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
Two ILs containing guanidinium cations (butylguanidinium chloride -CGu-Cl- and hexylguanidinium chloride -CGu-Cl-) were synthesized and characterized. Their cytotoxicity was also assessed, obtaining adequate CC values of 680 ± 99 mg·L for CGu-Cl and 135 ± 8 mg·L for CGu-Cl. Miniaturized aqueous biphasic systems (μ-ABSs) were developed using amounts lower than 1% (w/w) of these synthesized guanidinium-based ILs, KPO as salting-out agent, and ultrapure water. The phases diagrams of both systems were determined, and the CGu-Cl-based μ-ABS was selected for the development of a microextraction method in combination with high performance liquid chromatography (HPLC) with fluorescence detection (FD) for the determination of five polycyclic aromatic hydrocarbons (PAHs) as model analytes. A point of the biphasic region of the CGu-Cl-based μ-ABS corresponding to a mixture of 0.75% (w/w) of the IL, 37.7% (w/w) of KPO and 61.55% (w/w) of ultrapure water, and 30 min of equilibrium time, were selected as optimum conditions to obtain high enrichment factors and proper analytical microextraction performance. The CGu-Cl-based μ-ABS-HPLC-FD method exhibited low limits of detection, between 0.010 ng·L and 2.0 ng·L, average relative recoveries of 96.7%, high enrichment factors ranging from 44.1 to 60.4, average extraction efficiencies of 61.7%, and intermediate precision relative standard deviations lower than 17% for a concentration level of 12 ng·L. The developed method was applied successfully in the analysis of different tap water samples.
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Source |
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http://dx.doi.org/10.1016/j.talanta.2019.05.083 | DOI Listing |
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