Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Pharmaceutical Services Center, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Luminescence. 2019 May;34(3):375-381. doi: 10.1002/bio.3622. Epub 2019 Mar 18.
Sodium alendronate is the first in a pharmacological class known as bisphosphonates, used for treatment of various bone diseases. Assay of bisphosphonates by a spectroscopic technique is very challenging due to the fact that they lack chromophores and none of them are fluorescent. In this work, a simple method is presented for determination of alendronate in bulk and in pharmaceutical tablets using spectrofluorometry by exploiting the ability of alendronate to displace salicylate from the iron(III)-salicylate chelate, forming a non-fluorescent colorless iron(III)-alendronate complex. The liberated salicylate is fluorescent and is equivalent to the mount of alendronate added. The response was linear over the concentration range 20-90 μM and the proposed method was validated according to the guidelines of the International Conference on Harmonization. The correlation coefficient was found to be 0.995 and the limit of detection was 7.5 μM. The method was successfully applied for determination of alendronate in the commercially available Osteonate® tablets. The average percent recovery ± percent relative standard deviation was found to be 102.118 ± 2.033 which is congruent with the label claim of the dosage form. The results were also compared to a reported method using t-test and F-test at 95% confidence level; no significant differences were observed. The presented method is simple, fast, easy, cost-effective and suitable for routine pharmaceutical analysis.
阿仑膦酸钠是一类被称为双膦酸盐的药物中的第一种,用于治疗各种骨骼疾病。由于双膦酸盐缺乏生色团,并且它们都没有荧光,因此用光谱技术测定双膦酸盐非常具有挑战性。在这项工作中,提出了一种简单的方法,通过利用阿仑膦酸钠从铁(III)-水杨酸配合物中置换水杨酸的能力,利用荧光光谱法在原料药和药物片剂中测定阿仑膦酸钠,形成一种非荧光无色铁(III)-阿仑膦酸钠配合物。释放的水杨酸具有荧光性,与添加的阿仑膦酸钠的量相当。在 20-90 μM 的浓度范围内,响应呈线性,并且根据国际协调会议的指南对所提出的方法进行了验证。相关系数为 0.995,检测限为 7.5 μM。该方法成功地应用于市售 Osteonate®片剂中阿仑膦酸钠的测定。平均回收率 ± 相对标准偏差为 102.118 ± 2.033,与该剂型的标签声称相符。在 95%置信水平下,使用 t 检验和 F 检验将结果与报道的方法进行比较;未观察到显著差异。所提出的方法简单、快速、易于操作、具有成本效益,适合常规药物分析。