Literature DB >> 25418950

Do not drop: mechanical shock in vials causes cavitation, protein aggregation, and particle formation.

Theodore W Randolph1, Elise Schiltz, Donn Sederstrom, Daniel Steinmann, Olivier Mozziconacci, Christian Schöneich, Erwin Freund, Margaret S Ricci, John F Carpenter, Corrine S Lengsfeld.   

Abstract

Industry experience suggests that g-forces sustained when vials containing protein formulations are accidentally dropped can cause aggregation and particle formation. To study this phenomenon, a shock tower was used to apply controlled g-forces to glass vials containing formulations of two monoclonal antibodies and recombinant human growth hormone (rhGH). High-speed video analysis showed cavitation bubbles forming within 30 μs and subsequently collapsing in the formulations. As a result of echoing shock waves, bubbles collapsed and reappeared periodically over a millisecond time course. Fluid mechanics simulations showed low-pressure regions within the fluid where cavitation would be favored. A hydroxyphenylfluorescein assay determined that cavitation produced hydroxyl radicals. When mechanical shock was applied to vials containing protein formulations, gelatinous particles appeared on the vial walls. Size-exclusion chromatographic analysis of the formulations after shock did not detect changes in monomer or soluble aggregate concentrations. However, subvisible particle counts determined by microflow image analysis increased. The mass of protein attached to the vial walls increased with increasing drop height. Both protein in bulk solution and protein that became attached to the vial walls after shock were analyzed by mass spectrometry. rhGH recovered from the vial walls in some samples revealed oxidation of Met and/or Trp residues.
© 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.

Entities:  

Keywords:  oxidation; particle size; protein aggregation; protein formulation; simulations; stability

Mesh:

Substances:

Year:  2014        PMID: 25418950      PMCID: PMC4312221          DOI: 10.1002/jps.24259

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


  20 in total

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Review 5.  Antibody structure, instability, and formulation.

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7.  Classification and characterization of therapeutic antibody aggregates.

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  12 in total

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2.  The Effect of Container Surface Passivation on Aggregation of Intravenous Immunoglobulin Induced by Mechanical Shock.

Authors:  Sanli Movafaghi; Hao Wu; Irene M Francino Urdániz; David S Bull; Mary D Kelly; Theodore W Randolph; Andrew P Goodwin
Journal:  Biotechnol J       Date:  2020-06-08       Impact factor: 4.677

3.  Surface-Templated Nanobubbles Protect Proteins from Surface-Mediated Denaturation.

Authors:  David S Bull; Daniel F Kienle; Andres F Chaparro Sosa; Nathaniel Nelson; Shambojit Roy; Jennifer N Cha; Daniel K Schwartz; Joel L Kaar; Andrew P Goodwin
Journal:  J Phys Chem Lett       Date:  2019-05-08       Impact factor: 6.475

4.  Protein Nanoparticles Promote Microparticle Formation in Intravenous Immunoglobulin Solutions During Freeze-Thawing and Agitation Stresses.

Authors:  Neha N Pardeshi; Chen Zhou; Theodore W Randolph; John F Carpenter
Journal:  J Pharm Sci       Date:  2018-03-27       Impact factor: 3.534

5.  Comparative Effects of Metal-Catalyzed Oxidizing Systems on Carbonylation and Integrity of Therapeutic Proteins.

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6.  Shocking Data on Parcel Shipments of Protein Solutions.

Authors:  Christine Siska; Paul Harber; Bruce A Kerwin
Journal:  J Pharm Sci       Date:  2019-11-02       Impact factor: 3.534

7.  Parameters Influencing Cavitation Within Vials Subjected to Drop Shock.

Authors:  Rafael Valotta Rodrigues; Meagen Puryear; Donn Sederstrom; Corinne S Lengsfeld
Journal:  Sci Rep       Date:  2019-12-16       Impact factor: 4.379

Review 8.  Posttranslational Modifications and the Immunogenicity of Biotherapeutics.

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9.  Influence of cavitation and high shear stress on HSA aggregation behavior.

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Review 10.  Thiyl Radical Reactions in the Chemical Degradation of Pharmaceutical Proteins.

Authors:  Christian Schöneich
Journal:  Molecules       Date:  2019-11-28       Impact factor: 4.411

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