Herceptin-functionalized SK-BR-3 cell membrane-wrapped paclitaxel nanocrystals for enhancing the targeted therapy effect of HER2-positive breast cancer

[Display omitted] •HER2-positive breast cancer-targeting drug delivery nanosystem was designed.•HER2-positive breast cancer-targeting drug delivery nanosystem showed sustained release behavior.•HER2-positive breast cancer-targeting drug delivery nanosystem exhibited remarkable dual targeting ability...

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Veröffentlicht in:Materials & design 2022-07, Vol.219, p.110818, Article 110818
Hauptverfasser: Wu, Qian, Tong, Le, Zou, Zhiru, Li, Yingqiao, An, Jinyu, Shen, Wenwen, Gao, Yu, Liu, Ying, Wu, Chao
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Sprache:eng
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Zusammenfassung:[Display omitted] •HER2-positive breast cancer-targeting drug delivery nanosystem was designed.•HER2-positive breast cancer-targeting drug delivery nanosystem showed sustained release behavior.•HER2-positive breast cancer-targeting drug delivery nanosystem exhibited remarkable dual targeting ability. The objective of this study was to prepare Herceptin-functionalized SK-BR-3 cell membrane-wrapped paclitaxel nanocrystals (HCNCs) as a targeted delivery module for HER2-positive breast cancer. According to transmission electron microscopy (TEM) images, HCNCs presented a membrane-coated cubic shape with a particle size of approximately 220 nm. In vitro release test suggested that HCNCs had a certain sustained release effect of paclitaxel (PTX). Cell uptake experiments, in vivo imaging, and tissue distribution experiments demonstrated that HCNCs had excellent targeting ability to homologous tumor cells (SK-BR-3). The results of MTT, flow cytometry, Western blot, cell immunofluorescence staining, and in vivo antitumor experiments proved that HCNCs had a more significant ability to promote HER2-positive breast cancer cell apoptosis and inhibit its proliferation. These results clearly concluded that HCNCs were a promising nano-targeted preparation in anti-HER2-positive breast cancer.
ISSN:0264-1275
1873-4197
DOI:10.1016/j.matdes.2022.110818