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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
Uniform fluorescein isothiocyanate (FITC)-incorporated silica-coated core-shell SPIO nanoparticles (MNP@SiO2) with sizes of about 30 nm have been prepared by controlled hydrolysis of tetraethyl orthosilicateb. Monoclonal antibody nimotuzumab (h-R3) is labeled to the core-shell MNP@SiO2 for targeting to cancer cell A431 overexpressing epidermal growth factor receptor (EGFR). The result shows h-R3 labeled MNP@SiO2 nanoparticle (MNP@SiO2-mAb(h_R3)) has desired specificity to cancer cell A431. Compared to BSA labeled MNP@SiO2 nanoparticle (MNP@SiO2-BSA), MNP@SiO2-mAb(h_R3) could increase the cellular uptake of endocytosis and cytotoxicity due to h-R3 binding.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1166/jnn.2013.6640 | DOI Listing |
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