scholarly journals Determination of blood urea using cation exchange column solid phase extraction combined with HPLC.

1994 ◽  
Vol 43 (10) ◽  
pp. 805-807 ◽  
Author(s):  
Hideharu SHINTANI ◽  
Takashi INOUE
2001 ◽  
Vol 84 (2) ◽  
pp. 556-562 ◽  
Author(s):  
Michael S Young ◽  
Dorothy J Phillips ◽  
Pamela C Iraneta ◽  
Jim Krol

Abstract Solid-phase extraction (SPE) procedures were developed for rapid cleanup and determination of thiabendazole and carbendazim in orange, apple, and grape juices. Samples were prepared by using an SPE cartridge containing a mixed-mode sorbent with both reversed-phase and strong cation-exchange chemistries. Analysis was by liquid chromatography with photodiode-array UV detection. Orange juice was analyzed by mixed-mode cation-exchange extraction with reversed-phase cleanup; the other juices were analyzed by reversed-phase extraction with cation-exchange cleanup. Recoveries >80% for carbendazim and >90% for thiabendazole. Quantitation limits were 20 μg/L for both analytes.


2009 ◽  
Vol 72 (8) ◽  
pp. 1769-1773 ◽  
Author(s):  
PETER M. SCOTT ◽  
BARBARA NIEDZWIADEK ◽  
DOROTHEA F. K. RAWN ◽  
BEN P.-Y. LAU

β-N-Methylamino-l-alanine (BMAA) is a neurotoxin originally found in cycad seeds and now known to be produced by many species of freshwater and marine cyanobacteria. We developed a method for its determination in blue-green algae (BGA) food supplements, freshwater fish, and bottled water by using a strong cation-exchange, solid-phase extraction column for cleanup after 0.3 M trichloroacetic acid extraction of BGA supplements and fish. Bottled water was applied directly onto the solid-phase extraction column. For analysis of carbonated water, sonication and pH adjustment to 1.5 were needed. To determine protein-bound BMAA, the protein pellet left after extraction of the BGA supplement and fish was hydrolyzed by boiling with 6 M hydrochloric acid; BMAA was cleaned up on a C18 column and a strong cation-exchange, solid-phase extraction column. Determination of BMAA was by liquid chromatography of the fluorescent derivative formed with 9-fluorenylmethyl chloroformate. The method was validated by recovery experiments using spiking levels of 1.0 to 10 μg/g for BGA supplements, 0.5 to 5.0 μg/g for fish, and 0.002 μg/g for bottled water; mean recoveries were in the range of 67 to 89% for BGA supplements and fish, and 59 to 92% for bottled water. Recoveries of BMAA from spiked extracts of hydrolyzed protein from BGA supplements and fish ranged from 66 to 83%. The cleanup developed provides a useful method for surveying foods and supplements for BMAA and protein-bound BMAA.


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