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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/19940
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dc.contributor.authorDima, Ines-
dc.date.accessioned2022-02-03T11:31:57Z-
dc.date.available2022-02-03T11:31:57Z-
dc.date.issued2012-
dc.identifier.citationDIMA, Ines. Capillary electrophoresis method for monitoring donepezil hydrochoride in plasma of patients treated for Alzheimer’s disease. In: MedEspera: the 4th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2012, p. 243.en_US
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/19940-
dc.description.abstractIntroduction: Donepezil is a prescription drug to treat mild, moderate, and severe stages of Alzheimer’s disease. By its selective and reversible inhibition on acetylcholinesterase especially in the brain, the peripheral effects are minimal. These aspects together with its lack of hepatotoxicity represent the advantages of using donepezil towards other drugs, becoming the first line therapy for this pathology. The secundary effects involve muscarinic cholinergic symptoms (nausea, vomit, diarrhea), as well as nicotinic N, (insomnia) and N (muscular cramps). Aim: The paper aims to find and validate a sensitive method for the assay of donepezil in plasma using a non-aqueous capillary electrophoresis method. Matherials and methods: Donepezil hydrochloride (PhEur.), methanol (HPLC isocratic grade), acetonitrile (HPLC grade), hexane and ammonium acetate of analytical purity were bought from Sigma, human plasma was obtained from the Haematological Institute in Bucharest. Agilent AG1610 capillary electrophoresis with diode array detector was used as main analytical instrument. Human plasma samples spiked with known amounts of donepezil were used for the bioanalytical validation of the method, which was performed according to the EMA guidelines. The method was also tested on real samples tor patients treated with donepezil. Results: The non-aqueous capillary electrophoresis method for the donepezil assay in plasma was performed using as a running buffer a mixture of methanol: acetonitrile (70:30) with 15 mM ammonium acetate, a silica PVA coated capillary (64 cm length, 50pm i.d.), 10 minutes 50 mbarr hydrodynamic injection, 30kV applied voltage; detection was performed at 315 nm (which lacks spectral interference of proteins), but the 268 and 220 nm wavelengths were also monitored. The sample were extracted with hexane from alkalinized 1:10 diluted plasma, dried under nitrogen flow, and then re-dissolved in a small amount of mobile phase. Limit of detection obtained was 0.5 pg/mL. Conclusions: The method is sensitive and can be applied to monitor donepezil hydrochloride plasma levels in patients treated for Alzheimer’s disease.en_US
dc.language.isoenen_US
dc.publisherState Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association, Scientific Association of Students and Young Doctorsen_US
dc.relation.ispartofMedEspera: The 4th International Medical Congress for Students and Young Doctors, May 17-19, 2012, Chisinau, Republic of Moldovaen_US
dc.subjectdonepezil hydrochlorideen_US
dc.subjectplasmatic levelen_US
dc.subjectnon-aqueous capillary electrophoresisen_US
dc.subjecttherapeutic monitoringen_US
dc.titleCapillary electrophoresis method for monitoring donepezil hydrochoride in plasma of patients treated for Alzheimer’s diseaseen_US
dc.typeOtheren_US
Appears in Collections:MedEspera 2012



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