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
Glutathione (GSH) coated gold‑iron oxide core shell nanoparticles (GS-Au-FeO) were prepared by coating glutathione shell on nanoparticles to reduce the dose dependent behaviour of anticancer drug, doxorubicin (DOX). The resultant nanoparticles were characterized using XPS, FTIR, HR-TEM with STEM profile to analyze the GSH shell over the surface. The GS-Au-FeO nanoparticles were loaded with DOX and maximum drug entrapment capacity of 54% was observed in 48 h. In-vitro drug release were evaluated using UV-vis and Fluorescence spectroscopy. The results show that drug release is facilitated under acidic conditions as well as by extracellular glutathione spiking. Cytotoxicity and cellular uptake was studied on HeLa cells where GS-Au-FeO nanoparticles lead to significantly higher uptake of DOX as compared to free drug. The use of glutathione conjugation thus act as an efficient drug delivery vehicle which requires significantly low concentration of GS-Au-FeO nanoparticles for DOX release besides triggering drug release by using redox active GSH.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1016/j.msec.2019.03.031 | DOI Listing |
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