dc.contributor.author | Wang, Andrew Z | |
dc.contributor.author | Yuet, Kai | |
dc.contributor.author | Zhang, Liangfang | |
dc.contributor.author | Gu, Frank X | |
dc.contributor.author | Huynh-Le, Minh | |
dc.contributor.author | Radovic-Moreno, Aleksandar F | |
dc.contributor.author | Kantoff, Philip W | |
dc.contributor.author | Bander, Neil H | |
dc.contributor.author | Langer, Robert | |
dc.contributor.author | Farokhzad, Omid C | |
dc.date.accessioned | 2021-10-27T20:04:20Z | |
dc.date.available | 2021-10-27T20:04:20Z | |
dc.date.issued | 2010 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/134290 | |
dc.description.abstract | Aim: The development of chemoradiation - the concurrent administration of chemotherapy and radiotherapy - has led to significant improvements in local tumor control and survival. However, it is limited by its high toxicity. In this study, we report the development of a novel NP (nanoparticle) therapeutic, ChemoRad NP, which can deliver biologically targeted chemoradiation. Method: A biodegradable and biocompatible lipid-polymer hybrid NP that is capable of delivering both chemotherapy and radiotherapy was formulated. Results: Using docetaxel, indium111 and yttrium90 as model drugs, we demonstrated that the ChemoRad NP can encapsulate chemotherapeutics (up to 9% of NP weight) and radiotherapeutics (100 mCi of radioisotope per gram of NP) efficiently and deliver both effectively. Using prostate cancer as a disease model, we demonstrated the targeted delivery of ChemoRad NPs and the higher therapeutic efficacy of ChemoRad NPs. Conclusion: We believe that the ChemoRad NP represents a new class of therapeutics that holds great potential to improve cancer treatment. © 2010 Future Medicine Ltd. | |
dc.language.iso | en | |
dc.publisher | Future Medicine Ltd | |
dc.relation.isversionof | 10.2217/nnm.10.6 | |
dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | |
dc.source | PMC | |
dc.title | ChemoRad nanoparticles: a novel multifunctional nanoparticle platform for targeted delivery of concurrent chemoradiation | |
dc.type | Article | |
dc.identifier.citation | Wang, A. Z., et al. "Chemorad Nanopartides: A Novel Multifunctional Nanoparticle Platform for Targeted Delivery of Concurrent Chemoradiation." Nanomedicine 5 3 (2010): 361-68. | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemical Engineering | |
dc.contributor.department | Harvard University--MIT Division of Health Sciences and Technology | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | |
dc.relation.journal | Nanomedicine: Nanotechnology, Biology, and Medicine | |
dc.eprint.version | Author's final manuscript | |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
eprint.status | http://purl.org/eprint/status/PeerReviewed | |
dc.date.updated | 2019-08-22T18:50:30Z | |
dspace.orderedauthors | Wang, AZ; Yuet, K; Zhang, L; Gu, FX; Huynh-Le, M; Radovic-Moreno, AF; Kantoff, PW; Bander, NH; Langer, R; Farokhzad, OC | |
dspace.date.submission | 2019-08-22T18:50:31Z | |
mit.journal.volume | 5 | |
mit.journal.issue | 3 | |
mit.metadata.status | Authority Work and Publication Information Needed | |