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Rod‐Shaped Drug Particles for Cancer Therapy: The Importance of Particle Size and Participation of Caveolae Pathway
Author(s) -
He Wei,
Xin Xiaofei,
Li Yongji,
Han Xiaopeng,
Qin Chao,
Yin Lifang
Publication year - 2017
Publication title -
particle and particle systems characterization
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 56
eISSN - 1521-4117
pISSN - 0934-0866
DOI - 10.1002/ppsc.201600371
Subject(s) - endocytosis , caveolae , in vivo , paclitaxel , cytotoxicity , microbiology and biotechnology , in vitro , drug , chemistry , particle size , penetration (warfare) , biophysics , cancer research , pharmacology , cell , cancer , biology , medicine , biochemistry , operations research , engineering
It is disclosed how the sizes of rod‐shaped paclitaxel‐nanosuspensions (PTX‐Ns) that are less than 500 nm affect their in vitro and in vivo performances. A size reduction from 500 to 160 nm enhances the cellular uptake and subsequent cytotoxicity, due to the participation of caveolae‐mediated endocytosis; moreover, the ability of the PTX‐Ns to penetrate tumors is well correlated with the extent to which the caveolae pathway participates in cellular uptake, as their ability to target caveolae is markedly promoted as their size decreased to 160 nm. Also, the size reduction markedly alters the in vivo performance and tumor targeting. It is disclosed that via enhanced tumor penetration and retention but not simply increased tumor accumulation, size reduction of PTX‐Ns results in significant improvement in antitumor activities. Overall, this study highlights the importance of the size of the PTX‐Ns and the participation of caveolae‐mediated endocytosis in controlling their biological functions and will assist in the design and optimization of new nanosuspension formulations for disease therapy.