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 present study investigates the potential use of forsterite as an orthopedic biomaterial along with the role of strontium oxide (SrO) as a dopant. The degradation behavior was measured as a function of immersion time in simulated body fluid (SBF) for up to 8 weeks and was analyzed by micro computed tomography (μ-CT) and scanning electron microscopy (SEM). All the doped samples showed higher degradation than pure sample. The cytocompatibility study showed good cytocompatibility and proliferation of MC3T3-E1 cells on Sr-doped MgS samples. The experiments were carried out by implanting the ceramics in a rabbit femur for 30 and 90 days. The 3D μ-CT and SEM images of 2 and 3 wt % Sr-doped MgS showed increased bone regeneration around the implant materials compared with pure and 1 wt % Sr-doped MgS, which was further confirmed by quantitative oxytetracycline labeling. The histological examination of three major organs of heart, kidney, and liver confirmed that the degradation product of the MgS ceramics, with or without doping, had no toxicological side effects. These results indicate that Sr-doped MgS bioceramics exhibit enhanced degradability with the potential to be used for temporary bone regeneration.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acsbiomaterials.8b00788 | DOI Listing |
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