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Folate receptor targeting of radiolabeled liposomes reduces intratumoral liposome accumulation in human KB carcinoma xenografts
Content Provider | Scilit |
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Author | Christensen, Esben Henriksen, Jonas Rosager Jørgensen, Jesper Tranekjær Amitay, Yasmine Schmeeda, Hilary Gabizon, Alberto A. Kjær, Andreas Andresen, Thomas Lars Hansen, Anders Elias |
Copyright Year | 2018 |
Description | Folate receptor targeting of radiolabeled liposomes reduces intratumoral liposome accumulation in human KB carcinoma xenografts Esben Christensen,1–3 Jonas R Henriksen,2,4 Jesper T Jørgensen,3 Yasmine Amitay,5 Hilary Shmeeda,5 Alberto A Gabizon,5 Andreas Kjær,3 Thomas L Andresen,1,2 Anders E Hansen1–3 1Department of Micro- and Nanotechnology, DTU Nanotech, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark; 2Center for Nanomedicine and Theranostics, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark; 3Cluster for Molecular Imaging, Department of Biomedical Sciences and Department of Clinical Physiology, Nuclear Medicine & PET, University of Copenhagen and Rigshospitalet, DK-2200 & DK-2100, Copenhagen, Denmark; 4Department of Chemistry, DTU Chemistry, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark; 5Shaare Zedek Medical Center and Hebrew University – School of Medicine, Jerusalem, Israel Background: Active, ligand-mediated, targeting of functionalized liposomes to folate receptors (FRs) overexpressed on cancer cells could potentially improve drug delivery and specificity. Studies on folate-targeting liposomes (FTLs) have, however, yielded varying results and generally fail to display a clear benefit of FR targeting.Method: Tumor accumulating potential of FTLs and NTLs were investigated in a FR overexpressing xenograft model by positron emission tomography/computed tomography imaging.Results: Tumors displayed significantly lower activity of FTLs than NTLs. Furthermore, FTLs displayed worse circulating properties and increased liver-accumulation than NTLs. Conclusion: This study underlines that long-circulating properties of liposomes must be achieved to take advantage of EPR-dependent tumor accumulation which may be lost by functionalization. FR-functionalization negatively affected both tumor accumulation and circulation properties. Keywords: liposomes, folate, cancer, imaging, PET, EPR |
Related Links | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251465/pdf https://www.dovepress.com/getfile.php?fileID=46318 |
Ending Page | 7656 |
Page Count | 10 |
Starting Page | 7647 |
e-ISSN | 11782013 |
DOI | 10.2147/ijn.s182579 |
Journal | International Journal of Nanomedicine |
Volume Number | 13 |
Language | English |
Publisher | Informa UK Limited |
Publisher Date | 2018-11-01 |
Access Restriction | Open |
Subject Keyword | Journal: International Journal of Nanomedicine Oncology Epr Pet Cancer Folate Imaging Liposomes |
Content Type | Text |
Resource Type | Article |