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通过包封于丝素蛋白圆盘实现HIV抑制剂的稳定化与缓释

Stabilization and Sustained Release of HIV Inhibitors by Encapsulation in Silk Fibroin Disks.

作者信息

Zhang Li, Herrera Carolina, Coburn Jeannine, Olejniczak Natalia, Ziprin Paul, Kaplan David L, LiWang Patricia J

机构信息

Molecular Cell Biology, University of California Merced, 5200 North Lake Road, Merced, California 95343, United States.

Department of Medicine, St. Mary's Campus Imperial College, Room 460 Norfolk Place, London W2 1PG, United Kingdom.

出版信息

ACS Biomater Sci Eng. 2017;3(8):1654-1665. doi: 10.1021/acsbiomaterials.7b00167. Epub 2017 Jun 5.

Abstract

Topical microbicides have the potential to provide effective protection against sexual transmission of HIV. Challenges in developing microbicides include their application in resource-poor settings with high temperatures and a lack of refrigeration, and low user adherence to a rigorous daily regimen. Several protein-based HIV inhibitors show great promise as microbicides, being highly specific and not expected to lead to resistance that would affect the efficacy of current antiretroviral treatments. We show that four potent protein HIV inhibitors, 5P12-RANTES, 5P12-RANTES-L-C37, Grft, and Grft-L-C37 can be formulated into silk fibroin (SF) disks and remain functional for 14 months at 25, 37, and 50 °C. These HIV inhibitor-encapsulated SF disks show excellent inhibition properties in PBMC and in human colorectal and cervical tissue explants, and do not induce inflammatory cytokine secretion. Further, the SF provides a mechanically robust matrix with versatile material formats for this type of application. Finally, a formulation was developed to allow sustained release of functional Grft for 4 weeks at levels sufficient to inhibit HIV transmission. This work establishes the suitability of HIV inhibitor-encapsulated SF disks as topical HIV microbicides that can be further developed to allow easy insertion for extended protection.

摘要

局部用杀微生物剂有潜力提供针对艾滋病毒性传播的有效保护。开发杀微生物剂面临的挑战包括在高温且缺乏冷藏设备的资源匮乏环境中的应用,以及使用者对严格日常用药方案的依从性较低。几种基于蛋白质的艾滋病毒抑制剂作为杀微生物剂显示出巨大潜力,它们具有高度特异性,预计不会导致影响当前抗逆转录病毒治疗效果的耐药性。我们表明,四种有效的蛋白质艾滋病毒抑制剂,即5P12-RANTES、5P12-RANTES-L-C37、Grft和Grft-L-C37,可以配制成丝素蛋白(SF)圆盘,并在25、37和50°C下保持功能14个月。这些包封有艾滋病毒抑制剂的SF圆盘在PBMC以及人结肠和宫颈组织外植体中显示出优异的抑制特性,并且不会诱导炎性细胞因子分泌。此外,SF为这类应用提供了一种具有多种材料形式的机械坚固的基质。最后,开发了一种配方,使功能性Grft能够以足以抑制艾滋病毒传播的水平持续释放4周。这项工作确立了包封有艾滋病毒抑制剂的SF圆盘作为局部用艾滋病毒杀微生物剂的适用性,这种杀微生物剂可以进一步开发以便于插入以提供长期保护。

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