1980
DOI: 10.1002/jps.2600690412
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Digoxin Degradation in Acidic Dissolution Medium

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1982
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Cited by 20 publications
(5 citation statements)
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“…For dihydrodigoxigenin, the reported cross-reactivity for the FPIA method (91%) was considerably greater than that reported for RIA methods (Gault et al 1982). The FPIA method requires serum proteins to be precipitated with 5-sulphosalicylic acid (Skogen et al 1987) which has been suggested to result in the transformation of digoxin and its metabolites to digoxigenin and/or dihydrodigoxigenin (Sonobe et al 1980). It was therefore not surprising that the metabolites were not differentiated from the drug itself using this procedure.…”
Section: Discussionmentioning
confidence: 80%
“…For dihydrodigoxigenin, the reported cross-reactivity for the FPIA method (91%) was considerably greater than that reported for RIA methods (Gault et al 1982). The FPIA method requires serum proteins to be precipitated with 5-sulphosalicylic acid (Skogen et al 1987) which has been suggested to result in the transformation of digoxin and its metabolites to digoxigenin and/or dihydrodigoxigenin (Sonobe et al 1980). It was therefore not surprising that the metabolites were not differentiated from the drug itself using this procedure.…”
Section: Discussionmentioning
confidence: 80%
“…The activation energy and degradation rates were determined at various temperatures. Digoxin is known as very stable when kept in dark and well-closed containers, but it undergoes acid catalysed hydrolysis in water solutions [11,12]. The degradation products of digoxin hydrolysis are digoxigenin-bisdigitoxoside, digoxigenin-monotoxoside and digoxigenin.…”
Section: Introductionmentioning
confidence: 99%
“…Depending on analytical method used, it can be underestimated or overestimated. It has been reported in the literature that some of the drugs could be degraded during the dissolution study [9,11,12,14,16,21]. It is essential to know the amount of drug released and the amount of drug degraded during the dissolution study in the development of suitable formulation for the degrading drug and subsequent quality control of the developed product.…”
Section: Introductionmentioning
confidence: 99%
“…However, it is very difficult to measure the amount of degradation product accurately. Several mathematical approaches have been made to describe simultaneous dissolution and degradation [7,21].…”
Section: Introductionmentioning
confidence: 99%