CryoEM Laboratory of Soft Matter, Faculty of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.
Laboratory of Pharmaceutical Nanomaterials Science, Department of Materials Science and Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.
J Colloid Interface Sci. 2021 Jun 15;592:156-166. doi: 10.1016/j.jcis.2020.12.021. Epub 2021 Jan 1.
The antiretroviral (ARV) cocktailrevolved the treatment of the human immunodeficiency virus (HIV) infection. Drug combinations have been also tested to treat other infectious diseases, including the recentcoronavirus disease 2019 (COVID-19) outbreak. To simplify administration fixed-dose combinationshave been introduced, however, oral anti-HIV therapy still struggles with low oral bioavailability of many ARVs.This work investigated the co-encapsulation of two clinically relevant ARV combinations,tipranavir (TPV):efavirenz (EFV) anddarunavir (DRV):efavirenz (EFV):ritonavir (RTV),within the core of β-casein (bCN) micelles. Encapsulation efficiency in both systems was ~100%. Cryo-transmission electron microscopy and dynamic light scattering of the ARV-loaded colloidaldispersions indicatefull preservation of the spherical morphology, and x-ray diffraction confirm that the encapsulated drugs are amorphous. To prolong the physicochemical stabilitythe formulations were freeze-driedwithout cryo/lyoprotectant, and successfully redispersed, with minor changes in morphology.Then, theARV-loaded micelles were encapsulated within microparticles of Eudragit® L100, which prevented enzymatic degradation and minimized drug release under gastric-like pH conditionsin vitro. At intestinal pH, the coating polymer dissolved and released the nanocarriers and content. Overall, our results confirm the promise of this flexible and modular technology platform for oral delivery of fixed dose combinations.
抗逆转录病毒(ARV)鸡尾酒疗法改变了人类免疫缺陷病毒(HIV)感染的治疗方法。药物组合也已被测试用于治疗其他传染病,包括最近的 2019 年冠状病毒病(COVID-19)爆发。为了简化管理,已经引入了固定剂量组合,但是,许多 ARV 的口服生物利用度仍然很低,这使得口服抗 HIV 治疗仍然具有挑战性。这项工作研究了将两种临床相关的 ARV 组合,替拉那韦(TPV):依非韦伦(EFV)和达芦那韦(DRV):依非韦伦(EFV):利托那韦(RTV),共同包封在β-酪蛋白(bCN)胶束的核心内。在这两个系统中,包封效率均接近 100%。载有 ARV 的胶体分散体的冷冻透射电子显微镜和动态光散射表明,球形形态得到了完全保留,X 射线衍射证实包封的药物为无定形。为了延长物理化学稳定性,制剂在没有冷冻/保护剂的情况下进行了冷冻干燥,并成功重新分散,形态变化很小。然后,将载有 ARV 的胶束包封在 Eudragit®L100 的微粒中,这可以防止酶降解,并在体外模拟胃样 pH 条件下最小化药物释放。在肠内 pH 下,涂层聚合物溶解并释放纳米载体和内容物。总体而言,我们的结果证实了这种灵活的模块化技术平台在口服固定剂量组合中的应用前景。