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基于质量源于设计(QbD)理念开发用于氟比洛芬眼部给药的自纳米乳化药物递送系统

Quality by Design (QbD)-Based Development of a Self-Nanoemulsifying Drug Delivery System for the Ocular Delivery of Flurbiprofen.

作者信息

Jeong Ju-Hwan, Yoon Tae-Han, Ryu Si-Won, Kim Min-Gyeong, Kim Gu-Hae, Oh Ye-Jin, Lee Su-Jeong, Kwak Na-Woon, Bang Kyu-Ho, Kim Kyeong-Soo

机构信息

Department of Pharmaceutical Engineering, Gyeongsang National University, 33 Dongjin-ro, Jinju 52725, Republic of Korea.

出版信息

Pharmaceutics. 2025 May 9;17(5):629. doi: 10.3390/pharmaceutics17050629.

Abstract

: In this study, Quality by Design (QbD) was used to develop an optimized self-nanoemulsifying drug delivery system (SNEDDS) as an ophthalmic formulation of flurbiprofen (FLU). Using a Box-Behnken design (BBD), an optimal SNEDDS composition was crafted, targeting enhanced corneal permeability and increased bioavailability of the drug. : The levels of each factor(X) were established using a pseudo-ternary diagram, and the Box-Behnken design (BBD) was used to evaluate the components of oil (18.9 mg), surfactant (70.7 mg), and co-surfactant (10.0 mg) to optimize the SNEDDS formulation. The response(Y) considered were particle size, polydispersity index (PDI), transmittance, and stability. Transmission electron microscopy (TEM) and dynamic light scattering (DLS) were used to analyze the particle size and morphology. In vitro and ex vivo diffusion tests were conducted to assess drug flux and permeability. : Using a response optimization tool, the values of each X factor were optimized to achieve a small particle size (nm), a low polydispersity index (PDI), and high transmittance (%), resulting in a formulation prepared with 18.9 mg of oil, 70.7 mg of surfactant, and 10.0 mg of co-surfactant. The optimized SNEDDS exhibited a small particle size of 24.89 nm, a minimal PDI of 0.068, and a high transmittance of 74.85%. A transmission electron microscopy (TEM) analysis confirmed the presence of uniform spherical nanoemulsion droplets with an observed mean diameter of less than 25 nm, corroborating the dynamic light scattering (DLS) measurements. Furthermore, the SNEDDS demonstrated improved stability under the stress conditions of heating-cooling cycles, with no phase separation, creaming, or caking observed and no differences in its particle size, PDI, or transmittance. In vitro and ex vivo diffusion tests demonstrated that the flux of the optimized SNEDDS (2.723 ± 0.133 mg/cm, 5.446 ± 0.390 μg/cm) was about 2.5 and 4 times higher than that of the drug dispersion, and the initial diffusion was faster, which is suitable for the characteristics of eye drops. : Therefore, the formulation of a flurbiprofen-loaded SNEDDS (FLU-SNE) was successfully optimized using the QbD approach. The optimized FLU-SNE exhibited excellent stability and enhanced permeability, suggesting its potential effectiveness in treating various ocular inflammations, including uveitis and cystoid macular edema.

摘要

在本研究中,采用质量源于设计(QbD)方法开发了一种优化的自纳米乳化药物递送系统(SNEDDS),作为氟比洛芬(FLU)的眼用制剂。使用Box-Behnken设计(BBD)构建了最佳的SNEDDS组成,目标是提高药物的角膜渗透性和生物利用度。

每个因素(X)的水平通过伪三元相图确定,使用Box-Behnken设计(BBD)评估油(18.9mg)、表面活性剂(70.7mg)和助表面活性剂(10.0mg)的成分,以优化SNEDDS制剂。所考虑的响应(Y)包括粒径、多分散指数(PDI)、透光率和稳定性。使用透射电子显微镜(TEM)和动态光散射(DLS)分析粒径和形态。进行体外和离体扩散试验以评估药物通量和渗透性。

使用响应优化工具对每个X因素的值进行优化,以实现小粒径(nm)、低多分散指数(PDI)和高透光率(%),从而制备出含有18.9mg油、70.7mg表面活性剂和10.0mg助表面活性剂的制剂。优化后的SNEDDS表现出24.89nm的小粒径、0.068的最小PDI和74.85%的高透光率。透射电子显微镜(TEM)分析证实存在平均直径小于25nm的均匀球形纳米乳液滴,这与动态光散射(DLS)测量结果一致。此外,SNEDDS在加热-冷却循环的应力条件下表现出更好的稳定性,未观察到相分离、乳析或结块现象,其粒径、PDI或透光率也无差异。体外和离体扩散试验表明,优化后的SNEDDS的通量(2.723±0.133mg/cm,5.446±0.390μg/cm)分别比药物分散体高约2.5倍和4倍,且初始扩散更快,这适合滴眼液的特性。

因此,使用QbD方法成功优化了载氟比洛芬的SNEDDS(FLU-SNE)制剂。优化后的FLU-SNE表现出优异的稳定性和增强的渗透性,表明其在治疗包括葡萄膜炎和黄斑囊样水肿在内的各种眼部炎症方面具有潜在疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a3e/12115244/4c0dbba3a8b9/pharmaceutics-17-00629-g001.jpg

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