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多模态非线性光学成像用于多种药物固态形式和表面转变的灵敏检测。

Multimodal Nonlinear Optical Imaging for Sensitive Detection of Multiple Pharmaceutical Solid-State Forms and Surface Transformations.

机构信息

Division of Pharmaceutical Chemistry and Technology, University of Helsinki , Viikinkaari 5E, 00014 Helsinki, Finland.

Division of Pharmaceutical Biosciences, University of Helsinki , Viikinkaari 5E, 00014 Helsinki, Finland.

出版信息

Anal Chem. 2017 Nov 7;89(21):11460-11467. doi: 10.1021/acs.analchem.7b02639. Epub 2017 Oct 18.

Abstract

Two nonlinear imaging modalities, coherent anti-Stokes Raman scattering (CARS) and sum-frequency generation (SFG), were successfully combined for sensitive multimodal imaging of multiple solid-state forms and their changes on drug tablet surfaces. Two imaging approaches were used and compared: (i) hyperspectral CARS combined with principal component analysis (PCA) and SFG imaging and (ii) simultaneous narrowband CARS and SFG imaging. Three different solid-state forms of indomethacin-the crystalline gamma and alpha forms, as well as the amorphous form-were clearly distinguished using both approaches. Simultaneous narrowband CARS and SFG imaging was faster, but hyperspectral CARS and SFG imaging has the potential to be applied to a wider variety of more complex samples. These methodologies were further used to follow crystallization of indomethacin on tablet surfaces under two storage conditions: 30 °C/23% RH and 30 °C/75% RH. Imaging with (sub)micron resolution showed that the approach allowed detection of very early stage surface crystallization. The surfaces progressively crystallized to predominantly (but not exclusively) the gamma form at lower humidity and the alpha form at higher humidity. Overall, this study suggests that multimodal nonlinear imaging is a highly sensitive, solid-state (and chemically) specific, rapid, and versatile imaging technique for understanding and hence controlling (surface) solid-state forms and their complex changes in pharmaceuticals.

摘要

两种非线性成像模式,相干反斯托克斯拉曼散射(CARS)和和频产生(SFG),成功地结合用于药物片剂表面上的多种固态形式及其变化的敏感多模态成像。使用了两种成像方法并进行了比较:(i)与主成分分析(PCA)和 SFG 成像相结合的高光谱 CARS,和(ii)同时进行的窄带 CARS 和 SFG 成像。使用这两种方法,清晰地区分了吲哚美辛的三种不同固态形式 - 结晶的γ和α形式以及无定形形式。同时进行的窄带 CARS 和 SFG 成像速度更快,但高光谱 CARS 和 SFG 成像有可能应用于更广泛、更复杂的样品。这些方法进一步用于在两种存储条件下(30°C/23%RH 和 30°C/75%RH)研究吲哚美辛在片剂表面上的结晶过程。亚微米分辨率的成像表明,该方法可以检测到非常早期的表面结晶。在较低湿度下,表面逐渐结晶为主要(但不是唯一)γ形式,而在较高湿度下则结晶为α形式。总的来说,这项研究表明,多模态非线性成像技术是一种高度敏感、固态(和化学)特异性、快速和多功能的成像技术,可用于理解和控制药物中(表面)固态形式及其复杂变化。

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