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Therapeutic Efficacy Evaluation of Pegylated Liposome Encapsulated With Vinorelbine Plus 111In Repeated Treatments in Human Colorectal Carcinoma With Multimodalities of Molecular Imaging

机译:用血肠籽加上111林的聚乙二醇化脂质体的治疗疗效评价用分子成像的多重差异的人结直肠癌重复处理

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Background/Aim: In precision therapy, liposomal encapsulated chemotherapeutic drugs have been developed to treat cancers by achieving higher drug accumulation in the tumor compared to normal tissues/organs. Materials and Methods: We developed a novel chemoradiotherapeutic approach via nanoliposomes conjugated with vinorelbine (VNB) and 111In (111In-VNB-liposome) and examined their pharmacokinetics, biodistribution, maximum tolerance dose, and toxicity in a NOD/SCID mouse model. Results: Pharmacokinetic results showed that the area under the curve (AUC) of PEGylated liposomes was about 17-fold higher than that of the free radioisotope. Tumor growth inhibition by 111In-VNB-liposome was significantly higher than that of the control (p0.05). Conclusion: The tumors in NOD/SCID mice bearing HT-29/tk-luc xenografts were significantly suppressed by 111In-VNB-liposomes. The study proposed repeated treatments with a novel liposome-mediated radiochemotherapy and validation of therapeutic efficacy via imaging.
机译:背景/目的:在精密治疗中,通过在与正常组织/器官相比,通过在肿瘤中实现更高的药物积累来开发脂质体包封的化学治疗药物。材料和方法:我们开发了一种通过与Vinorelbine(VNB)和111in(111in-VNB-脂质体)缀合的纳米脂质体的新型化学调节治疗方法,并在点击/ SCID小鼠模型中检查其药代动力学,生物分布,最大耐受剂量和毒性。结果:药代动力学结果表明,聚乙二醇化脂质体的曲线(AUC)下的面积高于自由放射性同位素的约17倍。肿瘤生长抑制111英寸-VNB-脂质体显着高于对照(P <0.05)。结论:111英寸-VNB-脂质体显着抑制了HT-29 / TK-LUC异种移植物的NOD / SCID小鼠中的肿瘤。该研究提出了具有新型脂质体介导的放射性化学疗法的重复处理和通过成像验证治疗效果。

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