Smith, Keith, Li, Zhaoqiang, Yang, Jing-Jing, Weeks, Ian ORCID: https://orcid.org/0000-0002-6362-2929 and Woodhead, J. Stuart 2000. Synthesis and properties of novel chemiluminescent biological probes: substituted 4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulphonate. Journal of Photochemistry and Photobiology A: Chemistry 132 (3) , pp. 181-191. 10.1016/S1010-6030(00)00209-4 |
Abstract
Substituted aryl acridinium esters, 2,6-dimethyl-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulphonate (3), 2,6-dimethoxy-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulphonate (4), 2-methoxy-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulphonate (5) and 2,6-dibromo-4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulphonate (6), have been synthesised and coupled to immunoglobulinG(IgG). The chemiluminescent properties and hydrolytic stabilities of the conjugates have also been examined. The different substituents on the phenoxy ring affected the chemiluminescent efficiency and kinetics. All the human IgG conjugates of these substituted acridinium esters demonstrated much higher stability than the conjugate of the corresponding unsubstituted acridinium ester
Item Type: | Article |
---|---|
Status: | Published |
Schools: | Chemistry Medicine Systems Immunity Research Institute (SIURI) |
Subjects: | Q Science > QD Chemistry |
Uncontrolled Keywords: | Acridinium ester; Chemiluminescence; Chemiluminescence immunoassay |
Publisher: | Elsevier |
ISSN: | 1010-6030 |
Last Modified: | 18 Oct 2022 13:32 |
URI: | https://orca.cardiff.ac.uk/id/eprint/14290 |
Citation Data
Cited 23 times in Scopus. View in Scopus. Powered By Scopus® Data
Actions (repository staff only)
Edit Item |