Organic Modifier In Mobile Phase Research Articles

Selectivity comparison of acetonitrile-methanol-water ternary mobile phases on an octadecylsiloxane-bonded silica stationary phase.

The solvation parameter model was used in this study to investigate various intermolecular interactions that influence retention on the standard C18 stationary phase for the solvent system acetonitrile:methanol (ACN:MeOH, 1:1). In comparison to the organic mobile phase modifiers acetonitrile, acetone, methanol, 2-propanol, and tetrahydrofuran, the solvent strength for the ACN:MeOH (1:1) solvent system was evaluated. To facilitate the interpretation of various intermolecular interactions that contribute to retention on a standard C18 stationary phase for the solvent system ACN:MeOH (1:1), system maps were constructed and compared with those of acetone, tetrahydrofuran, acetonitrile, 2-propanol, and methanol. The solvation parameter models were constructed for the ternary solvent system ACN:MeOH (1:1)-water, and in the models constructed, the coefficient of determination values were from 0.998 to 0.999, the Fisher statistic values for the models were from 1687 to 4015, and the standard error of the estimate values ranged from 0.022 to 0.029. The solvent system ACN:MeOH (1:1) has retention properties more similar to methanol than acetonitrile, indicating methanol's influence is more dominant.

Comparative study for the retention of some benzodiazepines in reversed-phase liquid chromatography using C8, C18, C6H5 and CN stationary phases

The retention behavior of six benzodiazepines (alprazolam, bromazepam, diazepam, flunitrazepam, medazepam, and nitrazepam) was studied using four different stationary phases, under reversed-phase mechanism in high-performance liquid chromatography. Four stationary phases were used for evaluating the retention of these compounds at fixed temperature. Functional dependences of the retention factor on the content of the organic modifier (methanol, or acetonitrile) in the composition of mobile phase were calculated. The extrapolated values of the retention factor for zero content of the organic modifier in mobile phase were higher for acetonitrile than for methanol for all studied compounds and for the four types of stationary phases.

Dimethyl Carbonate as a Mobile-Phase Modifier for Normal-Phase and Hydrophilic Interaction Liquid Chromatography

We studied the use of dimethyl carbonate (DMC) as a non-toxic, aprotic modifier for hydrophilic liquid interaction chromatography (HILIC) and as a modifier for normal-phase liquid chromatography (LC). A comparison of ethyl acetate (EA) and DMC as organic mobile-phase modifiers in hexane for normal-phase LC of phthalates was conducted with a silica column and showed that retention factors (k) at the same modifier percentage were about a factor of two greater for DMC. Detection at 215 nm, possible with DMC, allowed for the better detection of the phthalates by a factor of 10, compared with EA detection, best at a 254 nm wavelength. Using a core-shell silica column, HILIC separations of trans-ferulic acid, syringic acid, and vanillic acid were compared between acetonitrile (MeCN) and DMC as the organic portion of the mobile phase, from 80–95%. The analyte retention for DMC, when compared to MeCN, was about 1.5 times greater, with only a moderate increase in back pressure. Plate count and peak asymmetry were somewhat better for the DMC chromatograms, compared to those with MeCN. Seven mono- and di-hydroxybenzoic acid positional isomers could be resolved effectively with DMC. Sorbate and benzoate preservatives in commercial drinks were also determined.

Unique selectivity of tetrahydrofuran-2-propanol-water ternary mobile phases on a superficially porous particle column in reversed-phase liquid chromatography

Three mixed mobile phase organic modifiers, tetrahydrofuran: 2-propanol 1:1 (v/v), tetrahydrofuran: 2-propanol: 1:3 (v/v), and tetrahydrofuran: 2-propanol: 3:1 (v/v) were studied at 20–70% (v/v) total organic solvent compositions. The solvent strength parameters for the three mixed organic modifiers and system properties were compared to those of more established binary solvent systems, acetonitrile-water and methanol-water. To interpret intermolecular interactions responsible for retention for the three mixed mobile phase organic modifiers, system maps were constructed and compared with acetonitrile and methanol. Three mixed organic mobile phase modifiers on one stationary phase chemistry (Kinetex C18) provide different selectivity than the more established acetonitrile and methanol mobile phase modifiers on the same stationary phase (Kinetex C18) as well as different stationary phase chemistries (Kinetex Biphenyl, Kinetex Phenyl-Hexyl, Kinetex F5, Kinetex XB-C18, and Kinetex EVO C18). The solvation parameter models for all three mixed mobile phase systems the coefficient of determination ranged from 0.991 to 0.999, the Fisher statistic from 338 to 1850, and the standard error of the estimate ranged from 0.024 to 0.097.

Dietary supplement mislabelling: case study on selected slimming products by developing a green isocratic HPLC method for their quality control

Nowadays, a huge population consumes Dietary supplements for losing weight. Products are often claimed as botanical blends, yet they aren't necessarily safe. Misleading labels are also very common. Thus, validated analytical methods for a wide range of slimming compounds are highly needed. Herein, we present a simple HPLC/PDA method for the quantitation of seven popular slimming ingredients. Studied compounds were Caffeine, Raspberry Ketone, trans-Resveratrol, p-Synephrine, p-Octopamine, p-Hordenine and 2-phenethylamine. After optimization, separation was carried out on a C18 column and mobile phase was a mixture of Acetonitrile:Water containing 0.1% phosphoric acid (50:50, %v/v). The last compound was eluted at 9.76 min. Separation was efficient showing baseline- separated symmetric peaks, without using any gradient programs, organic mobile phase modifiers or modified stationary phases. Method validation was done following ICH guidelines. Calibration curves were linear over wide concentration ranges and calculated LOD values were in the range 0.02–0.09 µg/mL. Method greenness was assessed using Analytical Eco-scale, GAPI and AGREE metric tools. Further, four random sample products purchased from online supplement stores were assayed. Results proved some mislabeling actions. To support our findings, standard addition was carried out and average % recoveries were 96.67 – 101.44% with standard deviation ≤ 2.83 between measurements.

A New Strategy for the Software-Assisted LC Separations of Ketoconazole and Its Impurities.

Analytical quality by design and the use of dissimilar chromatographic systems can be employed to accelerate chromatographic separations. Herein, a software (S-Matrix)-assisted platform was used to proficiently screen, optimize and select the optimal parameters for the chromatographic separation of ketoconazole and its related impurities. This approach evaluated the various chromatographic parameters in a stepwise manner based on the statistical tools and provided an in-depth understanding of the critical parameters influencing the peak selectivities and separations. It was demonstrated that dissimilar conditions, such as different stationary phases, mobile phase pH and organic modifiers (i.e., critical method variables), can improve the peak resolution, while the critical quality attributes can provide conditions appropriate for quantification purposes via a quality target analytical method. Furthermore, an orthogonal method was established to support the primary method. The orthogonality between the two methods was defined by the correlation matrix between the two systems using the Pearson correlation coefficient and was found to be 0.12. Using the optimized method, the primary method was validated as per International Council for Harmonization in the range of 0.05-1.0% for impurities and 80.0-120.0% for ketoconazole, thereby indicating the suitability of the method for use in quality control laboratories.

Environmentally friendly analytical method to assess enantioselective behaviour of pharmaceuticals and pesticides in river waters

Reported herein is the first enantioselective method for simultaneous separation of chiral pharmaceuticals and pesticides using ultra-high-performance liquid chromatography-tandem mass spectrometry. Separation was achieved using a ChiralPak IG-U® column (amylose tris(3-chloro-5-methylphenylcarbamate) stationary phase) and ethanol as a ‘green’ mobile phase organic modifier. Minimum enantiomer resolutions ranged from 0.5 to 6.9 for 28 pharmaceuticals, herbicides, fungicides and insecticides. The total run time was 26 min and is considerably shorter than other multi-residue enantioselective methods for similar numbers of pesticides, and is the first to facilitate simultaneous pharmaceutical separation. Direct injection of river water samples enabled omission of acetonitrile and methanol from the sample treatment step (and the whole methodology). This approach was considerably faster than enantioselective methodologies that rely on solid phase extraction and avoids the need for large sample volumes for analysis. The suitability of this approach was demonstrated by the method's sensitivity with enantiomer method quantitation limits in the range 0.005–0.6 μg L-1. The new method was applied to river water microcosms to investigate enantiospecific transformation of racemic pharmaceuticals and pesticides. The pharmaceutical omeprazole, fungicide prothioconazole and insecticide profenofos were all subject to enantioselective transformation under biotic conditions, represented by a change in enantiomeric fraction of ≥0.1 units. Individual enantiomer microcosms revealed chiral inversion of R-omeprazole to S-omeprazole in the environment for the first time. In conclusion, this method offers comparatively fast enantioselective analysis for a high number of pharmaceuticals and pesticides in river water, and is achieved in an environmentally friendlier way than previously reported liquid chromatography methods.

Development of LC-MS/MS method and application to bioequivalence study of a light sensitive drug montelukast

Objective The aim of the study was to develop a simple, highthroughput and sensitive LC-MS/MS method and apply to a bioequivalence study of montelukast, a light sensitive drug. Method The effects of organic modifiers in mobile phase, protein precipitation agent to plasma sample ratio, and light on montelukast stability in unprocessed and processed human plasma, were evaluated. Validation was conducted in accordance with European Medicines Agency Guideline on bioanalytical method validation. Results No interference peak was observed when acetonitrile was used as an organic modifier. Acetonitrile to plasma ratio of 4:1 produced clean plasma sample. Approximately 3 % of cis isomer was detected in unprocessed plasma samples while 21 % of cis isomer was detected in processed plasma samples after exposing to fluorescent light for 24h. The standard calibration curve was linear over 3.00–1200.00 ng/mL. All method validation parameters were within the acceptance criteria. Conclusion The validated method was successfully applied to a bioequivalence study of two montelukast formulations involving 24 healthy Malaysian volunteers. The light stability of a light sensitive drug in unprocessed and processed human plasma samples should be studied prior to pharmacokinetic/bioequivalence studies. Measures could then be taken to protect the analyte in human plasma from light degradation.

Parallel gradients in comprehensive multidimensional liquid chromatography enhance utilization of the separation space and the degree of orthogonality when the separation mechanisms are correlated.

Comprehensive two-dimensional liquid chromatography (LC×LC) offers increased peak capacity, resolution and selectivity compared to one-dimensional liquid chromatography. It is commonly accepted that the technique produces the best results when the separation mechanisms in the two dimensions are completely orthogonal, which necessitates the use of gradient elution for each second-dimension fraction. Recently, the use of similar separation mechanisms in both dimensions has been gaining popularity, but full or shifted gradients are still used for each second dimension fraction. Herein, we argue that when the separation mechanisms are correlated in the two dimensions, the best results can be obtained with the use of parallel gradients in the second dimension, which makes the technique nearly as user-friendly as comprehensive two-dimensional gas chromatography. This has been illustrated through the separation of a mixture of 39 pharmaceutical compounds using reversed phase in both dimensions. Different selectivity in the second dimension was obtained through the use of different stationary phase chemistries and/or mobile phase organic modifiers. The best coverage of the separation space was obtained when parallel gradients were applied in both dimensions, and the same was true for practical peak capacity.

Stress testing of crisaborole by a novel stability indicating RP-HPLC method

An isocratic reverse phase high performance liquid chromatographic method has been developed for the determination of crisaborole (CRB), a novel non-steroidal topical phosphodiesterase-4-inhibitor. The analyte was separated on an Agilent eclipse XDB-C18 (3.0 × 150 mm, 3.5 µm) analytical column using water: acetonitrile (30: 70 v/v) as the mobile phase at a flow rate of 0.75 ml/min under ambient temperature and PDA detection at 254 nm. Added to this, several validation parameters were exercised on the developed HPLC method as per ICH guidelines. Method variables, viz., mobile phase flow rate (0.75 ± 0.1 ml/min) and percentage of organic modifier in mobile phase (70 ± 5%) were studied by a central composite design for testing the robustness of the proposed method. The method was found to be linear in the concentration range of 2–100 µg/ml (r2 = 0.999) and precise (RSD ˂ 2%) satisfying regulatory criteria. The method was found to be robust and ambiguity of worst result for certain responses still are acceptable and likely to occur due to the effect of extreme experimental conditions. Stress testing of CRB was carried out under acid, base, thermal, photolysis, peroxide and neutral conditions. Separation of the forced degradation products from the main analyte was accomplished using a gradient elution of the mobile phase consisting acetonitrile from 0 to 100% in water at a flow rate of 1.2 ml/min.

A Stepwise Strategy Employing Automated Screening for Reversed-Phase Chromatographic Separation of Itraconazole and Its Impurities

The development of methods for the chromatographic separation of complex mixtures is often challenging, and an organized approach is required to rapidly achieve the desired separation. Herein, software (S-Matrix Fusion)-assisted platform is used to effectively screen, optimize, and select optimal parameters for the separation of itraconazole and its 15 impurities. The employed platform exploits dissimilar chromatographic systems, uses a diverse set of columns with enormous selectivity differences, and evaluates a wide range of aqueous mobile phase pH and organic modifiers for screening experiments. The wide range of selectivity ensures the identification and resolution of critical analytes, while the combination of dissimilar systems and automated screening statistical software increases the speed, efficiency, and level of understanding of critical parameters influencing separation. Automated screening using the described platform allows the establishment of a mass-compatible ultra-high-performance liquid chromatography method capable of separating all impurities. Multivariate robustness of critical parameters such as buffer concentration, flow rate, column temperature, and gradient is evaluated to identify the operational range of the method. Moreover, the optimized method is validated following the International Conference on Harmonization (ICH) guidelines, evaluated in terms of specificity, analysis repeatability, intermediate precision, linearity, accuracy, limit of quantification, limit of detection, solution stability, and range, and concluded to be fit for purpose in the quality control laboratories for release, stability, and investigation purposes.

Application of reversed-phase thin layer chromatography and QSRR modelling for prediction of protein binding of selected β-blockers

Chromatographic properties of sixteen β-blockers were studied using planar chromatography. The aim of presented study was to investigate influence of different organic solvents (acetonitrile, methanol, dioxin and tetrahydrofurane) on β-blockers’ retention on C18 bonded silica gel stationary phase. Group of sixteen, diverse in terms of structure, beta blockers was used as a model set. The main goal of this study was to compare chromatographically estimated lipophilicity parameters with values obtained with the use of computational methods. Furthermore, in order to understand molecular mechanisms of retention better, quantitative structure-retention relationships (QSRR) analysis was performed. The next step was focused on application of chromatographically obtained lipophilicity parameters for prediction of protein binding (PB), based on quantitative retention–activity relationships (QRAR) approach. The obtained results showed that reversed-phase thin layer chromatography (RP-TLC), especially with tetrafydrofurane used as an organic modifier of mobile phase, is a useful tool for lipophilicity estimation, as well as for prediction of β-blockers’ biological properties. The QRAR model included C0 parameters for tetrahydrofuran-water as a mobile phase, as well as maximal projection area, and can be easily applied for prediction of systematically synthesized β-blockers structures’ PB.

Simultaneous enantioselective determination of seven psychoactive drugs enantiomers in multi-specie animal tissues with chiral liquid chromatography coupled with tandem mass spectrometry

In stock farming, illegal use of antipsychotics has caused the food safety problem. This paper presents for the first time, a multi-residues method for the simultaneous enantioselective determination of seven antipsychotics in pork, beef and lamb muscles. The behaviors of Chiralpak AGP toward changes in pH and organic modifier in mobile phase were studied, and all analytes were rapidly separated within 30 min. The calibration curves of all enantiomers were linear in the range of 1–250 ng g−1, with correlation coefficient above 0.9931. The recoveries of the targeted compounds were higher than 82.1%, with repeatability and intermediate precision lower than 18.2% and 17.4%, respectively. In three matrices, the limit of detection and limit of quantification ranged from 0.20 to 0.65 ng g−1 and from 0.40 to 1.00 ng g−1, respectively. The proposed method can be used to provide additional information for the reliable risk assessment of chiral antipsychotics.

Enantioseparation, recognition mechanisms and binding of xanthones on human serum albumin by liquid chromatography.

Aim: To develop a method for enantioseparation of several chiral derivatives of xanthones (CDXs) by LC using a human serum albumin-chiral stationary phase (HSA-CSP) and screening CDX-HSA affinity. Additionally, recognition mechanisms were investigated. Materials & methods: The influence of organic modifier, buffer type, pH and ionic strength of mobile phase, and temperature were explored. The affinity was determined by measuring the retention times and further calculation of bound percentage. Chiral recognition mechanisms were investigated by docking. Results: Enantioselectivity and resolution values ranged from 1.40 to 9.16 and 1.51 to 4.97. Bound percentages ranged from 79.02 to 99.99%. Conclusion: LC systematic study and binding affinity of CDXs on HSA-CSP are presented here for the first time, expanding the applications of HSA-CSP for this class of compounds.

Separation of 1,4-Dihydropyridine Derivative and Its Oxidized Form

Derivatives of 1,4-dihydropyridine (DHP) still play an important role in treatment of cardiovascular diseases. Typical degradation of the DHP ring is aromatization to pyridine ring which occurs both chemically and biochemically. It is, therefore, important to have a reliable and robust analytical method for separation of DHPs from their oxidized counterparts. Separation of closely-related substances possessing similar hydrophobicity, such as DHP and its oxidized form, can be challenging on conventional alkyl-bonded sorbents. In this study, an impact of reversed-phase (RP) liquid chromatography conditions on separation of the DHP/Ox pair has been investigated. Initially, a systematic study has been performed on 33 commercial RP columns with mobile phase acetonitrile/water for separation of foridone and its corresponding oxidized form. The retention and selectivity are discussed in view of the hydrophobic-subtraction model. Best separation was found replacing conventional C18 sorbents with ones containing an embedded polar group due to polar interactions. Similarly, application of cyano columns resulted in efficient separation of analytes. Organic modifier of mobile phase (methanol vs. acetonitrile) contributed significantly to separation of foridone from its oxidized counterpart. Separation of six chemically diverse DHPs from corresponding oxidized forms was studied on seven RP columns (traditional C18 sorbent, alkyl sorbent with polar embedded group, two different aromatic phases, pentafluorophenylpropyl sorbent and sorbent with straight chain perfluorohexyl ligand). Both acetonitrile and methanol were applied as organic modifier. It was found that application of alkyl sorbent with an embedded polar group (column Zorbax Bonus RP) or cyano sorbent (column ACE CN) yields clear separation of chemically diverse DHPs from their oxidized forms.

Photografted methacrylate-based monolithic columns coated with cellulose tris(3,5-dimethylphenylcarbamate) for chiral separation in CEC.

A chiral capillary monolithic column for enantiomer separation in capillary electrochromatography was prepared by coating cellulose tris(3,5-dimethylphenylcarbamate) on porous glycidyl methacrylate-co-ethylene dimethacrylate monolith in capillary format grafted with chains of [2(methacryloyloxy)ethyl] trimethylammonium chloride. The surface modification of the monolith by the photografting of [2(methacryloyloxy)ethyl] trimethylammonium chloride monomer as well as the coating conditions of cellulose tris(3,5-dimethylphenylcarbamate) onto the grafted monolithic scaffold were optimized to obtain a stable and reproducible chiral stationary phase for capillary electrochromatography. The effect of organic modifier (acetonitrile) in aqueous mobile phase for the enantiomer separation by capillary electrochromatography was also investigated. Several pairs of enantiomers including acidic, neutral, and basic analytes were tested and most of them were partially or completely resolved under aqueous mobile phases. The prepared monolithic chiral stationary phases exhibited a good stability, repeatability, and column-to-column reproducibility, with relative standard deviations below 11% in the studied electrochromatographic parameters.

Characterization of the Retention of Artificial Sweeteners by Hydrophilic Interaction Liquid Chromatography

ABSTRACTThe aim of this work was to study the chromatographic behavior of polar artificial sweeteners on three hydrophilic interaction liquid chromatography (HILIC) columns: Kinetex HILIC (unbounded silica, core shell), ZIC HILIC (sulfoalkylbetain) and TSKgel Amide-80 (amide). The studied analytes were dipeptides (aspartame, neotame, advantame, alitame), sulfamates (acesulfame, saccharin, cyclamate), and sugars (sucralose, neohesperidin dihydrochalcone). Critical parameters such as the mobile phase pH, buffer concentration, column temperature, and organic modifier were studied for the investigation of the retention mechanism. Partition and adsorption models were also used. The retention mechanism of dipeptides seems to be partition for the aqueous layer and weak electrostatic interactions or hydrogen bonds. For the sulfamates, on Kinetex and ZIC HILIC columns, it is likely that partitioning to the aqueous layer is combined with the ERLIC phenomena at pH 5.5. For the TSKgel Amide, the partition and the hydrogen bonds formed between the analytes and carbamoyl groups of the stationary phase play an important role in the retention mechanism. For sucralose, partition seems to be the predominant mechanism in every column, while, for neohesperidin dihydrochalcone, both partition to aqueous layer and hydrogen bonding seems to contribute to the retention. This is also the first report of a method for the chromatographic determination of advantame, a new sweetener.

Impact of organic modifier and temperature on protein denaturation in hydrophobic interaction chromatography

The goal of this study was to better understand the chromatographic conditions in which monoclonal antibodies (mAbs) of broad hydrophobicity scale and a cysteine conjugated antibody-drug conjugate (ADCs), namely brentuximab-vedotin, could denaturate. For this purpose, some experiments were carried out in HIC conditions using various organic modifier in natures and proportions, different mobile phase temperatures and also different pHs. Indeed, improper analytical conditions in hydrophobic interaction chromatography (HIC) may create reversed-phase (RP) like harsh conditions and therefore protein denaturation. In terms of organic solvents, acetonitrile (ACN) and isopropanol (IPA) were tested with proportions ranging from 0 to 40%. It appeared that IPA was a less denaturating solvent than ACN, but should be used in a reasonable range (10–15%). Temperature should also be kept reasonable (below 40°C), to limit denaturation under HIC conditions. However, the combined increase of temperature and organic content induced denaturation of protein biopharmaceuticals in all cases. Indeed, above 30–40°C and 10–15% organic modifier in mobile phase B, heavy chain (HC) and light chain (LC) fragments dissociated. Mobile phase pH was also particularly critical and denaturation was significant even under moderately acidic conditions (pH of 5.4).Today, HIC is widely used for measuring drug-to-antibody ratio (DAR) of ADCs, which is a critical quality attribute of such samples. Here, we demonstrated that the estimation of average DAR can be dependent on the amount of organic modifier in the mobile phase under HIC conditions, due to the better recovery of the most hydrophobic proteins in presence of organic solvent (IPA). So, special care should be taken when measuring the average DAR of ADCs in HIC.

Fragmental Method KowWIN as the Powerful Tool for Prediction of Chromatographic Behavior of Novel Bioactive Urea Derivatives

A series of the new urea derivatives with antinociceptive activity has been chromatographically evaluated using reversed phase materials: Zorbax Extend-C18, Cogent UDC Cholesterol with organic-aqueous eluent systems with two organic modifiers (methanol and acetonitrile). The chromatographic lipophilicity parameters: log kw, S and φ0 were determined basing on linear relationship between log k values and concentration of organic mobile phase modifier. The structure-retention studies revealed that the retention mechanism for all studied urea derivatives is uniform for the proposed chromatographic systems. However, a few exceptions were noticed. Derivatives containing nonpolar substituents in the imidazole ring acted as outliers for cholesterol column. In turn, the derivative containing ester polar substituent acted as an outlier in conventional reversed-phase system. Quantitative relationships based on a wide set of established computational molecular descriptors and experimental chromatographic data were also developed. Through a systematic study, by using the principal component analysis, fragmental method KowWIN appeared to be the most powerful software to produce reliable estimations of experimental retention parameters obtained on cholesterol column.

Sensitive determination of atorvastatin in human plasma by dispersive liquid-liquid microextraction and solidification of floating organic drop followed by high-performance liquid chromatography.

A novel and sensitive dispersive liquid-liquid microextraction method based on the solidification of the floating organic drop combined with high-performance liquid chromatography and ultraviolet detection was used for the determination of atorvastatine in blood serum samples. The chromatographic separation of atorvastatin was carried out using methanol as the mobile phase organic modifier. Various parameters affecting the extraction efficiency were optimized, such as the kind and volume of extraction solvent (1-undecanol) and disperser solvent (acetonitrile), pH, and the extraction time. The calibration curve was linear in the range of 0.2-6000 μg/L of atorvastatin (r(2) = 0.995) with a limit of detection of 0.07 μg/L. The relative standard deviation for 100 μg/L of atorvastatin in human plasma was 8.4% (n = 4). The recoveries of plasma samples spiked with atorvastatin were in the range of 98.8-113.8%. The obtained results showed that the proposed method is fast, simple, and reliable for the determination of very low concentrations of atorvastatin in human plasma samples.