化学
白血病
细胞
癌症研究
骨髓
钙
生物物理学
化疗
纳米颗粒
细胞培养
细胞凋亡
药理学
药物输送
膜
细胞膜
生物化学
细胞生长
天冬酰胺酶
初生骨
细胞疗法
癌细胞
线粒体内膜
肿瘤微环境
细胞毒性
骨肉瘤
作者
Guangtao Gao,Junyi Che,Bing Chen,Yuanjin Zhao
标识
DOI:10.1186/s12951-025-03962-2
摘要
Chemotherapy is the primary clinical treatment for leukemia, while its effectiveness is often limited due to undesired off-target effects and the reduced sensitivity of leukemia cells to chemotherapeutic agents. Therapies capable of targeting the bone marrow and addressing the acidic tumor microenvironment are anticipated to improve treatment efficacy. Here, we presented biomimetic cell membrane-decorated calcium carbonate nanoparticles co-loaded with asparaginase and metformin (AMNPs@CM) for bone marrow-targeted therapy of leukemia. The biomimetic cell membrane coating facilitated significant accumulation of AMNPs@CM in the bone marrow, where the nanoparticles released the payloads in response to the acidic tumor microenvironment. The released asparaginase and metformin could synergically induce mitochondrial dysfunction in leukemia cells, leading to inhibited cell proliferation and enhanced apoptosis. Thus, our stratagem could effectively inhibit tumor burden and prolong survival in a C1498 leukemia-bearing mouse model. These results indicate the potential of the AMNPs@CM as a bone marrow-targeted delivery platform for combination therapy in the treatment of leukemia.
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