Determination of Methotrexate in pH-Sensitive Chitosan Nanoparticles by Validated RP-LC and UV Spectrophotometric Methods

dc.contributor.authorNogueira, Daniele R.
dc.contributor.authorMacedo, Letícia B.
dc.contributor.authorScheeren, Laís E.
dc.contributor.authorMitjans Arnal, Montserrat
dc.contributor.authorInfante Martínez-Pardo, Ma. Rosa
dc.contributor.authorRolim, Clarice M. B.
dc.contributor.authorVinardell Martínez-Hidalgo, Ma. Pilar
dc.date.accessioned2016-04-08T17:17:42Z
dc.date.available2016-04-08T17:17:42Z
dc.date.issued2014-12
dc.date.updated2016-04-08T17:17:47Z
dc.description.abstractNanotechnology-based drug delivery systems are in constant development and, therefore, it is of great importance to have rapid, efficient and accurate analytical methodology to quantify the encapsulated drugs. Here, simple and fast methods, by reversed-phase liquid chromatography (RP-LC) and UV spectrophotometry, were developed and validated for the determination of methotrexate (MTX) in pH-sensitive chitosan nanoparticles (CS-NPs). NPs were prepared using a modified ionotropic complexation process, in which was included a surfactant derived from Nα,Nε-dioctanoyl lysine with an inorganic sodium counterion. The RP-LC method was carried out on a Waters XBridgeTM C18 column (250 mm x 4.6 mm I.D., 5μm), with mobile phase consisted of potassium phosphate buffer (0.05 M, pH 3.2): acetonitrile (86:14, v/v), and UV detection set at 303 nm. The analyses of MTX content by the UV method were also accomplished at 303 nm, using 0.1 M sodium hydroxide as diluent. The measurements were linearly correlated with concentration for both methods in the 1 - 30 μg/mL range (r > 0.9999). The specificity tests showed that there was no interference of the NP components on the quantitative analyses. Precision (repeatability and intermediate precision) was demonstrated by a relative standard deviation lower than 1.5%, whereas the accuracy was assessed by the recovery of MTX from sample matrices, given mean value of ~99%. The proposed methods were applied for the analyses of MTX in different batches of NPs, and the results showed non-significant differences (p > 0.05) between the values obtained with both methodologies. Moreover, the RP-LC method was successfully used to determine the drug entrapment efficiency, and to quantify MTX during in vitro release assays and photolytic degradation studies. In conclusion, the validated methods are suitable to assay MTX in pH-sensitive CS-NPs without any interference from the polymer or surfactant.
dc.format.extent9 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec644826
dc.identifier.issn2309-4435
dc.identifier.urihttps://hdl.handle.net/2445/97209
dc.language.isoeng
dc.publisherPharma Publisher
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.14205/2309-4435.2014.02.02.3
dc.relation.ispartofJournal of Applied Biopharmaceutics and Pharmacokinetics , 2014, vol. 2, num. 2, p. 59-67
dc.relation.urihttp://dx.doi.org/10.14205/2309-4435.2014.02.02.3
dc.rightscc-by-nc (c) Nogueira D.R. et al., 2014
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es
dc.sourceArticles publicats en revistes (Bioquímica i Fisiologia)
dc.subject.classificationQuitosan
dc.subject.classificationNanopartícules
dc.subject.classificationMedicaments antineoplàstics
dc.subject.classificationMetotrexat
dc.subject.classificationAgents tensioactius
dc.subject.classificationCromatografia
dc.subject.classificationEspectroscòpia
dc.subject.otherChitosan
dc.subject.otherNanoparticles
dc.subject.otherAntineoplastic agents
dc.subject.otherMethotrexate
dc.subject.otherSurface active agents
dc.subject.otherChromatography
dc.subject.otherSpectrum analysis
dc.titleDetermination of Methotrexate in pH-Sensitive Chitosan Nanoparticles by Validated RP-LC and UV Spectrophotometric Methods
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Carregant...
Miniatura
Nom:
644826.pdf
Mida:
352.73 KB
Format:
Adobe Portable Document Format