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Nanostructured Lipid Carriers as Multifunctional Nanomedicine Platform for Pulmonary Co-Delivery of Anticancer Drugs and siRNA

机译:纳米脂质载体作为多功能抗癌药物和siRNA肺共同递送的纳米医学平台。

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摘要

We developed, synthesized, and tested a multifunctional nanostructured lipid nanocarrier-based system (NLCS) for efficient delivery of an anticancer drug and siRNA directly into the lungs by inhalation. The system contains: (1) nanostructured lipid carriers (NLC); (2) anticancer drug (doxorubicin or paclitaxel); (3) siRNA targeted to MRP1 mRNA as a suppressor of pump drug resistance; (4) siRNA targeted to BCL2 mRNA as a suppressor of nonpump cellular resistance and (5) a modified synthetic analog of luteinizing hormone-releasing hormone (LHRH) as a targeting moiety specific to the receptors that are overexpressed in the plasma membrane of lung cancer cells. The NLCS was tested in vitro using human lung cancer cells and in vivo utilizing mouse orthotopic model of human lung cancer. After inhalation, the proposed NLCS effectively delivered its payload into lung cancer cells leaving healthy lung tissues intact and also significantly decreasing the exposure of healthy organs when compared with intravenous injection. The NLCS showed enhanced antitumor activity when compared with intravenous treatment. The data obtained demonstrated high efficiency of proposed NLCS for tumor-targeted local delivery by inhalation of anticancer drugs and mixture of siRNAs specifically to lung cancer cells and, as a result, efficient suppression of tumor growth and prevention of adverse side effects on healthy organs.
机译:我们开发,合成和测试了一种基于多功能纳米结构脂质纳米载体的系统(NLCS),该系统可通过吸入将抗癌药物和siRNA直接有效地直接输送到肺部。该系统包含:(1)纳米结构脂质载体(NLC); (2)抗癌药(阿霉素或紫杉醇); (3)靶向MRP1mRNA的siRNA作为泵浦药物抗性的抑制剂; (4)靶向BCL2 mRNA的siRNA作为非泵细胞抗性的抑制剂,和(5)改良的黄体生成激素释放激素(LHRH)的合成类似物,作为肺癌细胞膜中过表达的受体的特异性靶向部分细胞。使用人肺癌细胞在体外测试NLCS,并使用人肺癌的小鼠原位模型在体内测试NLCS。吸入后,与静脉内注射相比,拟议的NLCS有效地将其有效载荷传递到肺癌细胞中,使健康的肺组织完整无损,并且还大大减少了健康器官的暴露。与静脉内治疗相比,NLCS显示出增强的抗肿瘤活性。获得的数据证明了拟议的NLCS通过向肺癌细胞吸入抗癌药和siRNA混合物特别有效地靶向肿瘤,从而有效地抑制了肿瘤的生长并防止了对健康器官的不良副作用。

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