In the triple-negative breast cancer MDA-MB-231 cell line, sulforaphane enhances the intracellular accumulation and anticancer action of doxorubicin encapsulated in liposomes.
Antibiotics, Antineoplastic
/ administration & dosage
Anticarcinogenic Agents
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
Cell Line, Tumor
Cell Survival
/ drug effects
Doxorubicin
/ administration & dosage
Drug Synergism
Female
Humans
Isothiocyanates
/ administration & dosage
Liposomes
Sulfoxides
Triple Negative Breast Neoplasms
/ drug therapy
Breast cancer
Doxorubicin
Intracellular distribution
Liposomes
Sulforaphane
Synergy
Journal
International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127
Informations de publication
Date de publication:
10 Mar 2019
10 Mar 2019
Historique:
received:
14
08
2018
revised:
03
12
2018
accepted:
02
01
2019
pubmed:
15
1
2019
medline:
14
6
2019
entrez:
15
1
2019
Statut:
ppublish
Résumé
A new combination of sulforaphane (a natural compound obtained from Brassicaceae vegetables) and the cytostatic drug doxorubicin was entrapped in nanometer-sized liposomes. In vitro experiments were performed to investigate the cytotoxicity of these structures on the human breast cancer cell line MDA-MB-231. Confocal microscopy studies revealed enhanced cellular endocytotic internalization, followed by the release of the examined combination from the lysosomes. The in vitro interaction analysis using the Chou-Talalay approach showed high synergistic activity of the examined combination. This synergistic activity enables a considerable reduction in cytostatic dosage and an increase in cancer treatment efficiency.
Identifiants
pubmed: 30641176
pii: S0378-5173(19)30034-1
doi: 10.1016/j.ijpharm.2019.01.008
pii:
doi:
Substances chimiques
Antibiotics, Antineoplastic
0
Anticarcinogenic Agents
0
Isothiocyanates
0
Liposomes
0
Sulfoxides
0
Doxorubicin
80168379AG
sulforaphane
GA49J4310U
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
311-318Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.