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Mass spectrometry fingerprinting of media used for in vitro production of bovine embryos
Authors:Christina Ramires Ferreira  Gustavo Henrique Martins Ferreira Souza  Maria Francesca Riccio  Rodrigo Ramos Catharino  José Henrique Fortes Pontes  Andréa Cristina Basso  José Carlos Ereno Júnior  Felipe Perecin  Marcos Nogueira Eberlin
Affiliation:1. In Vitro Brasil Ltda, Mogi Mirim‐SP, 13800‐970, Brazil;2. ThoMSon Mass Spectrometry Laboratory, Institute of Chemistry, State University of Campinas, UNICAMP, Campinas, SP, 13083‐970, Brazil;3. Faculty of Animal Sciences and Food Engineering, FZEA, Basic Science Department, University of S?o Paulo, USP, Pirassununga‐SP, 13635‐000, Brazil;4. Department of Pharmacology, Faculty of Medical Sciences, State University of Campinas, UNICAMP, Campinas‐SP, 13083‐970, Brazil;5. Department of Clinical Pathology, School of Medical Sciences, State University of Campinas, UNICAMP, Campinas, SP, 13083‐887, Brazil
Abstract:Using the bovine species as a biological model, direct infusion chip‐based nano‐electrospray ionization mass spectrometry (nano‐ESI‐MS) fingerprinting in the positive ion mode is used to obtain fast chemical profiles of media used for in vitro production of bovine embryos. Nano‐ESI‐MS fingerprinting is useful for characterization and routine quality control requiring no sample pre‐separation, being able to differentiate four different media (IVM, IVF, SOF and HSOF) via principal component analysis (PCA). For media stored at +4°C for up to 45 days, no significant (p > 0.05) variation was observed in cleavage and blastocyst rate development, as well as in the nano‐ESI‐MS chemical profiles. For media exposed to a heat shock (60°C for 3 h), no significant decrease (p > 0.05) in embryo development rates was observed, but nano‐ESI‐MS profiles were quite distant from fresh control media in the PCA. For frozen media (?70°C for 2 months), again no significant variation (p > 0.05) in embryo development was noticed, but nano‐ESI‐MS profiles from all media were significantly affected. These results indicate that nano‐ESI(+)‐MS fingerprinting was able to characterize different media based on their specific chemical profile. The technique seems therefore applicable as a routine quality control assay, detecting, for example, compositional changes after temperature variations that may affect post‐transfer embryo viability. Copyright © 2009 John Wiley & Sons, Ltd.
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