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991.
A new method applying sensitive and selective liquid chromatography coupled with mass spectrometry (LC/MS/MS) for analyzing
tertiary-butylhydroquinone (TBHQ) and its metabolites in rat serum was validated. Using an extracted ion chromatogram (EIC)
of m/z 149, free TBHQ was observed in rat serum after dosing TBHQ at 350 mg/kg to male and female Sprague–Dawley (SD) rats. Four
major metabolites of TBHQ were identified—a TBHQ-sulfate, two TBHQ-sulfate-derived substances and a TBHQ-glucuronide through
MSn spectra. Besides its simplicity, the sample treatment allows one to obtain a very good recovery of analysts, namely around
95%. This result suggests that the method described here is useful for the analysis of TBHQ and its metabolites in rat serum.
Moreover, the metabolism of TBHQ was investigated using the method. After oral administration, TBHQ appear to be more completely
absorbed and bio-transformed by males than females, which may result in higher acute oral toxicity of TBHQ for males than
females. 相似文献
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Li Wen Jin-Kun Fu Ping-Ying Gu Bing-Xing Yao Zhong-Hua Lin Jian-Zhang Zhou 《Applied catalysis. B, Environmental》2008,79(4):402-409
Monodispersed nano-Au/γ-Al2O3 catalysts for low-temperature oxidation of CO have been prepared via a modified colloidal deposition route, which involves the deposition of dodecanethiolate self-assembled monolayer (SAM)-protected gold nanoparticles (C12 nano-Au) in hexane on γ-Al2O3 at room temperature. The diameter of the gold nanoparticles deposited on the support is 2.5 ± 0.8 nm after thermal treatment, and their valence states comprise both the metallic and oxidized states. It is found that the thermal treatment temperature affects significantly the catalytic activity of the catalysts in the processing steps. The catalyst treated at 190 °C exhibits considerably higher activity as compared to catalysts treated at 165 and 250 °C. A 2.0-wt.% nano-Au/γ-Al2O3 catalyst treated at 190 °C for 15 h maintains the catalytic activity at nearly 100% CO oxidation for at least 800 h at 15 °C, at least 600 h at 0 °C, and even longer than 450 h at −5 °C. Evidently, the catalysts obtained using this preparation route show high catalytic activity, particularly at low temperatures, and a good long-term stability. 相似文献
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Nonwoven, biodegradable membranes fabricated by electrospinning have recently attracted a great deal of attention for biomedical applications. In this study, microporous, nonwoven membranes of poly(L ‐lactide) and its copolymers and blends were fabricated through electrospinning. The structures and morphologies of the electrospun membranes were investigated with scanning electron microscopy, differential scanning calorimetry, and X‐ray diffraction. Different polymer membranes, incorporated with carmofur, were fabricated, and their drug release profiles were investigated. Scanning electron microscopy images showed that the fiber diameters were down to the nanometer range. The diameters and morphologies of thenanofibers depended on processing parameters such as the solution properties (concentration and polymer molecular weight), applied electric voltage, solution feeding rate, and needle diameter. Differential scanning calorimetry showed that the crystallinity of the electrospun membranes was lower than that of the cast film. For all the membranes incorporated with the drug, there was a burst release in the first 10 h of incubation in phosphate‐buffered saline at 37°C. Poly(glycolide‐co‐lactide) membranes showed faster and more complete drug release than poly(L ‐lactide), and this could be attributed to its faster degradation. The incorporation of polylactide–poly(ethylene glycol) could shorten the drug release time. A combination of suitable degradable biomaterials with an appropriate electrospinning process could be useful in the fabrication of a new kind of membrane suitable for different biomedical applications such as tissue engineering and drug delivery. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献