化学
药品
药物输送
阿霉素
药理学
纳米颗粒
生物物理学
纳米技术
化疗
医学
有机化学
外科
材料科学
生物
作者
Santosh Aryal,Che‐Ming Jack Hu,Ronnie H. Fang,Diana Dehaini,Cody W. Carpenter,Dong‐Er Zhang,Liangfang Zhang
出处
期刊:Nanomedicine
[Future Medicine]
日期:2013-02-14
卷期号:8 (8): 1271-1280
被引量:200
摘要
Polymeric nanoparticles (NPs) cloaked by red blood cell membrane (RBCm) confer the combined advantage of both long circulation lifetime and controlled drug release. The authors carried out studies to gain a better understanding of the drug loading, drug-release kinetics and cell-based efficacy of RBCm-cloaked NPs.Two strategies for loading doxorubicin into the RBCm-cloaked NPs were compared: physical encapsulation and chemical conjugation. In vitro efficacy was examined using the acute myeloid leukemia cell line, Kasumi-1.It was found that the chemical conjugation strategy resulted in a more sustained drug release profile, and that the RBCm cloak provided a barrier, retarding the outward diffusion of encapsulated drug molecules. It was also demonstrated that RBCm-cloaked NPs exhibit higher toxicity in comparison with free doxorubicin.These results indicate that the RBCm-cloaked NPs hold great promise to become a valuable drug-delivery platform for the treatment of various diseases such as blood cancers.
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