Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
MicroRNA (miRNA) imaging in living cells is paramount for comprehending its dynamic functions and profiles, offering valuable insights into miRNA-related cellular processes. However, this remains challenging due to limited transfection agents and the low abundance of miRNAs. Herein, a smart nanosystem was proposed for miRNA imaging in living cells by ingeniously integrating cyclometalated ruthenium (II) nanoparticles (RuNPs) with a catalyzed hairpin assembly (CHA) strategy. Three cyclometalated ruthenium (II) complexes were synthesized and employed self-assembly technology to construct RuNPs. After evaluating their loading efficiency (L), fluorescence quenching rates (Q), and fluorescence recovery rates (R) for Hairpins, RuNPs-1 was selected to construct the Hairpins@RuNPs-1 nanosystem. With a detection limit of 1.5 pM, the Hairpins@RuNPs-1 nanosystem demonstrated high sensitivity for miR-25, live cell imaging confirmed its ability to detect intracellular miR-25 and differentiate its expression in various cells with excellent biocompatibility. We believe it has the potential to become an effective tool for nucleic acid research and would be poised to significantly influence the diagnosis and treatment of diseases.
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Source |
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http://dx.doi.org/10.1016/j.bios.2024.117090 | DOI Listing |
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