Synthesis of a Potential Tumor Imaging Agent by Oxidative Radioiodination of Aspirin and Its Preclinical Study


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

Aspirin, one of nonsteroidal anti-inflammatory analgesic drugs, was labeled with 125I with a labeling yield of 85.5% under the following conditions: pH 9, 100 mg of the substrate, 50 µg of Chloramine-T, 5–15 min, room temperature. The radiochemical yield of 125I-aspirin was determined by paper chromatography and electrophoresis, and the radiochemical purity was determined by HPLC.125I-aspirin was stable for at least 3 h. Biodistribution of 125I-aspirin in normal and tumor-bearing mice was studied. The uptake of 125I-aspirin in tumor sites makes it promising as a new radiopharmaceutical for tumor imaging.

作者简介

I. Ibrahim

Hot Laboratories Centre

编辑信件的主要联系方式.
Email: ismailtaha_73@yahoo.com
埃及, Cairo

K. Attallah

Hot Laboratories Centre; Pharmaceutics Department, Faculty of Pharmacy

Email: ismailtaha_73@yahoo.com
埃及, Cairo; Mecca

M. Elsaid

Biochemistry Department, Faculty of Pharmacy

Email: ismailtaha_73@yahoo.com
沙特阿拉伯, Buraydah

M. Fahmy

Hot Laboratories Centre

Email: ismailtaha_73@yahoo.com
埃及, Cairo

L. Abo Zaid

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy

Email: ismailtaha_73@yahoo.com
埃及, Mansoura; Gumassa


版权所有 © Pleiades Publishing, Inc., 2019
##common.cookie##