Development of a Monoclonal Antibody-Based Immunochemical Assay for Liquiritin and Its Application to the Quality Control of Licorice Products

2014 ◽  
Vol 62 (15) ◽  
pp. 3377-3383 ◽  
Author(s):  
Shunsuke Fujii ◽  
Osamu Morinaga ◽  
Takuhiro Uto ◽  
Shuichi Nomura ◽  
Yukihiro Shoyama
Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
T Kitisripanya ◽  
J Komaikul ◽  
K Jutathis ◽  
O Udomsin ◽  
H Tanaka ◽  
...  

1994 ◽  
Vol 9 (1) ◽  
pp. 43-47 ◽  
Author(s):  
G.C. Zucchelli ◽  
A. Pilo ◽  
M.R. Chiesa ◽  
S. Masini ◽  
A. Clerico

Immunoassays of the tumor markers CA 19.9, CA125 and CA 15.3 are generally acknowledged to be a useful tool in the management of cancer patients. As a consequence, many methods developed by different companies are now commercially available. However, discrepancies have been described in the results of marker determinations even when the same monoclonal antibody was used. An external quality assessment (EQA) was carried out; starting from 1989 about 110 laboratories participated; since December 1991 the program was linked with the interlaboratory program Oncocheck organized by the Service de Radiopharmacie et Radioanalyse, University of Lyon. At present more than 200 laboratories of many European countries are involved: cumulatively 47 quality control samples have been prepared and sent to the participants. This manuscript is a report on data collected for CA 19.9, CA 125, and CA 15.3.


2011 ◽  
Vol 8 (1) ◽  
pp. 60-65 ◽  
Author(s):  
Ming-Ying Shang ◽  
Min Tian ◽  
Hiroyuki Tanaka ◽  
Xiao-Wei Li ◽  
Shao-Qing Cai ◽  
...  

2021 ◽  
Vol 205 ◽  
pp. 114330
Author(s):  
Zhiqi Hao ◽  
Benjamin Moore ◽  
Chengfeng Ren ◽  
Monica Sadek ◽  
Frank Macchi ◽  
...  

2018 ◽  
Vol 157 ◽  
pp. 93-101
Author(s):  
Adriana Sierra González ◽  
Ana Luiza Guimarães Assmann ◽  
Celso Raul Romero Ramos ◽  
Miryam Marroquin Quelopana ◽  
Aline Carolina Aleixo Silva ◽  
...  

1987 ◽  
Vol 33 (5) ◽  
pp. 700-704 ◽  
Author(s):  
R A Felder ◽  
R H MacMillan ◽  
D E Bruns

Abstract Monoclonal antibody-based methods can provide clinically different impressions for some patients than does an earlier method involving a conventional antiserum. Therefore, performance of two commercial double-monoclonal-antibody methods for carcinoembryonic antigen (CEA) were studied further, those of Abbott Diagnostics and Roche Diagnostic Systems. The two methods showed similar precision. Total CVs over 20 days at three concentrations were 16, 6, and 6% in the Roche assay, and 15, 8, and 7% in the Abbott assay (n = 20). Within-run CVs for quality-control levels 1, 2, and 3, respectively, in the Roche assay were 14, 8, and 9%, and in the Abbott 15, 9, and 10% (n = 20). Mean CEA concentrations were consistently lower in the Roche assay than in the Abbott assay. Results of the two assays correlated significantly in patients with CEA-secreting carcinomas (r = 0.88), and in serial samples from cancer patients who had low, medium, or high CEA concentrations in their sera (r = 0.92 for all serial data). About 10% of values were false-positive (greater than 5.0 micrograms/L) by each of the two methods in 89 patients with various non-malignant conditions. The two methods appear to be more specific for tumor-associated CEA than are polyclonal antibody-based assays previously available from the two manufacturers.


2018 ◽  
Vol 66 ◽  
pp. 145-151 ◽  
Author(s):  
Zack C.F. Wong ◽  
Gallant K.L. Chan ◽  
Long Wu ◽  
Henry H.N. Lam ◽  
Ping Yao ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document