Experimental verification of sample-solvent induced modifier-solute peak interactions in biochromatography

被引:7
作者
Stroehlein, Guido
Aumann, Lars
Melter, Lena
Buescher, Klaus
Schenkel, Berthold
Mazzotti, Marco
Morbidelli, Massimo [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, Inst Chem & Bioengn, HCI, CH-8093 Zurich, Switzerland
[2] NOVARTIS Pharma AG, CH-4002 Basel, Switzerland
[3] ETH, Inst Proc Engn, CH-8092 Zurich, Switzerland
关键词
chromatography; equilibrium theory; gradient elution; system peaks; bioseparations;
D O I
10.1016/j.chroma.2006.03.081
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In a previous theoretical analysis based on equilibrium theory it has been shown how differences in the sample and elution modifier concentrations can lead to unexpected behavior of the solute eluted peaks such as retention time distortion, peak deformation and peak doubling. All these features are verified experimentally in this work using the polypeptide calcitonin and a variant of a specific monoclonal antibody as chromatographic model systems. For both experimental systems, the retention time distortion can be predicted with high accuracy by the solution of the equilibrium theory model. For the polypeptide, the predictions from the theory about the occurrence of peak deformation and double peaks has been successfully verified by a series of tailored experiments with positive as well as negative modifier perturbations. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 153
页数:8
相关论文
共 10 条
[1]   PEAK DISTORTION IN THE COLUMN LIQUID-CHROMATOGRAPHIC DETERMINATION OF OMEPRAZOLE DISSOLVED IN BORAX BUFFER [J].
ARVIDSSON, T ;
COLLIJN, E ;
TIVERT, AM ;
ROSEN, L .
JOURNAL OF CHROMATOGRAPHY, 1991, 586 (02) :271-276
[2]   COMPARISON BETWEEN EXPERIMENTAL AND THEORETICAL PROFILES OF HIGH-CONCENTRATION ELUTION BANDS AND LARGE SYSTEM PEAKS IN NONLINEAR CHROMATOGRAPHY [J].
FORNSTEDT, T ;
GUIOCHON, G .
ANALYTICAL CHEMISTRY, 1994, 66 (17) :2686-2693
[3]   EXPERIMENTAL-STUDY OF SYSTEM PEAKS AND ELUTION PROFILES FOR LARGE CONCENTRATION BANDS IN THE CASE OF A BINARY ELUENT CONTAINING A STRONGLY SORBED ADDITIVE [J].
GOLSHANSHIRAZI, S ;
GUIOCHON, G .
JOURNAL OF CHROMATOGRAPHY, 1989, 461 :19-34
[4]   EFFECT OF THE SAMPLE SOLVENT ON BAND PROFILES IN PREPARATIVE LIQUID-CHROMATOGRAPHY USING NONAQUEOUS REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
JANDERA, P ;
GUIOCHON, G .
JOURNAL OF CHROMATOGRAPHY, 1991, 588 (1-2) :1-14
[5]  
MELTER L, 2006, THESIS ETH ZUERICH Z
[6]  
Rhee H.K., 2001, First-Order Partial Differential Equations, V1
[7]   Experimental determination of single solute and competitive adsorption isotherms [J].
Seidel-Morgenstern, A .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1037 (1-2) :255-272
[8]   Modeling of modifier-solute peak interactions in chromatography [J].
Ströhlein, G ;
Morbidelli, M ;
Rhee, HK ;
Mazzotti, M .
AICHE JOURNAL, 2006, 52 (02) :565-573
[9]   Analysis of sample-solvent induced modifier-solute peak interactions in biochromatography using equilibrium theory and detailed simulations [J].
Ströhlein, G ;
Mazzotti, M ;
Morbidelli, M .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1091 (1-2) :60-71
[10]   SAMPLE-SOLVENT-INDUCED PEAK BROADENING IN THE REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OF ASPIRIN AND RELATED ANALGESICS [J].
WILLIAMS, KJ ;
LIWANPO, A ;
IRWIN, WJ .
JOURNAL OF CHROMATOGRAPHY, 1980, 194 (02) :217-223