Dosage Form Design Considerations

- Volume I

Forfatter: info mangler
Bog
  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

Dosage Form Design Parameters, Volume I, examines the history and current state of the field within the pharmaceutical sciences, presenting key developments. Content includes drug development issues, the scale up of formulations, regulatory issues, intellectual property, solid state properties and polymorphism. Written by experts in the field, this volume in the Advances in Pharmaceutical Product Development and Research series deepens our understanding of dosage form design parameters. Chapters delve into a particular aspect of this fundamental field, covering principles, methodologies and the technologies employed by pharmaceutical scientists. In addition, the book contains a comprehensive examination suitable for researchers and advanced students working in pharmaceuticals, cosmetics, biotechnology and related industries.

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Detaljer
  • SprogEngelsk
  • Sidetal820
  • Udgivelsesdato27-07-2018
  • ISBN139780128144237
  • Forlag Academic Press Inc
  • FormatHardback
Størrelse og vægt
  • Vægt2220 g
  • coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

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    Additives Pharmacokinetics Gastrointestinal Tract Bioavailability Safety Particle size determination Rheology Biopharmaceutics Patient compliance Cyclodextrins OPTIMIZATION Drug Discovery Pharmacodynamics Absorption Product Quality Cyclodextrin Drug transporters Product development Barriers Crystal Ionic Liquid Metabolic enzymes Interactions Mathematical explanations Drug disposition Evelopment Gras Pharmaceutical development Rheological Properties Quality by Design (QbD) Preformulation Preclinical Amorphous Dissolution Gut microbiota Clinical Studies Particle Size FDA Formulation development Pharmaceutical Prototyping Physicochemical properties Cytochrome P450 Drug Absorption Chemical stability Liquid Dosage Forms Absorption of drugs Bio-relevance Biopharmaceutical properties Biowaiver biological properties Complexation Cosolvent Enzyme induction Chemical nature of drug Dilation rheology drug properties Drug Product Performance enzyme inhibition Force degradation studies Controlled release delivery system CYP450 First-pass metabolism GIT fluids Distribution of drugs Drugs solubility Drug-excipient compatibility studies Environmental pH Excretion of drugs Meta-ion complex Factors affecting drug absorption Pharmaceutical product development Pharmaceutical scale-up P-Glycoprotein (p-GP) Physical stability physiological process Patented CRS Physiological factors Ich Guideline regulatory guideline Pharmaceutical product stability Protein binding kinetics Rheology measurements SUPAC Routes of administration Micromeritics Measuring protein binding Metabolism of drugs Rheology Modifiers Mucosal and nonmucosal barriers Pharmacokinetics parameters Physiological barriers Rheological features Pharmaceutical salts Plasma Protein Binding

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