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Quantification of circulating steroids in individual zebrafish using stacking to achieve nanomolar detection limits with capillary electrophoresis and UV-visible absorbance detection.


ABSTRACT: Capillary electrophoresis and UV-visible absorbance detection are used with sample stacking to achieve detection limits ranging from 0.2 to 2 ng/mL (0.8 to 6 nM) for steroids. Stacking is accomplished using negatively charged cyclodextrin steroid-carrier molecules at a discrete pH interface between the reconstituted sample and the separation electrolyte. Steroids are then separated in under 5 min using capillary electrophoresis that incorporates secondary equilibria via sodium dodecyl sulfate and cyclodextrin. The effectiveness of the method for measurements of multiple steroids in limited sample volumes is demonstrated in individual female fish with total circulating blood volumes of 5 ?L or less. Steroid recoveries from plasma following a sample processing method developed with commercial extraction cartridges range from 81 to 109 % for 17?,20?-dihydroxy-pregn-4-en-3-one, testosterone, 11-ketotestosterone, estrone, 17?-estradiol, and 17?-ethinyl estradiol. When applied to reproductively active female zebrafish, changes were detected in the levels of circulating steroids as a result of exposure to different solvents and 17?-estradiol.

SUBMITTER: Nyakubaya VT 

PROVIDER: S-EPMC4551537 | biostudies-literature | 2015 Sep

REPOSITORIES: biostudies-literature

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Quantification of circulating steroids in individual zebrafish using stacking to achieve nanomolar detection limits with capillary electrophoresis and UV-visible absorbance detection.

Nyakubaya Vincent T VT   Durney Brandon C BC   Ellington Marriah C G MC   Kantes Amber D AD   Reed Paige A PA   Walter Shaylyn E SE   Stueckle Jennifer Ripley JR   Holland Lisa A LA  

Analytical and bioanalytical chemistry 20150604 23


Capillary electrophoresis and UV-visible absorbance detection are used with sample stacking to achieve detection limits ranging from 0.2 to 2 ng/mL (0.8 to 6 nM) for steroids. Stacking is accomplished using negatively charged cyclodextrin steroid-carrier molecules at a discrete pH interface between the reconstituted sample and the separation electrolyte. Steroids are then separated in under 5 min using capillary electrophoresis that incorporates secondary equilibria via sodium dodecyl sulfate an  ...[more]

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