PLGA公司
材料科学
膜
血小板
纳米颗粒
共焦显微镜
流式细胞术
生物物理学
纳米技术
化学
生物化学
分子生物学
医学
免疫学
细胞生物学
生物
作者
Dandan Ren,Tianyu Xiao,Jiadong Lou,Rong Ren,Yuhan Ye,Li‐Min Zhu
出处
期刊:NANO
[World Scientific]
日期:2021-09-25
卷期号:16 (11)
标识
DOI:10.1142/s1793292021501289
摘要
In this study, poly (lactic acid-glycolic acid) (PLGA) nanoparticles loaded with anti-inflammatory drug ketoprofen (KET) were prepared and then coated with platelet membrane (PLTM) to form KET@PLTM-PLGA nano-particles (NPs). The particle size of the KET@PLTM-PLGA NPs is 176[Formula: see text]nm and the surface protein is the same as that of PLTM. The results of confocal microscopy and flow cytometry showed that the KET@PLTM-PLGA NPs uptake of RAW264.7 induced by LPS was significantly higher than that of KET@PLGA NPs, without PLTM, which was due to the binding of P-selectin to CD44 receptors on the surface of RAW264.7 cells induced by LPS on the surface of PLTM. Compared with other KET preparations, KET@PLTM-PLGA NPs have better anti-inflammatory effect.
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