Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 25: 1440-1443, 1979;
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Eberts, T. J.
Right arrow Articles by Ellis, G. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Eberts, T. J.
Right arrow Articles by Ellis, G. H.

Clinical Chemistry, Vol 25, 1440-1443, Copyright © 1979 by American Association for Clinical Chemistry

A simplified, colorimetric micromethod for xylose in serum or urine, with phloroglucinol

TJ Eberts, RH Sample, MR Glick and GH Ellis

We have developed a simplified xylose assay procedure that requires only 10 min and requires 50 microL of serum or 5 microL of urine. The reaction with phloroglucinol is more sensitive than the classic p- bromaniline color reaction, and requires only 4 min of heating for color development. A single reagent is mixed with the specimen directly, without prior protein precipitation. Analytical recovery of xylose added to serum was quantitative; precision studies resulted in a between-day coefficient of variation of 5.2%. Glucose, which has significant potential for interference in most other xylose procedures, reacts under the test conditions only to the extent of 70 mumol of apparent xylose per liter for a 5.5 mmol/L solution of glucose. The new procedure has been valuable in the assessment of malabsorption, especially in children and infants, where serum xylose is the preferred measurement.


The following articles in journals at HighWire Press have cited this article:


Home page
J. Clin. Endocrinol. Metab.Home page
M. Salehi, T. P. Vahl, and D. A. D'Alessio
Regulation of Islet Hormone Release and Gastric Emptying by Endogenous Glucagon-Like Peptide 1 after Glucose Ingestion
J. Clin. Endocrinol. Metab., December 1, 2008; 93(12): 4909 - 4916.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
A. Guijarro, S. Suzuki, C. Chen, H. Kirchner, F. A. Middleton, S. Nadtochiy, P. S. Brookes, A. Niijima, A. Inui, and M. M. Meguid
Characterization of weight loss and weight regain mechanisms after Roux-en-Y gastric bypass in rats
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 2007; 293(4): R1474 - R1489.
[Abstract] [Full Text] [PDF]


Home page
JPEN J Parenter Enteral NutrHome page
A. L. Buchman, J. Fryer, A. Wallin, C. W. Ahn, S. Polensky, and K. Zaremba
Clonidine Reduces Diarrhea and Sodium Loss in Patients With Proximal Jejunostomy: A Controlled Study
JPEN J Parenter Enteral Nutr, November 1, 2006; 30(6): 487 - 491.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
C. Hermida, G. Corrales, O. H. Martinez-Costa, A. Fernandez-Mayoralas, and J. J. Aragon
Noninvasive Evaluation of Intestinal Lactase with 4-Galactosylxylose: Comparison with 3- and 2-Galactosylxylose and Optimization of the Method in Rats
Clin. Chem., February 1, 2006; 52(2): 270 - 277.
[Abstract] [Full Text] [PDF]


Home page
JPEN J Parenter Enteral NutrHome page
S. J. Carlson, J. C. Deutsch, and R. M. Craig
Physiologic Response to a Protein, Carbohydrate, Fat Meal in Patients With Human Immunodeficiency Virus Who Underwent Small Intestinal Enteropathy as Characterized by a Kinetic Model of D-Xylose Absorption
JPEN J Parenter Enteral Nutr, January 1, 1998; 22(1): 27 - 30.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1979 by the American Association for Clinical Chemistry.