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首页> 外文期刊>Journal of food and drug analysis >Hantzsch pre-column derivatization for simultaneous determination of alendronate sodium and its pharmacopoeial related impurity: Comparative study with synchronous fluorometry using fluorescamine
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Hantzsch pre-column derivatization for simultaneous determination of alendronate sodium and its pharmacopoeial related impurity: Comparative study with synchronous fluorometry using fluorescamine

机译:汉茨预柱衍生化法同时测定阿仑膦酸钠及其药理相关杂质:同步荧光法与荧光胺的比较研究

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摘要

High performance liquid chromatographic (HPLC) method with a pre-column derivatization based on Hantzsch condensation reaction was applied for simultaneous determination of alendronate sodium (ALN) and its main related impurity, 4-Aminobutanoic acid (ABA) at its pharmacopeial limit. The separation of colored condensation products of ALN and ABA were achieved on Agilent Zobrax Eclipse SB-C18 analytical column (250?×?4.6?mm, 5?μm) using a mobile phase composed of acetonitrile–0.1?M acetate buffer, pH 5.0 (15:85, v/v). The flow rate was 1?mL?minsup?1/sup. The detection was carried out at 340?nm using photo-diode array detector. Peak areas were used for the linear regression line in the range of 10–500 and 0.2–40?μg?mLsup?1/sup for ALN and ABA, respectively. Different conditions for the optimization of the derivatization reactions as well as for the HPLC measurement were studied. The proposed method was validated for linearity, precision, accuracy, specificity and robustness. This method was used to check the purity of ALN in the presence of ABA (related impurity) at the pharmacopeial limit (0.5%). For comparison purpose, another method was proposed which involves synchronous fluorescence measurement after ALN reaction with fluorescamine . In this method, the third derivative synchronous spectra were estimated as peak to peak measurement from 339 to 370?nm for ALN determination with LOD and LOQ of 24 and 73?ng?mLsup?1/sup, respectively, showing very high sensitivity. Both methods have been applied for determination of the alendronate sodium (ALN) in bulk and pharmaceutical preparations without interference of additives in tablets or oral solution.
机译:采用基于Hantzsch缩合反应的柱前衍生化的高效液相色谱(HPLC)方法同时测定了阿仑膦酸钠(ALN)及其主要相关杂质,4-氨基丁酸(ABA)的限量。在Agilent Zobrax Eclipse SB-C18分析柱(250?×?4.6?mm,5?μm)上,使用乙腈–0.1?M乙酸盐缓冲液,pH 5.0分离ALN和ABA的彩色缩合产物(15:85,v / v)。流速为1?mL?min ?1 。使用光电二极管阵列检测器在340nm处进行检测。线性回归线的峰面积分别在ALN和ABA的10–500和0.2–40?ggmL / mL ?1 范围内。研究了优化衍生化反应以及进行HPLC测定的不同条件。所提出的方法的线性,精度,准确性,特异性和鲁棒性均得到验证。该方法用于检查在药典限量(0.5%)下存在ABA(相关杂质)的情况下ALN的纯度。为了进行比较,提出了另一种方法,该方法涉及在ALN与荧光胺反应后进行同步荧光测量。在此方法中,将三阶导数同步光谱估计为峰到峰测量值,范围从339至370nm,用于ALN测定,LOD和LOQ分别为24和73?ng?mL ?1 。很高的灵敏度。两种方法均已用于测定散装和药物制剂中的阿仑膦酸钠(ALN),而不会干扰片剂或口服溶液中的添加剂。

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