The cytotoxic effects of lipidic formulated gold porphyrin nanoparticles for the treatment of neuroblastoma.
暂无分享,去创建一个
C. Che | Xuelai Liu | Kenneth K. Y. Wong | W. Hao | J. Yan | Yifan Zhu | Puiyan Lee | Raymond Wy Sun
[1] L. Rybak,et al. Cisplatin ototoxicity and protection: clinical and experimental studies. , 2009, The Tohoku journal of experimental medicine.
[2] B. Wong,et al. Gold (III) porphyrin complexes induce apoptosis and cell cycle arrest and inhibit tumor growth in colon cancer , 2009, Cancer.
[3] T. Niidome,et al. The effects of PEG grafting level and injection dose on gold nanorod biodistribution in the tumor-bearing mice. , 2009, Journal of controlled release : official journal of the Controlled Release Society.
[4] P. Nathan,et al. Long-term outcomes in survivors of neuroblastoma: a report from the Childhood Cancer Survivor Study. , 2009, Journal of the National Cancer Institute.
[5] C. Che,et al. Inhibition of Akt sensitises neuroblastoma cells to gold(III) porphyrin 1a, a novel antitumour drug induced apoptosis and growth inhibition , 2009, British Journal of Cancer.
[6] C. Che,et al. The anti-cancer properties of gold(III) compounds with dianionic porphyrin and tetradentate ligands , 2009 .
[7] A. Casini,et al. Thioredoxin reductase: A target for gold compounds acting as potential anticancer drugs , 2009 .
[8] P. Tam,et al. Gold(III) porphyrin complex is more potent than cisplatin in inhibiting growth of nasopharyngeal carcinoma in vitro and in vivo , 2009, International journal of cancer.
[9] Wolfgang A. Weber,et al. Impact of tumor-specific targeting on the biodistribution and efficacy of siRNA nanoparticles measured by multimodality in vivo imaging , 2007, Proceedings of the National Academy of Sciences.
[10] Qing‐Yu He,et al. Gold(III) Porphyrin 1a Induced Apoptosis by Mitochondrial Death Pathways Related to Reactive Oxygen Species , 2005 .
[11] J. Oh,et al. Blood Compatibility of Cetyl Alcohol/Polysorbate-Based Nanoparticles , 2005, Pharmaceutical Research.
[12] Y. Sohn,et al. Selective tumor targeting by enhanced permeability and retention effect. Synthesis and antitumor activity of polyphosphazene-platinum (II) conjugates. , 2005, Journal of inorganic biochemistry.
[13] Tetsuro Tanaka,et al. Tumor targeting based on the effect of enhanced permeability and retention (EPR) and the mechanism of receptor-mediated endocytosis (RME). , 2004, International journal of pharmaceutics.
[14] Hongzhe Sun,et al. Gold(III) porphyrins as a new class of anticancer drugs: cytotoxicity, DNA binding and induction of apoptosis in human cervix epitheloid cancer cells. , 2003, Chemical communications.
[15] Lin Chen,et al. CpG-oligodeoxynucleotide rejection of a neuroblastoma in A/J mice does not induce a paraneoplastic disease , 2002, Neuroscience Letters.
[16] H. Maeda. The enhanced permeability and retention (EPR) effect in tumor vasculature: the key role of tumor-selective macromolecular drug targeting. , 2001, Advances in enzyme regulation.
[17] W. Middlesworth,et al. All angiogenesis is not the same: Distinct patterns of response to antiangiogenic therapy in experimental neuroblastoma and Wilms tumor. , 2001, Journal of pediatric surgery.
[18] K K Matthay,et al. Treatment of High-Risk Neuroblastoma with Intensive Chemotherapy, Radiotherapy, Autologous Bone Marrow Transplantation, and 13-cis-Retinoic Acid , 1999 .
[19] C. Shaw. Gold-Based Therapeutic Agents , 1999 .
[20] J. Pezzuto,et al. Betulinic acid induces apoptosis in human neuroblastoma cell lines. , 1997, European journal of cancer.
[21] R K Jain,et al. Vascular permeability in a human tumor xenograft: molecular size dependence and cutoff size. , 1995, Cancer research.
[22] P. Anderson,et al. Retroperitoneal inoculation of murine neuroblastoma results in a reliable model for evaluation of the antitumor immune response. , 1994, Journal of pediatric surgery.
[23] G. Zientara,et al. Exchange of macromolecules between plasma and peritoneal cavity in ascites tumor-bearing, normal, and serotonin-injected mice. , 1989, Cancer research.
[24] J. Kopeček,et al. Effect of molecular weight (Mw) of N-(2-hydroxypropyl)methacrylamide copolymers on body distribution and rate of excretion after subcutaneous, intraperitoneal, and intravenous administration to rats. , 1987, Journal of biomedical materials research.
[25] H. Maeda,et al. A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. , 1986, Cancer research.
[26] M. Grunze,et al. Lateral segregation of membrane lipids and formation of stable rod-shaped membrane projections in erythrocytes treated with long-chain alcohols. , 1982, Biochimica et biophysica acta.
[27] R. Mumper,et al. Preparation and characterization of novel coenzyme Q10 nanoparticles engineered from microemulsion precursors , 2008, AAPS PharmSciTech.
[28] Xiaogang Pan,et al. Reversal of multidrug resistance by transferrin-conjugated liposomes co-encapsulating doxorubicin and verapamil. , 2007, Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques.
[29] H. Maeda,et al. Tumoritropic and lymphotropic principles of macromolecular drugs. , 1989, Critical reviews in therapeutic drug carrier systems.