Synthesis of 99mTc(CO)3-mebrofenin via [99mTc(OH2)3(CO)3]+ precursor and comparative pharmacokinetics studies with 99mTc-mebrofenin
✍ Scribed by Kanchan Kothari; Sangeeta Joshi; Meera Venkatesh; N. Ramamoorthy; M.R.A. Pillai
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 134 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.704
No coin nor oath required. For personal study only.
✦ Synopsis
The organometallic precursor fac-[ 99m Tc(OH 2 ) 3 (CO) 3 ] + was reacted with trimethyl-bromoacetanilido-iminodiacetic acid (mebrofenin) in phosphate buffered saline (pH 7) at 708C for 1 h to produce the complex, 99m Tc(CO) 3mebrofenin, in >95% yields. High performance liquid chromatography analysis indicated the formation of a single species. In vitro studies of 99m Tc(CO) 3 -mebrofenin showed that the complex is stable for 24 h. No decomposition or alteration of the complex was observed in the presence of excess amount of cysteine and histidine. 99m Tc-mebrofenin was also prepared for comparative evaluation by the conventional method using a ready to use kit HPLC analysis of this complex showed presence of two species. Biodistribution studies in normal Swiss mice with 99m Tc(CO) 3 -mebrofenin showed hepatobiliary clearance. However, the retention in liver was higher (13% at 1 h p.i.) as compared to that of 99m Tc-mebrofenin (3.4% at 1 h p.i.).
📜 SIMILAR VOLUMES
Non-invasive determination of hypoxia is an important problem in clinical nuclear medicine. Although 18 F-fluoromisonidazole is used clinically for hypoxia determination, the short half-life (t 1/2 = 109.77 min), high cost and less availability of cyclotrone-produced 18 F make 99m Tc (t 1/2 = 6 h)-b
## Abstract __S__‐Alkylated cysteines are used as efficient tridentate N,O,S‐donor‐atom ligands for the __fac__‐[M(CO)~3~]^+^ moiety (M=^99m^Tc or Re). Reaction of (Et~4~N)~2~[ReBr~3~(CO)~3~] (3) with the model __S__‐benzyl‐L‐cysteine (2) leads to the formation of [Re(2′)(CO)~3~] (4) as the exclusi
## 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 A comparison of the preparation of Tc carbonyl complexes of a few ligands of interest through the conventional method as well as by using the recently introduced carbonyl kit method is described. Synthesis of [^99m^Tc(OH~2~)~3~(CO)~3~]^+^ precursor was carried out by the conventional me
## Abstract Dendrimer polyamidoamine generation five‐folic acid conjugate was synthesesed and radiolabelled with __fac__‐[^99m^Tc(CO)~3~(H~2~O)~3~]^+^, its __in vitro__ stability was evaluated further. Both of the labeling yield and radiochemical purity of the G5‐FA‐DTPA‐^99m^Tc(CO)~3~ conjugate ex