Biomedical subjects

Peter Schoenmakers

Publications and source records attributed to Peter Schoenmakers.

7 recordsLinked to original sources

PubMed2006

Preparation of monolithic columns with target mesopore-size distribution for potential use in size-exclusion chromatography.

The main factors affecting the mesopore porosity of methacrylate-ester based monolithic columns were investigated. We prepared 40 monolithic capillary columns with porosity controlled by varying the proportions of butyl methacrylate (BMA) and ethylene dimethacrylate (EDMA) monomers and of 1,4-butanediol (BUT) and 1-propanol (PROP) as the porogen solvent in the polymerisation mixtures by thermally initiated in situ polymerisation in fused-silica capillaries. Using mixture design software, we systematically varied the composition of the polymerisation mixtures to find significant factors affecting mesopore formation. Multivariate analysis of the experimental data obtained for the fabricated columns yielded a model for prediction of the mesopore porosity in monolithic beds as a function of the composition of the polymerisation mixture used to prepare polymethacrylate monolithic capillary columns. The mean absolute deviation of predicted porosities is 0.029 for most of the columns, with only eight columns showing deviations exceeding 0.050. The main factor affecting the mesopore porosity proved to be the combination of the concentration of hydrophobic monomer (BMA) and the concentration of the less-polar solvent, 1-propanol, in the porogen mixture. The proportion of mesopores in the monolithic capillary columns increases with increasing concentration of 1-propanol and with decreasing concentration ratios of the cross-linker (EDMA) to monomer (BMA) and of BUT to PROP porogenic solvents.

Chromatography, Gel↗

PubMed2006

Influence of pore size on the separation of random and block copolymers by interactive liquid chromatography.

Stationary phase materials with small pore diameters are often used for the separation of copolymers according to their chemical composition. The rationale for such a column selection is to minimize the influence of the molecular weight on the separation. In this paper, we describe a detailed study of the influence of the pore size on the retention and separation of poly(methylmethacrylate) (PMMA)-poly(butylmethacrylate) copolymers. We used normal-phase (NP) and reversed-phase (RP) columns with various pore diameters, as well as non-porous columns and a monolithic column. The pore size was found to affect the separation, especially for (co-)polymer molecules with characteristic diameters that roughly correspond to the exclusion limit of the column. Also possibilities to separate block copolymers according to block length are strictly investigated. The making of one block in a di-block (DB) copolymer "invisible" can only be fulfilled if the "invisible" block does not play any role in the separation.

Calibration↗

PubMed2005

Molar mass distributions by gradient liquid chromatography: predicting and tailoring selectivity.

Interactive liquid chromatography (iLC) for polymer analysis is usually applied to the characterisation of distributions other than molar mass. In particular, its use for the determination of chemical-composition, functionality-type and tacticity distributions has been demonstrated. The application of iLC for the determination of molar mass distributions (MMDs), however, has not yet been fully explored. An expanded version of the reversed-phase liquid chromatography model has been developed to describe and predict how the retention behaviour of polydisperse polystyrene samples changes with molar mass. The relationship between molar mass and the parameters of the model has been investigated in some detail and non-linear correlations were found. From the model and the relationships between the model parameters and molar mass, calibration curves (retention time versus molar mass) were constructed to predict changes in chromatographic selectivity across a given molar mass range. These calibration curves were compared to experimentally obtained curves and, in most cases, excellent agreement was found. The dramatic enhancement in selectivity that can be obtained with iLC in comparison to size-exclusion chromatography (SEC) was illustrated by measuring matrix-assisted laser desorption ionisation (MALDI) MS spectra of fractions collected during a gradient-LC separation. In the low-molar mass range, essentially monodisperse fractions were obtained. Calibration curves, predicted by the model and validated experimentally using narrow-dispersity standards and MALDI-MS spectra of fractions, were used to determine the molar mass distribution of some narrowly distributed polystyrene samples. Molar mass distributions for such standards were found to be somewhat lower than the values reported by the manufacturers. The results also deviated from those obtained by MALDI-MS.

Calibration↗

PubMed2004

Characterisation of fluorinated copolymers using liquid chromatography coupled on-line to mass spectrometry, with automated data interpretation.

A perfluorinated co-polyether was characterised in terms of the number and type of functional end groups present on the molecule. The polymer was separated chromatographically according to the polarity of the polymer end groups and the separation was coupled on-line to an electrospray ionisation time-of-flight mass spectrometer. Negative-mode electrospray ionisation of the relatively non-polar polymer was achieved by post-column addition of a polar constituent to the mobile phase. LC-MS analysis of polydisperse analytes is a highly data intensive technique and manual interpretation of the resulting data can be extremely complicated, especially for the characterisation of copolymers or polymers with end-group distributions. In order to overcome this problem, an automated data-analysis program was developed that allows the user to quickly determine the probability of the presence of a certain molecular compound. The program evaluated data in terms of the possible combinations of monomeric units and end groups that could be combined to make up the mass values present in the mass spectra. Using the program, the polymer can be characterised according to its molar-mass, chemical-composition and functionality-type distributions. A graphical representation of the LC-MS analyses is presented to give a clear overview of the two-dimensional separation. The identification of various end groups on the polymer is also presented graphically, as (a) a histogram (frequency of matches versus time), (b) a two-dimensional plot (masses that match the particular end group combination versus LC retention time) and (c) a plot of average chemical composition versus LC retention time.

Automation↗

PubMed2004

Accurate prediction of the retention behaviour of polydisperse macromolecules based on a minimum number of experiments.

This study illustrates how retention models can be used to accurately predict the retention behaviour of polydisperse macromolecules in LC separations. It highlights that the number of experiments required can be drastically reduced when the relationship between the model parameters and molecular structure parameters (e.g. molar mass) can be incorporated into one global model. A practical implication of this work is that an appropriate model can then be used for the determination of molar-mass distributions for polydisperse samples. The globalised model can predict retention time as a function of molar mass and gradient slope. Both the original and globalised versions of the model were rigorously validated in terms of the difference between the predicted and experimental retention times. The original model had very low residuals and there was no apparent dependence of the errors on the applied gradient, the molar mass or the retention times. Confidence intervals for the model parameters (S and ln k0) were determined using a bootstrapping analysis of the residual errors in the predicted retention times. Confidence intervals were seen to broaden significantly as the mass of the polymer increased. The parameters were also seen to be highly correlated. For the global model, retention-time residuals remained quite low, even when the number of experiments used to determine the model parameters was reduced from approximately 100 to 10.

Chromatography, High Pressure Liquid↗

PubMed2003

Application of the reversed-phase liquid chromatographic model to describe the retention behaviour of polydisperse macromolecules in gradient and isocratic liquid chromatography.

This paper illustrates how conventional models of chromatographic behaviour can be used to predict the separation behaviour of polydisperse macromolecules. Using polystyrene and polymethylmethacrylate homo- and co-polymeric standards, the models were validated by comparing experimental retention behaviour with that predicted by the chromatographic model. The experimental retention time of each of the samples was entered into a spreadsheet application, which calculated the parameters that best described retention (for a given model). When a correlation between the relevant parameters and molecular mass was established, that correlation was used to predict the change in retention behaviour over the molecular-mass range. An expression introduced in a previous paper, to calculate the critical mobile-phase composition of a homopolymer was validated using polystyrene homopolymers. A second expression, which can predict the elution behaviour of copolymers, was also validated. This expression can predict the retention of a copolymer, based solely onthe retention of the homopolymeric units that make up the copolymer.

Calibration↗

PubMed2002

Predicting the behaviour of polydisperse polymers in liquid chromatography under isocratic and gradient conditions.

In this paper we describe how the existing theories to describe retention and peak width in isocratic and gradient-elution liquid chromatography can be expanded to describe the retention behaviour of natural and synthetic repetitive polymers, which feature distributions of molecules with different masses (and often different structures) rather than unambiguous molecular formulas. For polydisperse samples, it is vital that the model accommodates (isocratic) elution of sample components before the onset of a gradient, elution during the gradient, and elution after the completion of the gradient. The expanded models can readily be implemented in standard spreadsheet software, such as Excel. We have created such spreadsheets based on the conventional model for retention in reversed-phase liquid chromatography (RPLC) and on two different models for retention in normal-phase liquid chromatography. The implementation allows an easy visualization of the theoretical concept. Up to three different polymeric series can be entered, with a total of up to 100 peaks being computed and displayed in isocratic or gradient-elution chromatograms. Also visualized are "retention models" (diagrams of isocratic retention vs. composition) and "calibration curves" (retention or elution composition vs. molecular mass or degree of polymerization). The coefficients in the isocratic retention model may be correlated, as has often been observed in RPLC. It is shown that under certain conditions such a correlation corresponds to the existence of so-called critical (isocratic) conditions, at which all the members of a given polymeric series (same composition and end groups, different number of repeat units) show co-elution.

Chromatography, Liquid↗