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A study of the stability of ranitidineHaywood, P. A. January 1987 (has links)
No description available.
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Shelf-life designing and analysing stability trials /Kiermeier, Andreas. January 2003 (has links)
Thesis (Ph.D.)--University of Adelaide, School of Agriculture and Wine, Biometrics SA, 2004. / "December 2003" Title from screen page; viewed 7 Feb 2005. Includes bibliographical references. Also available in print form.
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The hydrolysis of cirazoline and the mechanism of stabilization by SDDSJones, Christopher Buchan January 1988 (has links)
No description available.
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The degradation of drugs in formaldehydeJames, Devona Gwen, January 1999 (has links)
Thesis (M.S.)--West Virginia University, 1999. / Title from document title page. Document formatted into pages; contains xvi, 100 p. : ill. Vita. Includes abstract. Includes bibliographical references (p. 98-99).
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Empirical and Kinetic Models for the Determination of Pharmaceutical Product StabilityKhalifa, Nagwa 24 January 2011 (has links)
Drug stability is one of the vital subjects in the pharmaceutical industry. All drug products should be kept stable and protected against any chemical, physical, and microbiological degradation to ensure their efficacy and safety until released for public use. Hence, stability is very important to be estimated or predicted.
This work involved studying the stability of three different drug agents using three different mathematical models. These models included both empirical models (linear regression and artificial neural network), and mechanistic (kinetic) models. The stability of each drug in the three cases studied was expressed in terms of concentration, hardness, temperature and humidity. The predicted values obtained from the models were compared to the observed values of drug concentrations obtained experimentally and then evaluated by calculating the mean of squared.
Among the models used in this work, the mechanistic model was found to be the most accurate and reliable method of stability testing given the fact that it had the smallest calculated errors.
Overall, the accuracy of these mathematical models as indicated by the proximity of their stability measurements to the observed values, led to the assumption that such models can be reliable and time-saving alternatives to the analytical techniques used in practice.
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Empirical and Kinetic Models for the Determination of Pharmaceutical Product StabilityKhalifa, Nagwa 24 January 2011 (has links)
Drug stability is one of the vital subjects in the pharmaceutical industry. All drug products should be kept stable and protected against any chemical, physical, and microbiological degradation to ensure their efficacy and safety until released for public use. Hence, stability is very important to be estimated or predicted.
This work involved studying the stability of three different drug agents using three different mathematical models. These models included both empirical models (linear regression and artificial neural network), and mechanistic (kinetic) models. The stability of each drug in the three cases studied was expressed in terms of concentration, hardness, temperature and humidity. The predicted values obtained from the models were compared to the observed values of drug concentrations obtained experimentally and then evaluated by calculating the mean of squared.
Among the models used in this work, the mechanistic model was found to be the most accurate and reliable method of stability testing given the fact that it had the smallest calculated errors.
Overall, the accuracy of these mathematical models as indicated by the proximity of their stability measurements to the observed values, led to the assumption that such models can be reliable and time-saving alternatives to the analytical techniques used in practice.
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Mechanistic studies of physico-chemical stability of model therapeutic proteins using pharmaceutically relevant factors /Roy, Shouvik. January 2006 (has links)
Thesis (Ph.D. in Pharmaceutical Sciences) -- University of Colorado at Denver and Health Sciences Center, 2006. / Typescript. Includes bibliographical references (leaves 161-173). Free to UCDHSC affiliates. Online version available via ProQuest Digital Dissertations;
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Towards a mechanistic understanding of pharmaceutical protein stabilization in solution and the solid state /Katayama, Derrick S. January 2006 (has links)
Thesis (Ph.D. in Pharmaceutical Sciences) -- University of Colorado at Denver and Health Sciences Center, 2006. / Typescript. Includes bibliographical references (leaves 159-173). Free to UCDHSC affiliates. Online version available via ProQuest Digital Dissertations;
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Stability of drugs in pharmaceuticals : kinetics and mechanisms of hydrolysis in liposomal suspensions and aqueous solutions /D'Silva, Joseph B., January 1981 (has links)
No description available.
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The effects of temperature and admixture handling on lipid emulsion stability in centrally administered veterinary parenteral nutrition (PN) admixturesThomovsky, Elizabeth. January 2008 (has links)
Thesis (M.S.)--University of Missouri-Columbia, 2008. / "May 2008" The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Includes bibliographical references.
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