TY - JOUR
T1 - Raman imaging analysis of pharmaceutical tablets by two-dimensional (2D) correlation spectroscopy
AU - Shinzawa, Hideyuki
AU - Awa, Kimie
AU - Okumura, Takehiro
AU - Morita, Shin ichi
AU - Otsuka, Makoto
AU - Ozaki, Yukihiro
AU - Sato, Hidetoshi
N1 - Funding Information:
This work was financially supported by Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) Fellows. It was supported by ‘Open Research Center’ project (Research Center for Near Infrared Spectroscopy) for private universities: matching fund subsidy from MEXT (Ministry of Education, Culture, Sports, Science and Technology), 2001–2008 and SENTAN, Japan Science and Technology Agency (JST).
PY - 2009/9/18
Y1 - 2009/9/18
N2 - Chemical properties of active substances and insoluble excipient within tablets such as crystalline structures can be seen as an important index for solubility of ingredients. Spectroscopic imaging can potentially be a solid solution to understanding mechanisms at the molecular level and it may bring useful insight in terms of process analytical technique. In the present study, generalized two-dimensional (2D) correlation spectroscopy is utilized for the Raman image analysis of pharmaceutical tablets to reveal molecular interactions between chemical components. By using a spatial distance as a perturbation variable in 2D correlation scheme, synchronous and asynchronous correlation analysis becomes possible. Two kinds of pharmaceutical tablets, pentoxifylline (PTX) as an active substance and palmitic acid (PA) as an insoluble excipient, are prepared with different grinding times, 0.5 and 45 min. The 2D correlation analysis of Raman images of the tablets clearly reveals both physical and chemical effects of grinding process on the properties of the tablets. Asynchronous correlations indicate that a specific molecular structural change of PTX related to the crystallinity is induced by the grinding process. Namely, the crystallinity of PTX based on CH2 structure is a key factor to control the solubility of the tablets. Some properties of pharmaceutical tablets, i.e. solubility or distribution of components in turn may become possible by the simple grinding process. Detailed analysis of Raman images becomes possible by the 2D correlation spectroscopy. Crown
AB - Chemical properties of active substances and insoluble excipient within tablets such as crystalline structures can be seen as an important index for solubility of ingredients. Spectroscopic imaging can potentially be a solid solution to understanding mechanisms at the molecular level and it may bring useful insight in terms of process analytical technique. In the present study, generalized two-dimensional (2D) correlation spectroscopy is utilized for the Raman image analysis of pharmaceutical tablets to reveal molecular interactions between chemical components. By using a spatial distance as a perturbation variable in 2D correlation scheme, synchronous and asynchronous correlation analysis becomes possible. Two kinds of pharmaceutical tablets, pentoxifylline (PTX) as an active substance and palmitic acid (PA) as an insoluble excipient, are prepared with different grinding times, 0.5 and 45 min. The 2D correlation analysis of Raman images of the tablets clearly reveals both physical and chemical effects of grinding process on the properties of the tablets. Asynchronous correlations indicate that a specific molecular structural change of PTX related to the crystallinity is induced by the grinding process. Namely, the crystallinity of PTX based on CH2 structure is a key factor to control the solubility of the tablets. Some properties of pharmaceutical tablets, i.e. solubility or distribution of components in turn may become possible by the simple grinding process. Detailed analysis of Raman images becomes possible by the 2D correlation spectroscopy. Crown
KW - Generalized two-dimensional (2D) correlation spectroscopy
KW - Pharmaceutical tablet
KW - Raman imaging
KW - Raman spectroscopy
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U2 - 10.1016/j.vibspec.2008.11.011
DO - 10.1016/j.vibspec.2008.11.011
M3 - Article
AN - SCOPUS:67649172572
SN - 0924-2031
VL - 51
SP - 125
EP - 131
JO - Vibrational Spectroscopy
JF - Vibrational Spectroscopy
IS - 1
ER -