Application of 1,2-diethyl-3-hydroxypyridin-4-one to enhance tissue selectivity for photodynamic therapy of the bladder
暂无分享,去创建一个
Alexander J. MacRobert | Stephen G. Bown | Shi-Chung Chang | John B. Porter | Shi-Chung Chang | A. MacRobert | S. Bown | J. Porter
[1] A. Richter,et al. THE PLASMA DISTRIBUTION OF BENZOPORPHYRIN DERIVATIVE and THE EFFECTS OF PLASMA LIPOPROTEINS ON ITS BIODISTRIBUTION , 1990, Photochemistry and photobiology.
[2] H. Pass,et al. In vitro photodynamic therapy of human lung cancer: investigation of dose-rate effects. , 1989, Cancer research.
[3] T. Wieman,et al. Complications of whole bladder dihematoporphyrin ether photodynamic therapy. , 1989, The Journal of urology.
[4] M. Freedman,et al. Deferoxamine: a reversible S-phase inhibitor of human lymphocyte proliferation. , 1984, Blood.
[5] U. Nseyo,et al. Photodynamic therapy in the management of resistant lower urinary tract carcinoma , 1987, Cancer.
[6] J. Moan,et al. The distribution of porphyrins with different tumour localising ability among human plasma proteins. , 1989, British Journal of Cancer.
[7] D. Becton,et al. Antileukemic effects of deferoxamine on human myeloid leukemia cell lines. , 1989, Cancer research.
[8] A. Gräslund,et al. Continual presence of oxygen and iron required for mammalian ribonucleotide reduction: possible regulation mechanism. , 1983, Biochemical and biophysical research communications.
[9] J. Hindmarsh. The porphyrias: recent advances. , 1986, Clinical chemistry.
[10] Alexander J. MacRobert,et al. Biodistribution and photodynamic effect of protoporphyrin IX in rat urinary bladders after intravesical instillation of 5-aminolaevulinic acid , 1995, Other Conferences.
[11] T. Hasan,et al. Photoimmunotherapy of human ovarian carcinoma cells ex vivo. , 1991, Cancer research.
[12] J C Kennedy,et al. NON‐INVASIVE TECHNIQUE FOR OBTAINING FLUORESCENCE EXCITATION AND EMISSION SPECTRA IN VIVO , 1986, Photochemistry and photobiology.
[13] E. Reddi,et al. Liposome- or LDL-administered Zn (II)-phthalocyanine as a photodynamic agent for tumours. I. Pharmacokinetic properties and phototherapeutic efficiency. , 1990, British Journal of Cancer.
[14] A. Hoffbrand,et al. Orally active α‐ketohydroxy pyridine iron chelators intended for clinical use: in vivo studies in rabbits , 1986, British journal of haematology.
[15] Simple Synthesis of the Potent Iron Chelators 1-Alkyl-3-hydroxy-2-methylpyrid-4-ones , 1987 .
[16] P. Dobbin,et al. Iron mobilization from myocardial cells by 3-hydroxypyridin-4-one chelators: studies in rat heart cells in culture. , 1991, Blood.
[17] P. Reichard,et al. Reduction of ribonucleotides. , 1979, Annual review of biochemistry.