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基于质量源于设计理念的载氯替泼诺纳米制剂用于角膜给药:优化、表征及抗炎活性

Loteprednol-Loaded Nanoformulations for Corneal Delivery by Quality-by-Design Concepts: Optimization, Characterization, and Anti-inflammatory Activity.

作者信息

Uner Burcu, Ozdemir Samet, Tas Cetin, Uner Melike, Ozsoy Yildiz

机构信息

Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Turkey.

Faculty of Pharmacy, Yeditepe University, Atasehir, 34755, Istanbul, Turkey.

出版信息

AAPS PharmSciTech. 2023 Mar 28;24(4):92. doi: 10.1208/s12249-023-02551-6.

Abstract

Loteprednol etabonate (LE) is a topical corticosteroid that uses inflammatory conditions of the eye. It has a low ocular bioavailability and side effects such as corneal disorder, eye discharge, and ocular discomfort. Therefore, it was decided to select the delivery systems, which are solid lipid nanoparticles (SLN), nanostructured lipid carriers (NLC), and nanoemulsion (NE). Design of experiments (DoE) of SLN, NLC, and NE formulations were formulated by using the quality by design (QbD) approach. Precirol® ATO 5 and oleic acid were used as solid and liquid lipids, respectively, in SLN, NLC, and NE formulations. Physiochemical characterization was performed on the formulations. The optimized formulations' inflammatory effects have been appraised on human corneal epithelial cells employing the ELISA test. Physicochemical characterization studies and inflammatory effects were appraised. The sizes of optimized formulations of SLN, NLC, and NE were 86.19 nm, 82.38 nm, and 126.35 nm, respectively, with minimum polydispersity. The release behavior of the formulations is composed of both diffusion and erosion. ELISA test results proved that the formulations significantly reduced IL-1 and IL-6 levels (p < 0.05). D-optimal mixture experimental design allowed us to develop the most precise formulations of SLN, NLC, and NE. Furthermore, the optimized formulations could be promising candidates for treating an inflammation-based corneal disease of the eye.

摘要

氯替泼诺依碳酸酯(LE)是一种用于治疗眼部炎症性疾病的局部用皮质类固醇。它的眼部生物利用度较低,且会产生如角膜病变、眼部分泌物和眼部不适等副作用。因此,决定选择固体脂质纳米粒(SLN)、纳米结构脂质载体(NLC)和纳米乳剂(NE)等给药系统。采用质量源于设计(QbD)方法对SLN、NLC和NE制剂进行实验设计(DoE)。在SLN、NLC和NE制剂中,分别使用Precirol® ATO 5和油酸作为固体和液体脂质。对制剂进行了理化特性表征。采用ELISA试验评估了优化制剂对人角膜上皮细胞的炎症作用。评估了理化特性研究和炎症作用。SLN、NLC和NE优化制剂的粒径分别为86.19 nm、82.38 nm和126.35 nm,多分散性最小。制剂的释放行为由扩散和侵蚀共同构成。ELISA试验结果证明,这些制剂显著降低了IL-1和IL-6水平(p < 0.05)。D-最优混合实验设计使我们能够开发出最精确的SLN、NLC和NE制剂。此外,优化后的制剂有望成为治疗眼部基于炎症的角膜疾病的候选药物。

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