Literature DB >> 10460913

Instability, stabilization, and formulation of liquid protein pharmaceuticals.

W Wang1.   

Abstract

One of the most challenging tasks in the development of protein pharmaceuticals is to deal with physical and chemical instabilities of proteins. Protein instability is one of the major reasons why protein pharmaceuticals are administered traditionally through injection rather than taken orally like most small chemical drugs. Protein pharmaceuticals usually have to be stored under cold conditions or freeze-dried to achieve an acceptable shelf life. To understand and maximize the stability of protein pharmaceuticals or any other usable proteins such as catalytic enzymes, many studies have been conducted, especially in the past two decades. These studies have covered many areas such as protein folding and unfolding/denaturation, mechanisms of chemical and physical instabilities of proteins, and various means of stabilizing proteins in aqueous or solid state and under various processing conditions such as freeze-thawing and drying. This article reviews these investigations and achievements in recent years and discusses the basic behavior of proteins, their instabilities, and stabilization in aqueous state in relation to the development of liquid protein pharmaceuticals.

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Year:  1999        PMID: 10460913     DOI: 10.1016/s0378-5173(99)00152-0

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  125 in total

Review 1.  Protein instability in poly(lactic-co-glycolic acid) microparticles.

Authors:  M van de Weert; W E Hennink; W Jiskoot
Journal:  Pharm Res       Date:  2000-10       Impact factor: 4.200

2.  Effect of polyols on the conformational stability and biological activity of a model protein lysozyme.

Authors:  Somnath Singh; Jagdish Singh
Journal:  AAPS PharmSciTech       Date:  2003       Impact factor: 3.246

3.  Temperature- and pH-induced multiple partially unfolded states of recombinant human interferon-alpha2a: possible implications in protein stability.

Authors:  Vikas K Sharma; Devendra S Kalonia
Journal:  Pharm Res       Date:  2003-11       Impact factor: 4.200

4.  A novel in vitro delivery system for assessing the biological integrity of protein upon release from PLGA microspheres.

Authors:  Anne Aubert-Pouëssel; David C Bibby; Marie-claire Venier-Julienne; François Hindré; Jean-Pierre Benoît
Journal:  Pharm Res       Date:  2002-07       Impact factor: 4.200

5.  Preformulation development of recombinant pegylated staphylokinase SY161 using statistical design.

Authors:  Frank Bedu-Addo; Randall Moreadith; Siddharth J Advant
Journal:  AAPS PharmSci       Date:  2002

6.  Effect of vacuum drying on protein-mannitol interactions: the physical state of mannitol and protein structure in the dried state.

Authors:  Vikas K Sharma; Devendra S Kalonia
Journal:  AAPS PharmSciTech       Date:  2004-02-17       Impact factor: 3.246

7.  Solvent exchange method: a novel microencapsulation technique using dual microdispensers.

Authors:  Yoon Yeo; Alvin U Chen; Osman A Basaran; Kinam Park
Journal:  Pharm Res       Date:  2004-08       Impact factor: 4.200

8.  Rational design of solution additives for the prevention of protein aggregation.

Authors:  Brian M Baynes; Bernhardt L Trout
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

9.  Mapping site-specific changes that affect stability of the N-terminal domain of calmodulin.

Authors:  Mary E Krause; Talia T Martin; Jennifer S Laurence
Journal:  Mol Pharm       Date:  2012-02-15       Impact factor: 4.939

Review 10.  The importance of handling high-value biologicals: Physico-chemical instability and immunogenicity of monoclonal antibodies.

Authors:  Tomislav Laptoš; Jasna Omersel
Journal:  Exp Ther Med       Date:  2018-01-31       Impact factor: 2.447

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