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
The loading capacity of dsRNA by nanocarriers is a key parameter in the process of RNAi commercialisation. In this research, a sustainable, simple, and cheap method was developed to determine the dsRNA loading capacity by popular cationic nanocarriers. In this method, the fluorescence emission of the cationic nanocarrier + (dsRNA-DAPI) shows blue shift in comparison to that of dsRNA-DAPI. When dsRNA-DAPI is completely loaded by cationic nanocarriers, the fluorescence peak coincides with the emission wavelength of DNA-DAPI. The samples of nanocarrier + (dsRNA-DAPI) are simply tested in a fluorometer with no damage to the samples. The reported method is simpler, cheaper, and more sustainable than gel electrophoresis and HPLC, and will fulfill the industry need for reliable and quick quality administration/control in the production process.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1039/d4tb01393j | DOI Listing |
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