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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Gout is a joint disease caused by the deposition of monosodium urate, the incidence of which shows an escalating trend annually while demonstrating a propensity toward younger populations, whereas available pharmacological interventions frequently induce severe adverse effects. In this investigation, a highly sensitive electrochemical enzyme biosensor was constructed based on the pivotal role of xanthine oxidase (XO); the enzymatic activity was enhanced through chitosan - functionalized graphene oxide (CS@GO)-modified electrodes coupled with electrodeposited gold nanoparticles (AuNPs), which, when integrated with their superior electrical conductivity along with exceptional biocompatibility, facilitated the highly efficient screening of anti-gout components within natural products. Following optimization of critical parameters, evaluation of 14 compounds revealed five plant extracts (accounting for 28 % of samples) exhibiting XO inhibition exceeding 83 %, demonstrating superior efficacy compared to allopurinol (83.32 %). This methodology establishes an innovative strategy for rapid identification of highly potent yet minimally toxic anti-gout natural compounds, offering significant reference value regarding natural drug development.
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http://dx.doi.org/10.1016/j.bioelechem.2025.109032 | DOI Listing |