Bio-mediated synthesis of 5-FU based nanoparticles employing orange fruit juice: a novel drug delivery system to treat skin fibrosarcoma in model animals.
Animals
Antineoplastic Agents
/ pharmacology
Apoptosis
/ drug effects
Calorimetry, Differential Scanning
Caspase 9
/ metabolism
Citrus sinensis
/ chemistry
DNA Fragmentation
/ drug effects
Disease Models, Animal
Disease Progression
Drug Delivery Systems
Female
Fibrosarcoma
/ drug therapy
Fluorouracil
/ chemical synthesis
Fruit and Vegetable Juices
Kinetics
Male
Mice, Inbred BALB C
Nanoparticles
/ chemistry
Skin Neoplasms
/ drug therapy
Spectroscopy, Fourier Transform Infrared
Treatment Outcome
X-Ray Diffraction
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
23 08 2019
23 08 2019
Historique:
received:
20
05
2016
accepted:
19
02
2019
entrez:
25
8
2019
pubmed:
25
8
2019
medline:
22
10
2020
Statut:
epublish
Résumé
Nano-sized drug delivery systems (NDDS) have been widely exploited to achieve targeted delivery of pharmaco-materials. Traditional pharmaceutical approaches, implied in the synthesis of nano-formulations, are obscure owing to the incompatible physico-chemical properties of the core drug as well as some other factors crucial in development of NDDS. Infact, most of the existing methods used in development of NDDS rely on usage of additives or excipients, a special class of chemicals. Barring few exceptions, the usage of synthetic excipients ought to be curtailed because of several associated undesirable features. Such issues necessitate strategies that lead to development of the synthetic excipient free drug delivery system. Plant based extracts have great potential to induce synthesis of nano-sized particles. Considering this fact, here we propose a prototype employing orange fruit juice (OJ) to facilitate bio-mediated synthesis of nano-sized supra-molecular assemblies of 5-fluorouracil (5-FU), a potent anticancer drug. The as-synthesized 5-FU Nanoparticles (NPs) retained the anti-neoplastic efficacy of the parent compound and induced apoptosis in cancer cells. The novel 5-FU NPs formulation demonstrated enhanced efficacy against DMBA induced experimental fibrosarcoma in the mouse model when compared to the micro-sized crystals of parent 5-FU drug.
Identifiants
pubmed: 31444363
doi: 10.1038/s41598-019-48180-7
pii: 10.1038/s41598-019-48180-7
pmc: PMC6707153
doi:
Substances chimiques
Antineoplastic Agents
0
Caspase 9
EC 3.4.22.-
Fluorouracil
U3P01618RT
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
12288Références
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