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


     


Clinical Chemistry 29: 1974-1977, 1983;
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
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 Whitehouse, R. C.
Right arrow Articles by Cossack, Z. T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Whitehouse, R. C.
Right arrow Articles by Cossack, Z. T.

Clinical Chemistry, Vol 29, 1974-1977, Copyright © 1983 by American Association for Clinical Chemistry

Determination of ultrafiltrable zinc in plasma by flameless atomic absorption spectrophotometry

RC Whitehouse, AS Prasad and ZT Cossack

Ultrafiltrable zinc can be determined in small volumes of plasma by using Amicon ultrafiltration membrane cones and either flameless atomic absorption spectrophotometry or 65Zn. The ultrafiltration membrane cone is made sufficiently zinc-free by acid washing, followed by rinsing with de-ionized water. Within-run CVs were 12 and 10%, respectively, for the two methods. Matrix effects are compensated for by using standards in solutions with an inorganic matrix that simulates the sample matrix. Results for ultrafiltrable zinc by the two techniques agreed, and agreed with previously published data obtained by different ultrafiltration techniques. The mean (and SD) percentage of plasma zinc that was ultrafiltrable in 12 control subjects was 1.0 (0.5) by AAS and 0.7 (0.3) by 65Zn.


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


Home page
BloodHome page
N. Sheng, M. B. Fairbanks, R. L. Heinrikson, G. Canziani, I. M. Chaiken, D. M. Mosser, H. Zhang, and R. W. Colman
Cleaved high molecular weight kininogen binds directly to the integrin CD11b/CD18 (Mac-1) and blocks adhesion to fibrinogen and ICAM-1
Blood, June 15, 2000; 95(12): 3788 - 3795.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1983 by the American Association for Clinical Chemistry.