Inkjet-based multilayered growth factor-releasing nanofilms for enhancing proliferation of mesenchymal stem cells in vitro
[Display omitted] •By inkjet based LbL assembly, fabrication of bFGF/HEP nanofilms on a flexible PET substrate.•Active bFGFs were released from printed LbL nanofilms during 3days.•Printed LbL films can contain different amounts of bFGF through control of the number of deposited layers.•With active b...
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Published in | Journal of industrial and engineering chemistry (Seoul, Korea) Vol. 50; pp. 36 - 40 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
25.06.2017
한국공업화학회 |
Subjects | |
Online Access | Get full text |
ISSN | 1226-086X 1876-794X |
DOI | 10.1016/j.jiec.2017.02.014 |
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Abstract | [Display omitted]
•By inkjet based LbL assembly, fabrication of bFGF/HEP nanofilms on a flexible PET substrate.•Active bFGFs were released from printed LbL nanofilms during 3days.•Printed LbL films can contain different amounts of bFGF through control of the number of deposited layers.•With active bFGFs from nanofilms, the proliferation of rabbit BMSCs was improved.
We report the preparation and characterization of inkjet-based basic fibroblast growth factor (bFGF)-containing nanofilms on a flexible PET substrate. bFGF and heparin (HEP) were assembled by inkjet-based layer-by-layer (LbL) assembly driven by electrostatic interactions. The bFGF/HEP nano-assembly surface coatings were formed via alternating printing adsorption of positively charged bFGF and negatively charged HEP; the process was monitored by UV–vis spectroscopy and quartz crystal microbalance. The bFGF release profile could be controlled by altering the number of layers of printed LbL films. Mesenchymal stem cells, which are capable of extended proliferation in vitro, require a continuous supply of bFGF for proliferation. However, enhancing mesenchymal stem cell proliferation by continuous supplying bFGF is difficult, even with medium replacement, because of the instability of bFGF. Here, we established a novel system for releasing bioactive bFGF from a modified surface by using an inkjet-based nanofilm fabrication method. |
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AbstractList | We report the preparation and characterization of inkjet-based basicfibroblast growth factor (bFGF)-containing nanofilms on aflexible PET substrate. bFGF and heparin (HEP) were assembled by inkjet-basedlayer-by-layer (LbL) assembly driven by electrostatic interactions. The bFGF/HEP nano-assembly surfacecoatings were formed via alternating printing adsorption of positively charged bFGF and negativelycharged HEP; the process was monitored by UV–vis spectroscopy and quartz crystal microbalance. ThebFGF release profile could be controlled by altering the number of layers of printed LbLfilms.
Mesenchymal stem cells, which are capable of extended proliferation in vitro, require a continuous supplyof bFGF for proliferation. However, enhancing mesenchymal stem cell proliferation by continuoussupplying bFGF is difficult, even with medium replacement, because of the instability of bFGF. Here, weestablished a novel system for releasing bioactive bFGF from a modified surface by using an inkjet-basednanofilm fabrication method. KCI Citation Count: 6 [Display omitted] •By inkjet based LbL assembly, fabrication of bFGF/HEP nanofilms on a flexible PET substrate.•Active bFGFs were released from printed LbL nanofilms during 3days.•Printed LbL films can contain different amounts of bFGF through control of the number of deposited layers.•With active bFGFs from nanofilms, the proliferation of rabbit BMSCs was improved. We report the preparation and characterization of inkjet-based basic fibroblast growth factor (bFGF)-containing nanofilms on a flexible PET substrate. bFGF and heparin (HEP) were assembled by inkjet-based layer-by-layer (LbL) assembly driven by electrostatic interactions. The bFGF/HEP nano-assembly surface coatings were formed via alternating printing adsorption of positively charged bFGF and negatively charged HEP; the process was monitored by UV–vis spectroscopy and quartz crystal microbalance. The bFGF release profile could be controlled by altering the number of layers of printed LbL films. Mesenchymal stem cells, which are capable of extended proliferation in vitro, require a continuous supply of bFGF for proliferation. However, enhancing mesenchymal stem cell proliferation by continuous supplying bFGF is difficult, even with medium replacement, because of the instability of bFGF. Here, we established a novel system for releasing bioactive bFGF from a modified surface by using an inkjet-based nanofilm fabrication method. |
Author | Choi, Moonhyun Han, Uiyoung Hong, Jinkee Choi, Daheui |
Author_xml | – sequence: 1 givenname: Moonhyun surname: Choi fullname: Choi, Moonhyun – sequence: 2 givenname: Daheui surname: Choi fullname: Choi, Daheui – sequence: 3 givenname: Uiyoung surname: Han fullname: Han, Uiyoung – sequence: 4 givenname: Jinkee surname: Hong fullname: Hong, Jinkee email: jkhong@cau.ac.kr |
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CitedBy_id | crossref_primary_10_1016_j_apsusc_2023_156742 crossref_primary_10_3390_pharmaceutics13071083 crossref_primary_10_1021_acs_molpharmaceut_7b01099 crossref_primary_10_1016_j_jddst_2020_101519 crossref_primary_10_2139_ssrn_4190837 crossref_primary_10_1016_j_jiec_2017_07_040 crossref_primary_10_1186_s40824_018_0139_5 crossref_primary_10_1016_j_bprint_2018_e00031 crossref_primary_10_1016_j_cis_2020_102334 |
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Keywords | Nanofilms Basic fibroblast growth factor Mesenchymal stem cells (MSCs) Layer-by-layer (LbL) assembly Ink-jet printing |
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•By inkjet based LbL assembly, fabrication of bFGF/HEP nanofilms on a flexible PET substrate.•Active bFGFs were released from printed LbL... We report the preparation and characterization of inkjet-based basicfibroblast growth factor (bFGF)-containing nanofilms on aflexible PET substrate. bFGF and... |
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SubjectTerms | Basic fibroblast growth factor Ink-jet printing Layer-by-layer (LbL) assembly Mesenchymal stem cells (MSCs) Nanofilms 화학공학 |
Title | Inkjet-based multilayered growth factor-releasing nanofilms for enhancing proliferation of mesenchymal stem cells in vitro |
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