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Authors Sun Y, Zhao Y, Teng S, Hao F, Zhang H, Meng F, Zhao X, Zheng X, Bi Y, Yao Y, Lee RJ, Teng L
Received 24 July 2018
Accepted for publication 22 October 2018
Published 21 December 2018 Volume 2019:14 Pages 135—148
DOI https://doi.org/10.2147/IJN.S181296
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Govarthanan Muthusamy
Peer reviewer comments 2
Editor who approved publication: Dr Linlin Sun
Background: We
previously developed cabazitaxel (CTX)-loaded human serum albumin nanoparticles
(NPs-CTX) via a self-assembly method, and these NPs showed efficacy in prostate
cancer therapy. Many studies have shown that the levels of folic acid (FA)
receptor on the surface of various tumor cells are high. Therefore, FA-modified
NPs-CTX may have enhanced antitumor effects compared with unmodified NPs-CTX.
Methods: NPs-CTX
were first prepared via self-assembly, and FA was conjugated on the surface of
NPs-CTX through the -NH2 groups of the NPs to produce FA-NPs-CTX. The
FA-NPs-CTX were evaluated in tumor cells with high FA receptor (FR) expression
in vitro and in vivo.
Results: Both
NPs-CTX and FA-NPs-CTX exhibited good stability and morphology. Drug release
from the NPs was not affected by FA conjugation. Compared with CTX dissolved in
a mixture of Tween 80 and 13% ethanol (w/w) at a ratio of 1:4 (v/v)
(Tween-CTX), the two nanoformulations had lower lytic activity against normal
red blood cells. However, FA-NPs-CTX showed greater inhibition of tumor cells
with overexpressed FR, compared with NPs-CTX, in the cytotoxicity experiments.
Moreover, the cellular uptake of FA-NPs-CTX was enhanced through FR-mediated
endocytosis in HeLa cells in vitro and HeLa xenograft tumors in vivo. Although
Tween-CTX exhibited tumor growth inhibition similar to FA-NPs-CTX in vivo, this
inhibition also caused adverse side effects; the median lethal dose (LD50) of
Tween-CTX to mice was 5.68 mg/kg, while FA-NPs-CTX-treated mice survived at
doses exceeding 400 mg/kg.
Conclusion: The
results showed that FA-NPs-CTX caused inhibition of tumor growth in a manner
similar to that of Tween-CTX; however, the safety and tolerability of CTX were
greatly improved by FA conjugation compared with those of Tween-CTX. In
summary, FA-NPs-CTX have great potential in CTX delivery, and this formulation
is a promising candidate for the treatment of cancers with high FR levels.
Keywords: folic
acid, human serum albumin, nanoparticles, cabazitaxel, folic acid receptor
