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(99m)Tc-DTPA-CLP的设计及其在大鼠中的初步评价

Design of (99m) Tc-DTPA-CLP and preliminary evaluation in rats.

作者信息

Altıparmak Burcu, Lambrecht Fatma Y, Er Ozge

机构信息

Department of Nuclear Applications, Institute of Nuclear Science, Ege University, Bornova, Izmir, 35100, Turkey.

出版信息

Chem Biol Drug Des. 2014 Mar;83(3):362-6. doi: 10.1111/cbdd.12253. Epub 2014 Feb 1.

Abstract

Radiopharmaceuticals are localized in (malignant) tumor tissues by different mechanisms. One of these mechanisms, gelatinase enzyme activity, is associated with poor prognosis in cancer patients and potential targets for tumor imaging. There are some gelatinases to be associated with metastatic potential for tumor imaging to possibly predict metastases. In this study, a cyclic decapeptide conjugate, DTPA-CLP (DTPA-Cys-Leu-Pro-Gly-His-Trp-Gly-Phe-Pro-Ser-Cys), was selected as a peptide conjugate because of its selective inhibitory activity toward gelatinases. Peptide-conjugated DTPA-CLP was labeled with (99m) Tc with a radiolabeling efficiency of 97.0 ± 2.8%. After determining optimization conditions for radiolabeling, a biodistribution study of radiolabeled peptide in albino Wistar rats was performed. According to biodistribution data, (99m) Tc-DTPA-CLP showed high uptake in the lung, liver, uterus, and spleen. These results show that (99m) Tc-DTPA-CLP may be used for the imaging of gelatinase activity in metastatic tumors.

摘要

放射性药物通过不同机制在(恶性)肿瘤组织中聚集。其中一种机制,即明胶酶活性,与癌症患者的不良预后相关,也是肿瘤成像的潜在靶点。有一些明胶酶与肿瘤成像的转移潜能相关,可能用于预测转移。在本研究中,一种环十肽偶联物DTPA-CLP(DTPA-半胱氨酸-亮氨酸-脯氨酸-甘氨酸-组氨酸-色氨酸-甘氨酸-苯丙氨酸-脯氨酸-丝氨酸-半胱氨酸)因其对明胶酶的选择性抑制活性而被选为肽偶联物。用(99m)Tc标记肽偶联物DTPA-CLP,放射性标记效率为97.0±2.8%。在确定放射性标记的优化条件后,对白化Wistar大鼠体内放射性标记肽进行了生物分布研究。根据生物分布数据,(99m)Tc-DTPA-CLP在肺、肝、子宫和脾脏中摄取较高。这些结果表明,(99m)Tc-DTPA-CLP可用于转移性肿瘤中明胶酶活性的成像。

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