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Parallel imaging of active pharmaceutical ingredients in some tablets and blends on Raman and near-infrared mapping and imaging platforms

机译:在拉曼和近红外绘图和成像平台上对某些片剂和混合物中的活性药物成分进行并行成像

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Two types of tablets with the arbitrarily defined low and medium active pharmaceutical ingredient (API) loadings and a formulation blend with intentionally introduced large API agglomerate were inspected on Raman mapping and global imaging platforms as well as on the near-infrared (NIR) mapping platform. Only the API particles were identified and their images compared on the three systems. Several technical parameters were closely controlled such as spatial resolution in the images and acquisition times. The Raman mapping platform was found to be the most effective for determining the API in the low-loading formulation which was not analyzable by the other two methods. With regards to the medium loading of API in a tablet and the blend with an API agglomerate, the chemical images on all three platforms were found to be largely comparable with, in relative terms, the NIR mapping being the fastest and least complex to use.
机译:在拉曼制图和全球成像平台以及近红外(NIR)测绘平台上检查了两种类型的片剂,其中分别定义了低和中度活性药物成分(API)含量,并掺入了故意掺入的大型API团块的制剂。在三个系统上仅识别出API颗粒,并比较了它们的图像。几个技术参数受到严格控制,例如图像中的空间分辨率和采集时间。拉曼制图平台被发现是确定低负荷配方中API的最有效方法,而其他两种方法无法对其进行分析。关于片剂中API的中等负载量以及与API附聚物的共混物,相对而言,发现所有三个平台上的化学图像都可以与NIR作图进行比较,这是最快和最不复杂的。

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