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
Objective: To establish the determination method for polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans(PCDD/Fs) in human serum, and further to provide an operable and scientific determination protocal and basis for conducting human health risk assessment for PCDD/Fs.
Methods: The serum samples were pretreated by C18 column solid phase extraction, acid silica gel column and activated carbon column purification, separated by DB-5 MS capillary column(60 m×0. 25 mm×0. 25 μm), and PCDD/Fs was quantitative analyzed by high resolution mass spectrometry.
Results: The method detection limit was in the range of 0. 35-3. 26 pg/g lipid. This method was further validated using international serum standard reference material sample SRM 1958. According to the reference mass fraction values given for SRM 1958, the concentrations of 17 PCDD/Fs monomers were all in the range of reference mass fraction values, and the relative standard deviation was 2%-19%(n=3). This method was further applied to determination PCDD/Fs in actual serum of human body. The result showed that the recovery rate of isotope labeled PCDD/Fs internal standards were in the range of 61%-135%.
Conclusion: The performance of the method is highly sensitive, stable and highly accurate, which meets the requirements for the determination of PCDD/Fs in human serum and the method can be applied to human health risk assessment for PCDD/Fs in the future.
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Source |
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http://dx.doi.org/10.19813/j.cnki.weishengyanjiu.2021.01.018 | DOI Listing |
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