Rising horizon in circumventing multidrug resistance in chemotherapy with nanotechnology.
Effective chemotherapy, tumor-targeted delivery
Multidrug resistance
Nano-delivery
P-gp inhibition
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:
Aug 2019
Aug 2019
Historique:
received:
08
02
2019
revised:
24
03
2019
accepted:
02
04
2019
entrez:
29
4
2019
pubmed:
29
4
2019
medline:
20
8
2019
Statut:
ppublish
Résumé
Multidrug resistance (MDR) is one of the key barriers in chemotherapy, leading to the generation of insensitive cancer cells towards administered therapy. Genetic and epigenetic alterations of the cells are the consequences of MDR, resulted in drug resistivity, which reflects in impaired delivery of cytotoxic agents to the cancer site. Nanotechnology-based nanocarriers have shown immense shreds of evidence in overcoming these problems, where these promising tools handle desired dosage load of hydrophobic chemotherapeutics to facilitate designing of safe, controlled and effective delivery to specifically at tumor microenvironment. Therefore, encapsulating drugs within the nano-architecture have shown to enhance solubility, bioavailability, drug targeting, where co-administered P-gp inhibitors have additionally combat against developed MDR. Moreover, recent advancement in the stimuli-sensitive delivery of nanocarriers facilitates a tumor-targeted release of the chemotherapeutics to reduce the associated toxicities of chemotherapeutic agents in normal cells. The present article is focused on MDR development strategies in the cancer cell and different nanocarrier-based approaches in circumventing this hurdle to establish an effective therapy against deadliest cancer disease.
Identifiants
pubmed: 31029353
pii: S0928-4931(19)30494-1
doi: 10.1016/j.msec.2019.04.005
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Types de publication
Journal Article
Review
Langues
eng
Pagination
596-613Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.