Studies on the peparative capability of the horizontal flow-through coil planet centrifuge and high-performance liquid chromatography in the separation of polar compounds from Oxytropis ochrocephala Bunge

1991 ◽  
Vol 538 (1) ◽  
pp. 219-225 ◽  
Author(s):  
Ping Li ◽  
Tian-You Zhang ◽  
Xiang Hua ◽  
Yoichiro Ito
2020 ◽  
Author(s):  
Brittany Widner ◽  
Melissa C. Kido Soule ◽  
Frank Xavier Ferrer-Gonzalez ◽  
Mary Ann Moran ◽  
Elizabeth B. Kujawinski

Dissolved metabolites support microbial systems via nutritional and energetic utilization and chemical signaling. However, the full scope and magnitude of these processes in marine systems is unknown largely because the mass spectrometric identification and quantification of these compounds from saline matrices has been hampered by poor extraction of small, polar compounds using common solid phase extraction resins (e.g. PPL resin, Bond Elut, Agilent). Here we utilized pre-extraction derivatization to improve the extraction, quantification, and chromatographic resolution of targeted dissolved metabolites in seawater and saline culture medium detected with ultra-high performance liquid chromatography electrospray ionization tandem mass spectrometry (UHPLC-ESI-MSMS) with Orbitrap detection. Metabolites were derivatized with benzoyl chloride by their primary and secondary amine and alcohol functionalities and quantified using stable isotope-labeled internal standards (SIL-IS) produced from 13C-labeled benzoyl chloride. We optimized derivatization, extraction, and sample preparation for field and culture samples, and we evaluated matrix-derived biases. This method quantifies 73 metabolites in seawater, of which 50 have an extraction efficiency <2% without derivatization. This method is sensitive (detection limits = pM to nM) and substantially improves sample throughput by shortening processing time ~10-20x


1975 ◽  
Vol 58 (5) ◽  
pp. 888-897
Author(s):  
Howard W Ziegler ◽  
Thomas H Beasley ◽  
David W Smith

Abstract A method is described for the quantitative determination of morphine, codeine, cryptopine, thebaine, papaverine, and narcotine in opium by high-performance liquid chromatography. The alkaloids are isolated from a dilute acid extract by adsorption on an Amberlite XAD-2 resin column and eluted first with methanol and then with chloroform-methanol ( 3+1 ) . After solvent removal by reduced pressure evaporation, the alkaloids are redissolved in chloroformmethanol ( 3+1 ) . The sample solution, plus brucine as an internal standard, is injected onto a Corasil II column and eluted with hexane that is gradient programmed with a solution of chloroform-methanol-diethylamine ( 100+300+1). The absorbances of the separated alkaloids are continuously monitored at 254 nm, using a flow-through ultraviolet double-beam photometer.


2020 ◽  
Author(s):  
Brittany Widner ◽  
Melissa C. Kido Soule ◽  
Frank Xavier Ferrer-Gonzalez ◽  
Mary Ann Moran ◽  
Elizabeth B. Kujawinski

Dissolved metabolites support microbial systems via nutritional and energetic utilization and chemical signaling. However, the full scope and magnitude of these processes in marine systems is unknown largely because the mass spectrometric identification and quantification of these compounds from saline matrices has been hampered by poor extraction of small, polar compounds using common solid phase extraction resins (e.g. PPL resin, Bond Elut, Agilent). Here we utilized pre-extraction derivatization to improve the extraction, quantification, and chromatographic resolution of targeted dissolved metabolites in seawater and saline culture medium detected with ultra-high performance liquid chromatography electrospray ionization tandem mass spectrometry (UHPLC-ESI-MSMS) with Orbitrap detection. Metabolites were derivatized with benzoyl chloride by their primary and secondary amine and alcohol functionalities and quantified using stable isotope-labeled internal standards (SIL-IS) produced from 13C-labeled benzoyl chloride. We optimized derivatization, extraction, and sample preparation for field and culture samples, and we evaluated matrix-derived biases. This method quantifies 73 metabolites in seawater, of which 50 have an extraction efficiency <2% without derivatization. This method is sensitive (detection limits = pM to nM) and substantially improves sample throughput by shortening processing time ~10-20x


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