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Eliete Marçal Guimarães Raso Maria Esperanza Cortes Karina Imaculada Teixeira Milton Batista Franco Nelcy Della Santina Mohallem Ruben Dario Sinisterra 《Journal of inclusion phenomena and macrocyclic chemistry》2010,67(1-2):159-168
The purpose of this study was to prepare and characterize a controlled release system based on porous silica loaded with chlorhexidine (Cx) and its inclusion compounds in β-cyclodextrin (βcd), and to evaluate its antimicrobial activity. Acetate chlorhexidine (CxA), gluconate chlorhexidine (CxG), βcd:chlorhexidine acetate 2:1 (βcd:CxA) and βcd:chlorhexidine gluconate 2:1 (βcd:CxG) were incorporated into porous silica. Drug loading was characterized by FTIR, powder X-ray diffraction, thermal analysis and BET, and was shown to be in an amorphous state and porous matrix. The kinetics release parameter of the drug was established, which showed that the Cx systems release profile followed zero order release until 400 h and Higuchi model release until 750 h, after the burst effect at the first 8 h. Chlorhexidine therapeutic range was reached near first hour for all systems. The chlorhexidine porous silica system was biologically active against Enterococcus faecalis and Candida albicans in vitro. The systems showed an efficient Cx controlled release modulated by the presence of the β-cyclodextrin and by the porous silica matrices, providing effective antimicrobial activity. 相似文献
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2-Furoic acid (2FA), an organic third order nonlinear optical single crystal, has been synthesized and grown successfully by slow solvent evaporation technique. The space group and lattice parameters of the grown crystals were obtained by single crystal X-ray diffraction analysis. The presence of the functional groups was confirmed by Fourier Transform Infrared (FTIR) spectroscopy. Optical absorption studies reveal low absorption in the UV and visible regions and the UV cut-off wavelength is found to be at 240 nm. The thermal stability of the material examined by TGA analysis, reveals that the material is thermally stable up to 130 °C. The third order nonlinear optical parameters (nonlinear refractive index, nonlinear absorption coefficient and real and imaginary parts of the third order nonlinear optical susceptibility) were derived by Z-scan technique. This reveals that the crystal has a negative refractive index, which indicates the defocusing nature of the material. 相似文献
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Milton J. KiefelPradeep Chopra Paul D. MadgeAlex Szyczew Robin J. ThomsonI. Darren Grice Mark von Itzstein 《Tetrahedron letters》2011,52(1):98-100
Sialic acids are 9-carbon acidic sugars involved in a number of important biological processes and human diseases. As part of our ongoing interest in the development of novel sialic acids as biological probes, we have developed an efficient and simple synthesis of C-9 oxidised sialic acid derivatives. The key oxidative step involves the use of TEMPO under carefully controlled aqueous pH conditions. 相似文献
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Summary The complexestrans-[Ru(NH3)4(H2O)PPh3](PF6)2 and [Ru(NH3)5L](PF6)2, (L=AsPh3 or SbPh3) have been isolated and characterized by microanalysis, cyclic voltammetry and ultraviolet-visible spectroscopy. The specific rate constants for the aquation of [Ru(NH3)5L]2+ totrans-[Ru(NH3)4L(H2O)]2+ are (2.5±0.1)×10–5s–1 and (1.8±0.1)×10–5s–1 for L=AsPh3 and SbPh3, respectively, at 25.0±0.1°C; =0.10 mol dm–3, NaO2CCF3. Under the same conditions, the second-order rate constants for the substitution of water intrans-[Ru(NH3)4(H2O)L]2+ by isonicotinamide (isn) are 1.2±0.1, (6.3±0.3)×10–2 and (3.8±0.2)×10–2
m
–1s–1 for L=PPh3, AsPh3, and SbPh3, respectively, suggesting that the order of decreasingtrans-effect is: PPh3AsPh3>SbPh3. The formation constants for thetrans-[Ru(NH3)4L(isn)]2+ complexes are 75±3, (1.40±0.01)×103 and (1.80±0.02)×103M–1 for L=PPh3, AsPh3, and SbPh3, respectively, suggesting that the order of increasingtrans-influence is: SbPh33PPh3. 相似文献
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Fu R Truong M Saager RJ Cotten M Cross TA 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2007,188(1):41-48
A new two-dimensional scheme is proposed for accurate measurements of high-resolution chemical shifts and heteronuclear dipolar couplings in NMR of aligned samples. Both the (1)H chemical shifts and the (1)H-(15)N dipolar couplings are evolved in the indirect dimension while the (15)N chemical shifts are detected. This heteronuclear correlation (HETCOR) spectroscopy yields high-resolution (1)H chemical shifts split by the (1)H-(15)N dipolar couplings in the indirect dimension and the (15)N chemical shifts in the observed dimension. The advantages of the HETCOR technique are illustrated for a static (15)N-acetyl-valine crystal sample and a (15)N-labeled helical peptide sample aligned in hydrated lipid bilayers. 相似文献