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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
Intradermal injection of compound 48/80 into the nuchal area of the guinea pig in an adjuvant/water emulsion induced strong delayed hypersensitivity. Groups of 8 animals were injected weekly for 3 weeks with 100 microliter of 10%, 1%, 0.1% or 0% of compound 48/80 in the adjuvant/water emulsion. 6 of 8 animals in the highest concentration group died between 1 and 24 h after the first injection. The other concentrations produced no visible evidence of acute toxicity. 2 weeks after the last injection, the animals were challenged with an open topical application of 1%, 0.1%, 0.01%, and 0% of compound 48/80 in 3:7 propylene glycol/ethanol. The strongest reactions were found in the 0.1% induction group. Some degree of immunologic tolerance may have occurred in the 1% induction group resulting in somewhat weaker challenge responses.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1111/j.1600-0536.1985.tb02525.x | DOI Listing |
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