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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Spectrophotometric study of the reaction mechanism between DDQ as pi-acceptor and potassium iodate and flucloxacillin and dicloxacillin drugs and their determination in pure and in dosage forms
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Spectrophotometric study of the reaction mechanism between DDQ as pi-acceptor and potassium iodate and flucloxacillin and dicloxacillin drugs and their determination in pure and in dosage forms

机译:分光光度法研究DDQ作为pi受体与碘酸钾和氟氯西林和双氯西林药物之间的反应机理及其纯净和剂型测定

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Two simple and accurate spectrophotometric methods are presented for the determination of P-lactam drugs, flucloxacillin (Fluclox) and dicloxacillin (Diclox), in pure and in different pharmaceutical preparations. The charge transfer (CT) reactions between Fluclox and Diclox as electron donors and 2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ) pi-acceptor and potassium iodate via oxidation reduction reaction where the highly coloured complex species or the liberated iodine have been spectrophotometrically studied. The optimum experimental conditions have been studied carefully. Beer's law is obeyed over the concentration range of 2-450 mu g ml(-1) for Fluclox and 10-450 mu g ml(-1) for Diclox using DDQ reagent and at 50-550 mu g ml(-1) for Fluclox and 50-560 mu g ml(-1) for Diclox using iodate method, respectively. For more accurate results, Ringbom optimum concentration range is calculated and found to be 6-450 and 15-450 mu g ml(-1) for Fluclox and Diclox using DDQ, respectively, and 65-550 and 63-560 mu g ml(-1) for Fluclox and Diclox using iodine, respectively. The Sandell sensitivity is found to be 0.018 and 0.011 mu g cm(-1) for DDQ method and 0.013 and 0.011 mu g cm(-2) for iodate method for Fluclox and Diclox, respectively, which indicates the high sensitivity of both methods. Standard deviation (S.D. = 0.01-0.80 and 0.07-0.98) and relative standard deviation (R.S.D. = 0.13-0.44 and 0.11-0.82%) (n = 5) for DDQ and iodate methods, respectively, refer to the high accuracy and precision of the proposed methods. These results are also confirmed by between-day precision of percent recovery of 99.87-100.2 and 99.90-100% for Fluelox and Diclox by DDQ method and 99.88-100.1 and 99.30-100.2% for Fluclox and Diclox by iodate method, respectively. These data are comparable to those obtained by British and American pharmacopoeias assay for the determination of Fluclox and Diclox in raw materials and in pharmaceutical preparations. (c) 2005 Elsevier B.V. All rights reserved.
机译:提出了两种简单而准确的分光光度法测定纯和不同药物制剂中的β-内酰胺药物氟氯西林(Fluclox)和双氯西林(Diclox)。 Fluclox和Diclox作为电子供体与2,3-二氯-5,6-二氰基对苯醌(DDQ)pi受体和碘酸钾之间的电荷转移(CT)反应是通过氧化还原反应进行的,其中高度着色的复合物或已经用分光光度法研究了游离碘。最佳实验条件已经过仔细研究。使用DDQ试剂在Fluclox的浓度范围为2-450μgml(-1)和在Diclox的浓度范围为10-450μgml(-1)时,对于50-550μgml(-1)遵守比尔定律使用碘酸盐法分别将氟氯酸和50-560μg ml(-1)用于双氯芬酸。为了获得更准确的结果,Ringbom的最佳浓度范围经计算得出,使用DDQ的Fluclox和Diclox分别为6-450和15-450μgml(-1),以及65-550和63-560μgml( -1)分别使用碘的Fluclox和Diclox。发现DDQ方法的Sandell灵敏度分别为0.018和0.011μg cm(-1),碘伏特方法的Fluclox和Diclox灵敏度分别为0.013和0.011μgcm(-1),这表明这两种方法都具有很高的灵敏度。 DDQ和碘酸盐方法的标准偏差(SD = 0.01-0.80和0.07-0.98)和相对标准偏差(RSD = 0.13-0.44和0.11-0.82%)(n = 5)分别表示DDQ和碘酸盐方法的高精度和高精度建议的方法。这些结果还通过日间通过DDQ方法对Fluelox和Diclox的回收率分别为99.87-100.2和99.90-100%以及通过碘酸盐方法对Fluclox和Diclox的回收率分别为99.88-100.1和99.30-100.2%的精确度来证实。这些数据与通过英国和美国药典测定获得的数据相当,可用于测定原料和药物制剂中的Fluclox和Diclox。 (c)2005 Elsevier B.V.保留所有权利。

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