Handbook of Pharmaceutical Analysis by HPLC, 1st Edition,Satinder Ahuja,Michael Dong,ISBN9780120885473
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Volume 6: Handbook of Pharmaceutical Analysis by HPLC, 1st Edition

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Editor(s) : Ahuja  &   Dong  

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Imprint: Academic Press

ISBN: 9780120885473

Pages: 600

Dimensions: 240 X 165

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Key Features

* A complete reference guide to HPLC
* Describes best practices in HPLC and offers 'tricks of the trade' in HPLC operation and method development
* Reviews key HPLC pharmaceutical applications and highlights currents trends in HPLC ancillary techniques, sample preparations, and data handling

Description

High pressure liquid chromatography–frequently called high performance liquid chromatography (HPLC or, LC) is the premier analytical technique in pharmaceutical analysis and is predominantly used in the pharmaceutical industry. Written by selected experts in their respective fields, the Handbook of Pharmaceutical Analysis by HPLC Volume 6, provides a complete yet concise reference guide for utilizing the versatility of HPLC in drug development and quality control. Highlighting novel approaches in HPLC and the latest developments in hyphenated techniques, the book captures the essence of major pharmaceutical applications (assays, stability testing, impurity testing, dissolution testing, cleaning validation, high-throughput screening,

Readership

For laboratory analysts, researchers and managers in the pharmaceutical industry, academia and government agencies

Satinder Ahuja

Satinder Ahuja obtained his Ph.D. in analytical chemistry from the Philadelphia College of Pharmacy and Science. He serves as adjunct research professor at Pace University and is a consultant to pharmaceutical companies as president of Ahuja Consulting.

Affiliations and Expertise

Ahuja Consulting, Calabash, NC, USA

View additional works by Satinder Ahuja

Michael Dong

Affiliations and Expertise

Purdue Pharma, Ardsley, NY, USA

Handbook of Pharmaceutical Analysis by HPLC, 1st Edition

Overview (S. Ahuja).

Key concepts of HPLC in pharmaceutical analysis (R.D. Ornaf, M. Dong).

HPLC instrumentation: in pharmaceutical analysis: status, advances and trends (M. Dong).

HPLC columns for pharmaceutical analysis (U. Neue et al.).

Sample preparation for HPLC analysis of drug products (C.K. Choi, M.W. Dong).

HPLC method development (H.T. Rasmussen et al.).

Validation of HPLC methods in pharmaceutical analysis (A.S. Lister).

Ion Chromatography (C. Pohl).

How to be more successful with HPLC analysis:: practical aspects in HPLC operation (M.W. Dong).

Regulatory considerations in HPLC anaysis (C.F. Richardson, F. Erni).

HPLC system calibration for GMP compliance (M. Dong).

System validation: pre-installation, IQ, OQ and PQ (W.M. Reuter).

Assays and stability testing (A.W. Wong, A. Datla).

Impurity evaluation (T. Cecil, E. Shenin).

HPLC in dissolution testing (Q. Wang, V. Gray).

Cleaning validation using HPCL for analysis (A. Plasz).

LC/MS application in high throughput ADME screen (R. Kong).

Chiral separations (Y. Vander Heyden et al.).

Applications of LC/MS in pharmaceutical analysis (L.Z. Zhou).

Application of LC-MMR in Pharmaceutical Analysis (M-H. Wann).

Chromatography data systems (CDS) in the pharmaceutical laboratory; its history, advances and future direction (R. Mazzarese).

New developments in HPLC (D.M. Wagrowski-Diehl, S. Ahuja).
»
Handbook of Pharmaceutical Analysis by HPLC
 

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