Abstract

Two novel [ 99mTc] [ SNN/S] “3+1” mixed ligand complexes, where L 3H 2= o-methylthio-glycinanilide (A) or N-(1-methylthio-phenyl)-ethylenediamine (B) and L 1H= isopropanethiol, were synthesized using stannous chloride as reductant and glucoheptonate as transfer ligand. The identifications of [ 99mTc]-A and [ 99mTc]-B were established by thin layer chromatography. The radiochemical purity of both complexes was over 90%. The initial biodistribution study in mice demonstrated that both complexes can penetrate the intact blood–brain barrier and exhibit retention in mice brain. The brain uptake (%ID/g) values of [ 99mTc]-A were 1.68, 1.23, 1.24 and of [ 99mTc]-B were 1.76, 1.08, 0.90 at 2, 30 and 60 min i.v. postinjection, respectively.

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