光敏剂
脂质体
光动力疗法
癌症研究
癌细胞
佐剂
转移
细胞毒性
免疫系统
化学
癌症
细胞毒性T细胞
体内
药理学
医学
免疫学
体外
生物
生物化学
内科学
有机化学
生物技术
作者
Han Young Kim,Mikyung Kang,Yeon Woong Choo,Seokhyeong Go,Sung Pil Kwon,Seuk Young Song,Hee Su Sohn,Jihye Hong,Byung‐Soo Kim
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-07-12
卷期号:19 (8): 5185-5193
被引量:89
标识
DOI:10.1021/acs.nanolett.9b01571
摘要
Liposomes are clinically used as drug carriers for cancer therapy; however, unwanted leakage of the encapsulated anticancer drug and poor tumor-targeting efficiency of liposomes may generate toxic side effects on healthy cells and lead to failure of tumor eradication. To overcome these limitations, we functionalized liposomes with a photosensitizer (KillerRed, KR)-embedded cancer cell membrane (CCM). A lipid adjuvant was also embedded in the lipocomplex to promote the anticancer immune response. KR proteins were expressed on CCM and did not leak from the lipocomplex. Owing to the homotypic affinity of the CCM for the source cancer cells, the lipocomplex exhibited a 3.3-fold higher cancer-targeting efficiency in vivo than a control liposome. The liposome functionalized with KR-embedded CCM and lipid adjuvant generated cytotoxic reactive oxygen species in photodynamic therapy and effectively induced anticancer immune responses, inhibiting primary tumor growth and lung metastasis in homotypic tumor-bearing mice. Taken together, the lipocomplex technology may improve liposome-based cancer therapy.
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