comparable to that achieved in the IM control cohort (118.9 ng mL ). RPV is detected systemically, in lymph and vaginal tissue, indicating the potential to deliver RPV LA to primary sites of viral challenge and replication. This innovative research has future potential for patients and healthcare workers, particularly in low-resource settings.

摘要

抗逆转录病毒 (ARV) 药物多年来一直被用于预防和治疗人类免疫缺陷病毒 (HIV)。长效 (LA) ARV 的肌肉内 (IM) 注射正在临床开发中,但注射制剂需要定期获得医疗保健设施和锐器处理设施。开发一种离散的、自我管理的、自我失效的输送 ARV 的载体可以避免这些问题。本研究描述了含有 LA 纳米混悬剂的 ARV、利匹韦林 (RPV,RPV LA) 的溶解微阵列贴片 (MAP) 的制剂、机械特性和体内评价,用于阴道给药。这是首次将 MAP 应用于阴道组织的研究。RPV LA MAP 穿透离体皮肤和合成阴道皮肤模型,并能抵抗潜在的在合成阴道上皮上拖动运动的影响。在体内研究中,56 天终点时大鼠的 RPV 平均血浆浓度(116.5ng/mL)与 IM 对照组(118.9ng/mL)相当。RPV 被系统检测到,包括淋巴和阴道组织,表明有潜力将 RPV LA 递送到病毒攻击和复制的主要部位。这项创新性研究为患者和医护人员提供了未来的潜力,特别是在资源匮乏的环境中。

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