吡哆胺
化学
吡哆醇
荧光灯
吡哆醛
维生素
紫外线
荧光
白炽灯
荧光灯
色谱法
核化学
维生素b6
生物化学
光化学
材料科学
光学
酶
物理
光电子学
物理化学
出处
期刊:Journal - Association of Official Analytical Chemists
[Oxford University Press]
日期:1979-09-01
卷期号:62 (5): 1170-1173
被引量:11
标识
DOI:10.1093/jaoac/62.5.1170
摘要
Abstract Pyridoxine.HCl, pyridoxal.HCl, and pyridoxamine. 2HCl solutions were exposed to several laboratory light treatments, and the resulting vitamin retentions were determined by the AOAC microbiological method. The 5 treatments compared were total darkness, regular laboratory light, low actinic glass protection, yellow incandescent light, and golden fluorescent light. All treatments were imposed for 8 and 15 hr, and with the vitamin solutions at both a low and a high pH. Regular laboratory light was the most destructive to the vitamins, with greater destruction at higher pH and longer exposure time in all cases. Pyridoxine retentions ranged from 97 (pH 4.5, 8 hr) to 66% (pH 7, 15 hr); pyridoxal from 97 (pH 4.5, 8 hr) to 55% (pH 6, 15 hr); and pyridoxamine from 81 (pH 4.5, 8 hr) to 47% (pH 8, 15 hr). Retentions in low actinic glassware or in clear glassware under yellow or golden fluorescent light were essentially complete, ranging from 94 to 106% over all treatments and all 3 forms. Results showed that either of the 2 subdued light conditions, yellow or golden fluorescent light, is suitable in vitamin B6 assays and that low actinic glassware is suitable for storing sample solutions.
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