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首页> 外文期刊>British Journal of Cancer >The potential of carboxypeptidase G2: antibody conjugates as anti-tumour agents. II. In vivo localising and clearance properties in a choriocarcinoma model
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The potential of carboxypeptidase G2: antibody conjugates as anti-tumour agents. II. In vivo localising and clearance properties in a choriocarcinoma model

机译:羧肽酶G2:抗体偶联物作为抗肿瘤剂的潜力。二。绒毛膜癌模型的体内定位和清除特性

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The in vivo localising and clearance properties of conjugates of the folate-degrading enzyme carboxypeptidase G2 (CPG2) with anti-human chorionic gonadotrophin (W14A) were measured in nude mice bearing CC3 choriocarcinoma xenografts. Conjugates of W14A-F (ab')2 fragment coupled to CPG2 localised in tumour as effectively as native antibody alone but showed lower uptake in other major tissues. The clearance rates of conjugates prepared with intact antibody or F (ab')2 fragment were shown to be up to five-fold faster than for native antibody and two-fold compared to F (ab')2 fragment. Molecular weight analysis of residual conjugate in the blood showed that no degradation of conjugate to its component molecules occurred during circulation. It was concluded that F (ab')2: CPG2 conjugates offered the greatest potential for targeting applications.
机译:在携带CC3绒癌的异种移植裸鼠中,测定了叶酸降解酶羧肽酶G2(CPG2)与抗人绒毛膜促性腺激素(W14A)的结合物的体内定位和清除特性。与CPG2偶联的W14A-F(ab')2片段的缀合物与单独的天然抗体一样有效,但在其他主要组织中的摄取较低。与完整抗体或F(ab')2片段相比,用完整抗体或F(ab')2片段制备的缀合物的清除率显示最高快五倍,比F(ab')2片段快两倍。血液中残留结合物的分子量分析表明,在循环过程中结合物未降解为其组成分子。结论是,F(ab')2:CPG2共轭物为靶向应用提供了最大的潜力。

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