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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 ...
Handbook of Pharmaceutical excipients
(Libros Digitales - Pharmaceutical Press, 2009)
Pharmaceutical dosage forms contain both pharmacologically
active compounds and excipients added to aid the formulation
and manufacture of the subsequent dosage form for administration
to patients. Indeed, the properties ...
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 ...
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 ...
Preparation and characterization of purified Na-activated bentonite from Karak (Pakistan) for pharmaceutical use
(Middlesex, 2013)
The purpose of this paper was to prepare purified Na- bentonite with improved properties for use in the pharmaceutical industry. Calcium bentonite from the Shagia region of Karak district, Pakistan, was activated with ...
Bacterial nano cellulose as non-active pharmaceutical ingredient: Advances and perspectives
(MedCrave, 2018-11)
Nano Cellulose is commonly produced by the top-down enzymatic, mechanical and/or chemical treatments. In contrast, Bacterial Nano Cellulose (BNC) can be obtained by a bottom-up approach, where is biosynthesized from glucose ...
Propolis Standardized Extract (EPP-AF (R)), an Innovative Chemically and Biologically Reproducible Pharmaceutical Compound for Treating Wounds
(Ivyspring Int Publ, 2012-01-01)
The aim of this study was to develop a formulation, containing the propolis standardized extract (EPP-AF (R)), which can assist in the healing of skin lesions. To achieve this objective the antimicrobial activity and ...
Propolis Standardized Extract (EPP-AF (R)), an Innovative Chemically and Biologically Reproducible Pharmaceutical Compound for Treating Wounds
(Ivyspring Int Publ, 2012-01-01)
The aim of this study was to develop a formulation, containing the propolis standardized extract (EPP-AF (R)), which can assist in the healing of skin lesions. To achieve this objective the antimicrobial activity and ...
Analysis of low molecular weight compounds using MALDI- and LDI-TOF-MS: Direct detection of active pharmaceutical ingredients in different formulations
(2017-11-01)
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a high throughput, easy to use analytical technique. The simple sample preparation of this technique and its tolerance to the presence of contaminants ...