Literature DB >> 8660705

Physical factors affecting the storage stability of freeze-dried interleukin-1 receptor antagonist: glass transition and protein conformation.

B S Chang1, R M Beauvais, A Dong, J F Carpenter.   

Abstract

The effects of glass transition of, and protein conformation in, the dried solid on the storage stability of freeze-dried recombinant human interleukin-1 receptor antagonist (rhIL-1ra) were examined. Glass transition is a temperature-dependent phenomenon. Amorphous materials become hard and brittle at temperatures below their characteristic glass transition temperatures (Tg) such that diffusion of molecules along the matrix is not sufficient to cause large-scale structural changes. To ascertain the importance of the glass transition in protein storage stability, we compared 10 different lyophilized rhIL-1ra formulations, with Tgs ranging from 20 to 56 degrees C, during several weeks of storage at temperatures above and below the samples' Tgs. Protein degradation, both deamidation and aggregation, was greatly accelerated at temperatures above Tg, but for some formulations also arose below Tg. Thus, storage of dried proteins below the Tg is necessary but not sufficient to ensure long-term stability. To examine the effects of protein structure in the dried solid, we prepared formulations with various sucrose concentrations, all of which had a Tg = 66 +/- 2.5 degrees C. With infrared spectroscopy, we determined that the protein lyophilized with </=1% sucrose was unfolded in the initial dried solid. In contrast, in those formulations with >/=5% sucrose, conformational change was inhibited during lyophilization. When stored at 50 degrees C, degradation of the freeze-dried protein varied inversely with sucrose concentration. These results indicate that structural changes arising during the lyophilization process led to damage during subsequent storage, even if the storage temperature was less than the Tg. Together the results of these studies document that to obtain optimum stability of dried rhIL-1ra it was necessary to inhibit conformational change during lyophilization and to store at temperatures below the Tg of the dried formulation.

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Year:  1996        PMID: 8660705     DOI: 10.1006/abbi.1996.0305

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  20 in total

1.  High critical temperature above T(g) may contribute to the stability of biological systems.

Authors:  J Buitink; I J van den Dries; F A Hoekstra; M Alberda; M A Hemminga
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

2.  Effect of moisture on the stability of a lyophilized humanized monoclonal antibody formulation.

Authors:  E D Breen; J G Curley; D E Overcashier; C C Hsu; S J Shire
Journal:  Pharm Res       Date:  2001-09       Impact factor: 4.200

3.  The use of disaccharides in inhibiting enzymatic activity loss and secondary structure changes in freeze-dried β-galactosidase during storage.

Authors:  Ville Petteri Heljo; Kirsi Jouppila; Timo Hatanpää; Anne M Juppo
Journal:  Pharm Res       Date:  2010-10-22       Impact factor: 4.200

4.  Coupling between chemical reactivity and structural relaxation in pharmaceutical glasses.

Authors:  Sheri L Shamblin; Bruno C Hancock; Michael J Pikal
Journal:  Pharm Res       Date:  2006-08-29       Impact factor: 4.200

5.  Freeze-drying of proteins from a sucrose-glycine excipient system: effect of formulation composition on the initial recovery of protein activity.

Authors:  Wei Liu; D Q Wang; Steven L Nail
Journal:  AAPS PharmSciTech       Date:  2005-09-30       Impact factor: 3.246

6.  Preferential exclusion of sucrose from recombinant interleukin-1 receptor antagonist: role in restricted conformational mobility and compaction of native state.

Authors:  B S Kendrick; B S Chang; T Arakawa; B Peterson; T W Randolph; M C Manning; J F Carpenter
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

Review 7.  Rational design of stable lyophilized protein formulations: some practical advice.

Authors:  J F Carpenter; M J Pikal; B S Chang; T W Randolph
Journal:  Pharm Res       Date:  1997-08       Impact factor: 4.200

8.  X-ray-induced photo-chemistry and X-ray absorption spectroscopy of biological samples.

Authors:  Graham N George; Ingrid J Pickering; M Jake Pushie; Kurt Nienaber; Mark J Hackett; Isabella Ascone; Britt Hedman; Keith O Hodgson; Jade B Aitken; Aviva Levina; Christopher Glover; Peter A Lay
Journal:  J Synchrotron Radiat       Date:  2012-10-18       Impact factor: 2.616

9.  Characterization of dynamics in complex lyophilized formulations: II. Analysis of density variations in terms of glass dynamics and comparisons with global mobility, fast dynamics, and Positron Annihilation Lifetime Spectroscopy (PALS).

Authors:  Norman Chieng; Marcus T Cicerone; Qin Zhong; Ming Liu; Michael J Pikal
Journal:  Eur J Pharm Biopharm       Date:  2013-04-25       Impact factor: 5.571

10.  Stabilizing effect of four types of disaccharide on the enzymatic activity of freeze-dried lactate dehydrogenase: step by step evaluation from freezing to storage.

Authors:  Kiyoshi Kawai; Toru Suzuki
Journal:  Pharm Res       Date:  2007-05-08       Impact factor: 4.200

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