Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
The interaction between fluorescein-labeled propazine and antibodies against this hapten was studied in the reversed micelles of Aerosol OT in n-octane by a polarization fluoroassay. The effect of the hydration degree of micelles W0 (W0=[H2O]/[Surf]), which determines their size and surfactant concentration, on the binding of the antigen with antibodies was studied. A high hydration degree of the reversed micelles (W0 = 15-30) and low concentration of the surfactant (less than 50 microM) are optimal for binding. The binding efficacy depends upon the structure of the fluorescein-labeled hapten, particularly upon the length of the bridge binding fluorescein with propazine. It was shown that the polarization fluoroimmunoassay of propazine may be carried out in a reversed micellar system in nonpolar organic solvent (octane) with a detection limit of about 100 nM (20 microns/l). This is an order of magnitude higher than that achievable upon analysis in aqueous medium. The proposed polarization fluoroimmunoassay in a reversed micellar system makes it possible to detect haptens that are poorly soluble in water directly in organic extracts, e.g. in chloroform solutions.
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