Basavaiah Kanakapura, Ramakrishna Veeraiah, Kumar Urdigere Rangachar Anil
Department of Chemistry, University of Mysore, Manasagangotri, Mysore-570006, India.
Acta Pharm. 2007 Jun;57(2):211-20. doi: 10.2478/v10007-007-0017-5.
Two spectrophotometric methods are proposed for the assay of lansoprazole (LPZ) in bulk drug and in dosage forms using ceric ammonium sulphate (CAS) and two dyes, methyl orange and indigo carmine, as reagents. The methods involve addition of a known excess of CAS to LPZ in acid medium, followed by determination of residual CAS by reacting with a fixed amount of either methyl orange, measuring the absorbance at 520 nm (method A), or indigo carmine, measuring the absorbance at 610 nm (method B). In both methods, the amount of CAS reacted corresponds to the amount of LPZ and the measured absorbance was found to increase linearly with the concentration of LPZ, which is corroborated by the correlation coefficients of 0.9979 and 0.9954 for methods A and B, respectively. The systems obey Beer's law for 0.5-7.0 microg mL(-1) and 0.25-3.0 microg mL(-1) for methods A and B, respectively. The apparent molar absorptivities were calculated to be 3.0 x 10(4) and 4.4 x 10(4) L mol(-1) cm(-1) for methods A and B, respectively. The limits of detection (LOD) and quantification (LOQ) were calculated to be 0.08 and 0.25 microg mL(-1) for method A, and 0.09 and 0.27 microg mLs(-1) for method B, respectively. The intra-day and inter-day precision and accuracy of the methods were evaluated according to the current ICH guidelines. Both methods were of comparable accuracy (er < or = 2 %). Also, both methods are equally precise as shown by the relative standard deviation values < 1.5%. No interference was observed from common pharmaceutical adjuvants. The accuracy of the methods was further ascertained by performing recovery studies using the standard addition method. The methods were successfully applied to the assay of LPZ in capsule preparations and the results were statistically compared with those of the literature UV-spectrophotometric method by applying Student's t-test and F-test.
提出了两种分光光度法,用于原料药和剂型中兰索拉唑(LPZ)的测定,使用硫酸铈铵(CAS)以及两种染料甲基橙和靛蓝胭脂红作为试剂。这些方法包括在酸性介质中向LPZ中加入已知过量的CAS,然后通过与固定量的甲基橙反应(在520nm处测量吸光度,方法A)或靛蓝胭脂红反应(在610nm处测量吸光度,方法B)来测定残留的CAS。在两种方法中,反应的CAS量对应于LPZ的量,并且发现测量的吸光度与LPZ的浓度呈线性增加,方法A和B的相关系数分别为0.9979和0.9954,证实了这一点。方法A和B的体系分别在0.5 - 7.0μg mL⁻¹和0.25 - 3.0μg mL⁻¹范围内符合比尔定律。方法A和B的表观摩尔吸光系数分别计算为3.0×10⁴和4.4×10⁴L mol⁻¹ cm⁻¹。方法A的检测限(LOD)和定量限(LOQ)分别计算为0.08和0.25μg mL⁻¹,方法B的分别为0.09和0.27μg mL⁻¹。根据当前的ICH指南评估了方法的日内和日间精密度与准确度。两种方法的准确度相当(误差≤2%)。而且,如相对标准偏差值<1.5%所示,两种方法同样精确。未观察到常见药用辅料的干扰。通过使用标准加入法进行回收率研究进一步确定了方法的准确度。这些方法成功应用于胶囊制剂中LPZ的测定,并通过应用学生t检验和F检验将结果与文献紫外分光光度法的结果进行了统计学比较。