نتایج جستجو برای: wr 1065

تعداد نتایج: 4140  

Journal: :iranian journal of pharmaceutical research 0
nasim samiei department of pharmaceutics, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. seyed mohsen foroutan department of pharmaceutics, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. alireza shafaati - afshin zarghi department of pharmaceutical chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

a rapid, sensitive and reproducible hplc method was developed and validatedfor the analysis of amifostine (amf) and/or its metabolite, wr-1065 inhuman plasma. the method involves the alkylation of free sulfydryl group with iodoacetic acid followed by derivatization of the drug and its metabolite witho-phthaldialdehyde (opa) anduvdetection at 340 nm. the derivatized amf and wr-1065 were eluted i...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2012
Marleen Melis Roelf Valkema Eric P Krenning Marion de Jong

UNLABELLED Megalin-mediated renal retention of radiolabeled somatostatin analogs may lead to nephrotoxicity during peptide receptor radionuclide therapy (PRRT). The cytoprotective agent amifostine protected rats from long-term nephrotoxicity after PRRT with (177)Lu-DOTA,Tyr(3)-octreotate. This study describes the direct effect of amifostine on kidney and tumor uptake of (111)In-DOTA,Tyr(3)-octr...

2015
Nasim Samiei Seyed Mohsen Foroutan Alireza Shafaati Afshin Zarghi

A rapid, sensitive and reproducible HPLC method was developed and validated for the analysis of amifostine (AMF) and/or its metabolite, WR-1065 in human plasma. The method involves the alkylation of free sulfydryl group with iodoacetic acid followed by derivatization of the drug and its metabolite with o-phthaldialdehyde (OPA) and UVdetection at 340 nm. The derivatized AMF and WR-1065 were elut...

Journal: :Cancer research 2004
Roger F Martin Sam Broadhurst Monica E Reum Christopher J Squire George R Clark Pavel N Lobachevsky Jonathan M White Chris Clark Denise Sy Melanie Spotheim-Maurizot David P Kelly

New analogues of the minor groove binding ligand Hoechst 33342 have been investigated in an attempt to improve radioprotective activity. The synthesis, DNA binding, and in vitro radioprotective properties of methylproamine, the most potent derivative, are reported. Experiments with V79 cells have shown that methylproamine is approximately 100-fold more potent than the classical aminothiol radio...

Journal: :Journal of alternative and complementary medicine 2010
Tung-Kwang Lee Kevin F O'Brien Weidong Wang Roberta M Johnke Chao Sheng Sidi M Benhabib Tao Wang Ron R Allison

BACKGROUND Ionizing radiation (IR) initiates intracellular oxidative stress through enhanced formation of reactive oxygen species (ROS) that attack DNA leading to cell death. Because of the diversity of IR applied in medicine, agriculture, industry, and the growing threats of global terrorism, the acquisition of radioprotectors is an urgent need for the nation. However, the applicability of rad...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2002
Peter D Sadowitz Bradley A Hubbard James C Dabrowiak Jerry Goodisman Kirk A Tacka Mehmet K Aktas Mary J Cunningham Ronald L Dubowy Abdul-Kader Souid

DNA platination by cisplatin (CDDP) was investigated in peripheral blood mononuclear cells and ovarian cancer cells using atomic absorption spectroscopy. Plots showing the amount of platinum (Pt) bound to DNA versus the molar concentration of cisplatin in the incubation medium ([CDDP]) were nonlinear. For [CDDP] < about 5 microM, the amount of Pt bound to DNA increased slowly with added drug. H...

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