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
Ceramide molecules in water-based solutions readily attract each other to form molecular crystals, which seriously hampers to diversify their formulations. This paper describes a facile method that allows fabrication of stable ceramide emulsions through an effective molecular association with a lipid having an asymmetric molecular geometry. The lipid considered in this study is mannosylerythritol lipid (MEL). MEL is specialized in having a unique molecular structure containing sugar alcohol erythritol as a hydrophilic part and two alkyl chains with different number of carbons as hydrophobic moieties. Our particular interest has been focused on experimentally demonstrating how MEL interacts with pseudo-ceramide molecules by observing phase properties, emulsion morphology, and suspension stability. The pseudo-ceramide emulsions prepared with MEL show remarkably improved dispersion stability without either formation of molecular crystals or changes in particle sizes even after storing them for a long time. This suggests that MEL readily associates with the pseudo-ceramide due to the hydrophobic interaction, while it makes a break in the continuity of the molecular assembly of the pseudo-ceramide molecules themselves due to the geometric hindrance coming from MEL's asymmetric molecular structure.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1016/j.colsurfb.2013.10.022 | DOI Listing |
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