首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >1,4-Anthraquinone: A new useful pre-column reagent for the determination of N-acetylcysteine and captopril in pharmaceuticals by high performance liquid chromatography
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1,4-Anthraquinone: A new useful pre-column reagent for the determination of N-acetylcysteine and captopril in pharmaceuticals by high performance liquid chromatography

机译:1,4-蒽醌:通过高效液相色谱法测定药物中的N-乙酰半胱氨酸和卡托普利的新有用的预柱试剂

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1,4-Anthraquinone (ANQ) is proposed as a novel pre-column reagent for high performance liquid chromatography (HPLC) determination of N-acetylcysteine (NAC) and captopril (CAP) in pharmaceutical formulations. The derivatization reactions were carried out at room temperature: NAC at pH 8 for 1 min, while CAP at pH 7.5 for 20 min. Both reactions reached completeness at a reagent to thiol molar ratio of about 2.5. The synthesised derivatives were characterized by H-1 NMR and IR The chromatographic separations were performed on a C-18 Phenomenex Synergi Fusion 4 mu m (250 mm x 4.6 mm I.D.) stainless steel column with detection at lambda=300 nm. The mobile phase consisted of methanol/triethylammonium (TEA) phosphate buffer (pH 3; 0.05 mol/L) 75:25 (v/v) at a flow-rate of 0.4 mL/min for NAC and 88:12 (v/v), at a flow-rate of 0.6 mL/min for CAP. The validation parameters (linearity, sensitivity, accuracy, precision, specificity and stability) were highly satisfactory. Linear response was observed (determination coefficient >= 0.9996). Detection limits were about 8 and 18 ng/mL for NAC and CAP, respectively. Intra-day precision (relative standard deviation, R.S.D.) was <= 1.58%, for thiol to internal standard (IS) peak area ratio and <= 0.33%, for thiol and IS retention times (t(R)), without significant differences between intra- and inter-day data. Thiol recovery studies were satisfactory (99.50%) with R.S.D. <= 0.56%. The results highlight the high sensitivity of the method and the remarkable reactivity and selectivity of the reagent towards the thiol function. The developed method is suitable for the quality control of both thiols in commercial products. The method can be applied in any analytical laboratory not requiring a sophisticated instrumentation. (C) 2017 Elsevier B.V. All rights reserved.
机译:提出1,4-蒽醌(ANQ)作为高效液相色谱(HPLC)的新型预柱试剂(HPLC)测定药物制剂中的N-乙酰半胱氨酸(NAC)和卡托普利(帽)的含量。衍生化反应在室温下进行:NaC在pH8下1分钟,而pH 7.5的帽20分钟。两种反应在试剂中达到完全性,硫醇摩尔比为约2.5。合成的衍生物的特征在于H-1 NMR,并在C-18现象Synergi融合4μm(250mm×4.6mm I.D.)不锈钢柱上进行了色谱分离,在Lambda = 300nm处检测。流动相由NAC和88:12的流速为0.4ml / min的流速,由甲醇/三乙基铵(茶)磷酸盐缓冲液(pH3; 0.05mol / l)75:25(v / v)组成。(v / v ),以0.6ml / min的流速用于帽。验证参数(线性,灵敏度,准确性,精度,特异性和稳定性)非常令人满意。观察到线性响应(确定系数> = 0.9996)。对于NAC和帽,检测限度分别为约8至18ng / ml。对于硫醇的硫醇至内标(IS)峰面积比和硫醇的峰面积比和保留时间(T(r))而没有显着差异,为内标(相对标准偏差,RSD)<= 1.58%,对于内标(是)峰面积比和<= 0.33%(t(r)),无显着差异在日内和日内数据之间。硫醇恢复研究令人满意(99.50%),R.S.D. <= 0.56%。结果突出了该方法的高灵敏度和试剂对硫醇函数的显着反应性和选择性。开发方法适用于商业产品中硫醇的质量控制。该方法可以应用于不需要复杂仪器的任何分析实验室。 (c)2017年Elsevier B.V.保留所有权利。

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