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Mannan-Based Nanodiagnostic Agents for Targeting Sentinel Lymph Nodes and Tumors
M. Jirátová, A. Gálisová, M. Rabyk, E. Sticová, M. Hrubý, D. Jirák
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
16-30544a
the Grant Agency of the Ministry of Health
IN00023001
MH CR-DRO
18-07983S
the Czech Science Foundation
282216
the Charles University Grant Agency
NLK
Directory of Open Access Journals
od 1997
Free Medical Journals
od 1997
PubMed Central
od 2001
Europe PubMed Central
od 2001
ProQuest Central
od 1997-01-01
Open Access Digital Library
od 1997-01-01
Medline Complete (EBSCOhost)
od 2009-03-01
Health & Medicine (ProQuest)
od 1997-01-01
- MeSH
- apoptóza MeSH
- lidé MeSH
- lymfatické metastázy MeSH
- mannany chemie metabolismus MeSH
- myši inbrední BALB C MeSH
- myši inbrední C3H MeSH
- myši nahé MeSH
- myši MeSH
- nádorové buňky kultivované MeSH
- nádory prsu metabolismus patologie MeSH
- nanočástice aplikace a dávkování chemie MeSH
- optické zobrazování MeSH
- proliferace buněk MeSH
- sentinelová uzlina metabolismus patologie MeSH
- xenogenní modely - testy antitumorózní aktivity MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Early detection of metastasis is crucial for successful cancer treatment. Sentinel lymph node (SLN) biopsies are used to detect possible pathways of metastasis spread. We present a unique non-invasive diagnostic alternative to biopsy along with an intraoperative imaging tool for surgery proven on an in vivo animal tumor model. Our approach is based on mannan-based copolymers synergistically targeting: (1) SLNs and macrophage-infiltrated solid tumor areas via the high-affinity DC-SIGN (dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin) receptors and (2) tumors via the enhanced permeability and retention (EPR) effect. The polymer conjugates were modified with the imaging probes for visualization with magnetic resonance (MR) and fluorescence imaging, respectively, and with poly(2-methyl-2-oxazoline) (POX) to lower unwanted accumulation in internal organs and to slow down the biodegradation rate. We demonstrated that these polymer conjugates were successfully accumulated in tumors, SLNs and other lymph nodes. Modification with POX resulted in lower accumulation not only in internal organs, but also in lymph nodes and tumors. Importantly, we have shown that mannan-based polymer carriers are non-toxic and, when applied to an in vivo murine cancer model, and offer promising potential as the versatile imaging agents.
Department of Physiology Faculty of Science Charles University 128 00 Prague Czech Republic
Institute for Clinical and Experimental Medicine 140 21 Prague Czech Republic
Institute of Macromolecular Chemistry Czech Academy of Sciences 162 00 Prague Czech Republic
Citace poskytuje Crossref.org
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