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Download fileAlginate Bead Based Hexagonal Close Packed 3D Implant for Bone Tissue Engineering
journal contribution
posted on 2016-11-07, 00:00 authored by Tarun Agarwal, Prajna Kabiraj, Gautham Hari Narayana, Senthilguru Kulanthaivel, Uvanesh Kasiviswanathan, Kunal Pal, Supratim Giri, Tapas K. Maiti, Indranil BanerjeeSuccess
of bone tissue engineering (BTE) relies on the osteogenic microarchitecture
of the biopolymeric scaffold and appropriate spatiotemporal distribution
of therapeutic molecules (growth factors and drugs) inside it. However,
the existing technologies have failed to address both the issues together.
Keeping this perspective in mind, we have developed a novel three-dimensional
(3D) implant prototype by stacking hexagonal close packed (HCP) layers
of calcium alginate beads. The HCP arrangement of the beads lead to
a patterned array of interconnected tetrahedral and octahedral pores
of average diameter of 142.9 and 262.9 μm, respectively, inside
the implant. The swelling pattern of the implants changed from isotropic
to anisotropic in the z-direction in the absence
of bivalent calcium ions (Ca2+) in the swelling buffer.
Incubation of the implant in simulated body fluid (SBF) resulted in
a 2.7-fold increase in the compressive modulus. The variation in the
relaxation times as derived from the Weichert viscoelasticity model
predicted a gradual increase in the interactions among the alginate
molecules in the matrix. We demonstrated the tunability of the spatiotemporal
drug release from the implant in a tissue mimicking porous semisolid
matrix as well as in conventional drug release set up by changing
the spatial coordinates of the “drug loaded depot layer”
inside the implant. The therapeutic potential of the implant was confirmed
against Escherichia coli using metronidazole as the
model drug. Detailed analysis of cell viability, cell cycle progression,
and cytoskeletal reorganization using osteoblast cells (MG-63) proved
the osteoconductive nature of the implant. Expression of differentiation
markers such as alkaline phosphatase, runx2, and collagen type 1 in
human mesenchymal stem cell in vitro confirmed the
osteogenic nature of the implant. When tested in vivo, VEGF loaded implant was found capable of inducing angiogenesis
in a mice model. In conclusion, the bead based implant may find its
utility in non-load-bearing BTE.
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262.9 μ mWeichert viscoelasticity modelimplant prototypemodel drugoctahedral poresbody fluidcollagen type 1bone tissue engineeringcalcium alginate beadsPacked 3 D ImplantAlginate Beadosteoblast cellsosteogenic natureMGalginate moleculesosteoconductive naturespatiotemporal distributionBone Tissue Engineering Successbivalent calcium ionsVEGFEscherichia colibiopolymeric scaffoldmice modelSBFcell viabilitygrowth factorsdrug releaseHCP arrangementosteogenic microarchitecturespatiotemporal drug releasecytoskeletal reorganizationnon-load-bearing BTErelaxation timesdifferentiation markerscell cycle progressionsemisolid matrix