Analysis of Vitamin A in Jordanian Local Fresh Milk Samples Using Liquid Chromatography Tandem-Mass Spectrometry, LC/MS/MS
Ishaq Y. Habib, Isyaka Mohammed Sani, Fahad Danladi, Murtala Aliyu, Murtala Muhammad
Abstract
Ishaq Y. Habib, Isyaka Mohammed Sani, Fahad Danladi, Murtala Aliyu, Murtala Muhammad
Abstract
An auspicious method for the quantitative determination of vitamin A (retinol) was augmented in seven different Jordanian local fresh milk samples using liquid chromatography tandem -mass spectrometry (LC/MS/MS). The compound was separated with C18 Thermo fisher gold (4.50 x100 mm x 5 A) column through a flow rate of 1 mL/min with isocratic mobile phase. Vitamin A acetate was used as an internal standard .The method was validated using triplicate analyses, relative recovery experiment and statistical analysis. Liquid- liquid extraction was employed as a pre-concentration step with n-hexane -dichloromethane mixture (90%:10%) as an extraction solvent. The concentration range of the working standards was 0.0-1000.0 ng/mL. The correlation coefficient was found to be 0.9994. The limit 0f detection and limit of quantification were found to be 0.53 and 1.78 respectively. The 95% confidence interval was calculated to be 49.032 + 0.22. This technique showed reasonable recovery of 98.08%, coefficient of variation of 0.36%, standard deviation of 0.178 and error of -48.032. The ranges of the calculated concentrations of the vitamin A were found to be from 6.47 ng/mL- 46.35 ng/mL.
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An auspicious method for the quantitative determination of vitamin A (retinol) was augmented in seven different Jordanian local fresh milk samples using liquid chromatography tandem -mass spectrometry (LC/MS/MS). The compound was separated with C18 Thermo fisher gold (4.50 x100 mm x 5 A) column through a flow rate of 1 mL/min with isocratic mobile phase. Vitamin A acetate was used as an internal standard .The method was validated using triplicate analyses, relative recovery experiment and statistical analysis. Liquid- liquid extraction was employed as a pre-concentration step with n-hexane -dichloromethane mixture (90%:10%) as an extraction solvent. The concentration range of the working standards was 0.0-1000.0 ng/mL. The correlation coefficient was found to be 0.9994. The limit 0f detection and limit of quantification were found to be 0.53 and 1.78 respectively. The 95% confidence interval was calculated to be 49.032 + 0.22. This technique showed reasonable recovery of 98.08%, coefficient of variation of 0.36%, standard deviation of 0.178 and error of -48.032. The ranges of the calculated concentrations of the vitamin A were found to be from 6.47 ng/mL- 46.35 ng/mL.
Key concepts: Chromatography, Chemistry, Liquid chromatography–mass spectrometry, Coefficient of variation, Extraction (chemistry), Detection limit, Mass spectrometry, Tandem mass spectrometry