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Moreno, D., Zalba, S., Colom, H., Trocóniz, I.F., Tros de Ilarduya, C. and Garrido, M.J. (2009) Biopharmaceutic and pharmacodynamic modeling of the in vitro antiproliferative effect of new controlled delivery systems of cisplatin. European Journal of Pharmaceutical Sciences, 37, 341-350. doi:10.1016/j.ejps.2009.03.005
has been cited by the following article:
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TITLE:
Controlled release of cisplatin and cancer cell apoptosis with cisplatin encapsulated poly(lactic-co-glycolic acid) nanoparticles
AUTHORS:
A. Champa Jayasuriya, Anthony J. Darr
KEYWORDS:
Nanoparticles, Cisplatin; Poly(Lactic-co-Glycolic Acid); Controlled Release; Cancer; Apopotosis
JOURNAL NAME:
Journal of Biomedical Science and Engineering,
Vol.6 No.5,
May
27,
2013
ABSTRACT: The
goal of the present study is to utilize cis-diamminedichloroplatinum
(cisplatin) loaded polymer nanoparticles (NPs) to give a controlled, extended,
and local drug therapy for the treatment of cancer. We have used biodegradable
and biocompatible poly(lactic-co-glycolic
acid) (PLGA) to prepare the NPs by adjusting the double emulsion technique using poly(vinylalcohol) as a
surface active agent. The PLGA NPs were characterized for particle size and
shape, controlled release of cisplatin, and degradation. Cisplatin solubility
in deionized water was increased up to 4 mg/mL by simply changing the solution
parameters. Cisplatin encapsulated NPs were incubated in phosphate buffered
saline (PBS) at 37?C to study the release kinetics of cisplatin. Cisplatin
was released in a sustained manner with less than 20% release during a 3-day
period followed by 50% release during a 21-day period. A degradation study of
PLGA NPs demonstrated the loss of spherical shape during a 21-day period. We
also examined the cisplatin sensitive A2780 cell apoptosis when cells were
incubated with cisplatin encapsulated PLGA NPs. A large number of cell
apoptosis occurred as a result of cisplatin release from the PLGA NPs. These
results suggest that cisplatin encapsulated PLGA NPs can be used to treat the
cancer cells by injecting them into a localized site minimizing the side
effects.