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Authors Zhang Z, Qian HQ, Yang M, Li RT, Hu J, Li L, Yu LX, Liu BR, Qian XP
Received 10 November 2016
Accepted for publication 12 January 2017
Published 28 February 2017 Volume 2017:12 Pages 1593—1605
DOI https://doi.org/10.2147/IJN.S127256
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Alexander Kharlamov
Peer reviewer comments 2
Editor who approved publication: Dr Linlin Sun
Abstract: Gambogic acid (GA) is expected to be a potential new antitumor drug, but
its poor aqueous solubility and inevitable side effects limit its clinical
application. Despite these inherent defects, various nanocarriers can be used
to promote the solubility and tumor targeting of GA, improving antitumor
efficiency. In addition, a cell membrane-coated nanoparticle platform that was
reported recently, unites the customizability and flexibility of a synthetic
copolymer, as well as the functionality and complexity of natural membrane, and
is a new synthetic biomimetic nanocarrier with improved stability and biocompatibility.
Here, we combined poly(lactic-co -glycolic acid)
(PLGA) with red blood-cell membrane (RBCm), and evaluated whether GA-loaded
RBCm nanoparticles can retain and improve the antitumor efficacy of GA with
relatively lower toxicity in colorectal cancer treatment compared with free GA.
We also confirmed the stability, biocompatibility, passive targeting, and few
side effects of RBCm-GA/PLGA nanoparticles. We expect to provide a new drug
carrier in the treatment of colorectal cancer, which has strong clinical
application prospects. In addition, the potential antitumor drug GA and other
similar drugs could achieve broader clinical applications via this biomimetic
nanocarrier.
Keywords: gambogic acid, nanocarriers,
RBCm-GA/PLGA nanoparticles, colorectal cancer