体内
癌细胞
药理学
阿霉素
盐酸阿霉素
药物输送
核仁素
适体
体外
癌症研究
材料科学
癌症
医学
化疗
化学
纳米技术
生物
生物化学
分子生物学
内科学
细胞质
核仁
生物技术
作者
Li‐Hua Peng,Yuanhong Zhang,Han Lijie,Chenzhen Zhang,Jiahe Wu,Xia-Rong Wang,Jianqing Gao,Zhengwei Mao
标识
DOI:10.1021/acsami.5b05065
摘要
Systemic administration of chemotherapeutic agents can cause indiscriminate drug distribution and severe toxicity. Until now, encapsulation and targeting of drugs have typically relied on synthetic vehicles, which cannot minimize the clearance by the renal system and may also increase the risk of chemical side effects. Cell membrane capsules (CMCs) provide a generic and far more natural approach to the challenges of drug encapsulation and delivery in vivo. Here aptamer AS1411, which can recognize and bind overexpressed nucleolin on a cancer cell membrane, was chemically conjugated onto CMCs. As a result, AS1411 modified CMCs showed enhanced ingestion in certain cancer cells in vitro and accumulation in mouse cancer xenografts in vivo. Chemotherapeutics and contrast agents with therapeutically significant concentrations can be packaged into CMCs by reversible permeating their plasma membranes. The systematic administration of cancer targeting CMCs loaded with doxorubicin hydrochloride can significantly inhibit tumor growth in mouse xenografts, with significantly reduced toxicity compared to free drug. These findings suggest that cancer targeting CMCs may have considerable benefits in drug delivery and cancer treatment.
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