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Synthesis, labelling and animal experiments of the derivative of phenylpentadecanoic acid (CACPPA)

Synthesis, labelling and animal experiments of the derivative of phenylpentadecanoic acid (CACPPA)

Wu Chun-Ying
Ji Shu-Ren
Fang Ping
Zhou Xiang
Chen Zheng-Ping
Cao Guo-Xian
Nuclear Science and TechniquesVol.9, No.1pp.29-32Published in print 01 Feb 1998
32400

The synthesis and biodistribution were discribed for 99mTc labelled fatty acid, p-[(N,N'-di-carboxymethyl) aminomethyl carboxyamino]-phenylpentadecanoic acid (CACPPA). 99mTc-CACPPA was prepared by the reduction of Na99mTcO4 with stannous chloride in aqueous solution at pH 8.5〜9.5, the labelling yield and chemical purity were over 90% determined by TLC and HPLC. Biodistribution of 99mTc-CACPPA in mice demonstrated that the highest myocardial uptake of 99mTc-CACPPA was 18.17±2.67% ID/g. When blood disappearance of 99mTc-CACPPA was analysed with a biexponential model, an initial half time of 1.11 min and a late half time of 20.08 min were obtained. 99mTc-CACPPA exhibited high binding to HSA in vitro, and partition coefficients were 10.98 and 11.45 at pH7.00 and pH7.40, respectively.

99mTc labellingFatty acid/derivativeAnimal experimentMyocardial imaging agent
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