PMID- 27108739 OWN - NLM STAT- MEDLINE DCOM- 20180709 LR - 20181202 IS - 1944-8252 (Electronic) IS - 1944-8244 (Linking) VI - 8 IP - 19 DP - 2016 May 18 TI - Modulation of Protein Adsorption and Cell Proliferation on Polyethylene Immobilized Graphene Oxide Reinforced HDPE Bionanocomposites. PG - 11954-68 LID - 10.1021/acsami.6b00946 [doi] AB - The uniform dispersion of nanoparticles in a polymer matrix, together with an enhancement of interfacial adhesion is indispensable toward achieving better mechanical properties in the nanocomposites. In the context to biomedical applications, the type and amount of nanoparticles can potentially influence the biocompatibility. To address these issues, we prepared high-density polyethylene (HDPE) based composites reinforced with graphene oxide (GO) by melt mixing followed by compression molding. In an attempt to tailor the dispersion and to improve the interfacial adhesion, we immobilized polyethylene (PE) onto GO sheets by nucleophilic addition-elimination reaction. A good combination of yield strength (ca. 20 MPa), elastic modulus (ca. 600 MPa), and an outstanding elongation at failure (ca. 70%) were recorded with 3 wt % polyethylene grafted graphene oxide (PE-g-GO) reinforced HDPE composites. Considering the relevance of protein adsorption as a biophysical precursor to cell adhesion, the protein adsorption isotherms of bovine serum albumin (BSA) were determined to realize three times higher equilibrium constant (Keq) for PE-g-GO-reinforced HDPE composites as compared to GO-reinforced composites. To assess the cytocompatibility, we grew osteoblast cell line (MC3T3) and human mesenchymal stem cells (hMSCs) on HDPE/GO and HDPE/PE-g-GO composites, in vitro. The statistically significant increase in metabolically active cell over different time periods in culture for up to 6 days in MC3T3 and 7 days for hMSCs was observed, irrespective of the substrate composition. Such observation indicated that HDPE with GO or PE-g-GO addition (up to 3 wt %) can be used as cell growth substrate. The extensive proliferation of cells with oriented growth pattern also supported the fact that tailored GO addition can support cellular functionality in vitro. Taken together, the experimental results suggest that the PE-g-GO in HDPE can effectively be utilized to enhance both mechanical and cytocompatibility properties and can further be explored for potential biomedical applications. FAU - Upadhyay, Rahul AU - Upadhyay R AD - Laboratory for Biomaterials, Materials Research Center, Indian Institute of Science ,Bangalore 560012, India. FAU - Naskar, Sharmistha AU - Naskar S AD - Center for Biosystems Science and Engineering, Indian Institute of Science , Bangalore 560012, India. FAU - Bhaskar, Nitu AU - Bhaskar N AD - Laboratory for Biomaterials, Materials Research Center, Indian Institute of Science ,Bangalore 560012, India. FAU - Bose, Suryasarathi AU - Bose S AD - Department of Materials Engineering, Indian Institute of Science , Bangalore 560012, India. FAU - Basu, Bikramjit AU - Basu B AD - Laboratory for Biomaterials, Materials Research Center, Indian Institute of Science ,Bangalore 560012, India. AD - Center for Biosystems Science and Engineering, Indian Institute of Science , Bangalore 560012, India. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20160503 PL - United States TA - ACS Appl Mater Interfaces JT - ACS applied materials & interfaces JID - 101504991 RN - 27432CM55Q (Serum Albumin, Bovine) RN - 7782-42-5 (Graphite) RN - 9002-88-4 (Polyethylene) SB - IM MH - Animals MH - Cattle MH - Cell Line MH - Cell Proliferation/*drug effects MH - *Graphite/chemistry/pharmacology MH - Humans MH - Mesenchymal Stem Cells/cytology/*metabolism MH - Mice MH - Nanocomposites/*chemistry MH - Osteoblasts/cytology/*metabolism MH - *Polyethylene/chemistry/pharmacology MH - Serum Albumin, Bovine/*chemistry OTO - NOTNLM OT - HDPE OT - cytocompatibility OT - grafting OT - graphene oxide OT - hMSC OT - nanocomposites OT - osteoblast OT - toxicity EDAT- 2016/04/26 06:00 MHDA- 2018/07/10 06:00 CRDT- 2016/04/26 06:00 PHST- 2016/04/26 06:00 [entrez] PHST- 2016/04/26 06:00 [pubmed] PHST- 2018/07/10 06:00 [medline] AID - 10.1021/acsami.6b00946 [doi] PST - ppublish SO - ACS Appl Mater Interfaces. 2016 May 18;8(19):11954-68. doi: 10.1021/acsami.6b00946. Epub 2016 May 3.