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Preparation of floxuridine loaded polycation and its antitumor activity / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences ; (6): 53-58, 2009.
Article in Chinese | WPRIM | ID: wpr-310391
ABSTRACT
<p><b>OBJECTIVE</b>To develop a new prodrug of 5-fluorouracil-polyethylenimine-beta-cyclodextrin-floxuridine (PEI-beta-CyD-Fd) and to test its antitumor activity.</p><p><b>METHODS</b>Floxuridine was conjugated to polyethylenimine-beta-cyclodextrin to form prodrug PEI-beta-CyD-Fd. The structure of synthesized PEI-beta-CyD-Fd was confirmed by (1)H-NMR, FT-IR and UV. MTT assay and cell wound healing assay were performed on human hepatic carcinoma cell line HepG2.</p><p><b>RESULT</b>The drug loading was 2 %. The MTT assay and cell wound healing assay indicated that PEI-beta-CyD-Fd significantly inhibited proliferation and migration of HepG2 cells.</p><p><b>CONCLUSION</b>The synthesized prodrug PEI-CyD-Fd has a significant antitumor activity on HepG2 cells.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Polyethyleneimine / Prodrugs / Cell Movement / Floxuridine / Cell Line, Tumor / Beta-Cyclodextrins / Cell Proliferation / Fluorouracil Limits: Humans Language: Chinese Journal: Journal of Zhejiang University. Medical sciences Year: 2009 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Polyethyleneimine / Prodrugs / Cell Movement / Floxuridine / Cell Line, Tumor / Beta-Cyclodextrins / Cell Proliferation / Fluorouracil Limits: Humans Language: Chinese Journal: Journal of Zhejiang University. Medical sciences Year: 2009 Type: Article