Ugaonkar Shweta R, Clark Justin T, English Lexie B, Johnson Todd J, Buckheit Karen W, Bahde Robert J, Appella Daniel H, Buckheit Robert W, Kiser Patrick F
Department of Bioengineering, University of Utah, Salt Lake City, Utah, 84112.
Department of Biomedical Engineering, Northwestern University, Evanston, Illinois, 60208.
J Pharm Sci. 2015 Oct;104(10):3426-39. doi: 10.1002/jps.24551. Epub 2015 Jul 6.
Nucleocapsid 7 (NCp7) inhibitors have been investigated extensively for their role in impeding the function of HIV-1 replication machinery and their ability to directly inactivate the virus. A class of NCp7 zinc finger inhibitors, S-acyl-2-mercaptobenzamide thioesters (SAMTs), was investigated for topical drug delivery. SAMTs are inherently unstable because of their hydrolytically labile thioester bond, thus requiring formulation approaches that can lend stability. We describe the delivery of N-[2-(3,4,5-trimethoxybenzoylthio)benzoyl]-β-alaninamide (SAMT-10), as a single agent antiretroviral (ARV) therapeutic and in combination with the HIV-1 reverse-transcriptase inhibitor pyrimidinedione IQP-0528, from a hydrophobic polyether urethane (PEU) intravaginal ring (IVR) for a month. The physicochemical stability of the ARV-loaded IVRs was confirmed after 3 months at 40°C/75% relative humidity. In vitro, 25 ± 3 mg/IVR of SAMT-10 and 86 ± 13 mg/IVR of IQP-0528 were released. No degradation of the hydrolytically labile SAMT-10 was observed within the matrix. The combination of ARVs had synergistic antiviral activity when tested in in vitro cell-based assays. Toxicological evaluations performed on an organotypic EpiVaginal(™) tissue model demonstrated a lack of formulation toxicity. Overall, SAMT-10 and IQP-0528 were formulated in a stable PEU IVR for sustained release. Our findings support the need for further preclinical evaluation. © 2015 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 104:3426-3439, 2015.
核衣壳7(NCp7)抑制剂因其在阻碍HIV-1复制机制功能方面的作用以及直接使病毒失活的能力而受到广泛研究。一类NCp7锌指抑制剂,即S-酰基-2-巯基苯甲酰胺硫酯(SAMTs),被研究用于局部给药。SAMTs由于其硫酯键易水解而固有地不稳定,因此需要能提供稳定性的制剂方法。我们描述了将N-[2-(3,4,5-三甲氧基苯甲酰硫基)苯甲酰基]-β-丙氨酰胺(SAMT-10)作为单一抗逆转录病毒(ARV)疗法以及与HIV-1逆转录酶抑制剂嘧啶二酮IQP-0528联合,从一种疏水性聚醚聚氨酯(PEU)阴道环(IVR)中释放一个月的情况。在40°C/75%相对湿度下放置3个月后,确认了载有ARV的IVR的物理化学稳定性。在体外,释放出了25±3mg/IVR的SAMT-10和86±13mg/IVR的IQP-0528。在基质内未观察到易水解的SAMT-10发生降解。当在基于细胞的体外试验中进行测试时,ARV组合具有协同抗病毒活性。在一种器官型阴道上皮(EpiVaginal™)组织模型上进行的毒理学评估表明该制剂无毒性。总体而言,SAMT-10和IQP-0528被制成稳定的PEU IVR以实现持续释放。我们的研究结果支持进行进一步临床前评估的必要性。©2015威利期刊公司和美国药剂师协会《药物科学杂志》104:3426 - 3439,2015。