TY - JOUR
T1 - Nanospray liquid chromatography/tandem mass spectrometry analysis of steroids from gray whale blubber
AU - Hayden, Mary
AU - Bhawal, Ruchika
AU - Escobedo, John
AU - Harmon, Clinton
AU - O’hara, Todd M.
AU - Klein, David
AU - San-Francisco, Susan
AU - Zabet-Moghaddam, Masoud
AU - Godard-Codding, Céline A.J.
N1 - Funding Information:
This work was conducted under NMFS Office of Protected Resources’ Marine Mammal Health and Stranding Response Program (MMHSRP) permits 932-1905-MA-009526 and 18786. We thank Teri Rowles (National Marine Fisheries Service, Silver Spring, MD, USA) for assistance with the project and Frances Gulland (The Marine Mammal Center, Sausalito, CA, USA) for providing eastern gray whale tissues. We thank Margaret Castellini for assistance with sample processing and shipment. We also thank Azivy Aziz, Jennifer Dupont, and Lucie N’Guessan (ExxonMobil Upstream Research Co.), Mike Swindoll and Mike Scott (Exxon Neftegas Ltd), and Koen Broker (Shell Global Solutions International) for invaluable assistance in implementing this research project. This study was funded by Exxon Neftegas Limited (ENL) and Sakhalin Energy Investment Company (SEIC) and the TTU Center for Biotechnology and Genomics. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding parties.
Publisher Copyright:
© 2017 John Wiley & Sons, Ltd.
PY - 2017/7/15
Y1 - 2017/7/15
N2 - RATIONALE: Analysis of steroids from precious blubber biopsies obtained from marine mammals, especially endangered species, can provide valuable information on their endocrine status. Challenges with currently used ELISA methodology include lack of absolute quantitation and incompatibility with multiple steroids analysis due to limited biopsy mass. Development of a sensitive, accurate analytical method for this purpose is critical. METHODS: A nanospray liquid chromatography/tandem mass spectrometry (nanoLC/MS/MS) method was validated for sensitive, specific and quantitative analysis of three steroid hormones, without derivatization, extracted from 50 mg blubber samples. Data was acquired with an LTQ XL ion trap mass spectrometer in positive ion mode, using single reaction monitoring. All three steroids were analyzed in a single run. Cholic acid was used as a surrogate internal standard for quantitation due to its steroidal structure and lack of measurable endogenous levels in blubber. RESULTS: The lowest limits of quantitation for progesterone, testosterone, and hydrocortisone were significantly improved compared to previous studies using conventional LC/MS/MS. The lowest limit of detection was 7 fg/μL using a1μL injection volume. Calibration curves for steroid quantification showed good linearity (r2 >0.99) between 14 and 3620 fg/μL, and accuracy was <20% for interday and <10% for intraday. After validation, the method was successfully applied to quantification of steroids in gray whale blubber samples. CONCLUSIONS: The nanoLC/MS/MS method is more sensitive than traditional LC/MS/MS for steroid analysis. It is also compatible with other important biopsy analyses due to its small blubber mass requirement. This will benefit the reproductive and stress assessments for all marine mammals, particularly endangered populations.
AB - RATIONALE: Analysis of steroids from precious blubber biopsies obtained from marine mammals, especially endangered species, can provide valuable information on their endocrine status. Challenges with currently used ELISA methodology include lack of absolute quantitation and incompatibility with multiple steroids analysis due to limited biopsy mass. Development of a sensitive, accurate analytical method for this purpose is critical. METHODS: A nanospray liquid chromatography/tandem mass spectrometry (nanoLC/MS/MS) method was validated for sensitive, specific and quantitative analysis of three steroid hormones, without derivatization, extracted from 50 mg blubber samples. Data was acquired with an LTQ XL ion trap mass spectrometer in positive ion mode, using single reaction monitoring. All three steroids were analyzed in a single run. Cholic acid was used as a surrogate internal standard for quantitation due to its steroidal structure and lack of measurable endogenous levels in blubber. RESULTS: The lowest limits of quantitation for progesterone, testosterone, and hydrocortisone were significantly improved compared to previous studies using conventional LC/MS/MS. The lowest limit of detection was 7 fg/μL using a1μL injection volume. Calibration curves for steroid quantification showed good linearity (r2 >0.99) between 14 and 3620 fg/μL, and accuracy was <20% for interday and <10% for intraday. After validation, the method was successfully applied to quantification of steroids in gray whale blubber samples. CONCLUSIONS: The nanoLC/MS/MS method is more sensitive than traditional LC/MS/MS for steroid analysis. It is also compatible with other important biopsy analyses due to its small blubber mass requirement. This will benefit the reproductive and stress assessments for all marine mammals, particularly endangered populations.
UR - http://www.scopus.com/inward/record.url?scp=85050142536&partnerID=8YFLogxK
U2 - 10.1002/RCM.7884
DO - 10.1002/RCM.7884
M3 - Article
C2 - 28423207
AN - SCOPUS:85050142536
SN - 0951-4198
VL - 31
SP - 1088
EP - 1094
JO - Rapid Communications in Mass Spectrometry
JF - Rapid Communications in Mass Spectrometry
IS - 13
ER -