عنوان المقالة:التقدير الكمي للاسبرين وبعض الشوائب QUANTITATIVE ASSAY OF ASPIRIN AND (SALICYLIC ACID AND HEAVY METALS AS IMPURATIES) IN IRAQI’S MARKET ASPIRIN TABLETS USING DIFFERENT ANALYTICAL METHODS
AHMED MAHDI SAEED, MOHAMMED JASSIM HAMZAH, NOOR QASIM AHMED
الملخص العربي
تم تقدير الاسبريت وبعض الشوائب مثل حامض السالسليك والعناصر الثقيلة
الملخص الانجليزي
Objective: Easy and precise methods were developed for estimation of aspirin (ASP), impurities from such as salicylic acid (SAL) and heavy metal
ions (HMI) in ASP tablets that available in the Iraqi’s market using High-performance liquid chromatography (HPLC), UV–VIS spectrophotometry
and atomic absorption spectrophotometric (AAS).
Methods: HPLC separation was carried out using C18 as stationary phase and acetonitrile (ACN): water in the ratio of (10: 90 v/v) as a mobile
phase for HPLC method and as a solvent for UV-VIS spectrophotometric for quantitative ASP and SAL at 254 nm for HPLC, 226 and 296 nm for UV
measurements. AAS was used for HMI determination.
Results: ASP and SAL gave absorbance maxima at 226 and 296 nm in ACN: H2O solvent. The Beer’s law was obeyed in the range of 0.05-20 for ASP
and 0.02-8 μg/ml for SAL. Correlation coefficients (R2) were 0.9996 and 0.9992 for ASP and SAL respectively, for HPLC and LOD value was 0.006 for
ASP and 0.004 μg/ml for SAL. The % recovery for the developed method was found to be in the range of (98.80 to 101.26%) and (98.67 to 103.33%)
for ASP and SAL respectively, within the acceptable range, that approved by world health organization (WHO).
Conclusion: The proposed method can help research studies, quality control and routine analysis with lesser resources available. The results of the
assay of pharmaceutical formulation of the developed method are highly reliable and reproducible and is in good agreement with the label claim of
the medicines.
احمد مهدي سعيد محمد | Ahmed Mahdi Saeed Mohammed | 8558