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P W Carr

Publications and source records attributed to P W Carr.

At least 19 recordsLinked to original sources
PubMed2005

Column selectivity in reversed-phase liquid chromatography. VIII. Phenylalkyl and fluoro-substituted columns.

As reported previously, five solute-column interactions (hydrophobicity, steric resistance, hydrogen-bond acidity and basicity, ionic interaction) quantitatively describe column selectivity for 163 alkyl-silica, polar-group and cyano columns. In the present study, solute retention and column selectivity for 11 phenyl and 5 fluoro-substituted columns were compared with alkyl-silica columns of similar ligand length. It is concluded that two additional solute-column interactions may be significant in affecting retention and selectivity for the latter columns: (a) dispersion interactions of varying strength as a result of significant differences in bonded-phase polarizability or refractive index and (b) pi-pi interactions in the case of phenyl columns and aromatic solutes. These 16 phenyl and fluoro columns were also characterized in terms of hydrophobicity, steric resistance, hydrogen-bond acidity and basicity, and ionic interaction.

Chromatography, Liquid↗
PubMed2004

The hydrophobic-subtraction model of reversed-phase column selectivity.

A recently developed treatment of reversed-phase column selectivity (the hydrophobic-subtraction model) is reviewed and extended, including its characterization of the selectivity of different column types (e.g., C1-C30, cyano, phenyl, etc.). The application of this model to retention data for various solutes and columns has provided new insights into the nature of different solute-column interactions and their relative importance in affecting sample retention and separation. Reversed-phase columns can be characterized by five selectivity parameters (H, S*, A, B and C), values of which are summarized here for more than 300 different columns. The selection of columns of either equivalent or different selectivity is readily achievable on the basis of their values of H, S*, etc. The development of the hydrophobic-subtraction model, its use in characterizing the selectivity of different reversed-phase liquid chromatography (RP-LC) columns, and its application to various practical problems as described here began in 1998. The original inspiration for this project owes much to Jack Kirkland, who also contributed actively to the initial studies that laid the foundation of this model; he has since provided other important support to this project. Jack and one of the authors (LRS) have enjoyed a strong professional relationship and personal friendship for the past 35 years, and it is the privilege of the authors to dedicate this paper and the work that it represents to Jack. His contributions to HPLC column technology have extended from the mid-1960s into the present century, and it is impossible to conceive of present day HPLC practice without Jack's contributions over the years. In this and other ways, his position as a pioneer and key implementer of HPLC is widely recognized. We wish Jack well in the years to come.

Chromatography, Liquid↗
PubMed2004

Part II. Chromatography using ultra-stable metal oxide-based stationary phases for HPLC.

In this part of the review authors discuss methods used for modification of metal oxide surfaces. On the basis of literature data it is shown, that silanization of the surfaces do not form stable supports for chromatography. On the other hand, the success of polymer modified surfaces such as polybutadiene (PBD) and polystyrene (PS) is emphasized. Permanent modification of metal oxide surfaces with Lewis bases is also widely discussed. Chromatographic properties of polymer modified surfaces of zirconia are discussed in details. The perspectives of carbon-coated metal oxide surfaces in HPLC and high temperature separations are described.

Chromatography, High Pressure Liquid↗
PubMed2004

Part I. Chromatography using ultra-stable metal oxide-based stationary phases for HPLC.

The first part of the review contrasts the main drawbacks of silica-based packings such as their relative thermal and chemical instability with excellent stability of metal oxides. The paper concerns mainly ZrO2, TiO2 and Al2O3. Methods of preparation of spherical particles for HPLC are described. Surface chemistry of the oxides is, however, very different from that of silica. Ability of the oxides to ion- and ligand exchange is discussed from a chromatographic point of view.

Chromatography, High Pressure Liquid↗
PubMed2004

Column selectivity in reversed-phase liquid chromatography. V. Higher metal content (type-A) alkyl-silica columns.

Retention measurements involving 16 test solutes have been carried out for 38 type-A alkyl-silica columns and three bonded-zirconia columns. These measurements have been analyzed in terms of a model previously developed for type-B columns, so as to yield values of five column selectivity parameters (H, S*, A, B, C) for each type-A column. Overall differences in selectivity between type-A and -B columns can be related to the average values of H, S*, etc. for each column type. Compared to type-B columns, type-A columns provide generally stronger retention for carboxylic acids, while solutes that are more hydrophobic or less bulky are more retained on type-B columns. Hydrogen-bond acceptors (e.g. aliphatic amides) and cations (e.g. protonated bases) are strongly retained on type-A versus type-B columns. Compared to type-B columns, bonded-zirconia columns show much increased retention of cations and reduced retention of hydrogen-bond acceptors. Because of relatively large differences in the selectivity of bonded-zirconia, type-A, and type-B columns, it will prove difficult to find columns of different type (e.g. a type-A and a type-B column) which have equivalent selectivity. Type-A columns also tend to be more different from each other (in terms of selectivity) than is the case for type-B columns. As a result, the replacement of a given type-A column by an "equivalent" type-A column also appears unlikely, except for samples that do not contain ionized compounds.

Chromatography, Liquid↗
PubMed2002

Column selectivity in reversed-phase liquid chromatography III. The physico-chemical basis of selectivity.

Reversed-phase liquid chromatography (RP-LC) retention data for 23 additional solutes have been acquired to further test and evaluate a general relationship from part I: log alpha = log (k/kref) = eta'H(i) + sigma'S(ii) beta'S(iii) + alpha'B(iv) +kappa'C(v) The physico-chemical origin of terms i-v above is examined here by comparing values of (a) the solute parameters of Eq. (1) (eta', sigma', etc.) vs. solute molecular structure, and (b) the column parameters (H, S, etc.) vs. column properties (ligand length and concentration, pore diameter, end-capping). We conclude that terms i-v correspond, respectively, to hydrophobic (i), steric (ii), hydrogen bonding (iii, iv) and ionic (v) interactions between solute and stationary phase. While steric interaction (term ii) is superficially similar to what previously has been defined as "shape selectivity", the role of the solute and column in determining steric selectivity (term ii) appears more complex than previously proposed for "shape selectivity". Similarly, what has previously been called hydrogen bonding between donor solutes and an acceptor group in the stationary phase (term iv) is very likely an oversimplification.

Chromatography, Liquid↗
PubMed2002

Column selectivity in reversed-phase liquid chromatography I. A general quantitative relationship.

Retention factors k have been measured for 67 neutral, acidic and basic solutes of highly diverse molecular structure (size, shape, polarity, hydrogen bonding, pKa, etc.) on 10 different C18 columns (other conditions constant). These data have been combined with k values from a previous study (86 solutes, five different C8 and C18 columns) to develop a six-term equation for the correlation of retention as a function of solute and column. Values of k can be correlated with an accuracy of +/- 1-2% (1 standard deviation). This suggests that all significant contributions to column selectivity have been identified (and can be measured) for individual alkyl-silica columns which do not have an embedded polar group. That is, columns of the latter kind can be quantitatively characterized in terms of selectivity for use in the separation of any sample.

Chromatography, Liquid↗
PubMed2002

Column selectivity in reversed-phase liquid chromatography II. Effect of a change in conditions.

The isocratic retention of 67 widely-different solutes in reversed-phase liquid chromatography (RP-LC) has been investigated as a function of temperature and mobile phase composition (% B) for three different C18 columns. Similar studies were also carried out in a gradient mode, where temperature, gradient time and solvent type were varied. These results show that changes in retention with these conditions are similar for each of these three columns. This suggests that relative column selectivity as defined by experiments for one set of experimental conditions will be approximately applicable for other conditions, with the exception of changes in mobile phase pH-which can affect values of the column parameter C (a measure of silanol ionization). Column selectivity as a function of pH was explored for several columns.

Buffers↗
PubMed2001

Separation of selected basic pharmaceuticals by reversed-phase and ion-exchange chromatography using thermally tuned tandem columns.

The separation of basic pharmaceuticals is usually performed on C8 or C18 bonded silica supports. Silanolphilic interactions between basic analytes and surface silanol groups often lead to tailed peaks, poor efficiency, and irreproducible retention times. To solve these problems, many new types of silica-, zirconia-, and polymer-based columns, which provide unique selectivities, improved stability at high pH, or both, have been developed for the analysis of basic compounds. The essence of method development for the chromatographic analysis of basic compounds is to choose a system in which the band spacing can be varied dramatically, quickly, and conveniently while minimizing the tailing due to silanolphilic interactions. The thermally tuned tandem column (T3C) approach has been shown to provide an effective way to adjust stationary-phase selectivity for nonionic compounds. In this study, a tandem combination of an octadecylsilane (ODS) and a polybutadiene-coated zirconia (PBD-ZrO2) phase was used to separate nine antihistamines. Selectivity is tuned by independently adjusting the isothermal temperatures of the two columns. We found dramatic differences in the retention factors, elution sequences, and band spacing for the above set of basic drugs on the two types of columns. The T3C model has been used successfully to locate the optimal temperatures based on only four exploratory runs. The nine antihistamines were baseline separated on the tandem column combination even though they could not be separated on the individual phases. The effect of the buffer concentration on retention of the basic antihistamines was also studied. We conclude that cation-exchange interactions predominate on the PBD-ZrO2 phase, while reversed-phase interactions are more important on the ODS phase. Interestingly, an increase in column temperature causes a significant increase in the retention on the ODS column and a decrease of retention on the PBD-ZrO2 column. This can be explained by the change in the analyte's degree of ionization with temperature. The T3C combination of silica- and zirconia-based RPLC columns is demonstrated to be a powerful approach for the separation of this mixture of basic analytes.

Buffers↗
PubMed2001

A study of the Lewis acid-base interactions of vinylphosphonic acid-modified polybutadiene-coated zirconia.

Polybutadiene-coated zirconia (PBD-ZrO2) is very useful for reversed-phase separations under a wide variety of conditions. Its excellent chemical (pH = 1-13) and thermal (up to 150 degrees C) stability distinguish it from silica-based reversed phases. Just as with silica-based phases, zirconia's surface chemistry significantly influences the chromatography of certain classes of analytes. Zirconia's hard Lewis acid sites can be chromatographically problematic. Analytes such as carboxylic acids strongly interact with these sites on PBD-ZrO2 and do not elute. Addition of phosphate or other strong, hard Lewis bases to the eluent brings about elution, but the resulting peak is often tailed and broad. Typically, cationic solutes are more retained in the presence of phosphate or fluoride due to adsorption of the Lewis base additives and the concomitant development of a negative charge on the surface. This Coulombic interaction can be used to optimize selectivity, but the reversed-phase-cation-exchange retention can produce broad peaks with excessive retention. As an alternative to adding Lewis bases to the eluent, we studied the effect of permanently modifying PBD-ZrO2 by covalently attaching vinylphosphonic acid (VPA) to PBD which was predeposited in the pores of zirconia. We have investigated the chromatography of acids, bases, and small peptides on VPA-modified PBD-ZrO2 (VPA-PBD-ZrO2) and compared it to PBD-ZrO2. VPA-PBD-ZrO2 is a reversed-cation-exchange phase with properties quite different from PBD-ZrO2. The chemical stability of both phases led us to explore how low-pH (1.5-3), ultralow-pH (0), and high-pH (12) eluents effect the retention properties of these mixed-mode phases. Ultralow-pH eluents effectively separate small peptides on both phases. This approach gives lower retention, without sacrificing resolution, and much higher efficiency for small peptides than previously reported.

Anions↗
PubMed2001

Dependence of thermal mismatch broadening on column diameter in high-speed liquid chromatography at elevated temperatures.

In this paper, we compare a narrow-bore column (2.1-mm i.d.) to a conventional-bore column (4.6 mm i.d.) at elevated temperatures under conditions where thermal mismatch broadening is serious and show that narrow-bore columns offer significant advantages in terms of efficiency and peak shape at higher linear velocities. We conclude that the so-called thermal mismatch broadening effect is largely due to a radial retention factor gradient and not a radial viscosity gradient. The lower volumetric flow rates inherent with the use of narrower columns lead to lower linear velocity in the heater tubing and longer eluent residence times in the heater. Thus, with the same heater tubing at the same column linear velocity, narrow-bore columns give better thermal equilibration between the eluent and the column compared to wider bore columns. This means that high-temperature, ultrafast liquid chromatography no longer requires excessively long preheater tubing to thermally equilibrate the eluent to the column temperature. Consequently, the use of narrow-bore columns at high-temperature improves analysis speed and efficiency over wider bore columns. We also discuss the advantages of using liquid heat-transfer media as compared to air as the heat-transfer media. We show that an air bath ought not be used to heat the mobile phase because at high temperature (>80 degrees C) and high column linear velocity (> 1.5 cm/s) the length of tubing needed to heat the mobile phase to column temperature is prohibitively long. Using accurate, empirical heat-transfer correlations, we estimated the length of tubing needed to heat the eluent as a function of the column linear velocity for both air and liquid heat-transfer media.

Chromatography, Liquid↗
PubMed2001

Separation of barbiturates and phenylthiohydantoin amino acids using the thermally tuned tandem column concept.

There are many more choices of column type than of eluent type for method development in reversed-phase liquid chromatography. It is common to switch between different column types or between the same type from different suppliers to achieve the desired separations. The key difficulty in modulating band spacing by adjusting the column type is that it is a discontinuous, "hit or miss" proposition. The thermally tuned tandem column (T3C) concept effectively solves this problem by connecting two columns in series and independently controlling the two column temperatures. The columns are chosen to have distinctively different chromatographic selectivities (band spacing), so that the unresolved peaks on one column are separated by the other. The optimized separation in the T3C is achieved by simultaneously tuning the two column temperatures. In this study, we used the T3C combination of a carbon and a conventional bonded phase for the separation of barbiturates and phenylthiohydantoin amino acids (PTH-amino acids). Good peak shapes and comparable retention times were observed on the two phases at room temperature. The selectivities on the two phases are quite different. Baseline separations were easily achieved with the T3C set although neither column could individually resolve all the peaks. We further compared the separation of barbiturates optimized by the T3C approach with that optimized by adjusting the mobile phase. We found that T3C gave a better separation. We believe that the T3C combination of a carbon phase and a bonded conventional reversed-phase material provides a powerful and general method to optimize the separation of various mixtures.

Algorithms↗
PubMed2001

The solubility of gases and vapours in dry octan-1-ol at 298 K.

Ostwald solubility coefficients of 74 compounds in dry octan-1-ol at 298 K have been determined, and have been combined with literature values and additional values we have calculated from solubilities in dry octan-1-ol and vapour pressures to yield a total of 161 log L(OctOH) values at 298 K. These L(OctOH) values are identical to gas-to-dry octan-1-ol partition coefficients, often denoted as K(OA). Application of the solvation equation of Abraham to 124 values as a training set yielded a correlation equation with n = 124, S.D. = 0.125, r2 = 0.9970 and F = 7731. This equation was then used to predict 32 values of log L(OctOH) as a test set, giving a standard deviation, S.D. of 0.131, an average absolute deviation of 0.085 and an average deviation of -0.009 log units. The solvation equation for the combined 156 log L(OctOH) values was log L(OctOH) = -0.120 - 0.203R2 + 0.560pi2(H) + 3.560 sum(alpha2(H)) + 0.702 sum(beta2(H)) + 0.939 logL16, n =156, r2 = 0.9972, S.D. = 0.125, F = 10573, where, n is the number of data points (solutes), r the correlation coefficient, S.D. the standard deviation and F is the F-statistic. The independent variables are solute descriptors as follows: R2 is an excess molar refraction, pi2(H) the dipolarity/polarisability, sum(alpha2(H)) the overall or summation hydrogen-bond acidity, sum(beta2(H)) the overall or summation hydrogen-bond basicity and L16 is the Ostwald solubility coefficient on hexadecane at 298 K. The equation is consistent with similar equations for the solubility of gases and vapours into methanol, ethanol and propan-1-ol. It is suggested that the equation can be used to predict further values of log L(OctOH), for which the solute descriptors are known, to within 0.13 log units.

1-Octanol↗
PubMed2000

Fast enantioseparations of basic analytes by high-performance liquid chromatography using cellulose tris(3,5-dimethylphenylcarbamate)-coated zirconia stationary phases.

In this work, we study the influence of the mobile phase and column temperature on the enantioresolution of basic compounds on microparticulate porous zirconia coated with cellulose tris(3,5-dimethylphenylcarbamate) (CDMPC). The chiral analytes are amino compounds, including a number of beta-blockers. Analytes are eluted with hexane-alcohol mobile phases. We investigated the effect of alcohol (type and concentration), basic eluent additives, and column temperature on the parameters that control resolution (column efficiency, retention and selectivity). Conditions for achieving an adequate separation in the least time have been determined for numerous racemic mixtures. For most solutes, baseline resolution of the enantiomeric pair was achieved in less than 1 min; 12 of 13 pairs were separated in less than 2 min.

Carbamates↗
PubMed2000

A study of the enthalpy and entropy contributions of the stationary phase in reversed-phase liquid chromatography.

The goal of this study was to elucidate the roles played by the stationary and mobile phases in retention in reversed-phase liquid chromatography (RPLC) in terms of their individual enthalpic and entropic contribution to the Gibbs free energy of retention. The experimental approach involved measuring standard enthalpies of transfer of alkylbenzenes from typical mobile phases used in RPLC (methanol/water and acetonitrile/water mixtures), as well as from n-hexadecane (a simple analogue of the stationary phase) to the gas phase, using high-precision headspace gas chromatography. By combining the measured enthalpies with independently measured free energies of transfer, the entropies of transfer were obtained. This allowed us to examine more fully the contribution that each phase makes to the overall retention. It was found that the standard enthalpy of retention in RPLC (i.e., solute transfer from the mobile phase to the stationary phase) is favorable, due to the large and favorable stationary-phase contribution, which actually overcomes an unfavorable mobile-phase contribution to the enthalpy of retention. Further, the net free energy of retention is favorable due to the favorable enthalpic contribution to retention, which arises from the net interactions in the stationary phase. Entropic contributions to retention are not controlling. Therefore, to a great extent, retention is due to enthalpically dominated lipophilic interaction of nonpolar solutes with the stationary phase and not from solvophobic processes in the mobile phase. Further, our enthalpy data support a "partition-like" mechanism of retention rather than an "adsorption-like" mechanism. These results indicate that the stationary phase plays a very significant role in the overall retention process. Our conclusions are in direct contrast to the solvophobic model that has been used extensively to interpret retention in RPLC.

Journal Article↗
PubMed2000

Quaternized trimethylaminated polystyrene-coated zirconia as a strong anion exchange material for HPLC.

The synthesis and characterization of a new, base-stable, strong anion exchange phase by amination of polystyrene-coated zirconia (PS-ZrO2) are described. Even though the ion exchange capacity of the quaternized trimethylaminated PSZrO2 (QTMA-PS-ZrO2) is only 0.07 mequiv/g, it is able to separate various inorganic anions, benzoic acid derivatives, and nucleotides in their deprotonated states. The effects of ionic strength, eluent pH, and counterion type are discussed. In the presence of both phosphate and fluoride ions in the eluent, band broadening caused by Lewis acid/base interactions between zirconia and analytes is greatly suppressed. The mixed retention modes (ion exchange, hydrophobic interaction, and Lewis acid/base interactions) on QTMA-PS-ZrO2 offer a different selectivity toward various anionic analytes than do other zirconia- and nonzirconia-based ion exchangers.

Antiporters↗
PubMed2000

Use of spray-dried zirconia microspheres in the separation of immunoglobulins from cell culture supernatant.

A method suitable for the isolation of monoclonal antibodies (MAbs) on novel zirconia microspheres (20-30 microm) is described. Zirconia microspheres were generated by spray drying colloidal zirconia. Spray-dried zirconia microspheres were further classified and characterized by X-ray diffraction, BET porosimetry and scanning electron microscopy. Spray-dried zirconia microspheres were modified with ethylenediamine-N,N'-tetra(methylenephosphonic) acid (EDTPA) to create a cation-exchange chromatographic support. The chromatographic behavior of a semi-preparative column packed with EDTPA-modified zirconia microspheres was evaluated and implications for scale-up are provided. EDTPA-modified zirconia microspheres were further used to purify MAbs from cell culture supernatant. Analysis by enzyme linked immunosorbent assay and gel electrophoresis demonstrate that MAbs can be recovered from a cell culture supernatant at high yield (92-98%) and high purity (>95%) in a single chromatographic step.

Animals↗