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Nanocell

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surface of each cell is a lipid coat containing an anti-angiogenic drug. The technology makes use of the fact that a tumor's blood vessels have pores 600 _m in diameter and are much leakier than normal blood vessels, which have pores only around 50 _m in diameter. The nanocells circulate in the blood, and because of their size, they leak out of blood vessels only in tumors. Once there, the nanocells are degraded by enzymes produced by the tumor. Work remains to be done to win clinical approval for the technology, but results from Sengupta's lab indicate that the nanocells are more effective and less toxic than traditional chemotherapy.
658: 86: 292: 765: 1005: 286: 58:, and it begins to release growth factors to recruit new blood vessels that will supply it with oxygen. Inhibiting angiogenesis has been investigated as a means of preventing tumor growth but has not proven to be fully successful, for tumor cells cut off from the blood supply can eventually develop “reactive resistance” to hypoxia. These resistant cancer cells could be killed by 827: 531: 62:
drugs, but once the vasculature to the tumor has been cut off, there is no way for chemotherapy to be delivered. Nanotechnology offers a way to deliver chemotherapeutic drugs and anti-angiogenic drugs in the same vehicle so that as the blood supply is shut off, chemotherapy is present to prevent any
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Labs at MIT are in the process of developing nanocells capable of delivering both types of drugs. Each nanocell is between 120 and 200 _m in diameter and can be thought of as “a balloon within a balloon.” Inside each nanocell is a chemotherapeutic drug covalently bound to a polymer, and on the
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Sengupta S, Eavarone D, Capila I, Zhao G, Watson N, Kiziltepe T, Sasisekharan R. Temporal targeting of tumour cells and neovasculature with a nanoscale delivery system. Nature. 2005 Jul 28;436(7050):568-72.
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platform consisting of a polymer-bound chemotherapeutic drug combined with a lipid-bound anti-angiogenesis drug. Nanocells are currently being developed in the lab of Shiladitya Sengupta of
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This article is about biological cells. For cell phone technology, see
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Center for Integration of Medicine and Innovative Technology
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delivery devices 885:Transfersome vesicles 829: 767: 744:Intravesical infusion 660: 571:Metered-dose inhaler 556:Anesthetic vaporizer 996:Transdermal implant 956:(into tissue/blood) 733:Intrauterine device 614:Anaesthetic machine 609:Oxygen concentrator 1108:Nanocell injection 831: 769: 662: 516:Dry-powder inhaler 95:list of references 1131: 1130: 1127: 1126: 958: 920:Transdermal spray 915:Transdermal patch 905:Medicated shampoo 636: 635: 632: 631: 619:Medical inhalants 566:Medical inhalants 494:Respiratory tract 488: 487: 382: 381: 148: 147: 140: 1156: 1007: 963: 954: 541: 537: 533: 504: 433:Sublingual drops 406: 294: 288: 244: 230: 206: 199: 192: 183: 143: 136: 132: 129: 123: 118:this article by 109:inline citations 88: 87: 80: 60:chemotherapeutic 1164: 1163: 1159: 1158: 1157: 1155: 1154: 1153: 1134: 1133: 1132: 1123: 1103:Intraperitoneal 1075:musculoskeletal 1073: 1064: 1036: 1032:Intra-articular 1008: 999: 959: 953: 952: 928: 809: 747: 700: 645: 628: 586: 542: 539: 538: 535: 534: 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Index

microcell
drug delivery
MIT
Angiogenesis
blood vessels
tumor
hypoxic
chemotherapeutic
list of references
related reading
external links
inline citations
improve
introducing
Learn how and when to remove this message
Nanocell targets cancer
Nanocell's double hit on cancer
MIT engineers an anti-cancer smart bomb
Center for Integration of Medicine and Innovative Technology
v
t
e
Routes of administration
dosage forms
Oral
Digestive tract
enteral
Solids
Tablet
Capsule

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