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11.
Summary β-Cyclodextrin sulfate having heparin-mimicking activity was immobilized on a hydrophilic vinyl-polymer gel, TSKgel AF-Epoxy,
TOYOPEARL 650M. A column packed with this material could be used for high-performance affinity chromatographic separation
of heparin-binding substances such as growth factors, enzymes, coagulation factors and lipoproteins. The substances retained
on the column were recovered more easily than those on a heparin-immobilized column. Furthermore, the β-Cyclodextin sulfate-immobilized
gel was superior in stability to the heparin-immobilized gel when exposed to acidic and basic solutions. 相似文献
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Mutual annihilation of triplet excitons in Pt-phthalocyanine single crystal at 4.2 K has been studied under magnetic fields of up to 100 kG through the measurement of the phosphorescence decay by Q-switched ruby laser excitation. The maximum annihilation rate γ which is larger than that of zero magnetic field by 40–50% is obtained at magnetic fields of 30–40 kG. The annihilation rate γ is of the order of 10−12 cm3/s. 相似文献
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Sonoda Y Hirayama F Arima H Yamaguchi Y Saenger W Uekama K 《Chemical communications (Cambridge, England)》2006,(5):517-519
We describe a novel approach for the selective isolation of Ostwald's intermediate metastable polymorphs occurring during an early stage of crystallization, by utilizing the inclusion complex formed with a cyclic oligosaccharide derivative, 2,6-di-O-methyl-beta-cyclodextrin. 相似文献
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Hara T Hirayama F Arima H Yamaguchi Y Uekama K 《Chemical & pharmaceutical bulletin》2006,54(3):344-349
2-(N-Cyanoimino)-5-[(E)-4-styrylbenzylidene]-4-oxothiazolidine (FPFS-410) is a newly synthesized thiazolidine derivative having not only antidiabetic but also lipid-lowering activities. However, this compound has an extremely low aqueous solubility (2.8 (+/-0.33) x 10(-8) M (0.0094+/-0.0011 microg/ml) in 1.0 M phosphate buffer (pH 7.0) at 25 degrees C). In this study, we investigated the effect of various hydrophilic cyclodextrins (CyDs) on the solubility of FPFS-410 to select a CyD suitable for formulations of the compound. Among various CyDs, 2-hydroxypropyl-beta-CyD (HP-beta-CyD) had the highest solubilizing ability to FPFS-410, e.g., the solubility of the compound was increased 200000-fold by the addition of 40 mM HP-beta-CyD, which was attributable to the formation of the 1 : 2 (guest : host) inclusion complexes. The interaction of HP-beta-CyD with FPFS-410 was studied using 1H-nuclear magnetic resonance (NMR) spectroscopies including ROESY spectroscopy and a molecular modeling calculation. These results suggested that HP-beta-CyD forms a 1:2 (guest : host) inclusion complex with FPFS-410 by including both the stilbene and thiazolidine moieties. FPFS-410/HP-beta-CyD solid complexes with various stoichiometries were prepared by the spray drying and cogrinding methods, and confirmed by powder X-ray diffractometry that these complexes are in an amorphous state. The dissolution of FPFS-410 in water was significantly accelerated by the complexation with HP-beta-CyD. In vivo studies revealed that HP-beta-CyD markedly increases the bioavailability of FPFS-410 after oral administration in dogs. The present results suggest that HP-beta-CyD is useful for improvement of the extremely low bioavailability of FPFS-410. 相似文献