Hyperspectral coherent anti-Stokes Raman scattering microscopy for in situ analysis of solid-state crystal polymorphs

被引:2
作者
Garbacik, E. T. [1 ]
Fussell, A. L. [1 ]
Gueres, S. [3 ]
Korterik, J. P. [1 ]
Otto, C. [2 ]
Herek, J. L. [1 ]
Offerhaus, H. L. [1 ]
机构
[1] Univ Twente, Opt Sci Grp, MESA Inst Nanotechnol, POB 217, NL-7500 AE Enschede, Netherlands
[2] Univ Twente, MIRA Inst Biomed Technol & Tech Med, Med Cell Biophys Grp, NL-7500 AE Enschede, Netherlands
[3] Univ Dusseldorf, Inst Pharmaceut & Biopharmaceut, D-40225 Dusseldorf, Germany
来源
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES XIII | 2013年 / 8588卷
关键词
Coherent anti-Stokes Raman scattering; hyperspectral imaging; polymorphism; mannitol; theophylline; diprophylline; CARS; IDENTIFICATION; SPECTROSCOPY; DISSOLUTION; TISSUE; FORMS; BAND;
D O I
10.1117/12.2004522
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hyperspectral coherent anti-Stokes Raman scattering (CARS) microscopy is quickly becoming a prominent imaging modality because of its many advantages over the traditional paradigm of multispectral CARS. In particular, recording a significant portion of the vibrational spectrum at each spatial pixel allows image-wide spectral analysis at much higher rates than can be achieved with spontaneous Raman. We recently developed a hyperspectral CARS method, the driving principle behind which is the fast acquisition and display of a hyperspectral datacube as a set of intuitive images wherein each material in a sample appears with a unique trio of colors. Here we use this system to image and analyze two types of polymorphic samples: the pseudopolymorphic hydration of theophylline, and the packing polymorphs of the sugar alcohol mannitol. In addition to these solid-state form modifications we have observed spectral variations of crystalline mannitol and diprophylline as functions of their orientations relative to the optical fields. We use that information to visualize the distributions of these compounds in a pharmaceutical solid oral dosage form.
引用
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页数:11
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