Enhanced Antitumor Efficacy of Novel Biomimetic Platelet Membrane-Coated Tetrandrine Nanoparticles in Nonsmall Cell Lung Cancer

被引:7
|
作者
Jiang, Hui [1 ,2 ]
Tang, Chunming [2 ]
Wen, Yuanyuan [1 ]
Zhao, Qianqian [2 ]
Xu, Mingyuan [3 ,4 ]
Fan, Jinting [2 ]
Wang, Zhiji [2 ]
Wang, Lifeng [3 ,4 ]
Xu, Huae [1 ,2 ]
Chen, Gang [5 ]
机构
[1] Nanjing Med Univ, Affiliated Canc Hosp, Jiangsu Key Lab Mol & Translat Canc Res, Jiangsu Canc Hosp,Jiangsu Inst Canc Res, Nanjing 210009, Peoples R China
[2] Nanjing Med Univ, Sch Pharm, Dept Pharmaceut, Nanjing 211166, Peoples R China
[3] Nanjing Univ, Nanjing Drum Tower Hosp, Comprehens Canc Ctr, Med Sch, Nanjing 210093, Peoples R China
[4] Nanjing Univ, Clin Canc Inst, Med Sch, Nanjing 210093, Peoples R China
[5] Nanjing Med Univ, Affiliated Jiangning Hosp, Gen Surg Dept, Nanjing 210000, Peoples R China
基金
中国国家自然科学基金;
关键词
tetrandrine; platelet membranes; nonsmall celllung cancer; sustained release treatment; drug delivery; COMBINATION THERAPY; WNT/BETA-CATENIN; METASTASIS; APOPTOSIS; AUTOPHAGY; PROLIFERATION; LIPOSOMES; MIGRATION; GROWTH;
D O I
10.1021/acs.molpharmaceut.3c00310
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Nonsmall cell lung cancer (NSCLC) remains one of the leading causes of cancer-related death worldwide, posing a serious threat to global health. Tetrandrine (Tet) is a small molecule in traditional Chinese medicine with proven primary efficacy against multiple cancers. Although previous studies have demonstrated the potential anticancer effects of Tet on NSCLC, its poor water solubility has limited its further clinical application. Herein, a novel nanoparticle-based drug delivery system, platelet membrane (PLTM)-coated Tet-loaded polycaprolactone-b-poly-(ethylene glycol)-b-polycaprolactone nanoparticles (PTeNPs), is proposed to increase the potency of Tet against NSCLC. First, tetrandrine nanoparticles (TeNPs) are created using an emulsion solvent evaporation method, and biomimetic nanoparticles (PTeNPs) are prepared by coating the nanoparticles with PLTMs. When coated with PLTMs, PTeNPs are considerably less phagocytized by macrophages than Tet and TeNPs. In addition, compared with Tet and TeNPs, PTeNPs can significantly inhibit the growth and invasion of NSCLC both in vitro and in vivo. With reliable biosafety, this drug delivery system provides a new method of sustained release and efficient anticancer effects against NSCLC, facilitating the incorporation of Tet in modern nanotechnology.
引用
收藏
页码:5463 / 5475
页数:13
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