1998
DOI: 10.1016/s0142-9612(98)00021-0
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Three-dimensional culture of rat calvarial osteoblasts in porous biodegradable polymers

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Cited by 456 publications
(283 citation statements)
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“…Additionally, cells grown on TCPS exhibited similar temporal trends in ALP activity and mineralization as in a previous report [6], suggesting that PEEK-SP accelerated osteoblast differentiation rather than smooth PEEK and Ti6Al4V causing delayed differentiation. One potential explanation for the initially increased cell proliferation on PEEK-SP is that the increased surface area effectively decreased the seeding density of cells, which could have facilitated greater cell proliferation at early time points [20,54]. However, this increase in surface area and early proliferation did not translate to greater cell numbers at later time points (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, cells grown on TCPS exhibited similar temporal trends in ALP activity and mineralization as in a previous report [6], suggesting that PEEK-SP accelerated osteoblast differentiation rather than smooth PEEK and Ti6Al4V causing delayed differentiation. One potential explanation for the initially increased cell proliferation on PEEK-SP is that the increased surface area effectively decreased the seeding density of cells, which could have facilitated greater cell proliferation at early time points [20,54]. However, this increase in surface area and early proliferation did not translate to greater cell numbers at later time points (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The static method resulted in a statistically lower uniformity, consistent with the nonuniform spatial cell distributions reported by several groups. 4,6,21,22 This low uniformity may be explained by the difficulty in evenly distributing the small volume of cell suspension over the scaffold surface and by the intrinsically weak mechanism of infusion ͑i.e., via gravity and capillary action͒.…”
Section: Discussionmentioning
confidence: 99%
“…These were based on the utilization of supports, as gels and sponges of collagen type I, PLGA foam, DegraPol, agarose, Matrigel, or methylcellulose. 7,10,15,16,18,20,22,25,26,30,32,34,37,39 Normal human osteogenic cells, osteoblasts from prepubertal-age donors, or bone marrow stromal fibroblasts adhering to scaffolding of HAP/ TC, 16,20,25,26,30,34 collagraft, 26 collagen sponges, 15,39 or bone chips 5 were utilized to produce specifically 3D structures designed for direct implantation in vivo.…”
Section: Introductionmentioning
confidence: 99%