Department of Pharmaceutics and Drug Delivery, School of Pharmacy, University of Mississippi, University, Mississippi, USA.
National Center for Natural Products Research, University of Mississippi, University, Mississippi, USA.
J Ocul Pharmacol Ther. 2020 Jul/Aug;36(6):410-420. doi: 10.1089/jop.2019.0140. Epub 2020 Apr 21.
Natamycin (NTM) ophthalmic suspension is the only FDA-approved formulation commercially available for treating ocular fungal infections. However, precorneal residence times and losses/drainage remain the foremost challenges associated with current ocular antifungal pharmacotherapy. In our previous investigations, NTM loaded polyethylene glycol nanolipid carriers (NTM-PNLCs) showed enhanced corneal permeation, both and . To further improve the corneal retention of NTM-PNLCs, this study aimed to develop a gelling system composed of carboxyvinyl polymer, guar gum, and boric acid in which the NTM-PNLCs were loaded. A 2 factorial design was employed in formulating and optimizing the gelling system for NTM-PNLCs, where the independent factors were the gelling excipients (guar gum, boric acid, and Carbopol 940) and dependent variables were gelling time, gel depot collapse time, rheology, firmness, and work of adhesion. Optimized gel was evaluated for transcorneal permeation using rabbit cornea, ; and tear pharmacokinetics and ocular biodistribution in male New Zealand White rabbits, . Optimized NTM-PNLC-GEL was found to exhibit shear thinning rheology, adequate firmness, and spreadability, and formed a depot that did not collapse immediately. In addition, the transcorneal evaluation studies indicated that the NTM-PNLC-GEL exhibited a lower/slower flux and rate in comparison to Natacyn suspension. NTM-PNLC-GEL (0.3%), at a 16-fold lower dose, exhibited mean residence time and elimination half-life comparable to Natacyn (5%), and provided similar concentrations in the innermost tissues of the eye. The data indicate that the NTM-PNLC-GEL formulation could serve as an alternative during ophthalmic antifungal therapy.
那他霉素(NTM)眼用混悬剂是目前唯一获得美国食品和药物管理局(FDA)批准用于治疗眼部真菌感染的商业化制剂。然而,目前眼部抗真菌药物治疗仍面临的主要挑战是药物在眼前房的驻留时间和损失/排出。在我们之前的研究中,载有 NTM 的聚乙二醇纳米脂质载体(NTM-PNLCs)显示出增强的角膜渗透, 和 。为了进一步提高 NTM-PNLCs 的角膜滞留,本研究旨在开发一种由羧基乙烯基聚合物、瓜尔胶和硼酸组成的凝胶系统,其中载有 NTM-PNLCs。在配方和优化 NTM-PNLCs 的凝胶系统中采用了 2 因素设计,独立因素为凝胶赋形剂(瓜尔胶、硼酸和卡波姆 940),依赖变量为凝胶时间、凝胶储库塌陷时间、流变学、硬度和粘附功。使用兔角膜评价优化后的凝胶的经角膜渗透情况, ;并在雄性新西兰白兔中评价优化后的凝胶在泪液中的药代动力学和眼部生物分布, 。结果发现,优化后的 NTM-PNLC-GEL 表现出剪切稀化流变学特性、足够的硬度和铺展性,形成的储库不会立即塌陷。此外,经角膜评价研究表明,与 Natacyn 混悬剂相比,NTM-PNLC-GEL 的通量和速率较低/较慢。在低 16 倍剂量的情况下,NTM-PNLC-GEL(0.3%)表现出与 Natacyn(5%)相当的平均驻留时间和消除半衰期,并在眼部最内层组织中提供了相似的 浓度。数据表明,NTM-PNLC-GEL 制剂可作为眼部抗真菌治疗的替代方案。