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161.
Ioannis Papanastasiou Andrew Tsotinis George B. Foscolos S. Radhika Prathalingam John M. Kelly 《Journal of heterocyclic chemistry》2008,45(5):1401-1406
162.
The increasing interest in antioxidant properties of cereal and cereal-based products has prompted the development of a simple and reliable HPLC method for the simultaneous determination of important phytochemicals like tocopherols (T), tocotrienols (T3) and carotenoids. Separation was carried out on a Nucleosil 100 C(18) column, 5 μm (250 mm × 4.6 mm) thermostated at 25 °C, using a linear gradient elution system starting with methanol and ending with a mixture of methanol-isopropanol-acetonitrile. All separated compounds including the internal standard (α-tocopherol acetate) were eluted within 16 min and detected by dual detection: fluorescence for tocopherols and tocotrienols at 290 nm excitation and 320 nm emission and UV-vis photodiode array detection for lutein and β-carotene at 450 nm. Detection limits ranged from 0.2 μg/g (β-carotene) to 1.60 μg/g (α-tocopherol). The intra- and inter-assay coefficients of variation were calculated by using cereals with different levels of lipophilic antioxidants. The extraction method involved sample saponification and clean-up by solid-phase extraction (SPE). The extraction recoveries obtained using OASIS HLB SPE cartridges and dichloromethane as eluent were in the range of 90.2-110.1%, with RSD lower than 10%. The method was successfully applied to cereals: durum wheat, bread wheat, rice, barley, oat, rye, corn and triticale. 相似文献
163.
Papoutsis I Nikolaou P Athanaselis S Alevizopoulos G Pistos C Paraskevopoulou C Spiliopoulou C 《Journal of separation science》2011,34(21):3037-3042
Sildenafil (SDL) is a phosphodiesterase type 5 inhibitor and it is approved for the treatment of erectile dysfunction and pulmonary hypertension. SDL is extensively metabolized to its pharmacologically active metabolite, desmethyl‐sildenafil (DSDL). A sensitive and specific GC/MS method for the determination of SDL and DSDL in whole blood was developed and validated to support therapeutic drug monitoring of SDL patients. The combination of solid‐phase extraction with derivatization using BSTFA with 1% TMCS in acetonitrile efficiently reduced matrix effect and improved sensitivity of the method. In this assay, protriptyline was used as internal standard for both analytes. The LODs were 1.50 and 5.00 ng/mL for SDL and DSDL, respectively, whereas the respective LOQs were 5.00 and 15.0 ng/mL. The calibration curves were linear up to 500.0 ng/mL (SDL: R2 0.992, DSDL: R2 0.990). Absolute recovery values for both analytes ranged from 83.1 to 93.2%. Within‐ and between‐batch accuracy was less than 11.8 and 10.2%, respectively, whereas within‐ and between‐batch precision was less than 8.1 and 10.8%, correspondingly. The developed method is suitable for the determination of SDL and DSDL concentrations in blood samples obtained from patients under Viagra® treatment, for pharmacokinetic studies or for the investigation of related forensic cases. 相似文献
164.
A novel method for the simultaneous determination of six benzodiazepines (BZDs) and four tricyclic antidepressants (TCAs) in biological fluids by HPLC with UV detection at 240 nm has been developed. After a deproteinization step biological fluids were analyzed by direct injection. SPE on Nexus cartridges was also applied. Since two compounds, namely imipramine and diazepam, were coeluting, a sequential SPE protocol has been developed. BZDs were eluted by a mixture of methanol/ACN(1:1), followed by the elution of TCAs with methanol. Separation was performed on a Kromasil C8 column (250 x 64 mm(2) id, 5 microm) using a mobile phase of 0.05 MCH3COONH4/ACN/methanol (initial composition 55:15:30 v/v/v) at a flow rate of 1.0 mL/min delivered by a gradient program within 15 min. Colchicine was used as the internal standard (4 ng/microL). The method was linear for all analytes up to 20 ng/lL, with coefficients of regression between 0.996 and 0.99996. LODs and LOQs were 0.08-1.17 and 0.28-3.91 ng/lL, respectively. Recovery was in the range of 92.8-108.7% for within-day and 91.9-109.9% for between-day assays, with RSD values lower than 10.0% for all matrices. 相似文献
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168.
Dodecahydro‐ closo ‐dodecaborates of the Heavy Alkaline‐Earth Metals from Aqueous Solution: Ca(H2O)7[B12H12] · H2O, Sr(H2O)8[B12H12], and Ba(H2O)6[B12H12] The crystalline hydrates of the heavy alkaline earth metal dodecahydro‐closo‐dodecaborates (M[B12H12] · n H2O, n = 6–8; M = Ca, Sr, Ba) are easily accessible by reaction of an aqueous (H3O)2[B12H12] solution with an alkaline earth metal carbonate (MCO3). By isothermic evaporation of the respective aqueous solution we obtained colourless single crystals which are characterized by X‐ray diffraction at room temperature. The three compounds Ca(H2O)7[B12H12] · H2O (orthorhombic, P212121; a = 1161.19(7), b = 1229.63(8), c = 1232.24(8) pm; Z = 4), Sr(H2O)8[B12H12] (trigonal, R3; a = 1012.71(6), c = 1462.94(9) pm; Z = 3) and Ba(H2O)6[B12H12] (orthorhombic, Cmcm; a = 1189.26(7) pm, b = 919.23(5) pm, c = 1403.54(9) pm; Z = 4) are neither formula‐equal nor isostructural. The structure of Sr(H2O)8[B12H12] is best described as a NaCl‐type arrangement, Ba(H2O)6[B12H12] rather forms a layer‐like and Ca(H2O)7[B12H12] · H2O a channel‐like structure. In first sphere the alkaline earth metal cations Ca2+ and Sr2+ are coordinated by just seven and eight oxygen atoms from the surrounding water molecules, respectively. A direct coordinative influence of the quasi‐icosahedral [B12H12]2– cluster anions becomes noticeable only for the Ba2+ cations (CN = 12) in Ba(H2O)6[B12H12]. The dehydratation of the alkaline earth metal dodecahydro‐closo‐dodecaborate hydrates has been shown to take place in several steps. Thermal treatment leads to the anhydrous compounds Ca[B12H12], Sr[B12H12] and Ba[B12H12] at 224, 164 and 116 °C, respectively. 相似文献
169.
Tsakalof AK Bairachtari KA Aslani IS Chryssoulakis ID Kolisis FN 《Journal of separation science》2004,27(3):167-173
The materials and especially organic materials used for creation of art objects can be utilized by various microorganisms for their growth and facilitate the microbial colonization of the object. An understanding of the chemical alterations in artefacts caused by the presence of microorganisms can be crucial for correct identification of the materials initially used for the artefact creation--nowadays an important step in restoration and/or art-historical investigation of the art object. The present article describes a model experiment in which we investigated the possible chemical alterations in animal glue films used as substrate for growth of the fungus Aspergillus niger. The sterilized animal glue solution was poured into Petri dishes, inoculated with Aspergillus niger, and subsequently incubated at 15 degrees C for 0, 7, 9, 14, and 28 days. After interruption of incubation, the content of the Petri dish was analyzed for amino acid composition by the GC-MS based method. It was found that the growth of Aspergillus niger on animal glue films did not cause significant changes in the amino acid composition of the film and had no impact on animal glue identification. 相似文献
170.