2017
DOI: 10.5267/j.ccl.2017.4.003
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Carotenoid determination in recent marine sediments - practical problems during sample preparation and HPLC analysis

Abstract: An analytical procedure for the analysis of carotenoids in marine sediments rich in organic matter has been developed. Analysis of these compounds is difficult; the application of methods used by other authors required optimization for the samples studied here. The analytical procedure involved multiple ultrasound-assisted extraction with acetone followed by liquid-liquid extraction (acetone extract:benzene:water -15:1:10 v/v/v) and HPLC analysis. The influence of column temperature on pigment separation and t… Show more

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Cited by 8 publications
(5 citation statements)
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“…The pigment extraction, analysis, and quantification were carried out using the procedures described in detail elsewhere (Krajewska et al, ; Szymczak‐Żyła, ; Szymczak‐Żyła et al, , ). In brief, ultrasound‐assisted extraction of wet sediment samples with acetone was applied.…”
Section: Methodsmentioning
confidence: 99%
“…The pigment extraction, analysis, and quantification were carried out using the procedures described in detail elsewhere (Krajewska et al, ; Szymczak‐Żyła, ; Szymczak‐Żyła et al, , ). In brief, ultrasound‐assisted extraction of wet sediment samples with acetone was applied.…”
Section: Methodsmentioning
confidence: 99%
“…For exact analysis, separation of these molecules is necessary. Commonly used methods such as HPLC can discriminate molecules based on their mass and affinity to solvents and stationary phase but require chemical pretreatments, which can impair results, for example, dissolution in solvents 69 . Therefore, nondestructive analytical methods provide great advantages in studying samples in their natural states.…”
Section: Resultsmentioning
confidence: 99%
“…Zeaxanthin and canthaxanthin were extracted by acetone from either carotenoid-bound proteins or E. coli membranes as described earlier 5,48 . Absorbance spectra of carotenoids in organic solvents were registered on a Nanophotometer NP80 (Implen, Germany) using the following molar extinction coefficients: 121,300 M -1 cm -1 for βCar at 466 nm in DMSO 49 , 90,000 M -1 cm -1 for CAN at 472 nm in ethanol 50 , 125,000 M -1 cm -1 for AXT at 482 nm in DMSO 51 , 145,000 M -1 cm -1 for ZEA at 450 nm in methanol 52 . TRITC-conjugated phalloidin and Hoechst 33342 were purchased from Thermo Fisher (USA).…”
Section: Methodsmentioning
confidence: 99%