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Development of novel stability indic...

Bansal, Parveen.

Development of novel stability indicating methods using liquid chromatography

Record Type:	Electronic resources : Monograph/item
Title/Author:	Development of novel stability indicating methods using liquid chromatographyby Mukesh Maithani, Parveen Bansal.
Author:	Maithani, Mukesh.
other author:	Bansal, Parveen.
Published:	Singapore :Springer Singapore :2019.
Description:	xxii, 101 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	Liquid chromatography.
Online resource:	https://doi.org/10.1007/978-981-13-8723-4
ISBN:	9789811387234$q(electronic bk.)

Development of novel stability indicating methods using liquid chromatography
Maithani, Mukesh.

Development of novel stability indicating methods using liquid chromatography[electronic resource] /by Mukesh Maithani, Parveen Bansal. - Singapore :Springer Singapore :2019. - xxii, 101 p. :ill., digital ;24 cm.

Chapter 1. Introduction -- Chapter 2. Research Envisaged -- Chapter 3. Drug(s) Profile -- Chapter 4. Materials and Methods -- Chapter 5. Results and Discussion -- Chapter 6. Summary and Conclusion.

Reversed-phase high-performance liquid chromatography (RP-HPLC) has become the most widely used method for pharmaceutical analysis, as it ensures accuracy, specificity and reproducibility for the quantification of drugs, while avoiding interference from any of the excipients that are normally present in pharmaceutical dosage forms. This book presents a simple methodology for developing stability-indicating methods and offers a 'how-to guide' to creating novel stability-indicating methods using liquid chromatography. It provides the detailed information needed to devise a stability-indicating method for drug substances and drug products that comply with international regulatory guidelines. As such, it is a must-read for anyone engaged in analytical and bioanalytical chemistry: professionals at reference, test, and control laboratories; students and academics at research laboratories, and scientists working for chemical, pharmaceutical, and biotechnology companies.

ISBN: 9789811387234$q(electronic bk.)

Standard No.: 10.1007/978-981-13-8723-4doiSubjects--Topical Terms:

193947
Liquid chromatography.

LC Class. No.: QD79.C454 / M35 2019

Dewey Class. No.: 543.84

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505 0 $a Chapter 1. Introduction -- Chapter 2. Research Envisaged -- Chapter 3. Drug(s) Profile -- Chapter 4. Materials and Methods -- Chapter 5. Results and Discussion -- Chapter 6. Summary and Conclusion.
520 $a Reversed-phase high-performance liquid chromatography (RP-HPLC) has become the most widely used method for pharmaceutical analysis, as it ensures accuracy, specificity and reproducibility for the quantification of drugs, while avoiding interference from any of the excipients that are normally present in pharmaceutical dosage forms. This book presents a simple methodology for developing stability-indicating methods and offers a 'how-to guide' to creating novel stability-indicating methods using liquid chromatography. It provides the detailed information needed to devise a stability-indicating method for drug substances and drug products that comply with international regulatory guidelines. As such, it is a must-read for anyone engaged in analytical and bioanalytical chemistry: professionals at reference, test, and control laboratories; students and academics at research laboratories, and scientists working for chemical, pharmaceutical, and biotechnology companies.
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