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首页> 外文期刊>International Journal of Pharmaceutics >The application of novel nano-thermal and imaging techniques for monitoring drug microstructure and distribution within PLGA microspheres
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The application of novel nano-thermal and imaging techniques for monitoring drug microstructure and distribution within PLGA microspheres

机译:新型纳米热成像技术在PLGA微球中监测药物微观结构和分布的应用

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Poly (d,l-lactic-co-glycolic) acid (PLGA) based microspheres have been extensively used as controlled drug release systems. However, the burst effect has been a persistent issue associated with such systems, especially for those prepared by the double emulsion technique. An effective approach to preventing the burst effect and achieving a more ideal drug release profile is to improve the drug distribution within the polymeric matrix. Therefore, it is of great importance to establish a rapid and robust tool for screening and optimizing the drug distribution during pre-formulation. Transition Temperature Microscopy (TTM), a novel nano-thermal and imaging technique, is an extension of nano-thermal analysis (nano-TA) whereby a transition temperature is detected at a localized region of a sample and then designated a color based on a particular temperature/color palette, finally resulting in a coded map based on transition temperatures detected by carrying out a series of nanoTA measurements across the surface of the sample. In this study, we investigate the feasibility of applying the aforementioned technique combined with other thermal, imaging and structural techniques for monitoring the drug microstructure and spatial distribution within bovine serum albumin (BSA) loaded and nimodipine loaded PLGA microspheres, with a view to better predicting the in vitro drug release performance. (C) 2017 Elsevier B.V. All rights reserved.
机译:聚(d,1-乳酸 - 共 - 乙醇酸)(PLGA)微球的基于已被广泛地用作控制药物释放系统中。然而,突释效应已与这样的系统相关联的持久性问题,特别是对于那些由双乳液技术制备。一种有效的方法,以防止突释效应,并实现了更理想的药物释放曲线是改善聚合物基质中的药物分布。因此,它是非常重要的,建立快速而强大的工具,筛选和优化预配制过程中的药物分布。转变温度显微镜(TTM),一种新型的纳米热和成像技术,是纳米热分析的扩展(纳米-TA),由此的转变温度是在样品的局部区域中检测到,然后指定一个颜色基于一个特定的温度/调色板,最终导致基于过渡温度下具有编码图通过在样品的表面进行一系列nanoTA测量的检测。在这项研究中,我们探讨使用上述技术与其他热,成像和结构技术结合用于监控牛血清白蛋白(BSA)加载和尼莫地平PLGA微球,内的药物的微结构和空间分布,以更好地预测的可行性体外释药性能。 (c)2017年Elsevier B.V.保留所有权利。

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