Biophysical Characterization for Product Comparability - Spectroscopic methods such as circular dichroism can detect subtle differences in higher order structure before and after changes in process

ADVERTISEMENT

Biophysical Characterization for Product Comparability
Spectroscopic methods such as circular dichroism can detect subtle differences in higher order structure before and after changes in process and formulation.


BioPharm International Supplements


Acknowledgements

We thank James Carroll, John Steckert, and Ned Mozier for scientific discussion, and Zhaojiang Lu, Monica Brzezinski, Justin Sperry, Mike Dupuis, Min Huang, and Philip Boyle for technical assistance and material supply.

QIN ZOU, PHD, is a senior principal scientist in analytical research and development, BioTherapeutics Pharmaceutical Sciences, Pfizer Inc., Chesterfield, MO, 636.247.1257,
Yin Luo, PhD, is a director in analytical research and development, BioTherapeutics Pharmaceutical Sciences, Pfizer Inc., Andover, MA,

References

1. Rosenberg AS. Effects of protein aggregates: an immunologic perspective. AAPS J. 2006;8:E501–07.

2. US Food and Drug Administration. Guidance for Industry: Q5E Comparability of biotechnological/biological products subject to changes in their manufacturing process. Rockville, MD; 2005.

3. European Medical Association. Guideline on comparability of medical products containing biotechnology-derived proteins as active substance: quality issues. Geneva; Switzerland. 2003.

4. EMA. Guideline on similar biological medicinal products containg biotechnology-derived proteins as active substance: quality issues. Geneva, Switzerland; 2005.

5. Sreerama N, Woody RW. Estimation of protein secondary structure from circular dichroism spectra: Comparison of CONTIN, SELCON, and CDSSTR methods with an expanded reference set. Anal Biochem. 2000;287:252–60.

6. Tetin SY, et al. Accuracy of protein secondary structure determination from circular dichroism spectra based on immunoglobulin examples. Anal Biochem. 2000;321:183–7.

7. Khrapunov S. Circular dichroism spectroscopy has intrinsic limitations for protein secondary structure analysis. Anal Biochem. 2009;389:174–6.

8. Mächtle W. High-resolution, submicron particle size distribution analysis using gravitational-sweep sedimentation. Biophys J. 1999;76:1080–91.

9. Schuck P. Size-distribution analysis of macromolecules by sedimentation velocity ultracentrifugation and Lamm equation modeling. Biophys J. 2000;78:1606-19.

10. Stafford WF, Braswell EH. Sedimentation velocity, multi-speed method for analyzing polydisperse solutions. Biophys Chem. 2004;108:273–9.

11. Stafford WF, Sherwood PJ. Analysis of heterologous interacting systems by sedimentation velocity: Curve fitting algorithms for estimation of sedimentation coefficients, equilibrium and rate constants. Biophysical Chem. 2004;108:231–43.


blog comments powered by Disqus

ADVERTISEMENT

EMD Millipore Collaborates with PharmaCell on Large-Scale, Cell-Culture Systems
May 23, 2013
SCHOTT Introduces Cartridge Design for High-Speed Filling
May 23, 2013
Moscow Hosts IFPMA Biosimilars Conference
May 17, 2013
AbbVie and Alvine Will Collaborate on Celiac Disease Therapy
May 15, 2013
FDA Issues Pharmacoepidemiologic Safety Study Guidance
May 14, 2013
Upcoming Conferences
UPCOMING CONFERENCES

Access Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA | July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA | August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA | August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA | August 20-21, 2013
Request Brochure

See All Conferences >>

ADVERTISEMENT

Author Guidelines
FindPharma
Source: BioPharm International Supplements,
Click here