Application of Br-82 as a radioactive tracer isotope to study bromide ion-isotopic exchange reaction in strongly basic anion exchange resin Duolite A-161

2009 ◽  
Vol 83 (8) ◽  
pp. 1389-1394 ◽  
Author(s):  
R. S. Lokhande ◽  
P. U. Singare ◽  
S. R. D. Tiwari
2002 ◽  
Vol 35 (1) ◽  
pp. 32-39 ◽  
Author(s):  
Hiroyuki Yoshida ◽  
Steffen Oehlenschlaeger ◽  
Yuji Minami ◽  
Masaaki Terashima

2015 ◽  
Vol 36 (6) ◽  
pp. 391-398 ◽  
Author(s):  
Alina Zagorodnyaya ◽  
Zinesh Abisheva ◽  
Ainash Sharipova ◽  
Saltanat Sadykanova ◽  
Ata Akcil

2013 ◽  
Vol 53 (2) ◽  
pp. 515-523 ◽  
Author(s):  
Moonis Ali Khan ◽  
Zeid Abdullah ALOthman ◽  
Mu. Naushad ◽  
Mohammad Rizwan Khan ◽  
Mohammad Luqman

1968 ◽  
Vol 14 (6) ◽  
pp. 538-547 ◽  
Author(s):  
R L Jolley ◽  
M L Freeman

Abstract Automated carbohydrate analysis can be useful clinically in the research laboratory as an aid in understanding the fundamental role of carbohydrates in metabolism, including their pathologic significance. An analytic system being developed at our laboratory utilizes an automated carbohydrate analyzer to chromatograph borated physiologic fluids while using strongly basic anion-exchange resin. The eluted carbohydrates are detected by sulfuric acid-phenol colorimetry. The carbohydrate analyzer used in this experimental work should become a useful tool in the clinical laboratory. Normal and diabetic human urine and blood serum have been chromatographed and significant differences established. As many as 38 peaks have been observed in the complex urine chromatograms. Using cochromatographic technics, 14 peaks have been tentatively identified as sucrose, raffinose, N-acetylglucosamine, maltose, lactose, ribose, fructose, arabinose, fucose, galactose, xylose, mannoheptulose, glucose, and glucose-1-phosphate. All except fucose have been quantified. Blood serum chromatograms consist of a major glucose peak and several smaller peaks indicating traces of other sugars. Melibiose has been used as an internal standard in chromatograms to determine recovery, resolution, and reproducibility. With the present technic, the lower limit of detectable sugar in physiologic fluids is in the 1-µg. range.


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