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短期诱导性高血压可提高放射性标记单克隆抗体的肿瘤与非肿瘤比例。

Short-period-induced hypertension could improve tumor-to-nontumor ratios of radiolabeled monoclonal antibody.

作者信息

Kinuya S, Yokoyama K, Yamamoto W, Konishi S, Shuke N, Aburano T, Watanabe N, Takayama T, Michigishi T, Tonami N

机构信息

Department of Nuclear Medicine, Kanazawa University School of Medicine, Japan.

出版信息

Nucl Med Biol. 1997 Aug;24(6):547-51. doi: 10.1016/s0969-8051(97)00076-0.

Abstract

This study was undertaken to find optimum period of hypertensive treatment for the improvement of tumor targeting of 111In-labeled monoclonal antibody. Angiotensin II was infused into tumor-bearing mice at an infusion rate of 2.0 micrograms/kg/min determined by the dose-finding study. The infusion was continued for up to 72 h, and biodistribution of 111In-DTPA-A7, a murine IgG1, was observed 72 h postinjection. Tumor-to-nontumor ratios were best improved with the infusion for 0.5-3 h. However, with the longer infusion, the effect deteriorated by the increase of nontumor uptakes, and body-weight loss became remarkable. It could be concluded that hypertensive treatment for a short period could be safely performed to benefit targeting of radiolabeled monoclonal antibody.

摘要

本研究旨在寻找高血压治疗的最佳时长,以改善¹¹¹In标记的单克隆抗体的肿瘤靶向性。通过剂量探索研究确定,以2.0微克/千克/分钟的输注速率向荷瘤小鼠输注血管紧张素II。输注持续长达72小时,并在注射后72小时观察鼠IgG1¹¹¹In-DTPA-A7的生物分布。输注0.5 - 3小时时,肿瘤与非肿瘤的比值改善最佳。然而,随着输注时间延长,非肿瘤摄取增加导致效果恶化,体重减轻也变得显著。可以得出结论,短期高血压治疗可以安全进行,以利于放射性标记单克隆抗体的靶向性。

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