Show simple item record

dc.creatorMennickent C,Sigrid
dc.creatorYates K,Tamara
dc.creatorVega H,Mario
dc.creatorGodoy M,C Gloria
dc.creatorSaelzer F,Roberto
dc.date2002-04-01
dc.date.accessioned2020-02-17T15:28:52Z
dc.date.available2020-02-17T15:28:52Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0034-98872002000400008
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/128185
dc.descriptionBackground: The chemical stability of a pharmaceutical product depends, among other factors, on environmental factors during transport, storage and manipulation of the product. Aim: To study the chemical stability of acetylsalicylic acid (AAS) tablets during ten months of storage in five pharmacies of Concepción, Chile. Material and methods: Tablets were randomly collected at the beginning of the study and at the third, sixth and tenth month. Quantitative analyses of AAS tablets was carried out by instrumental thin layer chromatography (HPTLC). Results: AAS in tablets was between 99 and 109% at the beginning of the study, between 76 and 110% at three months, between 71% and 112% at six months and between 86 and 110% at ten months of storage. Conclusions: There was a progressive decrease in the content of acetylsalicylic acid in tables during storage, but it remained between the limits accepted by the United States Pharmacopoeia (USP) (90-110%) (Rev Méd Chile 2002; 130: 409-415)
dc.formattext/html
dc.languagees
dc.publisherSociedad Médica de Santiago
dc.relation10.4067/S0034-98872002000400008
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceRevista médica de Chile v.130 n.4 2002
dc.subjectAspirin
dc.subjectHigh performance thin layer chromatography
dc.subjectDrug stability
dc.subjectDrug delivery systems
dc.subjectDrug storage
dc.titleEstudio de la estabilidad química de comprimidos de ácido acetilsalicílico mediante un control de estanterías en farmacias de Concepción, Chile


This item appears in the following Collection(s)

Show simple item record