Development and Validation of Analytical Method for lower dosage form: Different Spectrophotometric and Chromatographic methods for Quantification of Rasagiline - Couverture souple

Vaishnani, Bhavinkumar

 
9783844384284: Development and Validation of Analytical Method for lower dosage form: Different Spectrophotometric and Chromatographic methods for Quantification of Rasagiline
Couverture souple
ISBN 10 : 3844384286 ISBN 13 : 9783844384284
Editeur : LAP LAMBERT Academic Publishing, 2011

Synopsis

To meet the emerging challenges of 21st century, the number of drugs introduced into the global pharmaceutical market is increasing every year. The focus on research and development of the drug molecule is to introduce either new entities or partial structural modification of the existing one to improve its potency and/or to reduce its adverse effect. Very often there is a time lag from the date of introduction of a drug into the market to the date of its inclusion in pharmacopoeias. This happens because of the possible uncertainties in the continuous and wider usage of these drugs, reports of new toxicities (resulting in their withdrawal from the market), development of patient resistance and introduction of better drugs by the competitors. Under these conditions, standard analytical procedures for these drugs may not be available in the pharmacopoeias. The analysis of high-potency, low-strength solid oral dosage forms poses a number of analytical challenges that can impact potency, purity and dissolution testing of the dosage form.

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Présentation de l'éditeur

To meet the emerging challenges of 21st century, the number of drugs introduced into the global pharmaceutical market is increasing every year. The focus on research and development of the drug molecule is to introduce either new entities or partial structural modification of the existing one to improve its potency and/or to reduce its adverse effect. Very often there is a time lag from the date of introduction of a drug into the market to the date of its inclusion in pharmacopoeias. This happens because of the possible uncertainties in the continuous and wider usage of these drugs, reports of new toxicities (resulting in their withdrawal from the market), development of patient resistance and introduction of better drugs by the competitors. Under these conditions, standard analytical procedures for these drugs may not be available in the pharmacopoeias. The analysis of high-potency, low-strength solid oral dosage forms poses a number of analytical challenges that can impact potency, purity and dissolution testing of the dosage form.

Biographie de l'auteur

Bhavinkumar K. Vaishnani, M.Pharmacy (Quality Assurance)from Rajiv Gandhi University of Health Science, Bangalore, INDIA

Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.

Éditeur
LAP LAMBERT Academic Publishing
Date d'édition
2011
Langue
anglais
ISBN 10 
3844384286
ISBN 13 
9783844384284
Reliure
Broché
Nombre de pages
188
Coordonnées du fabricant
non disponible
Personne responsable
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