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: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
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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γ-Glutamyl transpeptidase (GGT) is a membrane-bounded enzyme closely involved in a wide range of physiological and pathological processes. While numerous fluorescent probes have been developed to image GGT activity noninvasively, in vivo applications remain challenging. A key limitation lies in GGT's localization: activated fluorophores diffuse rapidly from sites of activation, significantly reducing contrast of image in living systems. To overcome this, we adopted the "one-to-multi" design to develop a novel NIR fluorescent probe for GGT. This probe, upon a single GGT activation, triggers a cascade of effects, including markedly reduced aqueous solubility, enhanced cellular permeability, covalent self-immobilization at the target site, and enhancement in near-infrared (NIR) fluorescence intensity. This design allows real-time and sensitive imaging of GGT activity in live cells and achieves high contrast in vivo imaging with long-lasting signal retention at tumor sites in living mice.
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http://dx.doi.org/10.1002/asia.70238 | DOI Listing |