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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Every 5 minutes, 50 people are bitten by a snake worldwide; four will be permanently disabled and one will die. Most approaches to treating and diagnosing snake envenomation, a World Health Organization (WHO)-neglected tropical disease, rely on antibody-based solutions derived from animals or cell culture. Here, we present the first proof of concept for a glycopolymer-based ultraviolet-visible (UV-vis) assay to detect snake venom, specifically Western Diamondback Rattlesnake () venom. This was achieved by synthesizing a library of glycan-terminated poly(hydroxyethyl acrylamide) functionalized gold nanoparticles. The library was analyzed using UV-vis spectroscopy and biolayer interferometry, with galactose-terminating systems found to demonstrate specificity for venom, versus model lectins and venom in UV-vis assays. This corroborates glycan array data in the literature and highlights our glycopolymer systems' potential as a diagnostic tool for snakebite, with the best particle system displaying a limit of detection of ∼20 μg·mL.
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Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12152936 | PMC |
http://dx.doi.org/10.1021/acs.biomac.5c00125 | DOI Listing |