2015
DOI: 10.1016/j.dental.2015.09.007
|View full text |Cite
|
Sign up to set email alerts
|

Effectiveness of non-biodegradable poly(2-hydroxyethyl methacrylate)-based hydrogel particles as a fibroblast growth factor-2 releasing carrier

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
8
0

Year Published

2017
2017
2021
2021

Publication Types

Select...
5
4

Relationship

3
6

Authors

Journals

citations
Cited by 17 publications
(8 citation statements)
references
References 48 publications
0
8
0
Order By: Relevance
“…Some carriers that have previously been proposed were collagen (Hu et al 1998, Kikuchi et al 2007, Bezerra Da Silva et al 2008, gelatin Ishimatsu et al 2009), agarose (Chaussain et al 2009), sodium alginate (Oliva-Rodriguez et al 2011), chitosan . Current in vitro evidence suggests other potential drug delivery systems for bioactive molecules, such as biodegradable polymer matrix of lactide and glycolide (Mathieu et al 2013), porous silk fibroin scaffolds (Yang et al 2015), poly-2-hydroxyethyl methacrylate (polyHEMA)-based hydrogel (Takeda et al 2015), tricalcium phosphate microsphere-hydrogel composite (Lee et al 2014). In addition, biomaterials that can be used as scaffolds for VPT have recently been suggested and could enhance proliferation and differentiation of human dental pulp cells, such as polycaprolactone/submicron bioactive glass hybrid composites (Wang et al 2016a), a chitosan-based scaffold (Bellamy et al 2016) and keratin hydrogel (Sharma et al 2016).…”
Section: Current Challenges and Future Directionsmentioning
confidence: 99%
“…Some carriers that have previously been proposed were collagen (Hu et al 1998, Kikuchi et al 2007, Bezerra Da Silva et al 2008, gelatin Ishimatsu et al 2009), agarose (Chaussain et al 2009), sodium alginate (Oliva-Rodriguez et al 2011), chitosan . Current in vitro evidence suggests other potential drug delivery systems for bioactive molecules, such as biodegradable polymer matrix of lactide and glycolide (Mathieu et al 2013), porous silk fibroin scaffolds (Yang et al 2015), poly-2-hydroxyethyl methacrylate (polyHEMA)-based hydrogel (Takeda et al 2015), tricalcium phosphate microsphere-hydrogel composite (Lee et al 2014). In addition, biomaterials that can be used as scaffolds for VPT have recently been suggested and could enhance proliferation and differentiation of human dental pulp cells, such as polycaprolactone/submicron bioactive glass hybrid composites (Wang et al 2016a), a chitosan-based scaffold (Bellamy et al 2016) and keratin hydrogel (Sharma et al 2016).…”
Section: Current Challenges and Future Directionsmentioning
confidence: 99%
“…As a non-biodegradable carrier suitable for delivery of proteins or antimicrobials 29,30) , we have developed poly(2-hydroxyethylmethacrylate)/trimethylolpropane trimethacrylate (polyHEMA/TMPT) particles. When FGF-2 was loaded into such particles, a sustained release of FGF-2 was maintained for up to 14 days 28) .…”
Section: Discussionmentioning
confidence: 99%
“…The non-biodegradable polyHEMA/TMPT particles described before can also act as a carrier for growth factors. Takeda et al 102) reported that fibroblast growth factor-2 (FGF-2) could be loaded into polymer particles composed of 90 (wt)% HEMA and 10 (wt)% TMPT, and FGF-2 adsorbed to the particles was released over 14 days and maintained its activity in increasing the proliferation of osteoblast-like cells. Additionally, when the FGF-2-loaded polymer particles were Each resin disc was placed in a 48-well plate, and MC3T3-E1 cells were seeded in each well at 5×10 3 cells/well and cultured for 3 days.…”
Section: Polymer Particles As a Reservoir Of Antimicrobialsmentioning
confidence: 99%