Literature DB >> 27017836

Pharmaceutical Perspective on Opalescence and Liquid-Liquid Phase Separation in Protein Solutions.

Ashlesha S Raut1, Devendra S Kalonia1.   

Abstract

Opalescence in protein solutions reduces aesthetic appeal of a formulation and can be an indicator of the presence of aggregates or precursor to phase separation in solution signifying reduced product stability. Liquid-liquid phase separation of a protein solution into a protein-rich and a protein-poor phase has been well-documented for globular proteins and recently observed for monoclonal antibody solutions, resulting in physical instability of the formulation. The present review discusses opalescence and liquid-liquid phase separation (LLPS) for therapeutic protein formulations. A brief discussion on theoretical concepts based on thermodynamics, kinetics, and light scattering is presented. This review also discusses theoretical concepts behind intense light scattering in the vicinity of the critical point termed as "critical opalescence". Both opalescence and LLPS are affected by the formulation factors including pH, ionic strength, protein concentration, temperature, and excipients. Literature reports for the effect of these formulation factors on attractive protein-protein interactions in solution as assessed by the second virial coefficient (B2) and the cloud-point temperature (Tcloud) measurements are also presented. The review also highlights pharmaceutical implications of LLPS in protein solutions.

Keywords:  B2; Tcloud; aggregation; crystallization; formulation; light scattering; liquid−liquid phase separation; opalescence; phase diagram; protein−protein interactions; stability; thermodynamics

Mesh:

Substances:

Year:  2016        PMID: 27017836     DOI: 10.1021/acs.molpharmaceut.5b00937

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  15 in total

1.  Predicting Protein-Protein Interactions of Concentrated Antibody Solutions Using Dilute Solution Data and Coarse-Grained Molecular Models.

Authors:  Cesar Calero-Rubio; Ranendu Ghosh; Atul Saluja; Christopher J Roberts
Journal:  J Pharm Sci       Date:  2017-12-21       Impact factor: 3.534

2.  Understanding the Role of Preferential Exclusion of Sugars and Polyols from Native State IgG1 Monoclonal Antibodies and its Effect on Aggregation and Reversible Self-Association.

Authors:  Chaitanya M Sudrik; Theresa Cloutier; Neil Mody; Hasige A Sathish; Bernhardt L Trout
Journal:  Pharm Res       Date:  2019-05-24       Impact factor: 4.200

3.  Nanobubbles in Reconstituted Lyophilized Formulations: Interaction With Proteins and Mechanism of Formation.

Authors:  Jared R Snell; N S Krishna Kumar; Raj Suryanarayanan; Theodore W Randolph
Journal:  J Pharm Sci       Date:  2019-05-13       Impact factor: 3.534

4.  Regulation of Transmembrane Signaling by Phase Separation.

Authors:  Lindsay B Case; Jonathon A Ditlev; Michael K Rosen
Journal:  Annu Rev Biophys       Date:  2019-04-05       Impact factor: 12.981

Review 5.  Methods for Physical Characterization of Phase-Separated Bodies and Membrane-less Organelles.

Authors:  Diana M Mitrea; Bappaditya Chandra; Mylene C Ferrolino; Eric B Gibbs; Michele Tolbert; Michael R White; Richard W Kriwacki
Journal:  J Mol Biol       Date:  2018-07-24       Impact factor: 5.469

6.  Evaluating the Effects of Hinge Flexibility on the Solution Structure of Antibodies at Concentrated Conditions.

Authors:  Marco A Blanco; Harold W Hatch; Joseph E Curtis; Vincent K Shen
Journal:  J Pharm Sci       Date:  2018-12-26       Impact factor: 3.534

7.  Predicting structural properties of fluids by thermodynamic extrapolation.

Authors:  Nathan A Mahynski; Sally Jiao; Harold W Hatch; Marco A Blanco; Vincent K Shen
Journal:  J Chem Phys       Date:  2018-05-21       Impact factor: 3.488

Review 8.  Multiple Modes of Protein-Protein Interactions Promote RNP Granule Assembly.

Authors:  Tanja Mittag; Roy Parker
Journal:  J Mol Biol       Date:  2018-08-09       Impact factor: 5.469

9.  Web-based display of protein surface and pH-dependent properties for assessing the developability of biotherapeutics.

Authors:  Max Hebditch; Jim Warwicker
Journal:  Sci Rep       Date:  2019-02-13       Impact factor: 4.379

10.  Stability of a high-concentration monoclonal antibody solution produced by liquid-liquid phase separation.

Authors:  Jack E Bramham; Stephanie A Davies; Adrian Podmore; Alexander P Golovanov
Journal:  MAbs       Date:  2021 Jan-Dec       Impact factor: 5.857

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