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1.
The suitability of acid- and enzymatically hydrolyzed birch hemicellulose as biotechnical raw material was studied usingCluconobacter oxydans, Fusarium oxysporum, andCandida utilis for production of xylonic acid, ethanol, and SCP, respectively. The fermentabilities of both hydrolyzates were rather similar
and inhibition was evident in all cases at xylose concentrations of 257–30 g/L and higher. Potential identified fermentation
inhibitors were the lignin-derived compounds sinapyl alcohol, coniferyl alcohol, vanillin, and syringaldehyde and the sugar
degradation products furfural and 5-hydroxymethyl furfural. 相似文献
2.
Kaisa Raninen Ringa Nenonen Elina Jrvel-Reijonen Kaisa Poutanen Hannu Mykknen Olavi Raatikainen 《Molecules (Basel, Switzerland)》2021,26(9)
Exhaled breath is a potential noninvasive matrix to give new information about metabolic effects of diets. In this pilot study, non-targeted analysis of exhaled breath volatile organic compounds (VOCs) was made by comprehensive two-dimensional gas chromatography–mass spectrometry (GCxGC-MS) to explore compounds relating to whole grain (WG) diets. Nine healthy subjects participated in the dietary intervention with parallel crossover design, consisting of two high-fiber diets containing whole grain rye bread (WGR) or whole grain wheat bread (WGW) and 1-week control diets with refined wheat bread (WW) before both diet periods. Large interindividual differences were detected in the VOC composition. About 260 VOCs were detected from exhaled breath samples, in which 40 of the compounds were present in more than half of the samples. Various derivatives of benzoic acid and phenolic compounds, as well as some furanones existed in exhaled breath samples only after the WG diets, making them interesting compounds to study further. 相似文献
3.
Linda Ahonen Pekka Keski-Rahkonen Taija Saarelainen Jenni Paviala Raimo A. Ketola Seppo Auriola Matti Poutanen Risto Kostianen 《Analytica chimica acta》2012
The feasibility of a microfluidic-based liquid chromatography-electrospray ionization/mass spectrometric system (HPLC-Chip/ESI/MS) was studied and compared to a conventional narrow-bore liquid chromatography-electrospray ionization/mass spectrometric (LC-ESI/MS) system for the analysis of steroids. The limits of detection (LODs) for oxime derivatized steroids, expressed as concentrations, were slightly higher with the HPLC-Chip/MS system (50–300 pM) using an injection volume of 0.5 μL than with the conventional LC-ESI/MS (10–150 pM) using an injection volume of 40 μL. However, when the LODs are expressed as injected amounts, the sensitivity of the HPLC-Chip/MS system was about 50 times higher than with the conventional LC-ESI/MS system. The results indicate that the use of HPLC-Chip/MS system is clearly advantageous only in the analysis of low-volume samples. Both methods showed good linearity and good quantitative and chromatographic repeatability. In addition to the instrument comparisons with oxime derivatized steroids, the feasibility of the HPLC-Chip/MS system in the analysis of non-derivatized and oxime derivatized steroids was compared. The HPLC-Chip/MS method developed for non-derivatized steroids was also applied to the quantitative analysis of 15 mouse plasma samples. 相似文献
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5.
Summary The MCGs measured in a case of an anterolateral myocardial infarction were compared with the corresponding simulated MCGs.
The most distinctive changes in the measured MCGs were observed in the upper and lower parts of the thorax as predicted by
the simulation.
Paper presented at the ?IV International Workshop on Biomagnetism?, held in Rome, September 14–16, 1982. 相似文献
6.
R. Hari A. Antervo T. Katila T. Poutanen M. Seppänen T. Tuomisto T. Varpula 《Il Nuovo Cimento D》1983,2(2):484-494
Summary Voluntary limb movements are preceded by MEG shifts beginning even as early as 1.2 s before the movement. These shifts reverse
polarity above the cortical motor representation area of the limb concerned.
Preliminary reports of this study have been presented (1,2). 相似文献
7.
Pekka Keski‐Rahkonen Kaisa Huhtinen Reena Desai D. Tim Harwood David J. Handelsman Matti Poutanen Seppo Auriola 《Journal of mass spectrometry : JMS》2013,48(9):1050-1058
Accurate measurement of estradiol (E2) is important in clinical diagnostics and research. High sensitivity methods are critical for specimens with E2 concentrations at low picomolar levels, such as serum of men, postmenopausal women and children. Achieving the required assay performance with LC–MS is challenging due to the non‐polar structure and low proton affinity of E2. Previous studies suggest that ionization has a major role for the performance of E2 measurement, but comparisons of different ionization techniques for the analysis of clinical samples are not available. In this study, female serum and endometrium tissue samples were used to compare electrospray ionization (ESI), atmospheric pressure chemical ionization (APCI) and atmospheric pressure photoionization (APPI) in both polarities. APPI was found to have the most potential for E2 analysis, with a quantification limit of 1 fmol on‐column. APCI and ESI could be employed in negative polarity, although being slightly less sensitive than APPI. In the presence of biological background, ESI was found to be highly susceptible to ion suppression, while APCI and APPI were largely unaffected by the sample matrix. Irrespective of the ionization technique, background interferences were observed when using the multiple reaction monitoring transitions commonly employed for E2 (m/z 271 > 159; m/z 255 > 145). These unidentified interferences were most severe in serum samples, varied in intensity between ionization techniques and required efficient chromatographic separation in order to achieve specificity for E2. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
8.
S. Bondestam A. Lamminen M. Komu V. -P. Poutanen A. Alanen J. Halavaara 《Magnetic resonance imaging》1992,10(6):989-995
A method for windowing specific T1 values is presented. A 1.0 T imager with two routine pulse sequences was employed: A T1-weighted spin echo (SE) sequence and a short tau inversion recovery STIR sequence (fat-suppressed IR). A T1 window for fat was obtained by subtracting the STIR image from the SE image. Negative values were coded black. The method was tested on a normal human thigh, on a human liver with confirmed fatty infiltration, and on the livers of four live burbots. The fat-containing tissues of the two human volunteers were well depicted. The differences in fat concentration among the burbot livers were also clearly shown. The fat intensity seen in the images correlated well with the chemically measured fat concentration. This subtraction method for windowing T1 values proved feasible for fat. The method could be used for tissues with other short T1 values as well. 相似文献
9.
Abstract The aim of this study was to compare three different test methods for assaying the biodegradability of starch-based materials. The materials tested included some commercial starch-based materials and thermoplastic starch film prepared by extrusion from native potato starch and glycerol. Enzymatic hydrolysis was performed using excess Bacillus licheniformis α-amylase and Aspergillus niger glucoamylase at 37°C. The degree of degradation was assayed by measuring the dissolved carbohydrates and the weight loss of the samples. The head-space test was based on carbon dioxide evolution using sewage sludge as an inoculum. The composting experiments were carried out in an insulated commercial composter bin. The degradation was evaluated visually at weekly intervals, and the weight loss of the samples was measured after composting. Good correlation was found among the three different test methods. 相似文献
10.
Ojala M Poutanen M Mattila I Ketola RA Kotiaho T Kostiainen R 《Rapid communications in mass spectrometry : RCM》2000,14(11):994-998
A method using purge-and-membrane mass spectrometry (PAM-MS) was developed for the analysis of residual solvents in pharmaceutical products. The method combines dynamic headspace and membrane inlet mass spectrometry. The limits of detection for the compounds studied, benzene, toluene, chloroform, 2-pentene and 2-methyl- and 3-methylpentane, were 0.05-0.1 mg/kg. In quantitative analysis the method showed good linearity (r(2) > 0.998) and acceptable within-day (RSD = 7.9-18%) and between-day (RSD = 6.8-10%) repeatability. The PAM-MS method combined with the custom-made Solver program was compared with a method using purge-and-trap gas chromatography/mass spectrometry (P&T-GC/MS) for identification of residual solvents from authentic samples. The results showed that PAM-MS/Solver provides reliable identification of the main volatile organic compounds (VOCs) in the pharmaceuticals, but VOCs with low concentrations (below 0.5 mg/kg) were better identified by P&T-GC/MS. Other advantages of the PAM-MS method were short analysis times and non-requirement for pre-treatment of samples. 相似文献