PolySciTech
division of Akina, Inc. (www.polyscitech.com)
provides a wide array of research products including biodegradable block
copolymer mPEG-PLGA. Recently, this polymer was used for generating
nanoparticles loaded with two chemotherapeutic drugs. These include paclitaxel,
an anti-mitotic drug derived from the Pacific yew tree commonly used in
treatment of cancer, and Temozolomide, a drug which acts to damage DNA of tumor
cells making it unreadable and triggering cell-death. The co-delivery of these chemotherapeutic agents
in a nanoparticle system was found to significantly reduce brain tumor cell growth
and proliferation in mice. Read more: Xu, Y., M. Shen, Y. Li, Y. Sun, Y. Teng,
Y. Wang, and Y. Duan. "The synergic antitumor effects of paclitaxel and
temozolomide co-loaded in mPEG-PLGA nanoparticles on glioblastoma cells."
Oncotarget (2016). http://europepmc.org/abstract/med/26956046
“Abstract: To get
better chemotherapy efficacy, the optimal synergic effect of Paclitaxel (PTX) and
Temozolomide (TMZ) on glioblastoma cells lines was investigated. A dual
drug-loaded delivery system based on mPEG-PLGA nanoparticles (NPs) was
developed to potentiate chemotherapy efficacy for glioblastoma. PTX/TMZ-NPs
were prepared with double emulsification solvent evaporation method and
exhibited a relatively uniform diameter of 206.3 ± 14.7 nm. The NPs showed
sustained release character. Cytotoxicity assays showed the best synergistic
effects were achieved when the weight ratios of PTX to TMZ were 1:5 and 1:100
on U87 and C6 cells, respectively. PTX/TMZ-NPs showed better inhibition effect
to U87 and C6 cells than single drug NPs or free drugs mixture. PTX/TMZ-NPs
(PTX: TMZ was 1:5(w/w)) significantly inhibited the tumor growth in the
subcutaneous U87 mice model. These results indicate that coordinate
administration of PTX and TMZ combined with NPs is an efficient method for
glioblastoma.”
No comments:
Post a Comment