Functionalization of Clinically Approved MRI Contrast Agents for the Delivery of VEGF.


Journal

Bioconjugate chemistry
ISSN: 1520-4812
Titre abrégé: Bioconjug Chem
Pays: United States
ID NLM: 9010319

Informations de publication

Date de publication:
17 04 2019
Historique:
pubmed: 13 3 2019
medline: 18 2 2020
entrez: 13 3 2019
Statut: ppublish

Résumé

In combining the two clinically approved substances ferumoxytol and VEGF-165 via peptide coupling, we propose a straightforward approach to obtain a potentially ready-to-use theranostic contrast agent for specific cardiovascular diseases. Clinical and preclinical magnetic resonance imaging (MRI) studies have shown that intravenously applied superparamagnetic ferumoxytol nanoparticles accumulate in acute ischemic myocardial tissue. On the other hand, growth factors such as VEGF-165 (vascular endothelial growth factor) play a major role during angiogenesis and vasculogenesis. Promising clinical studies with systemic application of VEGF-165 have been performed in the past. However, following untargeted systemic application, the biological half-life of VEGF-165 was too short to develop its full effect. Therefore, we hypothesized that ferumoxytol particles functionalized with VEGF-165 will accumulate in ischemic myocardial regions and can be detected by MRI, while the prolonged retention of VEGF-165 due to ferumoxytol-coupling will help to prevent adverse tissue remodeling. In addition, strategies such as magnetic targeting can be used to enhance targeted local accumulation. As a precondition for further preclinical research, we confirmed the successful coupling between ferumoxytol and VEGF-165 in detail (TEM, XPS, and IR spectroscopy), characterized the functionalized ferumoxytol particles (DLS, TEM, and MRI) and performed in vitro tests that showed their superior effect on cell growth and survival.

Identifiants

pubmed: 30860371
doi: 10.1021/acs.bioconjchem.9b00142
doi:

Substances chimiques

Contrast Media 0
VEGFA protein, human 0
Vascular Endothelial Growth Factor A 0
Ferrosoferric Oxide XM0M87F357

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1042-1047

Auteurs

Michael Bietenbeck (M)

Division of Cardiovascular Imaging, Department of Cardiology I , University Hospital Münster , Albert-Schweitzer-Campus 1 , 48149 Münster , Germany.

Sabrina Engel (S)

Organic Chemistry Institute and Center for Soft Nanoscience , Westfälische Wilhelms-Universität Münster , Corrensstrasse 40 , 48149 Münster , Germany.

Sebastian Lamping (S)

Organic Chemistry Institute and Center for Soft Nanoscience , Westfälische Wilhelms-Universität Münster , Corrensstrasse 40 , 48149 Münster , Germany.

Uwe Hansen (U)

Institute of Musculoskeletal Medicine , University Hospital Münster , Domagkstraße 3 , 48149 Münster , Germany.

Cornelius Faber (C)

Translational Research Imaging Center, Department of Clinical Radiology , University Hospital Münster , Albert-Schweitzer-Campus 1 , 48149 Münster , Germany.

Bart Jan Ravoo (BJ)

Organic Chemistry Institute and Center for Soft Nanoscience , Westfälische Wilhelms-Universität Münster , Corrensstrasse 40 , 48149 Münster , Germany.

Ali Yilmaz (A)

Division of Cardiovascular Imaging, Department of Cardiology I , University Hospital Münster , Albert-Schweitzer-Campus 1 , 48149 Münster , Germany.

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Classifications MeSH