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

被引:93
作者
Raut, Ashlesha S. [1 ]
Kalonia, Devendra S. [1 ]
机构
[1] Univ Connecticut, Dept Pharmaceut Sci, Storrs, CT 06269 USA
关键词
opalescence; liquid-liquid phase separation; aggregation; light scattering; thermodynamics; phase diagram; formulation; stability; protein-protein interactions; crystallization; B-2; T-cloud; 2ND VIRIAL-COEFFICIENT; HUMAN SERUM-ALBUMIN; MONOCLONAL-ANTIBODY; EXCLUDED-VOLUME; CONCENTRATED-SOLUTIONS; POLYETHYLENE-GLYCOLS; INTERMOLECULAR INTERACTIONS; CONCENTRATION FORMULATIONS; HOMOGENEOUS NUCLEATION; SALT CONCENTRATION;
D O I
10.1021/acs.molpharmaceut.5b00937
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 (B-2) and the cloud-point temperature (T-cloud) measurements are also presented. The review also highlights pharmaceutical implications of LLPS in protein solutions.
引用
收藏
页码:1431 / 1444
页数:14
相关论文
共 151 条
[71]   Application of a PEG precipitation method for solubility screening: A tool for developing high protein concentration formulations [J].
Li, Li ;
Kantor, Angela ;
Warne, Nicholas .
PROTEIN SCIENCE, 2013, 22 (08) :1118-1123
[72]  
[李玉书 Li Yushu], 2010, [分析仪器, Analytical Instrumentation], P63
[73]  
Lipatov I.U.r.S., 1988, COLLOID CHEM POLYM
[74]   ELECTROSTATIC SCREENING OF CHARGE AND DIPOLE INTERACTIONS WITH THE HELIX BACKBONE [J].
LOCKHART, DJ ;
KIM, PS .
SCIENCE, 1993, 260 (5105) :198-202
[75]   Cation-π Interaction: Its Role and Relevance in Chemistry, Biology, and Material Science [J].
Mahadevi, A. Subha ;
Sastry, G. Narahari .
CHEMICAL REVIEWS, 2013, 113 (03) :2100-2138
[76]   Protein Aggregation: Pathways, Induction Factors and Analysis [J].
Mahler, Hanns-Christian ;
Friess, Wolfgang ;
Grauschopf, Ulla ;
Kiese, Sylvia .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 98 (09) :2909-2934
[77]   Induction and analysis of aggregates in a liquid IgG1-antibody formulation [J].
Mahler, HC ;
Müller, R ;
Friess, W ;
Delille, A ;
Matheus, S .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 59 (03) :407-417
[78]   Thermodynamic instability in supersaturated lysozyme solutions: Effect of salt and role of concentration fluctuations [J].
Manno, M ;
Xiao, CD ;
Bulone, D ;
Martorana, V ;
San Biagio, PL .
PHYSICAL REVIEW E, 2003, 68 (01)
[79]   Opalescence of an IgG2 Monoclonal Antibody Solution as it Relates to Liquid-Liquid Phase Separation [J].
Mason, Bruce D. ;
Zhang, Le ;
Remmele, Richard L., Jr. ;
Zhang, Jifeng .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 100 (11) :4587-4596
[80]   Liquid-Liquid Phase Separation of a Monoclonal Antibody and Nonmonotonic Influence of Hofmeister Anions [J].
Mason, Bruce D. ;
Zhang-van Enk, Jian ;
Zhang, Le ;
Remmele, Richard L., Jr. ;
Zhang, Jifeng .
BIOPHYSICAL JOURNAL, 2010, 99 (11) :3792-3800