TY - JOUR
T1 - Antimicrobial cytocompatible pentaerythritol triacrylate-co- trimethylolpropane composite scaffolds for orthopaedic implants
AU - Smoak, Mollie
AU - Chen, Cong
AU - Qureshi, Ammar
AU - Garber, Leah
AU - Pojman, John A.
AU - Janes, Marlene E.
AU - Hayes, Daniel J.
N1 - Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 2014/11/15
Y1 - 2014/11/15
N2 - As of 2010, 5.3 million orthopedic surgeries are performed each year, and this number is expected to increase to 6.2 million by 2020. On average, 27.7% of all orthopedic surgeries result in infection which often leads to osteomyelitis and the loss of supporting bone. In this study, we describe two synthetic bone grafts, or augmentation methods, for a biodegradable, silver nanoparticle (SNPs) containing antimicrobial scaffolds composed of pentaerythritol triacrylate-co-trimethylolpropane tris (3-mercaptopropionate) (PETA) and hydroxyapatite (HA). This osteoinductive and degradable material is designed to stimulate proliferation of bone progenitor cells, and provide controlled release of antimicrobial components. The first method, denoted as the "incorporating method," involves dissolving SNPs in ethanol, butanol, or isopropanol and directly incorporating the particles into the scaffold prior to polymerization. The second method, "coating method," involves submerging fabricated scaffolds into their respective SNPs-solution and mixing for 24 h. The coating method allowed better distribution and release of SNPs from the surface of the composites when exposed to extracellular media. The in vitro release of silver for both methods was quantified by inductively coupled plasma optical emission spectroscopy (ICP-OES). The scaffolds made by means of the coating method showed increased release of silver with respect to time; no silver leached from the scaffolds formed by the incorporating method. Use of Alamar Blue assay demonstrated that the SNPs incorporation did not affect cell viability when tested with hASCs. The scaffolds formed by the coating method inhibited the proliferation of Staphylococcus aureus 99.5% and Escherichia coli by 99.9% within 24 h.
AB - As of 2010, 5.3 million orthopedic surgeries are performed each year, and this number is expected to increase to 6.2 million by 2020. On average, 27.7% of all orthopedic surgeries result in infection which often leads to osteomyelitis and the loss of supporting bone. In this study, we describe two synthetic bone grafts, or augmentation methods, for a biodegradable, silver nanoparticle (SNPs) containing antimicrobial scaffolds composed of pentaerythritol triacrylate-co-trimethylolpropane tris (3-mercaptopropionate) (PETA) and hydroxyapatite (HA). This osteoinductive and degradable material is designed to stimulate proliferation of bone progenitor cells, and provide controlled release of antimicrobial components. The first method, denoted as the "incorporating method," involves dissolving SNPs in ethanol, butanol, or isopropanol and directly incorporating the particles into the scaffold prior to polymerization. The second method, "coating method," involves submerging fabricated scaffolds into their respective SNPs-solution and mixing for 24 h. The coating method allowed better distribution and release of SNPs from the surface of the composites when exposed to extracellular media. The in vitro release of silver for both methods was quantified by inductively coupled plasma optical emission spectroscopy (ICP-OES). The scaffolds made by means of the coating method showed increased release of silver with respect to time; no silver leached from the scaffolds formed by the incorporating method. Use of Alamar Blue assay demonstrated that the SNPs incorporation did not affect cell viability when tested with hASCs. The scaffolds formed by the coating method inhibited the proliferation of Staphylococcus aureus 99.5% and Escherichia coli by 99.9% within 24 h.
UR - http://www.scopus.com/inward/record.url?scp=84923447104&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84923447104&partnerID=8YFLogxK
U2 - 10.1002/app.41099
DO - 10.1002/app.41099
M3 - Article
AN - SCOPUS:84923447104
SN - 0021-8995
VL - 131
JO - Journal of Applied Polymer Science
JF - Journal of Applied Polymer Science
IS - 22
M1 - 41099
ER -