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Vascular targeted nanoparticles for imaging and treatment of brain tumors.

Vascular targeted nanoparticles for imaging and treatment of brain tumors. Research Abstract Details 

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  • Vascular targeted nanoparticles for imaging and treatment of brain tumors. Abstract Text:

    g ramachandra reddyG Ramachandra Reddy,mahaveer s bhojaniMahaveer S Bhojani,patrick mcconvillePatrick McConville,jonathan moodyJonathan Moody,bradford a moffatBradford A Moffat,daniel e hallDaniel E Hall,gwangseong kimGwangseong Kim,yong-eun l kooYong-Eun L Koo,michael j woolliscroftMichael J Woolliscroft,james v sugaiJames V Sugai,timothy d johnsonTimothy D Johnson,martin a philbertMartin A Philbert,raoul kopelmanRaoul Kopelman,alnawaz rehemtullaAlnawaz Rehemtulla,brian d rossBrian D Ross,

    PURPOSE: Development of new therapeutic drug delivery systems is an area of significant research interest. The ability to directly target a therapeutic agent to a tumor site would minimize systemic drug exposure, thus providing the potential for increasing the therapeutic index. EXPERIMENTAL DESIGN: Photodynamic therapy (PDT) involves the uptake of a sensitizer by the cancer cells followed by photoirradiation to activate the sensitizer. PDT using Photofrin has certain disadvantages that include prolonged cutaneous photosensitization. Delivery of nanoparticles encapsulated with photodynamic agent specifically to a tumor site could potentially overcome the drawbacks of systemic therapy. In this study, we have developed a multifunctional polymeric nanoparticle consisting of a surface-localized tumor vasculature targeting F3 peptide and encapsulated PDT and imaging agents. RESULTS: The nanoparticles specifically bound to the surface of MDA-435 cells in vitro and were internalized conferring photosensitivity to the cells. Significant magnetic resonance imaging contrast enhancement was achieved in i.c. rat 9L gliomas following i.v. nanoparticle administration. Serial magnetic resonance imaging was used for determination of pharmacokinetics and distribution of nanoparticles within the tumor. Treatment of glioma-bearing rats with targeted nanoparticles followed by PDT showed a significant improvement in survival rate when compared with animals who received PDT after administration of nontargeted nanoparticles or systemic Photofrin. CONCLUSIONS: This study reveals the versatility and efficacy of the multifunctional nanoparticle for the targeted detection and treatment of cancer.

    Vascular targeted nanoparticles for imaging and treatment of brain tumors. Publishing Authors By Initials

    gr reddyGR Reddy,ms bhojaniMS Bhojani,p mcconvilleP McConville,j moodyJ Moody,ba moffatBA Moffat,de hallDE Hall,g kimG Kim,ye kooYE Koo,mj woolliscroftMJ Woolliscroft,jv sugaiJV Sugai,td johnsonTD Johnson,ma philbertMA Philbert,r kopelmanR Kopelman,a rehemtullaA Rehemtulla,bd rossBD Ross,

    For similar cells: cells, cultured: tumor cells, cultured research abstracts see: cells: cells, cultured: tumor cells, cultured research

    PUBMED ID PMID:

    MEDLINE DATE:

    Vascular targeted nanoparticles for imaging and treatment of brain tumors. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Clinical cancer research : an official journal of

    VOLUME: 12

    Page Numbers: 6677-86

    Journal Abbreviation: Clin. Cancer Res.

    ISSN: 1078-0432

    DAY: 15

    MONTH: Nov

    YEAR: 2006

    Vascular targeted nanoparticles for imaging and treatment of brain tumors. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9502500

    Vascular targeted nanoparticles for imaging and treatment of brain tumors. Keywords Mesh Terms:

    KEYWORDS: Tumor Cells, Cultured

    MESH TERMS: administration & dosage

    Chemical & Substance for Abstract: Vascular targeted nanoparticles for imaging and treatment of brain tumors. Information

    Substance Name: Dihematoporphyrin Ether

    Registry Number: 97067-70-4

    Grant and Affiliation Information for Vascular targeted nanoparticles for imaging and treatment of brain tumors.

    AFFILIATION: Molecular Therapeutics, Inc., Ann Arbor, MI 48109, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: R24CA83099

    ACRONYM: CA

    MEDLINETA: Clin Cancer Res

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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