Determination of Tetracycline in Pharmaceutical Preparation by Molecular and Atomic Absorption Spectrophotometry and High Performance Liquid Chromatography via Complex Formation with Au(III) and Hg(II) Ions in Solutions
Author(s) -
Ahlam Jameel Abdulghani,
Hadi Hassan Jasim,
Abbas Shebeeb Hassan
Publication year - 2013
Publication title -
international journal of analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.352
H-Index - 16
eISSN - 1687-8779
pISSN - 1687-8760
DOI - 10.1155/2013/305124
Subject(s) - metal ions in aqueous solution , spectrophotometry , extraction (chemistry) , ion , chemistry , tetracycline , atomic absorption spectroscopy , matrix (chemical analysis) , metal , analytical chemistry (journal) , nuclear chemistry , chromatography , physics , organic chemistry , biochemistry , quantum mechanics , antibiotics
UV-visible and atomic spectrophotometry and HPLC techniques were applied for the determination of tetracycline (TC) in pharmaceutical preparations via complexation of the drug with Au(III) and Hg(II) ions in solutions. The mole ratio of TC to metal ions was 1 : 1. Maximum peak absorption at λ 425 and 320 nm for the two ions, respectively, was optimized at heating temperature 75°C for 15 minutes at pH = 4 followed by the extraction with ethyl acetate. The percentage of extraction and stability constants for the two complexes was 95.247, 95.335% and 2.518 × 10 4 , 1.162 × 10 5 M −1 , respectively. HPLC method was applied without extraction process. The analytical data obtained from direct calibration curves of UV-visible absorption, FAAS, and HPLC for Au(III) complexes were recovery (100.78, 104.85, and 101.777%, resp.); detection limits (0.7403, 0.0997, and 2.647 μ g/ml, resp.); linearity (5–70, 5–30, and 10–150 μ g/ml, resp.), and correlation coefficient (0.9991, 0.9967, and 0.9986, resp.). The analytical data obtained from direct calibration curves for Hg(II) complexes by UV-visible spectrophotometry and HPLC were recovery (100.95 and 102.000%, resp.); detection limits (0.5867 and 2.532 μ g/ml, resp.); linearity (5–70 and 10–150 μ g/ml, resp.); and correlation coefficients (0.9989 and 0.9997, resp.).
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