Premium
UHMWPE‐MWCNT‐nHA based hybrid trilayer nanobiocomposite: Processing approach, physical properties, stem/bone cell functionality, and blood compatibility
Author(s) -
Naskar Sharmistha,
Panda Asish K.,
Jana Ashirbad,
Kanagaraj Subramani,
Basu Bikramjit
Publication year - 2020
Publication title -
journal of biomedical materials research part b: applied biomaterials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.665
H-Index - 108
eISSN - 1552-4981
pISSN - 1552-4973
DOI - 10.1002/jbm.b.34567
Subject(s) - materials science , nanocomposite , biocompatibility , composite number , composite material , mesenchymal stem cell , protein adsorption , carbon nanotube , nanoparticle , osteoblast , biomedical engineering , polymer , nanotechnology , chemistry , medicine , in vitro , biochemistry , metallurgy , biology , microbiology and biotechnology
Abstract The development of polymeric nanocomposites for biomedical applications remains a major challenge in terms of tailored addition of nanoparticles to realize the simultaneous enhancement of fracture resistance and cell/blood compatibility. To address this, the present work has been planned to determine whether small addition of surface functionalized multiwalled‐carbon‐nanotube, MWCNT (<1.5 wt%) and egg‐shell derived nanosized hydroxyapatite, nHA (<10 wt%) to ultrahigh‐molecular‐weight‐polyethylene (UHMWPE) can significantly improve the physical properties as well as biocompatibility. The difference in mouse osteoblast and human mesenchymal stem cell (hMSc) proliferation has been validated using both the monolithic composite and a trilayered composite with two different UHMWPE nanocomposites on either face with pure polymer at the middle. The combination of rheology and micro‐CT with fractography reveals the homogeneous dispersion of nanofillers, leading to mechanical property enhancement. The quantitative analysis of cell viability and cell spreading by immunocytochemistry method, using vinculin and vimentin expression, establish significant cytocompatibility with hMSc and osteoblast cells onto the trilayer hybrid nanobiocomposite substrates. The hemocompatibility of the investigated composites under the controlled flow of rabbit blood in a microfluidic device reveals the signature of reduced thrombogenesis with reduction of platelet activation on UHMWPE nanocomposite w.r.t. unreinforced UHMWPE. An attempt has been made to discuss the blood compatibility results in the backdrop of the bovine serum albumin adsorption kinetics. Summarizing, the present study establishes that the twin requirement of mechanical property and cyto/hemo‐compatibility can be potentially realized in developing trilayer composites in UHMWPE‐nHA‐MWCNT system.