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Multicomponent Chemical Imaging of Pharmaceutical Solid Dosage Forms with Broadband CARS Microscopy

机译:宽带CARS显微镜对药物固体剂型的多组分化学成像

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摘要

We compare a coherent Raman imaging modality, broadband coherent anti-Stokes Raman scattering (BCARS) microscopy, with spontaneous Raman microscopy for quantitative and qualitative assessment of multicomponent pharmaceuticals. Indomethacin was used as a model active pharmaceutical ingredient (API) and was analyzed in a tabulated solid dosage form, embedded within commonly used excipients. In comparison with wide-field spontaneous Raman chemical imaging, BCARS acquired images 10× faster, at higher spatiochemical resolution and with spectra of much higher SNR, eliminating the need for multivariate methods to identify chemical components. The significant increase in spatiochemical resolution allowed identification of an unanticipated API phase that was missed by the spontaneous wide-field method and bulk Raman spectroscopy. We confirmed the presence of the unanticipated API phase using confocal spontaneous Raman, which provided spatiochemical resolution similar to BCARS but at 100× slower acquisition times.
机译:我们比较了相干拉曼成像方式,宽带相干抗斯托克斯拉曼散射(BCARS)显微镜和自发拉曼显微镜对多组分药物的定量和定性评估。吲哚美辛用作模型活性药物成分(API),并以制成表格的固体剂型进行分析,包埋在常用的赋形剂中。与宽视野自发拉曼化学成像相比,BCARS以更高的时空化学分辨率和具有更高SNR的光谱更快地获取了10倍的图像,从而无需使用多元方法来识别化学成分。时空化学分辨率的显着提高使得可以识别出自发的宽视场方法和本体拉曼光谱法遗漏的未预期的API相。我们使用共聚焦自发拉曼证实了未预料到的API阶段的存在,它提供了类似于BCARS的时空化学分辨率,但采集时间慢了100倍。

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