Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165
Vascularization is a key issue for the success of tissue engineering to repair damaged tissue. In this study, we report a composite scaffold delivering angiogenic factor for this purpose. Vascular endothelial growth factor (VEGF) was loaded on mesoporous silica nanoparticle (MSN), which was then inc...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2016-01-01
|
Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2016/9676934 |
id |
doaj-1b6e936fe10249b1ac8f9149f1c0a911 |
---|---|
record_format |
Article |
spelling |
doaj-1b6e936fe10249b1ac8f9149f1c0a9112020-11-24T23:25:24ZengHindawi LimitedBioMed Research International2314-61332314-61412016-01-01201610.1155/2016/96769349676934Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165Joong-Hyun Kim0Tae-Hyun Kim1Min Sil Kang2Hae-Won Kim3Institute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan, Republic of KoreaInstitute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan, Republic of KoreaInstitute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan, Republic of KoreaInstitute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan, Republic of KoreaVascularization is a key issue for the success of tissue engineering to repair damaged tissue. In this study, we report a composite scaffold delivering angiogenic factor for this purpose. Vascular endothelial growth factor (VEGF) was loaded on mesoporous silica nanoparticle (MSN), which was then incorporated within a type I collagen sponge, to produce collagen/MSN/VEGF (CMV) scaffold. The CMV composite scaffold could release VEGF sustainably over the test period of 28 days. The release of VEGF improved the cell proliferation. Moreover, the in vivo angiogenesis of the scaffold, as studied by the chick chorioallantoic membrane (CAM) model, showed that the VEGF-releasing scaffold induced significantly increased number of blood vessel complexes when compared with VEGF-free scaffold. The composite scaffold showed good biocompatibility, as examined in rat subcutaneous tissue. These results demonstrate that the CMV scaffold with VEGF-releasing capacity can be potentially used to stimulate angiogenesis and tissue repair.http://dx.doi.org/10.1155/2016/9676934 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Joong-Hyun Kim Tae-Hyun Kim Min Sil Kang Hae-Won Kim |
spellingShingle |
Joong-Hyun Kim Tae-Hyun Kim Min Sil Kang Hae-Won Kim Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165 BioMed Research International |
author_facet |
Joong-Hyun Kim Tae-Hyun Kim Min Sil Kang Hae-Won Kim |
author_sort |
Joong-Hyun Kim |
title |
Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165 |
title_short |
Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165 |
title_full |
Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165 |
title_fullStr |
Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165 |
title_full_unstemmed |
Angiogenic Effects of Collagen/Mesoporous Nanoparticle Composite Scaffold Delivering VEGF165 |
title_sort |
angiogenic effects of collagen/mesoporous nanoparticle composite scaffold delivering vegf165 |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2016-01-01 |
description |
Vascularization is a key issue for the success of tissue engineering to repair damaged tissue. In this study, we report a composite scaffold delivering angiogenic factor for this purpose. Vascular endothelial growth factor (VEGF) was loaded on mesoporous silica nanoparticle (MSN), which was then incorporated within a type I collagen sponge, to produce collagen/MSN/VEGF (CMV) scaffold. The CMV composite scaffold could release VEGF sustainably over the test period of 28 days. The release of VEGF improved the cell proliferation. Moreover, the in vivo angiogenesis of the scaffold, as studied by the chick chorioallantoic membrane (CAM) model, showed that the VEGF-releasing scaffold induced significantly increased number of blood vessel complexes when compared with VEGF-free scaffold. The composite scaffold showed good biocompatibility, as examined in rat subcutaneous tissue. These results demonstrate that the CMV scaffold with VEGF-releasing capacity can be potentially used to stimulate angiogenesis and tissue repair. |
url |
http://dx.doi.org/10.1155/2016/9676934 |
work_keys_str_mv |
AT joonghyunkim angiogeniceffectsofcollagenmesoporousnanoparticlecompositescaffolddeliveringvegf165 AT taehyunkim angiogeniceffectsofcollagenmesoporousnanoparticlecompositescaffolddeliveringvegf165 AT minsilkang angiogeniceffectsofcollagenmesoporousnanoparticlecompositescaffolddeliveringvegf165 AT haewonkim angiogeniceffectsofcollagenmesoporousnanoparticlecompositescaffolddeliveringvegf165 |
_version_ |
1725557701604278272 |