| 1. |
- Liu, Yu-peng, et al.
(författare)
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应用酶热生物分析仪快速测量血糖的研究分析
- 2013
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Ingår i: Journal of Clinical and Experimental Medicine. ; 12:8, s. 579-581
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Tidskriftsartikel (refereegranskat)abstract
- Objective To compare the enzyme thermistor bioanalysis equipment with blood glucose meter which is analyzed by automatic biochemical analyzer, validate the correct rate of this equipment. The long-term aim of the project was to develop a prototype for a bedside monitor system for semi-continuous monitoring of the blood glucose concentration. This was made possible by using the special advantage of the thermal sensor technique in combination with the adjustment of flow. Methods 150 patients were collected in our department. The glucose level was determined using a single channel enzyme thermistor device. Then the results were compared with lab biochemistry analysator. Results There was no significant difference between these two methods (P>0.05). The measuring method with single channel enzyme thermistor device is a reliable method in determining blood glucose level. Single channel enzyme thermistor keep a coincidence with automatic biochemical analyzer. The assay cycle time was 3 minutes. Comparative analysis between our device and the clinical system device showed an excellent correlation for 150 patient blood samples. The device was stabile for hundreds of injections over a period of 45 days. Conclusion Determined glucose in whole blood using a single channel Enzyme Thermistor device can be used to assess the severity of an illness and for evaluating therapeutic efficacy. The ability of the device to analyze whole blood without any pretreatment makes it possible to develop real-time analysis.
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| 2. |
- Gao, Aiping, et al.
(författare)
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Asymmetric oxidation of sulfides catalyzed by vanadium(IV) complexes of dibromo- and diiodo-functionalized chiral Schiff bases
- 2006
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Ingår i: Cuihuà xuébào. - 0253-9837 .- 1872-2067. ; 27:8, s. 743-748
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Tidskriftsartikel (refereegranskat)abstract
- The catalyst system of VO(acac)(2) and Schiff base ligands derived from 3,5-dibromo- or 3,5-diiodosalicylaldehyde and inexpensive chiral amino alcohols was prepared. This catalyst displayed good yields and moderate to high enantioselectivity for the asymmetric oxidation of aryl methyl sulfides at room temperature when 1% catalyst (VO(acac)(2)/ligand molar ratio of 1: 2) and H2O2 Oxidant were used. The ligands derived from ( S)valinol exhibited considerably higher enantioselectivity than those ligands derived from ( S)-phenylalaninol and (R)-leucinol. The enantiomeric excess values were improved up to 88% for methyl phenyl sulfoxide and 92% for methyl p-bromophenyl sulfoxide by slow dropwise addition of H2O2 with the ligand prepared from 3 15-diiodosalicylaldehyde and (s)-valinol. The present study showed that the catalytic efficiency of VO(acac)(2) /Schiff base systems could not be improved by the addition of carboxylic acids or carboxylate salts.
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