4.7 Article

The influences of polycaprolactone-grafted nanoparticles on the properties of polycaprolactone composites with enhanced osteoconductivity

期刊

COMPOSITES SCIENCE AND TECHNOLOGY
卷 83, 期 -, 页码 64-71

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.compscitech.2013.04.020

关键词

Nanoparticles; Polymer-matrix composites (PMCs); Mechanical properties; Scanning electron microscopy (SEM); Osteoconductivity

资金

  1. Chang Gung Memorial Hospital [CMRPG3C0251]
  2. National Science Council [101-2221-E-182A-079-MY2]
  3. Laboratory Animal Center
  4. Molecular Imaging Center
  5. Expensive Advanced Instrument Core Laboratory, Chang Gung Memorial Hospital, Linkou

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Bioceramic or inorganic nanoparticles made of SiO2, TiO2, SrO, and hydroxyapatite (HAP) have been reported to improve cell adhesion onto polymers. However, direct mixing of these nanoparticles with polymers often leads to their aggregation within the polymer matrix and subsequent deterioration of the material's mechanical strength. A novel method for modifying the surfaces of the nanoparticles by grafting epsilon-caprolactone using a ring-opening condensation reaction was developed to improve the interconnection of the nanoparticles within the polymer matrix. The mechanical studies showed that adding grafted nanoparticles into the polycaprolactone (PCL) matrix improved the initial mechanical strength. MTT assay and a live/dead stain showed higher cell viability in the tablets with grafted SiO2, TiO2, and HAP nanoparticles, except the SrO-containing tablets. The cell adhesion and alkaline phosphatase activity assay confirmed that the composite tablets with PCL-grafted HAP nanopartides had better osteoconductivity. HE stains showed that composite tablets with PCL-grafted SiO2, TiO2, and HAP nanoparticles produce less immune response than the pure PCL. We thus conclude that a PCL matrix incorporating PCL-grafted HAP nanopartides has enhanced mechanical strength, improved osteoconductivity, and a slower degradation rate than pure nanoparticles. (C) 2013 Elsevier Ltd. All rights reserved.f

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