Control of Enantiomeric purity of Pharmaceuticals
using Liquid Chromatography
(Sprache: Englisch)
Dosage concentration of a racemic drug is an illusion to the patients as well to the practicing physicians because they are not aware of the fact that the two enantiomers have different pharmacodynamics and pharmacokinetics. Thus, the production and...
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Dosage concentration of a racemic drug is an illusion to the patients as well to the practicing physicians because they are not aware of the fact that the two enantiomers have different pharmacodynamics and pharmacokinetics. Thus, the production and marketing of pure enantiomeric drug is of critical importance. USFDA and other regulatory agencies require complete information on both the enantiomers along with the details of methods of separation and control of enantiomeric purity before a new enantiomeric mixture is approved. Therefore, the development of reliable and sensitive analytical methods are gaining importance and are the need of the hour. This publication reports several such new methods using liquid chromatography.
Autoren-Porträt von Manisha Singh
Singh, ManishaDr. Manisha Singh has completed her Ph.D (Chemistry) from Indian Institute of Technology Roorkee, Roorkee, India. She has received M.Sc in Organic Chemistry from Deen Dayal Upadhyaya Gorakhpur University, Gorakhpur, India. She is currently working as an Assistant Professor in Lovely Professional University Phagwara, Punjab.
Bibliographische Angaben
- Autor: Manisha Singh
- 2018, 136 Seiten, Maße: 22 cm, Kartoniert (TB), Englisch
- Verlag: LAP Lambert Academic Publishing
- ISBN-10: 6139867371
- ISBN-13: 9786139867370
Sprache:
Englisch
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