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Delivery of disulfiram into breast cancer cells using folate-receptor-targeted PLGA-PEG nanoparticles: in vitro and in vivo investigations
by
Ghavamzadeh, Ardeshir
, Esfandyari-Manesh, Mehdi
, Moradian, Hanieh
, Fasehee, Hamidreza
, Dinarvand, Rassoul
, Faghihi, Shahab
, Ghaffari, Seyed Hamidollah
in
Biotechnology
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - metabolism
/ Cell Line, Tumor
/ Cell Survival - drug effects
/ Chemistry
/ Chemistry and Materials Science
/ Disulfiram - administration & dosage
/ Drug Carriers - administration & dosage
/ Female
/ Folate Receptors, GPI-Anchored - metabolism
/ Folic Acid - administration & dosage
/ Folic Acid - analogs & derivatives
/ Folic Acid - metabolism
/ Humans
/ Lactic Acid - administration & dosage
/ MCF-7 Cells
/ Molecular Medicine
/ Nanoparticles - administration & dosage
/ Nanotechnology
/ Particle Size
/ Polyethylene Glycols - administration & dosage
/ Polyglycolic Acid - administration & dosage
2016
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Delivery of disulfiram into breast cancer cells using folate-receptor-targeted PLGA-PEG nanoparticles: in vitro and in vivo investigations
by
Ghavamzadeh, Ardeshir
, Esfandyari-Manesh, Mehdi
, Moradian, Hanieh
, Fasehee, Hamidreza
, Dinarvand, Rassoul
, Faghihi, Shahab
, Ghaffari, Seyed Hamidollah
in
Biotechnology
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - metabolism
/ Cell Line, Tumor
/ Cell Survival - drug effects
/ Chemistry
/ Chemistry and Materials Science
/ Disulfiram - administration & dosage
/ Drug Carriers - administration & dosage
/ Female
/ Folate Receptors, GPI-Anchored - metabolism
/ Folic Acid - administration & dosage
/ Folic Acid - analogs & derivatives
/ Folic Acid - metabolism
/ Humans
/ Lactic Acid - administration & dosage
/ MCF-7 Cells
/ Molecular Medicine
/ Nanoparticles - administration & dosage
/ Nanotechnology
/ Particle Size
/ Polyethylene Glycols - administration & dosage
/ Polyglycolic Acid - administration & dosage
2016
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Delivery of disulfiram into breast cancer cells using folate-receptor-targeted PLGA-PEG nanoparticles: in vitro and in vivo investigations
by
Ghavamzadeh, Ardeshir
, Esfandyari-Manesh, Mehdi
, Moradian, Hanieh
, Fasehee, Hamidreza
, Dinarvand, Rassoul
, Faghihi, Shahab
, Ghaffari, Seyed Hamidollah
in
Biotechnology
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - metabolism
/ Cell Line, Tumor
/ Cell Survival - drug effects
/ Chemistry
/ Chemistry and Materials Science
/ Disulfiram - administration & dosage
/ Drug Carriers - administration & dosage
/ Female
/ Folate Receptors, GPI-Anchored - metabolism
/ Folic Acid - administration & dosage
/ Folic Acid - analogs & derivatives
/ Folic Acid - metabolism
/ Humans
/ Lactic Acid - administration & dosage
/ MCF-7 Cells
/ Molecular Medicine
/ Nanoparticles - administration & dosage
/ Nanotechnology
/ Particle Size
/ Polyethylene Glycols - administration & dosage
/ Polyglycolic Acid - administration & dosage
2016
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Delivery of disulfiram into breast cancer cells using folate-receptor-targeted PLGA-PEG nanoparticles: in vitro and in vivo investigations
Journal Article
Delivery of disulfiram into breast cancer cells using folate-receptor-targeted PLGA-PEG nanoparticles: in vitro and in vivo investigations
2016
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Overview
Background
A folate-receptor-targeted poly (lactide-co-Glycolide) (PLGA)-Polyethylene glycol (PEG) nanoparticle is developed for encapsulation and delivery of disulfiram into breast cancer cells. After a comprehensive characterization of nanoparticles, cell cytotoxicity, apoptosis induction, cellular uptake and intracellular level of reactive oxygen species are analyzed. In vivo acute and chronic toxicity of nanoparticles and their efficacy on inhibition of breast cancer tumor growth is studied.
Results
The folate-receptor-targeted nanoparticles are internalized into the cells, induce reactive oxygen species formation, induce apoptosis and inhibit cell proliferation more efficiently compared to the untargeted nanoparticles. The acute and toxicity test show the maximum dose of disulfiram equivalent of nanoparticles for intra-venous injection is 6 mg/kg while show significant decrease in the breast cancer tumor growth rate.
Conclusion
It is believed that the developed formulation could be used as a potential vehicle for successful delivery of disulfiram, an old and inexpensive drug, into breast cancer cells and other solid tumors.
Graphical abstract
Disulfiram, an old and inexpensive drug, is encapsulated in folate-targeted PLGA-PEG nanoparticles and delivered into breast cancer cells using passive and active targeting to inhibit tumor growth in mice
Publisher
BioMed Central,Springer Nature B.V
Subject
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - metabolism
/ Cell Survival - drug effects
/ Chemistry and Materials Science
/ Disulfiram - administration & dosage
/ Drug Carriers - administration & dosage
/ Female
/ Folate Receptors, GPI-Anchored - metabolism
/ Folic Acid - administration & dosage
/ Folic Acid - analogs & derivatives
/ Humans
/ Lactic Acid - administration & dosage
/ Nanoparticles - administration & dosage
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