Derivative absorbance spectroscopy and protein phase diagrams as tools for comprehensive protein characterization: A bGCSF case study

被引:103
作者
Kueltzo, LA
Ersoy, B
Ralston, JP
Middaugh, CR
机构
[1] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66047 USA
[2] Univ Kansas, Dept Phys & Astron, Lawrence, KS 66047 USA
关键词
absorption spectroscopy; biophysical models; calorimetry (DSC); circular dichroism; fluorescence spectroscopy; infrared spectroscopy; protein formulation; protein structure; protein aggregation; UV/Vis spectroscopy;
D O I
10.1002/jps.10439
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In protein and macromolecule pharmaceutical formulation development, the amount of information initially gathered about a drug's physical and chemical properties under different conditions is often quite limited. This generally requires more intensive studies using a variety of techniques if problems arise later in the development process. We propose a supplementary approach involving a comprehensive examination of a protein by derivative absorbance spectroscopy in conjunction with other methods and the subsequent construction of a phase diagram that permits the determination of optimal formulation conditions. Using bovine granulocyte colony stimulating factor (bGCSF) as a model protein, a thorough characterization is performed using high-resolution second-derivative absorbance spectroscopy. Derivative ultraviolet absorbance data are used to construct an empirical phase diagram for bGCSF using a multidimensional phase space approach. Between pH 2 and 7, and from 10degrees to 90degreesC, bGCSF is found to adopt more than six distinct structural phases. Surprisingly, the combination of the phase diagram approach with derivative absorbance data identifies phase boundaries that are not apparent upon initial examination of complementary biophysical data (previous article in this issue). The simplicity and pharmaceutical utility of this approach are discussed. (C) 2003 Wiley-Liss, Inc. and the American Pharmacists.
引用
收藏
页码:1805 / 1820
页数:16
相关论文
共 18 条
[1]  
[Anonymous], 1997, ELEMENTARY DIFFERENT
[2]   2ND-DERIVATIVE SPECTROSCOPY OF PROTEINS - METHOD FOR QUANTITATIVE-DETERMINATION OF AROMATIC AMINO-ACIDS IN PROTEINS [J].
BALESTRIERI, C ;
COLONNA, G ;
GIOVANE, A ;
IRACE, G ;
SERVILLO, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1978, 90 (03) :433-440
[3]   Data visualization: Picture this [J].
Ball, P .
NATURE, 2002, 418 (6893) :11-13
[4]   SOLID-PHASE AGGREGATION OF PROTEINS UNDER PHARMACEUTICALLY RELEVANT CONDITIONS [J].
COSTANTINO, HR ;
LANGER, R ;
KLIBANOV, AM .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 83 (12) :1662-1669
[5]  
Donovan J W, 1973, Methods Enzymol, V27, P497
[6]  
Herman A.C., 1996, Characterization, Formulation, and Stability of Neupogen (filgrastim), a Recombinant Human GranulocyteColony Stimulating FactorFormulation, Characterization, and Stability of Protein Drugs, P303, DOI [10.1007/0-306-47452-2_7, DOI 10.1007/0-306-47452-2_7]
[7]   2ND DERIVATIVE SPECTROPHOTOMETRY AS AN EFFECTIVE TOOL FOR EXAMINING PHENYLALANINE RESIDUES IN PROTEINS [J].
ICHIKAWA, T ;
TERADA, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 494 (01) :267-270
[8]   ESTIMATION OF STATE AND AMOUNT OF PHENYLALANINE RESIDUES IN PROTEINS BY 2ND DERIVATIVE SPECTROPHOTOMETRY [J].
ICHIKAWA, T ;
TERADA, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 580 (01) :120-128
[9]   Sustained in vivo activity of recombinant bovine granulocyte colony stimulating factor (rbG-CSF) using HEPES buffer [J].
Kasraian, K ;
Kuzniar, A ;
Earley, D ;
Kamicker, BJ ;
Wilson, G ;
Manion, T ;
Hong, JY ;
Reiber, C ;
Canning, P .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2001, 6 (03) :441-447
[10]   Conformational lability of herpesvirus protein VP22 [J].
Kueltzo, LA ;
Normand, N ;
O'Hare, P ;
Middaugh, CR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) :33213-33221