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Homotypic Cell Membrane-Cloaked Biomimetic Nanocarrier for the Targeted Chemotherapy of Hepatocellular Carcinoma

机译:同型细胞膜包裹的仿生纳米载体的肝癌靶向化疗。

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Goals: Hepatocellular carcinoma (HCC) has been reported to be the third most common malignant tumor and has the highest rate of mortality. To increase the chemotherapy efficacy of HCC, a drug delivery system featured with desirable active targeting ability, delivery efficiency and immune evasion is in high demand. Methods: We have developed a drug nanocarrier by utilizing a homotypic cancer cell membrane for targeted chemotherapy of HCC. Structurally, the homotypic HepG2 cell membrane was used as the cloak, and a poly (lactic- co -glycolic acid) (PLGA) nanoparticle as the core, resulting in the nanocarrier HepM-PLGA . Results: The HepM-PLGA nanoparticles exhibit excellent targeting ability toward HepG2 cells. Doxorubicin (Dox) carried by HepM-PLGA possesses high delivery efficiency and a remarkable in vitro therapeutic effect. In in vivo experiments, HepM-PLGA delivers Dox directly to the tumor lesion of nude mice, and tumor volume decreases by approximately 90% after treatment. Conclusion: We have developed a drug nanocarrier by utilizing a homotypic cancer cell membrane for targeted chemotherapy of HCC with excellent active targeting ability. This biomimetic platform not only effectively treats HCC but also provides a sound strategy for the treatment of other cancers via changes in the corresponding homotypic cancer cell membrane.
机译:目标:据报道,肝细胞癌(HCC)是第三大最常见的恶性肿瘤,死亡率最高。为了增加HCC的化学疗法功效,对具有期望的主动靶向能力,递送效率和免疫逃逸的特征的药物递送系统的需求很高。方法:我们已经利用同型癌细胞膜开发了一种药物纳米载体,用于HCC的靶向化疗。从结构上讲,同型HepG2细胞膜用作披风,聚乳酸-乙醇酸(PLGA)纳米颗粒为核心,从而形成纳米载体HepM-PLGA。结果:HepM-PLGA纳米颗粒表现出对HepG2细胞的出色靶向能力。 HepM-PLGA携带的阿霉素(Dox)具有较高的递送效率和出色的体外治疗效果。在体内实验中,HepM-PLGA将Dox直接递送给裸鼠的肿瘤病变,治疗后肿瘤体积减少约90%。结论:我们已经利用同型癌细胞膜开发了具有良好的主动靶向能力的药物纳米载体,用于肝癌的靶向化疗。该仿生平台不仅有效治疗HCC,而且还通过相应同型癌细胞膜的变化为其他癌症的治疗提供了合理的策略。

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