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顺序半挥发性溶剂蒸汽冲击扫描分析研究纳曲酮从聚(丙交酯-共-乙交酯)微球中的释放。

Scanning Analysis of Sequential Semisolvent Vapor Impact To Study Naltrexone Release from Poly(lactide-co-glycolide) Microparticles.

机构信息

Akina, Inc., West Lafayette, Indiana 47906, United States.

Biomedical Engineering and Pharmaceutics, Purdue University, West Lafayette, Indiana 47907, United States.

出版信息

Mol Pharm. 2022 Nov 7;19(11):4286-4298. doi: 10.1021/acs.molpharmaceut.2c00595. Epub 2022 Sep 27.

Abstract

Poly(lactide-co-glycolide) (PLGA)-based microparticle formulations have been a mainstay of long-acting injectable drug delivery applications for decades. Despite a long history of use, tools and techniques to analyze and understand these formulations are still under development. Recently, a new characterization method was introduced known as the surface analysis after sequential semisolvent impact using sequential semisolvent vapors. The vapor-based technique is named, for convenience, surface analysis of (semisolvent) vapor impact (SAVI). In the SAVI method, discretely controlled quantities of selected organic semisolvents in the vapor phase were applied to PLGA microparticles to track particle morphological changes by laser scanning confocal microscopy. Subsequently, the morphological images were analyzed to calculate mean peak height (), core height (), kurtosis (), dale void volume (), the density of peaks (), maximum height (), and the shape ratio (). Here, the SAVI method was applied to naltrexone-loaded microparticles manufactured internally and Vivitrol, a commercial formulation. SAVI analysis of these microparticles indicated that the two primary mechanisms controlling the naltrexone release were the formation of discrete, self-crystallized portions of naltrexone within the PLGA structure and the degradation of PLGA chains through nucleophilic substitution. The relatively higher amounts of naltrexone crystals resulted in prolonged release than lower amounts of crystals. Data from gel permeation chromatography, differential scanning calorimetry, and in vitro release measurements all point to the importance of naltrexone crystal formation. This study highlights the utility of SAVI for gaining further insights into the microstructure of PLGA formulations and using SAVI data to support research, product development, and quality control applications for microparticle formulations of pharmaceuticals.

摘要

聚(乳酸-共-乙醇酸)(PLGA)为基础的微粒制剂已成为长效注射药物递送应用的主要支柱数十年。尽管使用历史悠久,但分析和理解这些制剂的工具和技术仍在不断发展。最近,引入了一种新的表征方法,称为顺序半溶剂蒸气冲击后的表面分析。为方便起见,这种蒸气基技术命名为(半溶剂)蒸气冲击的表面分析(SAVI)。在 SAVI 方法中,离散地控制数量的选择有机半溶剂在蒸气相中被应用于 PLGA 微粒,以通过激光扫描共聚焦显微镜跟踪颗粒形态变化。随后,对形态图像进行分析,以计算平均峰高()、核心高度()、峰度()、凹陷空隙体积()、峰密度()、最大高度()和形状比()。在这里,SAVI 方法被应用于内部制造的纳曲酮负载微粒和 Vivitrol,一种商业制剂。对这些微粒的 SAVI 分析表明,控制纳曲酮释放的两个主要机制是纳曲酮在 PLGA 结构内形成离散的、自结晶部分和通过亲核取代降解 PLGA 链。相对较高量的纳曲酮晶体导致释放时间延长,而较低量的晶体则导致释放时间缩短。凝胶渗透色谱、差示扫描量热法和体外释放测量的数据都表明纳曲酮晶体形成的重要性。这项研究强调了 SAVI 用于深入了解 PLGA 制剂的微观结构的实用性,并利用 SAVI 数据支持药物微粒制剂的研究、产品开发和质量控制应用。

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