• Something wrong with this record ?

Development of a nanomedicine-loaded hydrogel for sustained delivery of an angiogenic growth factor to the ischaemic myocardium

J. O'Dwyer, R. Murphy, EB. Dolan, L. Kovarova, M. Pravda, V. Velebny, A. Heise, GP. Duffy, SA. Cryan,

. 2020 ; 10 (2) : 440-454. [pub] -

Language English Country United States

Document type Journal Article, Research Support, Non-U.S. Gov't

The 5-year mortality rate for heart failure borders on 50%. The main cause is an ischaemic cardiac event where blood supply to the tissue is lost and cell death occurs. Over time, this damage spreads and the heart is no longer able to pump efficiently. Increasing vascularisation of the affected area has been shown to reduce patient symptoms. The growth factors required to do this have short half-lives making development of an efficacious therapy difficult. Herein, the angiogenic growth factor Vascular Endothelial Growth Factor (VEGF) is complexed electrostatically with star-shaped or linear polyglutamic acid (PGA) polypeptides. Optimised PGA-VEGF nanomedicines provide VEGF encapsulation of > 99% and facilitate sustained release of VEGF for up to 28 days in vitro. The star-PGA-VEGF nanomedicines are loaded into a percutaneous delivery compliant hyaluronic acid hydrogel. Sustained release of VEGF from the composite nano-in-gel system is evident for up to 35 days and the released VEGF has comparable bioactivity to free, fresh VEGF when tested on both Matrigel® and scratch assays. The final star-PGA-VEGF nanomedicine-loaded hydrogel is biocompatible and provides sustained release of bioactive VEGF. Therefore, we report the development of novel, self-assembling PGA-VEGF nanomedicines and their incorporation into a hyaluronic acid hydrogel that is compatible with medical devices to enable minimally invasive delivery to the heart. The final star-PGA-VEGF nanomedicine-loaded hydrogel is biocompatible and provides sustained release of bioactive VEGF. This formulation provides the basis for optimal spatiotemporal delivery of an angiogenic growth factor to the ischaemic myocardium.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc20028300
003      
CZ-PrNML
005      
20210114153448.0
007      
ta
008      
210105s2020 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s13346-019-00684-5 $2 doi
035    __
$a (PubMed)31691161
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a O'Dwyer, Joanne $u Drug Delivery & Advanced Materials Team, School of Pharmacy & Biomolecular Sciences, Royal College of Surgeons in Ireland (RCSI), Dublin 2, Ireland. Tissue Engineering Research Group, Department of Anatomy & Regenerative Medicine, RCSI, 1st Floor, Ardilaun House (Block B), St. Stephen's Green, Dublin 2, Ireland. Trinity Centre for Biomedical Engineering, Trinity College Dublin (TCD), Dublin 2, Ireland.
245    10
$a Development of a nanomedicine-loaded hydrogel for sustained delivery of an angiogenic growth factor to the ischaemic myocardium / $c J. O'Dwyer, R. Murphy, EB. Dolan, L. Kovarova, M. Pravda, V. Velebny, A. Heise, GP. Duffy, SA. Cryan,
520    9_
$a The 5-year mortality rate for heart failure borders on 50%. The main cause is an ischaemic cardiac event where blood supply to the tissue is lost and cell death occurs. Over time, this damage spreads and the heart is no longer able to pump efficiently. Increasing vascularisation of the affected area has been shown to reduce patient symptoms. The growth factors required to do this have short half-lives making development of an efficacious therapy difficult. Herein, the angiogenic growth factor Vascular Endothelial Growth Factor (VEGF) is complexed electrostatically with star-shaped or linear polyglutamic acid (PGA) polypeptides. Optimised PGA-VEGF nanomedicines provide VEGF encapsulation of > 99% and facilitate sustained release of VEGF for up to 28 days in vitro. The star-PGA-VEGF nanomedicines are loaded into a percutaneous delivery compliant hyaluronic acid hydrogel. Sustained release of VEGF from the composite nano-in-gel system is evident for up to 35 days and the released VEGF has comparable bioactivity to free, fresh VEGF when tested on both Matrigel® and scratch assays. The final star-PGA-VEGF nanomedicine-loaded hydrogel is biocompatible and provides sustained release of bioactive VEGF. Therefore, we report the development of novel, self-assembling PGA-VEGF nanomedicines and their incorporation into a hyaluronic acid hydrogel that is compatible with medical devices to enable minimally invasive delivery to the heart. The final star-PGA-VEGF nanomedicine-loaded hydrogel is biocompatible and provides sustained release of bioactive VEGF. This formulation provides the basis for optimal spatiotemporal delivery of an angiogenic growth factor to the ischaemic myocardium.
650    _2
$a aplikace kožní $7 D000279
650    _2
$a léky s prodlouženým účinkem $7 D003692
650    _2
$a endoteliální buňky pupečníkové žíly (lidské) $7 D061307
650    _2
$a lidé $7 D006801
650    _2
$a hydrogely $7 D020100
650    _2
$a ischemická choroba srdeční $x farmakoterapie $7 D017202
650    _2
$a nanočástice $7 D053758
650    _2
$a kyselina polyglutamová $x chemie $7 D011099
650    _2
$a statická elektřina $7 D055672
650    _2
$a vaskulární endoteliální růstový faktor A $x chemie $x farmakologie $7 D042461
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Murphy, Robert $u Department of Chemistry, RCSI, Dublin 2, Ireland.
700    1_
$a Dolan, Eimear B $u Drug Delivery & Advanced Materials Team, School of Pharmacy & Biomolecular Sciences, Royal College of Surgeons in Ireland (RCSI), Dublin 2, Ireland. Tissue Engineering Research Group, Department of Anatomy & Regenerative Medicine, RCSI, 1st Floor, Ardilaun House (Block B), St. Stephen's Green, Dublin 2, Ireland.
700    1_
$a Kovarova, Lenka $u R&D Department, Contipro, Dolni Dobrouc 401, 561 02, Dolni Dobrouc, Czech Republic. Faculty of Chemistry, Institute of Physical Chemistry, Brno University of Technology, Purkynova 464/118, 612 00, Brno, Czech Republic.
700    1_
$a Pravda, Martin $u R&D Department, Contipro, Dolni Dobrouc 401, 561 02, Dolni Dobrouc, Czech Republic.
700    1_
$a Velebny, Vladimir $u R&D Department, Contipro, Dolni Dobrouc 401, 561 02, Dolni Dobrouc, Czech Republic.
700    1_
$a Heise, Andreas $u Department of Chemistry, RCSI, Dublin 2, Ireland. CÚRAM, SFI Research Centre for Medical Devices, National University of Ireland Galway (NUIG) & RCSI, Galway, Ireland. AMBER, the SFI Centre for Advanced Materials and Bioengineering, NUIG, RCSI & TCD, Dublin, Ireland.
700    1_
$a Duffy, Garry P $u Tissue Engineering Research Group, Department of Anatomy & Regenerative Medicine, RCSI, 1st Floor, Ardilaun House (Block B), St. Stephen's Green, Dublin 2, Ireland. Trinity Centre for Biomedical Engineering, Trinity College Dublin (TCD), Dublin 2, Ireland. CÚRAM, SFI Research Centre for Medical Devices, National University of Ireland Galway (NUIG) & RCSI, Galway, Ireland. AMBER, the SFI Centre for Advanced Materials and Bioengineering, NUIG, RCSI & TCD, Dublin, Ireland. Anatomy, School of Medicine, College of Medicine, Nursing and Health Sciences, NUIG, Galway, Ireland.
700    1_
$a Cryan, Sally Ann $u Drug Delivery & Advanced Materials Team, School of Pharmacy & Biomolecular Sciences, Royal College of Surgeons in Ireland (RCSI), Dublin 2, Ireland. scryan@rcsi.ie. Tissue Engineering Research Group, Department of Anatomy & Regenerative Medicine, RCSI, 1st Floor, Ardilaun House (Block B), St. Stephen's Green, Dublin 2, Ireland. scryan@rcsi.ie. Trinity Centre for Biomedical Engineering, Trinity College Dublin (TCD), Dublin 2, Ireland. scryan@rcsi.ie. CÚRAM, SFI Research Centre for Medical Devices, National University of Ireland Galway (NUIG) & RCSI, Galway, Ireland. scryan@rcsi.ie. AMBER, the SFI Centre for Advanced Materials and Bioengineering, NUIG, RCSI & TCD, Dublin, Ireland. scryan@rcsi.ie.
773    0_
$w MED00197253 $t Drug delivery and translational research $x 2190-3948 $g Roč. 10, č. 2 (2020), s. 440-454
856    41
$u https://pubmed.ncbi.nlm.nih.gov/31691161 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20210105 $b ABA008
991    __
$a 20210114153445 $b ABA008
999    __
$a ok $b bmc $g 1608635 $s 1119480
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 10 $c 2 $d 440-454 $e - $i 2190-3948 $m Drug delivery and translational research $n Drug Deliv Transl Res $x MED00197253
LZP    __
$a Pubmed-20210105

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...