Analytical Method Development
Protein Characterization
Solid-State Characterization
Stability-Indicating Analytical Methods
Identification of Impurities and Degradation Products
Additional Analytical Applications


>
CASE STUDY 1
Parenteral dosage form development of a highly insoluble molecule
>
CASE STUDY 2
Salt form optimization and lyophilized parenteral formulation development
>
CASE STUDY 3
Oral liquid formulation development
>
CASE STUDY 4
Accelerated stability studies to support a screening IND
>
CASE STUDY 5
Lead Optimization: Solubility and formulation screen for efficacy and PK studies

Analytical Method Development

Analytical support is required for a variety of purposes: at different stages of a drug development cycle, in synthesis and manufacturing, for quality control and assurance, and for other applications. 

Wolfe Laboratories Inc. develops and qualifies many types of analytical methods for its clients and the methods are tailored to project requirements.  For example, qualitative assessment of solubility properties among a series of analogous compounds may be appropriate for a pre-nomination program.  The data generated with such a method will be used to construct a relative rank-order of compounds in a series.  Alternatively, rigorous quantitative measurement of properties of a compound nominated for clinical development may be needed.  WLI excels at determination of thermodynamic solubility properties of compounds during pre-formulation and formulation development.

Typical analytical methods consist of two components: separation and detection.  The majority of analytical methods used at Wolfe Laboratories are based on liquid chromatographic separation using common separation techniques.  These include reverse and normal phase chromatography, size exclusion chromatography, and ion-exchange chromatography.  Several types of detectors are available and their use is determined by properties of the analyte. 

 

© 2004 Wolfe Laboratories, Inc. All rights reserved.