نتایج جستجو برای: 111in dota antiher2

تعداد نتایج: 3276  

Journal: :Cancer research 2011
Damian Wild Michael Frischknecht Hanwen Zhang Alfred Morgenstern Frank Bruchertseifer Julie Boisclair Anne Provencher-Bolliger Jean-Claude Reubi Helmut R Maecke

Recurrent prostate cancer presents a challenge to conventional treatment, particularly so to address micrometastatic and small-volume disease. Use of α-radionuclide therapy is considered as a highly effective treatment in such applications due to the shorter range and exquisite cytotoxicity of α-particles as compared with β-particles. (213)Bi is considered an α-emitter with high clinical potent...

2013
Jürgen Grünberg Simone Jeger Dikran Sarko Patrick Dennler Kurt Zimmermann Walter Mier Roger Schibli

Site-specific enzymatic reactions with microbial transglutaminase (mTGase) lead to a homogenous species of immunoconjugates with a defined ligand/antibody ratio. In the present study, we have investigated the influence of different numbers of 1,4,7,10-tetraazacyclododecane-N-N'-N''-N'''-tetraacetic acid (DOTA) chelats coupled to a decalysine backbone on the in vivo behavior of the chimeric mono...

2004
Hung-Jen Huang

C-aryl derivatives of DOTA (N,N’,N”,N”’-tetrakis(carboxymethyl)1,4,7,10-tetraazacyclododecane) including phenyl-DOTA and 3-NO2Ph-DOTA were synthesized by a template reductive reaction. GaCl3 or GaCl3 was taken and transformed into Ga-acetylacetone (Ga(acac)3) before labeling to the DOTA derivatives. The Ga or Ga labeled complexes were generated by ligand-ligand exchange of acetylacetonate with ...

Journal: :The Journal of pharmacology and experimental therapeutics 1999
Y Yabe M Nishikawa A Tamada Y Takakura M Hashida

Four types of bovine liver catalase (CAT) derivatives, succinylated (Suc-CAT), galactosylated (Gal-CAT), mannosylated (Man-CAT), and polyethylene glycol conjugate (PEG-CAT), were synthesized and their pharmacokinetics and therapeutic potential in a hepatic ischemia/reperfusion injury model were studied in mice. About 90% of the CAT enzymatic activity was retained after chemical modification. Bi...

2017
Neel Patel Sarah Able Danny Allen Emmanouil Fokas Bart Cornelissen Fergus V Gleeson Adrian L Harris Katherine A Vallis

BACKGROUND The ability to image vascular endothelial growth factor (VEGF) could enable prospective, non-invasive monitoring of patients receiving anti-angiogenic therapy. This study investigates the specificity and pharmacokinetics of 111In-bevacizumab binding to VEGF and its use for assessing response to anti-angiogenic therapy with rapamycin. Specificity of 111In-bevacizumab binding to VEGF w...

2015
Ying-Hsia Shih Cheng-Liang Peng Shin-Yu Lee Ping-Fang Chiang Cheng-Jung Yao Wuu-Jyh Lin Tsai-Yueh Luo Ming-Jium Shieh

Colorectal adenocarcinoma is a common cause death cancer in the whole world. The aim of this study is to define the 111In-cetuximab as a diagnosis tracer of human colorectal adenocarcinoma. In this research, cell uptake, nano-SPECT/CT scintigraphy, autoradiography, biodistribution and immunohitochemical staining of EGF receptor were included. HCT-116 and HT-29 cell expressed a relatively high a...

Journal: :Nuclear medicine communications 1996
W J Oyen O C Boerman G Storm L van Bloois E B Koenders D J Crommelin J W van der Meer F H Corstens

Indium-111 (111In) and technetium-99m (99Tcm) Stealth liposomes were compared with 111In- and 99Tcm-labelled white blood cells (WBC) in experimental infection in a rabbit model. Preformed polyethylene glycol-coated liposomes and separated WBC were radiolabelled with either 111In-oxine or 99Tcm-hexamethylpropyleneamine oxime (99TcM-HMPAO). After the intravenous administration of one of the four ...

Journal: :Nuclear medicine review. Central & Eastern Europe 2011
Eftychia Koumarianou Dariusz Pawlak Agnieszka Korsak Renata Mikolajczak

BACKGROUND 44Sc as a positron emitter can be an interesting alternative to 68Ga (T½=67.71 min) due to its longer half-life (T½=3.97 h). Moreover, the b-emitter 47Sc can be used for therapy when attached to the same biomolecule vectors. DOTA as a chelating agent has been proven suitable for the radiolabelling of peptides recognising tumour cell receptors in vivo with M3+ radiometals. DOTA-deriva...

Journal: :Nuclear medicine and biology 2011
Kazuma Ogawa Kenichiro Takai Hiroya Kanbara Tatsuto Kiwada Yoji Kitamura Kazuhiro Shiba Akira Odani

INTRODUCTION (68)Ga is a radionuclide of great interest as a positron emitter for positron emission tomography (PET). To develop a new bone-imaging agent with radiogallium, 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) was chosen as a chelating site and Ga-DOTA complex-conjugated bisphosphonate, which has a high affinity for bone, was prepared and evaluated. Although we are in...

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