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Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis

Angiogenesis is essential for tumor growth and metastatic potential and for that reason considered an important target for tumor treatment. Noninvasive imaging technologies, capable of visualizing tumor angiogenesis and evaluating the efficacy of angiostatic therapies, are therefore becoming increas...

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Autores principales: Strijkers, Gustav J., Kluza, Ewelina, Van Tilborg, Geralda A. F., van der Schaft, Daisy W. J., Griffioen, Arjan W., Mulder, Willem J. M., Nicolay, Klaas
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911540/
https://www.ncbi.nlm.nih.gov/pubmed/20390447
http://dx.doi.org/10.1007/s10456-010-9165-1
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author Strijkers, Gustav J.
Kluza, Ewelina
Van Tilborg, Geralda A. F.
van der Schaft, Daisy W. J.
Griffioen, Arjan W.
Mulder, Willem J. M.
Nicolay, Klaas
author_facet Strijkers, Gustav J.
Kluza, Ewelina
Van Tilborg, Geralda A. F.
van der Schaft, Daisy W. J.
Griffioen, Arjan W.
Mulder, Willem J. M.
Nicolay, Klaas
author_sort Strijkers, Gustav J.
collection PubMed
description Angiogenesis is essential for tumor growth and metastatic potential and for that reason considered an important target for tumor treatment. Noninvasive imaging technologies, capable of visualizing tumor angiogenesis and evaluating the efficacy of angiostatic therapies, are therefore becoming increasingly important. Among the various imaging modalities, magnetic resonance imaging (MRI) is characterized by a superb spatial resolution and anatomical soft-tissue contrast. Revolutionary advances in contrast agent chemistry have delivered versatile angiogenesis-specific molecular MRI contrast agents. In this paper, we review recent advances in the preclinical application of paramagnetic and fluorescent liposomes for noninvasive visualization of the molecular processes involved in tumor angiogenesis. This liposomal contrast agent platform can be prepared with a high payload of contrast generating material, thereby facilitating its detection, and is equipped with one or more types of targeting ligands for binding to specific molecules expressed at the angiogenic site. Multimodal liposomes endowed with contrast material for complementary imaging technologies, e.g., MRI and optical, can be exploited to gain important preclinical insights into the mechanisms of binding and accumulation at angiogenic vascular endothelium and to corroborate the in vivo findings. Interestingly, liposomes can be designed to contain angiostatic therapeutics, allowing for image-supervised drug delivery and subsequent monitoring of therapeutic efficacy.
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spelling pubmed-29115402010-08-09 Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis Strijkers, Gustav J. Kluza, Ewelina Van Tilborg, Geralda A. F. van der Schaft, Daisy W. J. Griffioen, Arjan W. Mulder, Willem J. M. Nicolay, Klaas Angiogenesis Article Angiogenesis is essential for tumor growth and metastatic potential and for that reason considered an important target for tumor treatment. Noninvasive imaging technologies, capable of visualizing tumor angiogenesis and evaluating the efficacy of angiostatic therapies, are therefore becoming increasingly important. Among the various imaging modalities, magnetic resonance imaging (MRI) is characterized by a superb spatial resolution and anatomical soft-tissue contrast. Revolutionary advances in contrast agent chemistry have delivered versatile angiogenesis-specific molecular MRI contrast agents. In this paper, we review recent advances in the preclinical application of paramagnetic and fluorescent liposomes for noninvasive visualization of the molecular processes involved in tumor angiogenesis. This liposomal contrast agent platform can be prepared with a high payload of contrast generating material, thereby facilitating its detection, and is equipped with one or more types of targeting ligands for binding to specific molecules expressed at the angiogenic site. Multimodal liposomes endowed with contrast material for complementary imaging technologies, e.g., MRI and optical, can be exploited to gain important preclinical insights into the mechanisms of binding and accumulation at angiogenic vascular endothelium and to corroborate the in vivo findings. Interestingly, liposomes can be designed to contain angiostatic therapeutics, allowing for image-supervised drug delivery and subsequent monitoring of therapeutic efficacy. Springer Netherlands 2010-04-14 2010 /pmc/articles/PMC2911540/ /pubmed/20390447 http://dx.doi.org/10.1007/s10456-010-9165-1 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Strijkers, Gustav J.
Kluza, Ewelina
Van Tilborg, Geralda A. F.
van der Schaft, Daisy W. J.
Griffioen, Arjan W.
Mulder, Willem J. M.
Nicolay, Klaas
Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
title Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
title_full Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
title_fullStr Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
title_full_unstemmed Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
title_short Paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
title_sort paramagnetic and fluorescent liposomes for target-specific imaging and therapy of tumor angiogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911540/
https://www.ncbi.nlm.nih.gov/pubmed/20390447
http://dx.doi.org/10.1007/s10456-010-9165-1
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