Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Microdroplet chemistry has recently gained much attention, as reactions can be greatly accelerated in microdroplets. This study reports its first application in pharmaceutical bioanalysis settings to measure glucose homeostasis with unprecedented speed and sensitivity. Quantifying metabolic flux is critical for understanding drug action, but traditional isotope kinetic assays face challenges including the need of lengthy sample preparation and using radioactive tracers. To tackle these challenges, we used microdroplet reaction to facilitate on-the-fly derivatization in microseconds during mass spectrometry (MS) analysis, which increased sample throughput and sensitivity and avoided the use of radioactive tracers. This technique allowed us to elucidate a mechanism through which Semaglutide affects the levels of endogenous C-glucose and exogenous [U-C]glucose in mouse plasma and to quantify Pioglitazone-mediated changes of glucose uptake in mouse hearts. Such microdroplet-based bioanalysis would have an immediate high impact in characterizing disease phenotypes and guiding a mechanistic understanding of new drug discovery.
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http://dx.doi.org/10.1021/acs.analchem.5c01759 | DOI Listing |