Chromatography Research International

Analytical Method Development and Validation of Pharmaceutical Analysis Using Chromatographic Techniques


Publishing date
13 Jul 2012
Status
Published
Submission deadline
13 Jan 2012

Lead Editor

1Department of Analytical Chemistry, Faculty of Pharmacy, Ankara University, Tandogan, 06100 Ankara, Turkey

2Division of BioMolecular Analysis, Faculty of Sciences, VU University Amsterdam, De Boelelaan, 1081 HV Amsterdam, The Netherlands

3Biochemistry Division, Defence R&D Establishment (DRDE), Ministry of Defence, Government of India, Gwalior, India


Analytical Method Development and Validation of Pharmaceutical Analysis Using Chromatographic Techniques

Description

The science of separation and means for the development of chromatographic methods have continued to encourge study by numerous groups around the world. Since 1970, a large body of new and valuable information has become available. This has led to important insights and improvements relating to chromatographic column and method development. Many of the pioneers in this field have moved on to other areas, such as capillary electrophoresis, liquid, gas, and supercritical fluid chromatography, and field-flow fractionation.

Liquid chromatography can be applied to a greater variety of samples than any other separation techniques and is applicable to the extremely complex mixtures that scientists encounter in pharmaceutical and biological systems. Methods used in chromatographic pharmaceutical analysis must be sufficiently accurate, specific, sensitive, and precise to conform to the regulatory requirements as set out in the relevant guidelines of “The International Conference of Technical Requirements for the Registration of Pharmaceuticals for Human Use” (ICH), which are applied by the licensing authorities and by some pharmacopoeias. The implementation of concepts for rapid optimization should equally aid and support the planning of effective method development strategies as in daily practice at the laboratory bench.

Therefore, we invite authors to contribute original research articles as well as review articles in the following potential topics that include, but are not limited to:

  • LC method development
  • Chromatographic analysis of pharmaceuticals
  • Analysis of biochemical samples: proteins, nucleic acids, carbohydrates, and related compounds
  • Chiral separation
  • Quality control in pharmaceuticals, impurities, metabolites, and degradation products
  • Quantitation and method validation in chromatography

Before submission authors should carefully read over the journal's Author Guidelines, which are located at http://www.hindawi.com/journals/cri/guidelines/. Prospective authors should submit an electronic copy of their complete manuscript through the journal Manuscript Tracking System at http://mts.hindawi.com/ according to the following timetable:


Articles

  • Special Issue
  • - Volume 2012
  • - Article ID 948129
  • - Editorial

Analytical Method Development and Validation of Pharmaceutical Analysis Using Chromatographic Techniques

Bengi Uslu | Henk Lingeman | ... | Burcu Dogan-Topal
  • Special Issue
  • - Volume 2012
  • - Article ID 713273
  • - Research Article

Analysis of Some Biogenic Amines by Micellar Liquid Chromatography

Irena Malinowska | Katarzyna E. Stępnik
  • Special Issue
  • - Volume 2012
  • - Article ID 356216
  • - Research Article

Stability-Indicating RP-TLC/Densitometry Determination of Raloxifene Hydrochloride in Bulk Material and in Tablets

A. A. Shirkhedkar | J. K. Rajput | ... | S. J. Surana
  • Special Issue
  • - Volume 2012
  • - Article ID 806068
  • - Research Article

Development and Validation of Stability-Indicating GC-FID Method for the Quantitation of Memantine Hydrochloride and Its Nonchromophoric Impurities in Bulk and Pharmaceutical Dosages

Sanjay A. Jadhav | Shashikant B. Landge | ... | Vijayavitthal T. Mathad
  • Special Issue
  • - Volume 2012
  • - Article ID 162302
  • - Research Article

A Validated LC Method for Separation and Determination of Tetralone-4-O-β-D-Glucopyranoside and 4-Hydroxy-α-Tetralone in Ammannia multiflora

Harish C. Upadhyay | Ram K. Verma | Santosh K. Srivastava
  • Special Issue
  • - Volume 2012
  • - Article ID 437075
  • - Research Article

Pharmacokinetics of Single-Dose and Multi-Dose of Lovastatin/Niacin ER Tablet in Healthy Volunteers

Yan-yan Jia | Song Ying | ... | Yan-rong Zhu
  • Special Issue
  • - Volume 2012
  • - Article ID 610427
  • - Research Article

Development and Validation of Dissolution Test for Fluconazole Capsules by HPLC and Derivative UV Spectrophotometry

Josilene Chaves Ruela Corrêa | Cristina Duarte Vianna-Soares | Hérida Regina Nunes Salgado
  • Special Issue
  • - Volume 2012
  • - Article ID 157916
  • - Research Article

Development and Validation of Selective High-Performance Liquid Chromatographic Method Using Photodiode Array Detection for Estimation of Aconitine in Polyherbal Ayurvedic Taila Preparations

Nitin Dubey | Nidhi Dubey | Rajendra Mehta
  • Special Issue
  • - Volume 2012
  • - Article ID 846574
  • - Research Article

A Validated RP-HPLC Method for the Estimation of Pizotifen in Pharmaceutical Dosage Form

M. V. Basaveswara Rao | A. V. D Nagendrakumar | ... | N. Chandrasekhar

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