Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13485
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dc.contributor.authorChittasupho C.
dc.contributor.authorThongnopkoon T.
dc.contributor.authorKewsuwan P.
dc.date.accessioned2021-04-05T03:24:15Z-
dc.date.available2021-04-05T03:24:15Z-
dc.date.issued2016
dc.identifier.issn15672018
dc.identifier.other2-s2.0-84964076400
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13485-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84964076400&doi=10.2174%2f1567201812666150904144241&partnerID=40&md5=30c90d3f81f4ae94fe389ef425ecb8af
dc.description.abstractPoly(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.
dc.subjectcarboxymethylcellulose
dc.subjectdoxorubicin
dc.subjectnanoparticle
dc.subjectpolyglactin
dc.subjectstabilizing agent
dc.subjectcarboxymethylcellulose
dc.subjectdrug carrier
dc.subjectexcipient
dc.subjectlactic acid
dc.subjectnanoparticle
dc.subjectpolyglycolic acid
dc.subjectpolylactic acid-polyglycolic acid copolymer
dc.subjectadsorption
dc.subjectArticle
dc.subjectcell viability
dc.subjectcolloid
dc.subjectcolorimetry
dc.subjectcontrolled study
dc.subjectdifferential scanning calorimetry
dc.subjectdispersion
dc.subjecthuman
dc.subjecthuman cell
dc.subjectinfrared spectroscopy
dc.subjectparticle size
dc.subjectpriority journal
dc.subjectsurface property
dc.subjectzeta potential
dc.subjectA-549 cell line
dc.subjectcell survival
dc.subjectchemistry
dc.subjectdrug delivery system
dc.subjectdrug effects
dc.subjectdrug stability
dc.subjectprocedures
dc.subjecttumor cell line
dc.subjectA549 Cells
dc.subjectAdsorption
dc.subjectCarboxymethylcellulose Sodium
dc.subjectCell Line, Tumor
dc.subjectCell Survival
dc.subjectDrug Carriers
dc.subjectDrug Delivery Systems
dc.subjectDrug Stability
dc.subjectExcipients
dc.subjectHumans
dc.subjectLactic Acid
dc.subjectNanoparticles
dc.subjectParticle Size
dc.subjectPolyglycolic Acid
dc.titleSurface modification of poly(D,L-lactic-co-glycolic acid) nanoparticles using sodium carboxymethyl cellulose as colloidal stabilizer
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationCurrent Drug Delivery. Vol 13, No.1 (2016), p.95-104
dc.identifier.doi10.2174/1567201812666150904144241
Appears in Collections:Scopus 1983-2021

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