2005
DOI: 10.4028/www.scientific.net/kem.284-286.509
|View full text |Cite
|
Sign up to set email alerts
|

Accelerated Formation of Bone-Like Apatite on Biodegradable Polymer Substrates

Abstract: Using an acellular simulated body fluid (SBF), bone-like apatite can be formed on a variety of biomaterials, bioactive or bioinert, after these materials have undergone appropriate treatment(s). This biomimetic apatite-forming process is now applied to tissue engineering scaffolds in an attempt to make the scaffolds osteoconductive. In the current investigation, to form bone-like apatite on polymers such as poly(L-lactic acid) (PLLA) and poly(glycolic acid) (PGA) which degrade fast in aqueous environment, a so… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0

Year Published

2006
2006
2022
2022

Publication Types

Select...
2
1
1

Relationship

1
3

Authors

Journals

citations
Cited by 4 publications
(3 citation statements)
references
References 5 publications
0
3
0
Order By: Relevance
“…The PGA meshes were maintained at the air-solution interface of a supersaturated solution of Ca(HCO 3 ) 2 and heat-treated at 33 °C for 6 h. The saturation gradient that formed due to evaporation and CO 2 degassing enabled the heterogeneous nucleation/growth of CaCO 3 along the PGA mesh at the air-solution interface. This technique overcomes several challenges presented by the existing techniques to coat PGA with hard minerals: the deposition temperature is below the onset of the glass transition temperature of PGA (35 °C) [1], and the exposure time is relatively short, thereby avoiding hydrolytic degradation [11], 12,13].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The PGA meshes were maintained at the air-solution interface of a supersaturated solution of Ca(HCO 3 ) 2 and heat-treated at 33 °C for 6 h. The saturation gradient that formed due to evaporation and CO 2 degassing enabled the heterogeneous nucleation/growth of CaCO 3 along the PGA mesh at the air-solution interface. This technique overcomes several challenges presented by the existing techniques to coat PGA with hard minerals: the deposition temperature is below the onset of the glass transition temperature of PGA (35 °C) [1], and the exposure time is relatively short, thereby avoiding hydrolytic degradation [11], 12,13].…”
Section: Discussionmentioning
confidence: 99%
“…The low onset of the glass transition temperature of PGA (35 °C [1]) represents a key technical challenge in forming a mineral coating on the mesh. Hence, lowtemperature wet chemical techniques are a common way to coat PGA with apatite [11], 12,13]. However, these methods typically require extended exposure (up to 16 days) to simulated bodily fluids (SBF), which could severely compromise the mechanical strength of PGA due to hydrolytic degradation [14].…”
Section: Introductionmentioning
confidence: 99%
“…However, as polymers such as PLA degrades fast in the aqueous environment, normal biomimetic processes that have been developed for coating apatite on metals or ceramics [19] are not suitable for these polymers. Therefore, an accelerated biomimetic process was developed to coat PLLA scaffolds with a thin layer of apatite [20,21] . Apatite was found to form on PGA meshes and PLLA scaffolds (Fig.7), and with a dynamic environment, biomimetic apatite coatings could be produced on pores inside the scaffolds.…”
Section: Coating the Polymer Scaffold With An Apatite Layermentioning
confidence: 99%