Enhancing ovarian cancer conventional chemotherapy through the combination with cannabidiol loaded microparticles.
Animals
Antineoplastic Agents, Phytogenic
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Cannabidiol
/ administration & dosage
Cell Line, Tumor
Cell Survival
/ drug effects
Chick Embryo
Dose-Response Relationship, Drug
Drug Carriers
/ administration & dosage
Female
Humans
Microspheres
Ovarian Neoplasms
/ drug therapy
Paclitaxel
/ administration & dosage
Polylactic Acid-Polyglycolic Acid Copolymer
/ administration & dosage
Antitumor
CAM model
Cannabinoids
Combination therapy
Drug delivery
Gynecological cancer
Microparticles
Paclitaxel
Journal
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778
Informations de publication
Date de publication:
Sep 2020
Sep 2020
Historique:
received:
14
03
2020
revised:
25
06
2020
accepted:
10
07
2020
pubmed:
20
7
2020
medline:
3
6
2021
entrez:
20
7
2020
Statut:
ppublish
Résumé
In this work, we evaluated, for the first time, the antitumor effect of cannabidiol (CBD) as monotherapy and in combination with conventional chemotherapeutics in ovarian cancer and developed PLGA-microparticles as CBD carriers to optimize its anticancer activity. Spherical microparticles, with a mean particle size around 25 µm and high entrapment efficiency were obtained. Microparticles elaborated with a CBD:polymer ratio of 10:100 were selected due to the most suitable release profile with a zero-order CBD release (14.13 ± 0.17 μg/day/10 mg Mps) for 40 days. The single administration of this formulation showed an in vitro extended antitumor activity for at least 10 days and an in ovo antitumor efficacy comparable to that of CBD in solution after daily topical administration (≈1.5-fold reduction in tumor growth vs control). The use of CBD in combination with paclitaxel (PTX) was really effective. The best treatment schedule was the pre + co-administration of CBD (10 µM) with PTX. Using this protocol, the single administration of microparticles was even more effective than the daily administration of CBD in solution, achieving a ≈10- and 8- fold reduction in PTX IC
Identifiants
pubmed: 32682943
pii: S0939-6411(20)30211-3
doi: 10.1016/j.ejpb.2020.07.008
pii:
doi:
Substances chimiques
Antineoplastic Agents, Phytogenic
0
Drug Carriers
0
Cannabidiol
19GBJ60SN5
Polylactic Acid-Polyglycolic Acid Copolymer
1SIA8062RS
Paclitaxel
P88XT4IS4D
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
246-258Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.