Kinuya S, Yokoyama K, Yamamoto W, Konishi S, Shuke N, Aburano T, Watanabe N, Takayama T, Michigishi T, Tonami N
Department of Nuclear Medicine, Kanazawa University School of Medicine, Japan.
Nucl Med Biol. 1997 Aug;24(6):547-51. doi: 10.1016/s0969-8051(97)00076-0.
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.
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。