3,134 publications from this institution
Abstract Scope: The aim of this study was to investigate the interaction between polyphenols and bovine γ‐globulin. Methods and results: The relationship between the structural properties of natural polyphenols and their affinities for bovine γ‐globulin were investigated by fluorescence titration analysis. Methylation of hydroxyl groups on flavonoids weakened the affinities for γ‐globulin by 1.20–38.0 times. Hydroxylation on rings A, B, and C of flavonoids also significantly affected the affinity for γ‐globulin. Glycosylation of flavonoids slightly affected the affinity depending on the conjugation site and the class of sugar moiety. Hydrogenation of the C2C3 double bond on flavonoids decreased the binding affinities. Galloylated catechins and catechol‐type catechins exhibited higher binding affinities for γ‐globulin than non‐galloylated and pyrogallol‐type catechins. The glycosylation of resveratrol decreased its affinity for γ‐globulin. Conclusion: The binding process with γ‐globulin was strongly influenced by the structural differences of polyphenols.
A rapid revised phase high performance liquid chromatographic method for the determination of organic acids in bauxite was reported. Oxalic, malonic, acetic, succinic, glutaric and adipic acid were separated and quantified in 10 min. First time repeatability, reproducibility and recoveries were determined for these acids in bauxite. The organic acids were removed from bauxite using a solid phase extraction procedure with anion exchange cartridges. The chromatographic separation was achieved with only one Kromasil RP-C18 column thermostated at 25°C. Organic acids were detected with a UV VIS detector (215 nm). The precision results showed that the relative standard deviations of the repeatability and reproducibility were, <2·13 and, <3·24% respectively. The accuracy of the method was confirmed with an average recovery ranging between 89·2 and 114·7%. Under optimum conditions the detection limits ranged from 0·042 to 10·36 mg L−1.
Multipod Au nanoparticles (nanostars) with single crystalline tips were synthesized in extremely high yield through the reduction of HAuCl(4) in a concentrated solution of poly(vinylpyrrolidone) (PVP) in N,N-dimethylformamide (DMF), in the presence of preformed Au nanoparticle seeds, but with no need for external energy sources. Nanostar dispersions display a well-defined optical response, which was found (through theoretical modeling) to comprise a main mode confined within the tips and a secondary mode confined in the central body. Calculations of the surface enhanced Raman scattering (SERS) response additionally show that this morphology will be relevant for sensing applications.
Hermida, R. C.1; Ayala, D. E.1; Calvo, C.2; Mojon, A.1; Fernandez, J. R.1; Alonso, I.1; Dominguez, M. J.2; Covelo, M.2; Lopez, J. E.2 Author Information
A Rayleigh light scattering technique to determine ciprofloxacin lactate (CPFL) in drugs by tetraphenylboron sodium (TPB) was developed. Ciprofloxacin lactate was found to bind B(C6H5)4− anion and transformed to CPFL–TPB aggregate which displayed intense Rayleigh scattering light. Effects of factors such as wavelength, acidity, stabilizers and interferents on the RLS of CPFL–TPB were investigated in detail. The RLS intensity of the CPFL–TPB suspension was obtained in acetate buffer (0.50 mol L−1, pH = 4.0). The Rayleigh scattering light intensity at the maximum RLS peak of 408 nm was linear to the concentration of ciprofloxacin lactate in the range of 8.0–20.0 µg mL−1 with a detection limit of 6.0 µg mL−1. Good results were also obtained with the recovery range of 93.68–104.06%. The method was applied to determine ciprofloxacin lactate in injections, eye drops and tablets, showing high sensitivity and accuracy compared with the high performance liquid chromatography method (HPLC) according to Chinese Pharmacopoeia.