Noninvasive imaging of osteoclasts in parathyroid hormone–induced osteolysis using a 64Cu-labeled RGD peptide

JE Sprague, H Kitaura, W Zou, Y Ye… - Journal of Nuclear …, 2007 - Soc Nuclear Med
Bone diseases are often a result of increased numbers of osteoclasts, or bone-resorbing
cells. Bone metastases are a significant cause of morbidity in many types of cancer. An …

Integrin αvβ3 as a PET Imaging Biomarker for Osteoclast Number in Mouse Models of Negative and Positive Osteoclast Regulation

A Zheleznyak, TJ Wadas, CD Sherman… - Molecular imaging and …, 2012 - Springer
Purpose The goal of this study was to determine the specificity of 64 Cu-CB-TE2A-c
(RGDyK)(64 Cu-RGD) for osteoclast-related diseases, such as Paget's disease or …

Targeting the αvβ3 integrin for small-animal PET/CT of osteolytic bone metastases

TJ Wadas, H Deng, JE Sprague… - Journal of Nuclear …, 2009 - Soc Nuclear Med
This article describes the evaluation of the radiopharmaceutical 64Cu-CB-TE2A-c
(RGDyK)(64Cu-RGD) as an imaging agent for osteolytic bone metastases and their …

[HTML][HTML] Clinical study of 99mTc-3P-RGD2 peptide imaging in osteolytic bone metastasis

G Shao, W Gu, M Guo, S Zang, J Fu, S Liu, F Wang… - Oncotarget, 2017 - ncbi.nlm.nih.gov
Objective To investigate the value of integrin α v β 3 targeted imaging with 99m Tc-HYNIC-
PEG 4-E [PEG 4-c (RGDfk)] 2 (99m Tc-3P-RGD 2) as a radiotracer in dectecting osteolytic …

[HTML][HTML] Development of novel radiogallium-labeled bone imaging agents using oligo-aspartic acid peptides as carriers

K Ogawa, A Ishizaki, K Takai, Y Kitamura, T Kiwada… - PLoS …, 2013 - journals.plos.org
68Ga (T 1/2= 68 min, a generator-produced nuclide) has great potential as a radionuclide
for clinical positron emission tomography (PET). Because poly-glutamic and poly-aspartic …

An osteoclast-targeting agent for imaging and therapy of bone metastasis

W Liu, A Hajibeigi, M Lin, CL Rostollan… - Bioorganic & medicinal …, 2008 - Elsevier
A hybrid compound (DO3A-BP) featuring a radiometal bifunctional chelator (1, 4, 7, 10-
tetraazacyclotetradecane-N, N′, N ″, N‴-tetraacetic acid, DOTA) and an osteoclast …

Development of [90Y] DOTA-conjugated bisphosphonate for treatment of painful bone metastases

K Ogawa, H Kawashima, K Shiba, K Washiyama… - Nuclear medicine and …, 2009 - Elsevier
INTRODUCTION: Based on the concept of bifunctional radiopharmaceuticals, we have
previously developed 186Re-complex-conjugated bisphosphonate analogs for palliation of …

Rhemium-186-monoaminemonoamidedithiol-conjugated bisphosphonate derivatives for bone pain palliation

K Ogawa, T Mukai, Y Arano, A Otaka, M Ueda… - Nuclear medicine and …, 2006 - Elsevier
To develop a radiopharmaceutical for the palliation of painful bone metastases based on the
concept of bifunctional radiopharmaceuticals, we synthesized a bisphosphonate derivative …

[HTML][HTML] Evaluation of Ga-DOTA-(D-Asp)n as bone imaging agents: D-aspartic acid peptides as carriers to bone

K Ogawa, A Ishizaki, K Takai, Y Kitamura, A Makino… - Scientific Reports, 2017 - nature.com
Abstract 67Ga-DOTA-(L-Asp) 11 and 67Ga-DOTA-(L-Asp) 14, which have been developed
as bone imaging agents, showed a high accumulation in bone and a rapid blood clearance …

The addition of DTPA to [177Lu-DOTA0,Tyr3]octreotate prior to administration reduces rat skeleton uptake of radioactivity

WA Breeman, K van der Wansem, BF Bernard… - European journal of …, 2003 - Springer
Peptide receptor-targeted radionuclide therapy is nowadays also being performed with
DOTA-conjugated peptides, such as [DOTA 0, Tyr 3] octreotate, labelled with radionuclides …