dc.creatorRosasco, María Ana
dc.creatorBonafede, Silvina Laura
dc.creatorFaudone, Sonia Nerina
dc.creatorSegall, Adriana Ines
dc.date.accessioned2020-03-05T20:34:37Z
dc.date.accessioned2022-10-15T07:52:01Z
dc.date.available2020-03-05T20:34:37Z
dc.date.available2022-10-15T07:52:01Z
dc.date.created2020-03-05T20:34:37Z
dc.date.issued2018-12
dc.identifierRosasco, María Ana; Bonafede, Silvina Laura; Faudone, Sonia Nerina; Segall, Adriana Ines; Compatibility study of tobramycin and pharmaceutical excipients using differential scanning calorimetry, FTIR, DRX, and HPLC; Springer; Journal of Thermal Analysis and Calorimetry; 134; 3; 12-2018; 1929-1941
dc.identifier1388-6150
dc.identifierhttp://hdl.handle.net/11336/98880
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4362527
dc.description.abstractDifferential scanning calorimetry (DSC), isothermal stress testing–Fourier transform infrared spectroscopy (IST–FTIR), isothermal stress testing–high-performance liquid chromatography, and powder X-ray diffraction (PDRX) were used as screening techniques for assessing the compatibility of tobramycin with some currently employed ophthalmic excipients. In the first phase of the study, DSC was used as a tool to detect any interaction. The absolute value of the difference between the enthalpy of the pure tobramycin melting peak and that of its melting peak in the different analyzed mixtures was chosen as a parameter of the drug–excipient interaction degree. DSC results demonstrated that benzalkonium chloride, monobasic sodium phosphate, boric acid, edetate disodium, sodium metabisulfite, thimerosal, and potassium sorbate interact with tobramycin. Taking into account these results, it could be suggested that some of the changes observed in the IST–FTIR spectra of binary blends of tobramycin and some of the excipients would account for a possible interaction between the mixture component. In this study, PDRX did not provide much information, since only tobramycin–thimerosal interactions could be detected. DSC and IST–FTIR are suitable and simple methods for the detection of potential incompatibilities between active pharmaceutical ingredient (API) and excipients.
dc.languageeng
dc.publisherSpringer
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s10973-018-7282-z
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs10973-018-7282-z
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCOMPATIBILITY STUDIES
dc.subjectDSC
dc.subjectIST–FTIR
dc.subjectIST–HPLC
dc.subjectPDRX
dc.subjectTOBRAMYCIN
dc.titleCompatibility study of tobramycin and pharmaceutical excipients using differential scanning calorimetry, FTIR, DRX, and HPLC
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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