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
Liposomes of various phospholipids were prepared using an improved supercritical reverse phase evaporation (ISCRPE) method that utilizes supercritical carbon dioxide (scCO(2)) as an alternative to organic solvents. Using this method, in the absence of any organic solvent including ethanol, the maximum trapping efficiency of glucose reached 36% for 20 mM l-alpha-dioleoylphosphatidylcholine (DOPC), compared to less than 10% using the Bangham method. Liposomes prepared by the ISCRPE method were highly stable for one month at room temperature. Freeze fractured TEM observations, osmotic shrinkage measurements, and DSC measurements revealed that the liposomes prepared by the ISCRPE method are unilamellar vesicles with loosely packed phospholipids. Comparison of nitrogen with scCO(2) revealed that the presence of CO(2) is necessary for the formation of liposomes.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/la051654u | DOI Listing |
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