Dual stimuli-responsive ursolic acid-embedded nanophytoliposome for targeted antitumor therapy.
Animals
Antineoplastic Agents, Phytogenic
/ chemistry
Apoptosis
/ drug effects
Cell Line, Tumor
Cell Proliferation
/ drug effects
Drug Compounding
Drug Liberation
Female
Humans
Hyaluronan Receptors
/ metabolism
Hyaluronic Acid
/ chemistry
Liposomes
Mice, Inbred BALB C
Mice, Nude
Nanoparticles
Neoplasms
/ drug therapy
Polylysine
/ chemistry
Stimuli Responsive Polymers
/ chemistry
Tissue Distribution
Triterpenes
/ chemistry
Ursolic Acid
Anticancer effect
Nanophytoliposome
Nanosystem
Stimuli responsiveness
Ursolic acid
Journal
International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127
Informations de publication
Date de publication:
30 May 2020
30 May 2020
Historique:
received:
31
12
2019
revised:
23
03
2020
accepted:
10
04
2020
pubmed:
17
4
2020
medline:
20
2
2021
entrez:
17
4
2020
Statut:
ppublish
Résumé
The hindrances in achieving clinically translatable anticancer platforms are being tackled through nanotechnology-based formulations. In this study, stimuli-responsive, phytoactive constituent-loaded nanophytoliposomes were fabricated for designing a specific antitumor platform. Ursolic acid (UA)-loaded nanophytoliposomes (UA-PLL-HA.P) enwrapped in a poly-L-lysine (PLL) coat and hyaluronic acid (HA) were nanosized; these nanophytoliposomes had spherical morphology, slightly negative charge, and an in-range polydispersity index (~0.25). Successful fabrication of the nanosystem was proven through several characterization methods and the pH- and enzyme-responsiveness of the nanosystem was assessed through a release study. The cellular internalization in CD44 receptor-expressing cell lines was amplified by enhanced permeation and retention as well as by active targeting. In vitro antitumor behavior was confirmed through in vitro cytotoxic and apoptotic activity of the nanosystem. Similarly, in vivo imaging showed exceptional biodistribution in the tumor in agreement with the in vitro findings. Moreover, the tumor inhibitory rate of UA-PLL-HA.P was significantly higher, and was ascribed to the targeting potential and stimuli-responsiveness. In summary, UA-PLL-HA.P exhibited pronounced anticancer effect and could open a number of possibilities for discovering novel phytoconstituent-incorporated nanoformulations.
Identifiants
pubmed: 32298743
pii: S0378-5173(20)30314-8
doi: 10.1016/j.ijpharm.2020.119330
pii:
doi:
Substances chimiques
Antineoplastic Agents, Phytogenic
0
CD44 protein, human
0
Hyaluronan Receptors
0
Liposomes
0
Stimuli Responsive Polymers
0
Triterpenes
0
Polylysine
25104-18-1
Hyaluronic Acid
9004-61-9
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
119330Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.