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
98%
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Infectious diseases are prevalent in resource-limited regions with restricted access to health care. Nucleic acid testing is the gold standard for pathogen diagnosis. However, traditional methods are resource-intensive, which limits their use in point-of-care settings. Microfluidic technologies, such as the immiscible phase filtration-assisted system (IFAST) using paramagnetic particles (PMPs), simplify nucleic acid extraction but face barrier stability issues. The interface between the aqueous and oil phases in current IFAST systems is destabilized under the conditions required for efficient RNA extraction. These conditions include the use of reagents containing high concentrations of surfactants and organic solvents, as well as thermal treatment, which reduces the operational stability, reproducibility, and compatibility of the current IFAST systems. We developed a high-transition-temperature (HTT) paraffin-embedded IFAST-based device to improve barrier stability and extraction efficiency. HTT paraffin remains semi-solid at 65 °C, providing a robust barrier during the thermal lysis and RT-LAMP processes. At 75 °C, the device maintained compartment integrity and reduced carryover during the nucleic acid-bound magnetic particle transfer. Testing with SARS-CoV-2 samples showed detection of as little as 1 copy/μL of the viral genome without false positives. By integrating RNA extraction and colorimetric RT-LAMP detection, this device provided rapid on-site testing, advancing accessible and effective disease management in regions that require rapid diagnostics.
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http://dx.doi.org/10.1016/j.bios.2025.117314 | DOI Listing |