发明名称 RADIOTRACER COMPOSITIONS AND METHODS
摘要 The present invention relates to the field of radiopharmaceuticals for in vivo imaging, in particular to radiotracer compositions which comprises 18F-labelled c-Met binding peptides. The invention provides said compositions, as well as associated automated methods of preparation and cassettes.
申请公布号 US2016303263(A1) 申请公布日期 2016.10.20
申请号 US201415102952 申请日期 2014.12.18
申请人 GE HEALTHCARE LIMITED 发明人 Engell Torgrim;Getvoldsen Gareth Simon;Meijer Andreas Richard;KHAN IMTIAZ Ahmed;Nairne Robert James;McRobbie Graeme
分类号 A61K51/08;C07B59/00;A61K51/04 主分类号 A61K51/08
代理机构 代理人
主权项 1. A radiopharmaceutical composition which comprises: (i) a radiotracer that has a radioactive concentration of 500-700 MBq/mL and which comprises a c-Met binding peptide of Formula I labelled with 18F: Z1-[cMBP]-Z2   (I) (ii) a radioprotectant which comprises 4-aminobenzoic acid, or a salt thereof with a biocompatible cation; (iii) a biocompatible carrier which comprises aqueous ethanol having an ethanol content of 0.1 to 10% v/v;in a form suitable for mammalian administration; where: cMBP is the c-Met binding peptide having the amino acid sequence:Ala-Gly-Ser-Cysa-Tyr-Cysc-Ser-Gly-Pro-Pro-Arg-Phe-Glu-Cysd-Trp-Cysb-Tyr-Glu-Thr-Glu-Gly-Thr-Gly-Gly-Gly-Lys wherein Cysa-d are each cysteine residues such that residues a and b as well as c and d are cyclised to form two separate disulfide bonds; Z1 is attached to the N-terminus of cMBP, and is MIG; Z2 is attached to the C-terminus of cMBP and is MIG, MIG is independently a metabolism inhibiting group which is a biocompatible group which inhibits or suppresses in vivo metabolism of the cMBP peptide; the Lys residue of the cMBP is labelled with 18F.
地址 Little Chalfont Buckinghamshire GB