Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/35113
標題: Enhanced cytotoxicity of saporin by polyamidoamine dendrimer conjugation and photochemical internalization
作者: Lai, P.S.
賴秉杉
Pai, C.L.
Peng, C.L.
Shieh, M.J.
Berg, K.
Lou, P.J.
關鍵字: ribosome-inactivating protein
saporin
photochemical internalization
polyamidoamine dendrimer
cancer therapy
ribosome-inactivating proteins
copolymer-bound doxorubicin
liposome-mediated delivery
ovarian-carcinoma cells
epidermal
growth-factor
in-vitro
monoclonal-antibody
pamam dendrimers
drug-delivery
cancer-cells
期刊/報告no:: Journal of Biomedical Materials Research Part A, Volume 87A, Issue 1, Page(s) 147-155.
摘要: Because of the lack of membrane binding subunit, type I ribosome-inactivating proteins (RIPs) are not very toxic to cells unless action is taken to allow for toxin internalization to the cytosol. To overcome the potential barriers that greatly hinder the cellular uptake and intracellular release of saporin, a type I RIP, we used generation 4 polyamidoamine (PAMAM) dendrimer as the carrier to improve its endocytic uptake, passive tumor targeting, and implemented the photochemical internalization (PCI) technology to facilitate its cytosolic release. Our results showed that the cellular uptake of saporin was increased after conjugation with the PAMAM dendrimer and the cytotoxic effect was improved by more than I order of magnitude. The cytotoxicity of free saporin and PAMAM-saporin was further enhanced by the PCI technology. PCI changed the mechanism of cellular uptake of free saporin and then caused more saporin entering into the cells. After the PCI treatment, PAMAM-saporin was not only internalized into the cytosol but also efficiently entered the nuclei. Our results indicated that conjugating to PAMAM dendrimer is a possible approach to enhance the cellular uptake of saporin. PCI is a promising technology to significantly enhance the cytotoxicity of both free saporin and PAMAM-saporin. Combining both polymer conjugation and PCI approaches may improve the efficacy of RIPs in cancer therapy. (C) 2007 Wiley Periodicals, Inc.
URI: http://hdl.handle.net/11455/35113
ISSN: 1549-3296
文章連結: http://dx.doi.org/10.1002/jbm.a.31760
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