2002
DOI: 10.1016/s1570-0232(01)00598-0
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Supercritical fluid extraction of steroids from biological samples and first experience with solid-phase microextraction–liquid chromatography

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Cited by 17 publications
(16 citation statements)
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“…Additional possibilities are manipulating the pressure and/or temperature or the use of modifiers into the obtained fluid which changes the solvating power of the supercritical fluid. Carbon dioxide (CO 2 ) is the most frequently used supercritical fluid [58,69]. Few papers described the use of SFE for residue analysis of steroid hormones.…”
Section: Advanced Extraction and Purification Techniquesmentioning
confidence: 99%
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“…Additional possibilities are manipulating the pressure and/or temperature or the use of modifiers into the obtained fluid which changes the solvating power of the supercritical fluid. Carbon dioxide (CO 2 ) is the most frequently used supercritical fluid [58,69]. Few papers described the use of SFE for residue analysis of steroid hormones.…”
Section: Advanced Extraction and Purification Techniquesmentioning
confidence: 99%
“…Stolker et al [58] developed a multi-analyte (megestrol acetate, medroxyprogesterone acetate, chlormadinone acetate, melengestrol acetate), multi-matrix (skin, meat and fat) method for the routine determination of steroids in animal tissues coupling SFE to SPE. Kurečková et al [69] concluded that SFE is suitable as a sample preparation technique for monitoring trace levels of corticosteroids in animal tissue. As reviewed by Ridgway et al [72] one of the main problems with SFE is the robustness of the method compared to other extraction techniques.…”
Section: Advanced Extraction and Purification Techniquesmentioning
confidence: 99%
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“…Analytical determination was then performed by micro-HPLC on a column based on a new continuous polymer bed technology. Two papers have reported the determination of steroids in biological samples [57,58]. Volmer et al developed an SPME-LC-MS method for the determination of eleven corticosteroids and two steroid conjugates in urine, using the CW/TPR fiber; the method was characterized by LOD in the low ng mL -1 range, good linearity over three concentration decades, and precision, as RSD, never worse than 11% when an internal standard was used.…”
Section: Biological Samplesmentioning
confidence: 99%