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Impurities and Forced Degradation Studies: A Review
(Bentham Science Publ Ltd, 2016-01-01)
The safety of pharmaceuticals is dependent not only on the intrinsic toxicological properties of the active ingredient, but also on the impurities and degradation products that it may contain. The presence of impurities ...
Impurities and forced degradation studies: A review
(2016-01-01)
The safety of pharmaceuticals is dependent not only on the intrinsic toxicological properties of the active ingredient, but also on the impurities and degradation products that it may contain. The presence of impurities ...
Assessment of Pharmaceutical Equivalence: Difference Test or Equivalence Test?
(COLEGIO FARMACEUTICOS PROVINCIA DE BUENOS AIRESLA PLATA, 2012)
Pharmaceutical equivalence is an important step towards the confirmation of similarity and Interchangeability among pharmaceutical products, particularly regarding those that win not be tested for bioequivalence. The aim ...
Chemometrics coupled to vibrational spectroscopy and spectroscopic imaging for the analysis of solid-phase pharmaceutical products: A brief review on non-destructive analytical methods
(Elsevier, 2018-11)
This brief review reports on selected case studies aimed at verifying the authenticity of medicinal products, content uniformity of tablets and polymorphic forms in final products, and monitoring pharmaceutical cocrystallization ...
Identification of rupatadine fumarate polymorphic crystalline forms in pharmaceutical raw materials
(2018)
Polymorphism analysis of pharmaceutical raw materials is considered one of the most relevant
evaluations that should be done. As we know, different crystal forms from the same molecule have
differences in terms of their ...
Advances and challenges in nanocarriers and nanomedicines for veterinary application
(2020-04-30)
To ensure success in the development and manufacturing of nanomedicines requires forces of an interdisciplinary team that combines medicine, engineering, chemistry, biology, material and pharmaceutical areas. Numerous ...
DEVELOPMENT AND ASSESSMENT OF SPECTROSCOPY METHODOLOGIES AND CHEMOMETRICS STRATEGIES TO DETECT PHARMACEUTICALS BLEND ENDPOINT IN A PHARMACEUTICAL POWDER BLEND
(SOC CHILENA QUIMICA, 2021)
Manufacturing pharmaceutical products is one of the most regulated industrial processes due to the importance of its effects on human health. These processes require many physical and chemical determinations through ...
Spectrophotometric determination of methyldopa in pharmaceutical formulations
(2005-07-01)
A new, simple, precise, rapid and low-cost spectrophotometric method for methyldopa determination in pharmaceutical preparations is described. This method is based on the complexation reaction of methyldopa with molybdate. ...
Spectrophotometric determination of methyldopa in pharmaceutical formulations
(2005-07-01)
A new, simple, precise, rapid and low-cost spectrophotometric method for methyldopa determination in pharmaceutical preparations is described. This method is based on the complexation reaction of methyldopa with molybdate. ...