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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:分子成像多模式评价长春瑞滨加111包裹的聚乙二醇化脂质体在人大肠癌重复治疗中的疗效

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摘要

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 In ( In-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 In-VNB-liposome was significantly higher than that of the control (p<0.05). Conclusion: The tumors in NOD/SCID mice bearing HT-29/tk-luc xenografts were significantly suppressed by In-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:在精密疗法中,与正常组织/器官相比,脂质体封装的化学治疗药物已通过在肿瘤中实现更高的药物蓄积来开发用于治疗癌症的药物。材料和方法:我们通过与长春瑞滨(VNB)和In(In-VNB-脂质体)偶联的纳米脂质体开发了一种新颖的化学放射治疗方法,并在NOD / SCID小鼠模型中检查了它们的药代动力学,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下面积(AUC)比游离放射性同位素高约17倍。 In-VNB-脂质体对肿瘤的生长抑制作用明显高于对照组(p <0.05)。结论:In-VNB-脂质体可显着抑制携带HT-29 / tk-luc异种移植物的NOD / SCID小鼠的肿瘤。该研究提出用新型脂质体介导的放射化学疗法重复治疗,并通过成像验证治疗效果。

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