Publication: Surface modification of poly(D,L-lactic-co-glycolic acid) nanoparticles using sodium carboxymethyl cellulose as colloidal stabilizer
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Issued Date
2016
Resource Type
File Type
application/pdf
ISSN
15672018
Other identifier(s)
2-s2.0-84964076400
Rights Holder(s)
มหาวิทยาลัยศรีนครินทรวิโรฒ
Bibliographic Citation
Current Drug Delivery. Vol 13, No.1 (2016), p.95-104
Suggested Citation
Chittasupho C., Thongnopkoon T., Kewsuwan P. Surface modification of poly(D,L-lactic-co-glycolic acid) nanoparticles using sodium carboxymethyl cellulose as colloidal stabilizer. Current Drug Delivery. Vol 13, No.1 (2016), p.95-104. doi:10.2174/1567201812666150904144241 Retrieved from: https://hdl.handle.net/20.500.14740/5694
Author(s)
Abstract
Poly(D,L-lactic-co-glycolic acid) nanoparticles (PLGA NPs) have been widely used as drug delivery systems for both small molecules and macromolecules. However, the colloidal stability problem remains unsolved. This study aims to investigate the possibility of using sodium carboxymethyl cellulose (SCMC) as a stabilizing agent of PLGA NPs. In this study, PLGA NPs were fabricated using various concentrations of SCMC (0.01, 0.1 and 0.5% w/v) by solvent displacement method. SCMC coated NPs were characterized using DLS, FTIR, DSC, colorimetric method. Particle size, polydispersity index, zeta potential values and SCMC adsorption increased with SCMC concentration. FTIR spectra, DSC thermograms and results of colorimetry suggested the interaction of SCMC and PLGA NPs. The stability of SCMC coated PLGA NPs was observed during the storage of three weeks in water. The stability of SCMC coated NPs in serum was also evaluated. Cell viability study revealed that there was no toxicity increased when SCMC was used as a stabilizing agent up to a concentration of 0.1% w/v. SCMC coated PLGA NPs bound A549 cells in a time dependent manner and with a greater extent than uncoated PLGA NPs. In conclusion, SCMC can be used to stabilize PLGA NPs by adsorbing on the surface of NPs. © 2016 Bentham Science Publishers.
Subject(s)
Carboxymethylcellulose
Doxorubicin
Nanoparticle
Polyglactin
Stabilizing agent
Carboxymethylcellulose
Drug carrier
Excipient
Lactic acid
Nanoparticle
Polyglycolic acid
Polylactic acid-polyglycolic acid copolymer
Adsorption
Article
Cell viability
Colloid
Colorimetry
Controlled study
Differential scanning calorimetry
Dispersion
Human
Human cell
Infrared spectroscopy
Particle size
Priority journal
Surface property
Zeta potential
A-549 cell line
Cell survival
Chemistry
Drug delivery system
Drug effects
Drug stability
Procedures
Tumor cell line
A549 Cells
Adsorption
Carboxymethylcellulose Sodium
Cell Line, Tumor
Cell Survival
Drug Carriers
Drug Delivery Systems
Drug Stability
Excipients
Humans
Lactic Acid
Nanoparticles
Particle Size
Polyglycolic Acid
Doxorubicin
Nanoparticle
Polyglactin
Stabilizing agent
Carboxymethylcellulose
Drug carrier
Excipient
Lactic acid
Nanoparticle
Polyglycolic acid
Polylactic acid-polyglycolic acid copolymer
Adsorption
Article
Cell viability
Colloid
Colorimetry
Controlled study
Differential scanning calorimetry
Dispersion
Human
Human cell
Infrared spectroscopy
Particle size
Priority journal
Surface property
Zeta potential
A-549 cell line
Cell survival
Chemistry
Drug delivery system
Drug effects
Drug stability
Procedures
Tumor cell line
A549 Cells
Adsorption
Carboxymethylcellulose Sodium
Cell Line, Tumor
Cell Survival
Drug Carriers
Drug Delivery Systems
Drug Stability
Excipients
Humans
Lactic Acid
Nanoparticles
Particle Size
Polyglycolic Acid
