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Non-destructive analysis of drug content in polymer coatings with Raman spectroscopy : Current Directions in Biomedical Engineering

机译:用拉曼光谱法对聚合物涂层中药物含量进行无损分析:生物医学工程的最新方向

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The analysis of device drug content typically is carried out by means of chromatographic methods such as high performance liquid chromatography (HPLC) or liquid chromatography-mass spectrometry (LCMS). These approved methods are particularly fast, cost-efficient and ubiquitous in chemical-analytical laboratories. However, these quantitative methods necessitate the drug being eluted, which represents a destructive process. A novel alternative to these well-established methods [1, 2] is the Raman spectroscopy, which is fast and cost-efficient, as well [3]. Additionally, it offers the advantage of nondestructive analysis without the need for a special sample preparation. Within the current investigation we applied Raman spectroscopy for the qualitative and quantitative analysis of dexamethasone (DMS), a glucocorticoid, incorporated in a silicone matrix. The investigation was conducted in a rectangular area on the sample surface. The required number of measuring points (spectra) was determined. Calibration was performed with samples containing different amounts of DMS. The evaluation of Raman spectra is based on the analysis of the peak areas of the bands at 795 rel. cm-1(silicone) and 1,663 rel. cm-1(DMS). Remarkably, next to a precise overview of DMS distribution, an exact and reproducible quantification of incorporated DMS could be obtained.
机译:装置药物含量的分析通常通过色谱方法进行,例如高效液相色谱(HPLC)或液相色谱-质谱(LCMS)。这些批准的方法在化学分析实验室中特别快速,经济高效并且无处不在。但是,这些定量方法需要洗脱药物,这代表了破坏过程。这些完善的方法[1、2]的一种新颖替代方法是拉曼光谱法,它也快速且具有成本效益[3]。此外,它具有无损分析的优点,而无需特殊的样品制备。在当前的研究中,我们将拉曼光谱法用于定性和定量分析地塞米松(DMS)(一种糖皮质激素),并掺入了有机硅基质中。研究是在样品表面的矩形区域进行的。确定了所需的测量点数(光谱)。使用包含不同量DMS的样品进行校准。拉曼光谱的评估是基于对795 rel处谱带峰面积的分析。 cm-1(硅酮)和1,663 rel。 cm-1(DMS)。值得注意的是,在对DMS分布进行精确概述的同时,还可以对掺入的DMS进行精确且可重复的定量。

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