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Jul 4, 2009

Analytical

Dynamic avalanching accurately assesses flowability and quality

01 July 2009

Cefaclor is a β-lactam cephalosporin antibiotic that has a wide particle size distribution. Because of the nonporous nature of the material, the specific surface area value accounts for a significant amount of fine particles possibly present in the samples under analysis.

Particle size analysis

01 April 2009

An expert on diffraction systems offers insight on particle size specifications and analysis.

Characterizing amorphous materials with gravimetric vapour sorption techniques

01 April 2009

Even small amounts of amorphous materials can have a significant effect on the drug product. Are gravimetric vapour sorption techniques an effective solution to characterize amorphous materials?

LC–MS/MS method for the determination of Vitamin D3 in human plasma

01 March 2009

An LC–MS/MS method for the quantitative determination of vitamin D3 in human plasma has been developed and validated with positive atmospheric chemical ionization sources.

Ensuring raw material quality

01 March 2009

This month's expert examines the most appropriate technique for checking raw material quality. What technique would you recommend for quality checking of raw materials?

Breaking down the barriers

01 December 2008

The expanding role for X-ray powder diffraction in the pharmaceutical industry.

The counterfeit detective

01 September 2008

As counterfeiters become more cunning and technologically advanced, spotting their handiwork is increasingly difficult. Can surface analysis techniques be used to outwit them?

Handling difficult samples in bio-analytical chemical analysis

01 June 2008

There are two ways in which 'difficult' samples are usually categorized: either by the problems posed by the physical nature of the post-vivo sample matrix containing the chemical entity to be analysed, or...

The Problem with Stents

01 April 2008

Our company is involved in developing and manufacturing APIs that can be utilized with drug-eluting stents (DES). Despite ensuring constancy in pharmaceutical composition, we are experiencing issues with variations in drug release during in vitro studies. We are working closely with a stent manufacturer to develop the system, but could surface analysis techniques investigate the problem further?

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