Literature DB >> 20845460

Determination of the influence of primary drying rates on the microscale structural attributes and physicochemical properties of protein containing lyophilized products.

Andrew Parker1, Shellie Rigby-Singleton, Mark Perkins, David Bates, Delphine Le Roux, Clive J Roberts, Claire Madden-Smith, Lavinia Lewis, Dirk L Teagarden, Robert E Johnson, Saleem S Ahmed.   

Abstract

This work investigated the impact of primary drying conditions on the microstructure and protein stability of bovine serum albumin (BSA) containing lyophilized cakes. Two primary drying conditions were employed (termed 'conservative', slower drying rate and 'aggressive', higher drying rate) at two protein loadings (5 and 50 mg mL(-1)). The cake attributes were characterized using micro-X-ray computed tomography (micro-CT), scanning electron microscopy, manometric temperature measurements, Fourier transform infrared spectroscopy (FTIR) and size exclusion chromatography (SEC). The combination of analytical techniques revealed that although the aggressive drying conditions produced intact cakes which retained their macrostructure, they had undergone various degrees of microcollapse. The study demonstrates the applicability of micro-CT for resolving microstructural attributes of the freeze-dried cakes such as residual porosity, pore size distribution and connectivity. Micro-CT data showed significant differences in residual porosity and matrix connectivity between aggressively and conservatively dried cakes. The FTIR data show that at each protein loading, there is no observable difference in the secondary structure of the protein and the SEC data show comparable stability in the cakes produced under different primary drying conditions. Good content uniformity was observed with respect to BSA and sucrose distribution in the cakes.
© 2010 Wiley-Liss, Inc. and the American Pharmacists Association

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Year:  2010        PMID: 20845460     DOI: 10.1002/jps.22185

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  5 in total

1.  Characterizing the freeze-drying behavior of model protein formulations.

Authors:  Lavinia M Lewis; Robert E Johnson; Megan E Oldroyd; Saleem S Ahmed; Liji Joseph; Ilie Saracovan; Sandipan Sinha
Journal:  AAPS PharmSciTech       Date:  2010-11-06       Impact factor: 3.246

2.  Studying the morphology of lyophilized protein solids using X-ray micro-CT: effect of post-freeze annealing and controlled nucleation.

Authors:  Ken-ichi Izutsu; Etsuo Yonemochi; Chikako Yomota; Yukihiro Goda; Haruhiro Okuda
Journal:  AAPS PharmSciTech       Date:  2014-05-31       Impact factor: 3.246

3.  Effects of Drying Process on an IgG1 Monoclonal Antibody Using Solid-State Hydrogen Deuterium Exchange with Mass Spectrometric Analysis (ssHDX-MS).

Authors:  Ehab M Moussa; Nathan E Wilson; Qi Tony Zhou; Satish K Singh; Sandeep Nema; Elizabeth M Topp
Journal:  Pharm Res       Date:  2018-01-03       Impact factor: 4.200

4.  Process and Formulation Effects on Protein Structure in Lyophilized Solids Using Mass Spectrometric Methods.

Authors:  Lavanya K Iyer; Gregory A Sacha; Balakrishnan S Moorthy; Steven L Nail; Elizabeth M Topp
Journal:  J Pharm Sci       Date:  2016-04-01       Impact factor: 3.534

5.  Optical coherence tomography-based freeze-drying microscopy.

Authors:  Mircea Mujat; Kristyn Greco; Kristin L Galbally-Kinney; Daniel X Hammer; R Daniel Ferguson; Nicusor Iftimia; Phillip Mulhall; Puneet Sharma; Michael J Pikal; William J Kessler
Journal:  Biomed Opt Express       Date:  2011-12-07       Impact factor: 3.732

  5 in total

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