Gemcitabine and betulinic acid co-encapsulated PLGA-PEG polymer nanoparticles for improved efficacy of cancer chemotherapy.
Apoptosis
Cell Line, Tumor
Deoxycytidine
/ analogs & derivatives
Drug Carriers
/ chemistry
Drug Delivery Systems
Humans
Nanoparticles
/ chemistry
Particle Size
Pentacyclic Triterpenes
Polyesters
/ chemistry
Polyethylene Glycols
/ chemistry
Reactive Oxygen Species
/ metabolism
Triterpenes
/ chemistry
Betulinic Acid
Gemcitabine
Betulinic acid
Co-delivery
Gemcitabine
Nanoparticles
Solid tumor
Journal
Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
27
08
2018
revised:
28
11
2018
accepted:
07
01
2019
entrez:
1
3
2019
pubmed:
1
3
2019
medline:
14
6
2019
Statut:
ppublish
Résumé
The present study demonstrated the development of gemcitabine and betulinic acid co-encapsulated PLGA-PEG polymer nanoparticles for enhancing the chemotherapeutic response. This combinatorial PLGA-PEG nanoparticle was formulated using double emulsion and had size <200 nm. The developed nanoparticles were characterized using dynamic light scattering and transmission electron microscopy for their size and shape, respectively. The in vitro release of the drugs from combinatorial nanoparticles was predominantly followed by Fickian diffusion phenomenon. Study on hemocompatibilty approved the administration of this combinatorial nanoparticle for animal study. In vitro cytotoxicity study on Panc1 cells using MTT assay, reactive oxygen species production and cellular apoptotic assay demonstrated that combinatorial nanoparticle was more cytotoxic compared to native drugs solution. Furthermore, the combinatorial nanoparticle suppressed tumor growth more efficiently in Ehrlich (solid) tumor model than the native gemcitabine and betulinic acid at the same concentrations. These findings indicated that PLGA-PEG nanoparticle might be used to co-deliver multiple chemotherapeutic drugs with different properties for enhancing antitumor efficacy.
Identifiants
pubmed: 30813082
pii: S0928-4931(18)32589-X
doi: 10.1016/j.msec.2019.01.026
pii:
doi:
Substances chimiques
Drug Carriers
0
Pentacyclic Triterpenes
0
Polyesters
0
Reactive Oxygen Species
0
Triterpenes
0
polyethylene glycol-poly(lactide-co-glycolide)
0
Deoxycytidine
0W860991D6
Polyethylene Glycols
3WJQ0SDW1A
Betulinic Acid
4G6A18707N
Gemcitabine
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
764-771Informations de copyright
Copyright © 2019. Published by Elsevier B.V.