## Abstract The bis(__N__‐cyclopentyl dithiocarbamato) nitrido technetium‐99m complex ^99m^TcN(CPEDTC)~2~ was synthesized by the reduction of ^99m^TcO into [^99m^Tc≡N]^2+^ with stannous chloride in the presence of succinic dihydrazide and propylenediamine tetraacetic acid, followed by the addition
Preparation and biodistribution of novel 99mTc(CO)3-CNR complexes for myocardial imaging
✍ Scribed by Guiyang Hao; Jianying Zang; Boli Liu
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- French
- Weight
- 126 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
We evaluated lipophilicity and biodistribution of a series of 99m Tc(CO) 3 -ether isonitrile complexes to determine whether different lipophilicity and structure of isonitrile ligands would improve the imaging properties of the radiopharmaceutical for the heart. Novel 99m Tc(CO) 3 -MIBI analogs were prepared and analyzed by radio-HPLC, and their lipophilicity was determined. These new complexes could be bi-or tri-substituted in specified pH conditions like 99m Tc(CO) 3 -MIBI. These new complexes exhibited low liver, lungs and blood uptake compared with [ 99m Tc(CO) 3 (MIBI) 3 ] + though their heart uptake was not so high. Among these complexes, [ 99m Tc(CO) 3 (EPI) 2 (OH 2 )] + showed higher target to non-target ratios at 5 and 30 min post-injection than that of [ 99m Tc(CO) 3 (MIBI) 3 ] + . Copyright
📜 SIMILAR VOLUMES
## Abstract This work reports the synthesis, radiolabeling, and preliminary biodistribution results in tumor‐bearing mice of ^99m^Tc(CO)~3~(IDA‐CPT). The novel camptothecin (CPT) derivate was successfully synthesized by conjugation of iminodiacetic acid (IDA) to camptothecin via a short carbonyl‐me
## Abstract Labeling of sparafloxacin with technetium‐99m using stannous chloride as a reducing agent was investigated. Dependence of the yield of ^99m^Tc‐sparafloxacin complex on the concentration of sparafloxacin, reducing agent, pH and reaction time was studied. Under optimum conditions, the lab
## Abstract Coagulation in blood is initiated when coagulation factor VII (FVII) binds to exposed TF and is activated to FVIIa, and the TF/FVIIa complex may therefore provide a marker of vascular injury potentially applicable in diagnostic imaging of acute gastrointestinal (GI) bleeding. Methods: R