International Journal of Molecular Sciences | |
Structural Analysis of Crystalline R(+)-α-LipoicAcid-α-cyclodextrin Complex Based on Microscopic and Spectroscopic Studies | |
Seiichi Matsugo1  Tomoyuki Mizukami1  Kenji Takahashi1  Shota Hosomi1  Masayuki Okuno1  Takatsugu Endo1  Shoji Arai1  Shiori Tanaka2  Noriko Ogawa2  Keita Setou2  Hiromitsu Yamamoto2  Naoko Ikuta3  Keiji Terao3  | |
[1] College of Science and Engineering, Kanazawa University, Kanazawa 920-1192, Japan;Department of Pharmaceutical Engineering, School of Pharmacy, Aichi Gakuin University,Nagoya 464-8650, Japan;Graduate School of Medicine, Kobe University, Kobe 650-0017, Japan; | |
关键词: cyclodextrin; lipoic acid; ATR/FT-IR; microscopic Raman; solid-state NMR; | |
DOI : 10.3390/ijms161024614 | |
来源: DOAJ |
【 摘 要 】
R(+)-α-lipoic acid (RALA) is a naturally-occurring substance, and itsprotein-bound form plays significant role in the energy metabolism in the mitochondria. RALA is vulnerable to a variety of physical stimuli, including heat and UV light, which prompted us to study the stability of its complexes with cyclodextrins (CDs). In this study, we have prepared and purified a crystalline RALA-αCD complex and evaluated its properties in the solid state. The results of 1H NMR and PXRD analyses indicated thatthe crystalline RALA-αCD complex is a channel type complex with a molar ratio of 2:3 (RALA:α-CD). Attenuated total reflection/Fourier transform infrared analysis of the complex showed the shift of the C=O stretching vibration of RALA due to the formation of the RALA-αCD complex. Raman spectroscopic analysis revealed the significant weakness of the S–S and C–S stretching vibrations of RALA in the RALA-αCD complex implying that the dithiolane ring of RALA is almost enclosed in glucose ring of α-CD. Extent of this effect was dependent on the direction of the excitation laser to the hexagonal morphology of the crystal. Solid-state NMR analysis allowed for the chemical shift of the C=O peak to be precisely determined. These results suggested that RALA was positioned in the α-CD cavity with its 1,2-dithiolane ring orientated perpendicular to the plane of the α-CD ring.
【 授权许可】
Unknown