Rapid Identification and Characterization of Formulated Protein Products by Raman Spectroscopy Coupled with Discriminant Analysis

PDA J Pharm Sci Technol. 2016 Jan-Feb;70(1):62-75. doi: 10.5731/pdajpst.2015.005769. Epub 2016 Jan 21.

Abstract

The rapid identification of protein drug products for packaging and receiving can significantly reduce disposition cycle time, and thereby improve the efficiency and productivity of the supply chain to better meet the needs of patients. In this feasibility study, we demonstrate a novel methodology that combines Raman spectroscopy with discriminant analysis that can be used for rapid identification or verification of finished products. With this methodology, Raman spectra of formulated therapeutic proteins were collected non-invasively with the samples either in a quartz cuvette or in the original glass vials, and analyzed without subtraction of buffer or placebo solutions. The algorithm used for the discriminant analysis was Mahalanobis distance by principal component analysis with residuals. In addition to product identification, the methodology has the potential to be used for characterizing formulated proteins when exposed to external stresses based on the changes of Mahalanobis distances.

Lay abstract: The rapid identification of protein drug products for packaging and receiving can significantly reduce disposition cycle time, and thereby improve the efficiency and productivity of the supply chain. In this study, we demonstrate a novel methodology that combines Raman spectroscopy with discriminant analysis to rapidly identify formulated proteins non-invasively.

Keywords: Discriminant analysis; Formulated protein products; Mahalanobis distance; Principal component analysis; Raman spectroscopy; Rapid characterization; Rapid identification.

MeSH terms

  • Discriminant Analysis
  • Drug Compounding
  • Humans
  • Immunoglobulin G / analysis
  • Proteins / analysis*
  • Proteins / chemical synthesis
  • Recombinant Fusion Proteins / analysis
  • Spectrum Analysis, Raman / methods*
  • Time Factors

Substances

  • Immunoglobulin G
  • Proteins
  • Recombinant Fusion Proteins
  • peptibody A