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PROCÉDÉS DESTINÉS À LA SYNTHÈSE MULTI-DOSE DU [F-18]FDDNP DESTINÉS À DES CONTEXTES CLINIQUES
专利权人:
The Regents of the University of California
发明人:
SATYAMURTHY, Nagichettiar,LIU, Jie,BARRIO, Jorge R.
申请号:
EP17869521
公开号:
EP3538161A4
申请日:
2017.11.08
申请国别(地区):
EP
年份:
2020
代理人:
摘要:
A method of manufacturing 2-(1-{6-[(2-[F-18]fluoroethyl)(methyl)amino]-2-naphthyl}ethylidene)-malononitrile ([F-18]FDDNP) utilizes a semi-automated module that is used to perform fluorination, pre-purification, separation, product extraction, and formulation. The method is able to produce [F-18]FDDNP with high yields and ready for human administration under existing FDA regulations, and without the need for hazardous organic solvents such as dichloromethane (DCM), methanol (MeOH), and tetrahydrofuran (THF). The method also improves the speed with which [F-18]FDDNP can be synthesized with the method being able to generate a final product within about 90 to 100 minutes. This synthesis method is easily adaptable to FDA registered and approved automated synthesis systems.
来源网站:
中国工程科技知识中心
来源网址:
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