Department of Analytical Chemistry, School of Pharmacy with Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia in Katowice, Jagiellońska 4, 41-200 Sosnowiec, Poland.
Molecules. 2018 Nov 28;23(12):3115. doi: 10.3390/molecules23123115.
A new, simple, and cost-effective TLC-densitometric method has been established for the simultaneous quantitative determination of acetylsalicylic acid and ascorbic acid in combined effervescent tablets. Separation was performed on aluminum silica gel 60F plates using chloroform-ethanol-glacial acid at a volume ratio of 5:4:0.03 as the mobile phase. UV densitometry was performed in absorbance mode at 200 nm and 268 nm for acetylsalicylic acid and ascorbic acid, respectively. The presented method was validated as per ICH guidelines by specificity, linearity, accuracy, precision, limit of detection, limit of quantification, and robustness. Method validations indicate a good sensitivity with a low value of LOD and LOQ of both examined active substances. The linearity range was found to be 1.50⁻9.00 μg/spot and 1.50⁻13.50 μg/spot for acetylsalicylic and ascorbic acid, respectively. A coefficient of variation that was less than 3% confirms the satisfactory accuracy and precision of the proposed method. The results of the assay of combined tablet formulation equal 97.1% and 101.6% in relation to the label claim that acetylsalicylic acid and ascorbic acid fulfill pharmacopoeial requirements. The developed TLC-densitometric method can be suitable for the routine simultaneous analysis of acetylsalicylic acid and ascorbic acid in combined pharmaceutical formulations. The proposed TLC-densitometry may be an alternative method to the modern high-performance liquid chromatography in the quality control of above-mentioned substances, and it can be applied when HPLC or GC is not affordable in the laboratory.
一种新的、简单且具有成本效益的 TLC 比色法定量测定了复方泡腾片中的阿司匹林和抗坏血酸。在铝硅胶 60F 板上,以氯仿-乙醇-冰醋酸(5:4:0.03)为流动相进行分离。分别在 200nm 和 268nm 处对乙酰水杨酸和抗坏血酸进行紫外分光光度法检测。该方法按照 ICH 指南进行了验证,包括专属性、线性、准确性、精密度、检测限、定量限和稳健性。方法验证表明,该方法具有良好的灵敏度,两种被检活性物质的检测限和定量限均较低。线性范围分别为 1.50⁻9.00μg/斑点和 1.50⁻13.50μg/斑点。低于 3%的变异系数证实了该方法具有令人满意的准确性和精密度。复方片剂制剂的测定结果分别为 97.1%和 101.6%,与标签声称的乙酰水杨酸和抗坏血酸符合药典要求相符。所开发的 TLC 比色法可适用于复方药物制剂中阿司匹林和抗坏血酸的常规同时分析。与现代高效液相色谱法相比,所提出的 TLC 比色法可能是上述物质质量控制的替代方法,并且可以在实验室无法负担高效液相色谱法或气相色谱法时应用。