采用静态混合技术制备的醋酸曲安奈德微球的配方与表征

Huan-Huan Du, Li-Rong Wang, Xin-Hong Wu, Xue-Ai Liu, Ming-Wei Huo, Xiang-Xiang Huang, Ling-Zhi Shi, Yawen Liu, Min Tang, Li-Li Shi, Qing-Ri Cao
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引用次数: 0

摘要

目的:通过喷雾干燥法生产微球的可重复性和规模化生产面临重大挑战。本研究采用新型静态混合法制备了醋酸曲安奈德(TAA)生物可降解微球,并以聚乳酸-聚乙二醇酸(PLGA)作为缓释载体:方法:采用静态混合技术制备了负载TAA的微球(TAA-MSs)。从TAA-MSs的粒径、载药量(DL)和包封效率(EE)的角度优化了PLGA浓度、聚乙烯醇浓度(PVA)、油/水相比例和水/固相比例。使用扫描电子显微镜(SEM)检查了 TAA-MSs 的形态,并通过 X 射线衍射(XRD)、差示扫描量热仪(DSC)和傅立叶变换红外光谱(FT-IR)评估了其理化性质。在 pH 值为 7.4、温度为 37°C 的介质中,采用水浴振荡法比较了 TAA-MSs 与纯药物(TAA)的体外释放情况:制备TAA-MSs的配方组成和制备条件优化如下:PLGA浓度为1%,油(二氯甲烷)/水(PVA溶液)相比为1:3,水(PVA溶液)/固化相比为1:2。优化后的 TAA-MS 呈球形颗粒,粒径范围为 30-70 μm,DL 值和 EE 值分别为 27.09% 和 98.67%。此外,载药微球表现出显著的持续释放性,在 28 天内释放了 20% 的药物。XRD 结果表明,微球中的 TAA 晶体已部分转化为无定形形式。DSC 和傅立叶变换红外光谱结果表明,TAA 与 PLGA 之间发生了一些相互作用,这表明药物被有效地包裹在 PLGA 微球中:结论:通过静态混合技术成功制备了负载 TAA 的 PLGA 微球,其 EE 和缓释效果均有所提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Characterization of Triamcinolone Acetonide Acetate-Loaded Microspheres Prepared by a Static Mixing Technique.

Purpose: Reproducibility and scale-up production of microspheres through spray drying present significant challenges. In this study, biodegradable microspheres of Triamcinolone Acetonide Acetate (TAA) were prepared using a novel static mixing method by employing poly( lactic-co-glycolic acid) (PLGA) as the sustained-release carrier.

Methods: TAA-loaded microspheres (TAA-MSs) were prepared using a static mixing technique. The PLGA concentration, polyvinyl alcohol concentration (PVA), phase ratio of oil/water, and phase ratio of water/solidification were optimized in terms of the particle size, drug loading (DL), and encapsulation efficiency (EE) of TAA-MSs. The morphology of TAA-MSs was examined using Scanning Electron Microscopy (SEM), while the physicochemical properties were evaluated through X-ray diffraction (XRD), Differential Scanning Calorimetry (DSC), and Fourier Transform Infrared Spectroscopy (FT-IR). The in vitro release of TAA-MSs was compared to that of the pure drug (TAA) using a water-bath vibration method in the medium of pH 7.4 at 37°C.

Results: The formulation composition and preparation condition for the preparation of TAA-MSs were optimized as follows: the PLGA concentration was 1%, the phase ratio of oil(dichloromethane) /water (PVA solution) was 1:3, the phase ratio of water (PVA solution)/solidification was 1:2. The optimized TAA-MSs displayed spherical particles with a size range of 30-70 μm, and DL and EE values of 27.09% and 98.67%, respectively. Moreover, the drug-loaded microspheres exhibited a significant, sustained release, with 20% of the drug released over a period of 28 days. The XRD result indicated that the crystalline form of TAA in microspheres had been partly converted into the amorphous form. DSC and FT-IR results revealed that some interactions between TAA and PLGA occurred, indicating that the drug was effectively encapsulated into PLGA microspheres.

Conclusion: TAA-loaded PLGA microspheres have been successfully prepared via the static mixing technique with enhanced EE and sustained-release manner.

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