Rapid determination of molecular parameters of synthetic polymers by precipitation/redissolution high-performance liquid chromatography using ?molded? monolithic column (original) (raw)
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Journal of Chromatography A, 1984
The separation of synthetic polymers of different molecular weight by nonaqueous, gradient liquid chromatography does not follow traditional chromatographic mechanisms. As a result one can produce separations where late eluting solutes have narrower bandwidths than early eluting solutes, where shorter columns result in higher resolution than identical longer columns, and where the selectivity and resolution are independent of the type of stationary phase used. These results are explained for polystyrene, poly-a-methylstyrene and polyisoprene using recently developed theory. The results of this work are not only pertinent to the practice and theory of chromatography but also to the study of polymers.
2019
Poly (lactide-co-glycolide acid) ( PLGA) is an extraordinary well-described polymer and has excellent pharmaceutical properties like high biocompatibility and good biodegradability. Hence, it is one of the most used materials for drug delivery and biomedical systems, also being present in several US Food and Drug Administration approved carrier systems and therapeutic devices. For both applications, the quantification of polymer is important. During the development of the production process, parameters like yield or loading efficacy are essential to be determined. Although PLGA is a well-defined biomaterial, it still lacks a sensitive and convenient quantification approach for PLGA-based systems. Thus, we present a new method for fast and precise quantification of PLGA by HPLC-SEC. The method includes a shorter run time of 20 minutes with a size exclusion column of 300mm x 8.0mm diameter, tetrahydrofuran as mobile phase and diluent, the detection was carried out using the refractive...
Chemical Papers, 2006
A novel liquid chromatographic procedure is presented. It is based on differences in the transport velocities of the fast-moving, pore-excluded macromolecules and slow-progressing, pore-permeating small molecules of an auxiliary liquid. A barrier of small molecules selectively decelerates certain kind of macromolecules while other kind remains unhindered. As a result, polymers of different nature are efficiently separated. In this new approach, the barrier is formed by a zone of a nonsolvent injected immediately before the sample solution. The resulting method is denoted liquid chromatography under limiting conditions of insolubility.
Studies on high-performance size-exclusion chromatography of synthetic polymers
Journal of Chromatography A, 2005
Macromolecules, which stay adsorbed within the active size-exclusion chromatography (SEC) column packings may strongly reduce effective volume of the separation pores. This brings about a decrease of retention volumes of the non-retained polymer samples and results in the increased apparent molar mass values. The phenomenon has been demonstrated with a series of poly(methyl methacrylate)s (PMMA) and a polyethylenoxide (PEO) fully retained by adsorption within macroporous silica gel SEC column from toluene or tetrahydrofuran, respectively. The non-retained probes were polystyrenes (PS) in toluene and both PS and PMMA in THF eluents. The errors in the peak molar mass values determined for the non-retained polymer species using a column saturated with adsorbed macromolecules and considering calibration curves monitored for the original "bare" column packing assumed up to several hundreds of percent. Errors may appear also in the weight and number averages of molar masses calculated from calibration dependences obtained with columns saturated with adsorbed macromolecules. Moreover, the SEC peaks of species eluted from the polymer saturated columns were broadened and in some cases even split. These results demonstrate a necessity not only to periodically re-calibrate the SEC columns but also to remove macromolecules adsorbed within packing in the course of analyses.
Liquid chromatography of polymers under limiting conditions of desorption
Journal of Chromatography A, 2005
Liquid chromatography under limiting conditions of desorption (LC LCD) is a method which allows molar mass independent elution of various synthetic polymers. A narrow, slowly moving zone of small molecules, which promotes full adsorption of one kind of polymer species within column (an adsorli) acts as an impermeable barrier for the fast moving macromolecules. The latter accumulate on the barrier edge and elute nearly in total volume of liquid within column. At the same time, transport of less adsorptive macromolecules is not hampered so that these are eluted in the size exclusion (SEC) mode. As result, polymers differing in their polarity and adsorptivity can be easily separated without molar mass interference. Three methods of barrier creation are discussed and compared. It is shown that a fraction of sample may elute unretained if the adsorli sample solvent is used as a barrier in connection with a narrow-pore column packing. One part of excluded macromolecules likely breaks-out from the adsorli zone and this results in partial loss of sample and distortion of the LC LCD peaks. This problem can be avoided if the adsorli zone is injected immediately before sample solution. Applicability of the LC LCD method for polymer separation has been demonstrated with a model mixture of poly(methyl methacrylate) (adsorbing polymer) and polystyrene (non adsorbing polymer) using bare silica gel as a column packing with a combination of tetrahydrofuran (a desorption promoting liquid-a desorli) and toluene (adsorli). It has been shown that the LC LCD procedure with tandem injection allows simple and fast discrimination of polymer blend components with good repeatability and high sample recovery. For quantitative determination of molar masses of both LC LCD and SEC eluted polymers, an additional size exclusion chromatographic column can be applied either in a conventional way or in combination with a multi-angle light scattering detector. A single eluent is used in the latter column, which separates the mixed mobile phase, system peaks and the desorli zone from the polymer peaks so that measurements are free from disturbances caused by the changing eluent composition. The resulting LC LCD × SEC procedure has been successfully applied to poly(methyl methacrylate) samples.
Macromolecules, 2002
A novel liquid chromatographic procedure is presented. It is based on differences in the transport velocities of the fast-moving, pore-excluded macromolecules and slow-progressing, pore-permeating small molecules of an auxiliary liquid. A barrier of small molecules selectively decelerates certain kind of macromolecules while other kind remains unhindered. As a result, polymers of different nature are efficiently separated. In this new approach, the barrier is formed by a zone of a nonsolvent injected immediately before the sample solution. The resulting method is denoted liquid chromatography under limiting conditions of insolubility.
JPC - Journal of Planar Chromatography - Modern TLC, 2013
A repeatable separation of polystyrenes according to MW, from 1920 to 520000 u.m.a, has been obtained under adsorption conditions using a method that comprises the use of Lichrospher HPTLC plates, and a controlled, isocratic elution with a 78:22 (v/v) mixture of cyclohexane (Cy)-tetrahydrofuran (THF). Likewise, UV-densitometric quantification of polystyrenes in mixtures can be achieved, by an intra-plate or an inter-plate procedure, using the corresponding polystyrene calibration curve. In the case or overlapped, unresolved peaks, an average curve of the corresponding polystyrenes can be used. Migration of polystyrenes strongly varies with slight variations in the relative proportion of Cy and THF in the mobile phase. This allows different ranges of MW to be separated as a function of mobile phase composition. Other factors influencing repeatability have been identified. Some reasons have been advanced to explain the current lack of activity in the research on polymer characterization by HPTLC. Old literature results concerning polystyrene separation have also been discussed in the light of modern HPTLC instrumentation. Developed method provides similar information on Molecular Weight Distribution (MWD) to that obtained using Gel Permeation Chromatography (GPC). Advantages and limitations of HPTLC for obtaining polymer MWD have also been discussed.
HPLC analysis of synthetic polymers on short monolithic columns
Journal of Separation Science, 2013
Ultrashort monolithic columns (disks) were thoroughly studied as efficient stationary phases for precipitation-dissolution chromatography of synthetic polymers. Gradient elution mode was applied in all chromatographic runs. The mixtures of different flexible chain homopolymers, such as polystyrenes, poly(methyl methacrylates), and poly(tert-butylmethacrylates) were separated according to their molecular weights on both commercial poly(styrene-codivinylbenzene) disks (12 id × 3 mm and 5 × 5 mm) and lab-made monolithic columns (4.6 id × 50 mm) filled with supports of different hydrophobicity. The experimental conditions were optimized to reach fast and highly efficient separation. It was observed that, similar to the separation of monoliths of other classes of (macro)molecules (proteins, DNA, oligonucleotides), the length of column did not affect the peak resolution. A comparison of the retention properties of the poly(styrene-co-divinylbenzene) diskshaped monoliths with those based on poly(lauryl methacrylate-co-ethylene dimethacrylate), poly(butyl methacrylate-co-ethylene dimethacrylate), and poly(glycidyl methacrylateco-ethylene dimethacrylate) supports demonstrated the obvious effect of surface chemistry on the resolution factor. Additionally, the results of the discussed chromatographic mode on the fast determination of the molecular weights of homopolymers used in this study were compared to those established by SEC on columns packed with sorbent beads of a similar nature to the monoliths.
The separation of a mixture of three poly(styrene-block-t-butyl methacrylate) copolymers (PS-b-PtBMA), consisting of polystyrene (PS) blocks of similar length and t-butyl methacrylate (PtBMA) blocks of different lengths, was performed using various chromatographic techniques, that is, a gradient liquid chromatography on reversed-phase (C18 and C8) and normalphase columns, a liquid chromatography under critical conditions for polystyrene as well as a fully automated two-dimensional liquid chromatography that separates block copolymers by chemical composition in the first dimension and by molar mass in the second dimension. The results show that a partial separation of the mixture of PS-b-PtBMA copolymers can be achieved only by gradient liquid chromatography on reversed-phase columns. The coelution of the two block copolymers is ascribed to a much shorter PtBMA block length, compared to the PS block, as well as a small difference in the length of the PtBMA block in two of these copolymers, which was confirmed by SEC-MALS and NMR spectroscopy.
Journal of Chromatography A, 2011
A very simple and readily performed method is described for the preparation of poly(styrenedivinylbenzene-methacrylic acid) monolithic columns for capillary liquid chromatography. The effect of the methacrylic acid content on the morphological and chromatographic properties has been investigated. Methacrylic acid is shown to be essential for isocratic separations of small organic analytes by capillary liquid chromatography. Column efficiencies of about 28,000 theoretical plates/m have been obtained for all the test compounds. The batch-to-batch and run-to-run repeatability of the retention times is better than 1.5%.