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Voltammetric investigation of macrolides by an HPLC-coulometric assay.

机译:通过HPLC-电量分析法对大环内酯类进行伏安研究。

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摘要

Voltammograms of macrolides, including anhydroerythromycin A, azithromycin, erythromycin A, erythromycin A enol ether, pseudoerythromycin A enol ether, oleandomycin and tylosin have been investigated using a dual electrode cell in combination with a high-throughput LC method. The half-wave potentials (E(1/2)) of the seven macrolides investigated ranged from 0.734 to 0.866V, and the current responses reached the maxima at over 1.0V. The current response of the downstream electrode displayed a non-linear behavior at high potentials over +0.75V, probably because of polarization of solvent components, e.g., water. The HPLC-coulometric assay was optimized with the potentials of the upstream and downstream electrodes at +0.65 and +0.85V, respectively. This method is suitable for detection of 14- and 15-membered macrolides (sensitivity<0.05mugml(-1)), but not for a 16-membered macrolide, tylosin (sensitivity>0.1mugml(-1)). The assay shows interferences from biomatrices in rat's blood plasma and serum, and human urine, but they were effectively removed by a cold acetonitrile extraction method.
机译:使用双电极池结合高通量LC方法研究了大环内酯类化合物的伏安图,包括脱水红霉素A,阿奇霉素,红霉素A,红霉素A烯醇醚,假红霉素A烯醇醚,oleandomycin和tylosin。研究的七个大环内酯类化合物的半波电势(E(1/2))在0.734至0.866V范围内,电流响应在1.0V以上达到最大值。下游电极的电流响应在高于+ 0.75V的高电势下显示出非线性行为,这可能是由于溶剂成分(例如水)的极化所致。用上游和下游电极的电位分别在+0.65和+ 0.85V时对HPLC库仑法进行了优化。此方法适用于检测14和15元大环内酯类药物(灵敏度<0.05mugml(-1)),但不适用于16元大环内酯泰乐菌素(灵敏度> 0.1mugml(-1))。该测定法显示了生物基质对大鼠血浆,血清和人尿的干扰,但是通过冷乙腈提取方法可以有效地去除它们。

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