2005
DOI: 10.1016/j.jchromb.2005.07.004
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An improved HPLC method for determination of carotenoids in human serum

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Cited by 44 publications
(50 citation statements)
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“…The calculated LOD (0.38-0.91 μg mL -1 ) and LOQ (1.15-2.77 μg mL -1 ) were similar to those of β-carotene and lycopene (LOD: 0.127-0.511 μg mL -1 and LOQ: 0.511-1.55 μg mL -1 ) reported by Rajendran et al 27 These authors also calculated the limits using parameters of the analytical curves, but another solvent system consisting of MeOH and dichloromethane was applied for carotenoid separation in HPLC. 27 On the other hand, LOD and LOQ values reported by Chisté and Mercadante 18 were lower (LOD: 0.1 μg mL -1 and LOQ: 0.5 μg mL -1 ) for a set of carotenoids (i.e., (9Z)-neoxanthin, (all-E)-violaxanthin, (all-E)-antheraxanthin, (all-E)-lutein, (all-E)-zeaxanthin, and (all-E)-β-carotene) using the same equipment and similar mobile phases and gradient elution as applied in the present work. In the latter work, authors also calculated the limits from the parameters of analytical curves; however, different concentration ranges of carotenoids were evaluated, which could have influenced the calculated limits.…”
Section: Resultssupporting
confidence: 82%
“…The calculated LOD (0.38-0.91 μg mL -1 ) and LOQ (1.15-2.77 μg mL -1 ) were similar to those of β-carotene and lycopene (LOD: 0.127-0.511 μg mL -1 and LOQ: 0.511-1.55 μg mL -1 ) reported by Rajendran et al 27 These authors also calculated the limits using parameters of the analytical curves, but another solvent system consisting of MeOH and dichloromethane was applied for carotenoid separation in HPLC. 27 On the other hand, LOD and LOQ values reported by Chisté and Mercadante 18 were lower (LOD: 0.1 μg mL -1 and LOQ: 0.5 μg mL -1 ) for a set of carotenoids (i.e., (9Z)-neoxanthin, (all-E)-violaxanthin, (all-E)-antheraxanthin, (all-E)-lutein, (all-E)-zeaxanthin, and (all-E)-β-carotene) using the same equipment and similar mobile phases and gradient elution as applied in the present work. In the latter work, authors also calculated the limits from the parameters of analytical curves; however, different concentration ranges of carotenoids were evaluated, which could have influenced the calculated limits.…”
Section: Resultssupporting
confidence: 82%
“…Although there are other good reversed-phase HPLC methods for determining carotenoids, retinoids, and sometimes tocopherols in plasma, these methods require more time and solvent usage (ranging from 32 to 70 min and 30 to 100 mL per sample) [19,20,22,32,48]. They also often use gradient HPLC, which requires more expensive systems than isocratic HPLC and more time for instrument re-equilibrium (although they can be useful for elaborate isomeric separations) [20,22,32,48].…”
Section: Rapid Isocratic Hplc Methods and Sample Extraction Proceduresmentioning
confidence: 99%
“…Several HPLC methods for the analysis of retinol (R), retinyl palmitate (RP) and β-carotene (β-C) levels in tissues and blood serum are described, including UV/DAD [23,25,[27][28][29][30], fluorescence detection [31][32][33][34] and electrochemical detection [35][36][37][38]. Carotenoids and retinoids can be monitored by UV/ DAD detectors, retinoids by fluorescence detection, and carotenoids by electrochemical detection.…”
Section: Introductionmentioning
confidence: 99%