Handbook of pharmaceutical analysis /
edited by Lena Ohannesian, Anthony J. Streeter.
- New York : Marcel Dekker, c2002.
- xii, 585 p. : ill. ; 24 cm.
- Drugs and the pharmaceutical sciences ; v. 117 .
Rev. ed. of: Pharmaceutical analysis / edited by James W. Munson. c1981-1984.
Includes bibliographical references and indexes.
Form selection of pharmaceutical compounds --
Preparation of drug samples for analysis --
High-performance liquid chromatography --
Mass spectroscopy in pharmaceutical analysis --
Ultraviolet-visible spectroscopy --
Immunoassay techniques --
Application of capillary electrophoresis technology in the pharmaceutical industry --
Atomic spectroscopy --
uminescence spectroscopy --
Solid-state nuclear magnetic resonance spectroscopy --
Vibrational spectroscopy --
Statistical considerations in pharmaceutical process development and validation. Table of contents
Summary:
Exploring the analysis of pharmaceuticals, including polymorphic forms. This book discusses regulatory requirements in pharmaceutical product development and pharmaceutical testing. It covers methods of drug separation and procedures such as capillary electrophoresis for chromatographic separation of molecules.
0824704622 (alk. paper) 9780824704629
2001052780
Drugs--Analysis.
Pharmaceutical Preparations--analysis.
Chromatography--methods.
Spectrum Analysis--methods.
RS189 / .P44 2002
615.1901 / HAN 2002
W1 / DR893B v.117 2002 QV 25 / H2367 2002
Rev. ed. of: Pharmaceutical analysis / edited by James W. Munson. c1981-1984.
Includes bibliographical references and indexes.
Form selection of pharmaceutical compounds --
Preparation of drug samples for analysis --
High-performance liquid chromatography --
Mass spectroscopy in pharmaceutical analysis --
Ultraviolet-visible spectroscopy --
Immunoassay techniques --
Application of capillary electrophoresis technology in the pharmaceutical industry --
Atomic spectroscopy --
uminescence spectroscopy --
Solid-state nuclear magnetic resonance spectroscopy --
Vibrational spectroscopy --
Statistical considerations in pharmaceutical process development and validation. Table of contents
Summary:
Exploring the analysis of pharmaceuticals, including polymorphic forms. This book discusses regulatory requirements in pharmaceutical product development and pharmaceutical testing. It covers methods of drug separation and procedures such as capillary electrophoresis for chromatographic separation of molecules.
0824704622 (alk. paper) 9780824704629
2001052780
Drugs--Analysis.
Pharmaceutical Preparations--analysis.
Chromatography--methods.
Spectrum Analysis--methods.
RS189 / .P44 2002
615.1901 / HAN 2002
W1 / DR893B v.117 2002 QV 25 / H2367 2002