Run-to-run reproducibility and efficiency of SDS and L-AlaC4Lac for the simultaneous separation of NSAIDs. Conditions: 100 mM Tris/10 mM tetraborate decahydrate pH 8, applied voltage 30 kV, temperature 20 °C (for SDS) and 35 °C (for L-AlaC4Lac), detection wavelength 200 nm .
Ionic liquids (ILs) are unique solvents with melting points at or below 100 ºC. They have drawn scientific interest due to their unique properties that involve good thermal stability, miscibility in different solvents, tunable viscosity, conductivity, negligible vapor pressure, non-flammability, and low toxicity. They have often been called
In the last few years, a big number of chiral ILs (CILs), have been designed, synthesized and used for applications in electrophoretic and chromatographic chiral discrimination [4, 6]. They play a key role in enantioselective analysis because they combine the advantages of ILs with the properties of a chiral moiety, which can be anionic and/or cationic. Their utility in separation science as chiral selectors, additives, chiral ligands, and chiral stationary phases is becoming increasingly important .
Although a large number of reviews have been provided on the synthesis of CILs [8-10], a surprisingly limited number of articles have been published on their utility in analytical separations, and particularly in electrophoretic separations [7, 11]. Capillary electrophoresis (CE) has been extensively used in chiral separations by using various chiral selectors, such as cyclodextrins (CDs), cyclofructans, oligo-and polysaccharides, polymeric surfactants, and others . Some of the problems that limit their use involve low solubility, instability at high temperatures and/or low pH values, time-consuming organic synthesis procedures and high cost. The use of CILs is considered a potential alternative because they can dissolve various polar and nonpolar analytes, they may provide chiral selectivity, and their synthesis procedure is simple. In CE, the CILs are mainly used as BGE additives, and secondarily as chiral ligands and chiral selectors.
A new class of CILs, called amino acid ester-based ILs (AAILs), was synthesized and characterized in 2005 by Tao
In this chapter, the ability of AAILs to be used as chiral and achiral media in CE is investigated. In particular, some representative studies that involve the utility of AAILs as background electrolyte (BGE) additives and as sole chiral selectors in electrophoretic separations are reported and discussed. These studies involve synthesis procedure, establishment of optimum separation conditions and method validation. The first part of this chapter involves the application of AAILs as BGE additives and the evaluation of their performance in both chiral and achiral analysis, while the second part demonstrates their chiral recognition ability for the enantioseparation of 1,1’-binaphthyl-2,2-diylhydrogenphosphate (BNP).
2. AAILs as background electrolyte additives
Most of the applications of AAILs (Figure 1) in electrophoretic separations have been as additives in BGEs [15-23]. Hadjistasi
2.1. Chiral analysis
The use of AAILs as BGE additives, for improved resolutions, selectivity factors, and efficiencies in chiral analysis, is demonstrated further here by providing a more in-depth analysis of a research work that was performed by Zhang
The synthesis of both AAILs was accomplished by use of a one-step anion exchange reaction of the corresponding amino acid ester chloride and the bis(trifluoromethane)sulfonimide lithium salt . Briefly, an appropriate amount of L-alanine and L-valine
The main objective of their study was to evaluate the synergistic effect of the AAILs with the β-CD derivatives. It was proven to be significant for half of the analytes examined, and particularly for naproxen, pranoprofen and warfarin. Figure 2 demonstrates the electropherograms obtained when β-CD derivatives were used as the sole chiral selectors [(a)], and when AAILs were used as additives [(b) and (c)].
The novel synergistic system was optimized by using methyl-β-CD/AAILs as model systems. An important factor affecting the enantioseparation is the concentration of the chiral selector and the CIL, since both concentrations will determine the equilibria between the chiral selector, the CIL and the enantiomers. Initially, at a fixed concentration of 20 mM methyl-β-CD, as the concentrations of L-AlaC4NTf2 and L-ValC4NTf2 increased from 5 to 15 mM both resolution and effective selectivity factor improved. However, at the concentration of 20 mM, no peak was observed, even at 60 min. The electrophoretic mobility decreased dramatically, possibly due to the adsorption of the CIL cations onto the capillary walls.
The effect of the chiral selector´s concentration on enantioseparation was also studied by varying the concentration of methyl-β-CD from 10 to 50 mM. In the single methyl-β-CD separation system, resolution values increased upon increasing the concentration, due to an increase in the complexation between the chiral selector and the enantiomers. On the other hand, in the methyl-β-CD/AAILs systems, resolution was initially increased, and then decreased mainly due to the gradual complex saturation. Therefore, the optimum concentration of methyl-β-CD is lower with the presence of the synergistic effect in comparison to the single methyl-β-CD system.
The optimum BGE composition was also determined by examining two different systems (sodium sodium acetate-acetic acid and citrate-citric acid). The first BGE provided deformed peaks, while the use of the second one resulted in better peak shapes and better resolutions. The BGE pH was also investigated for the chiral recognition process, because the degree of protonation in the analytes and the AAILs depends on this parameter. It was observed that at pH values below 4.4 or above 5.6, resolutions of all the understudy chiral compounds were reduced. Therefore, a pH value of 5.0 was considered the optimum. According to the authors, at the particular optimum pH, in the present system of analyte/AAIL/methyl-β-CD, the following bindings occur: (a) hydrogen bonding among the hydroxyl function in methyl-β-CD, carboxyl group in the drug compounds and amino function in the AAILs and (b) ionic interactions between the carboxyl group in the analytes and the amino function in the AAILs.
Another important observation, in this study, was the improvement of both resolution and effective selectivity factor with the addition of an organic modifier, possibly due to a decrease in electroosmotic mobility, which, in turn, increases the interactions between the AAIL, methyl-β-CD and analyte. Other parameters, such as composition and pH of buffer system and applied voltage were also examined, and the optimum conditions included 15 mM AAIL, 20 mM methyl-β-CD, 30 mM sodium citrate/citric acid (pH 5), and 20 kV.
2.2. Achiral analysis
In a different study, the synergistic effect of sodium dodecyl sulfate (SDS) and L-alanine
For the synthesis of L-AlaC4Lac, appropriate amounts of the corresponding amino acid ester hydrochloride and silver lactate were separately mixed with methanol. The amino acid ester solution and the suspended silver lactate were then mixed and stirred. Subsequently, the precipitate was filtered and removed, and the remained solution was evaporated
In the single SDS system, separation is achieved by differential partitioning of analytes between the hydrophilic core of the surfactant and the bulk aqueous phase via electrostatic and hydrophobic interactions, and hydrogen bonding. SDS was initially examined as a sole additive, by varying its concentration from 10 to 30 mM. It was observed from Figure 4 that, even though the migration times of all analytes increased along with the increase of SDS concentration, resolution values decreased dramatically. At 30 mM, a coelution of indoprofen and ketoprofen was observed, and carprofen did not elute, even at 30 min. This is because the predominant population, at pH 8, is in the anionic form, which is expected to be repelled by the negatively charged headgroup of the anionic surfactant.
For comparison purposes and for further optimization of the separation, an AAIL was used as an additive. The effect of its concentration on the separation of NSAIDs was first examined. The optimum concentration was determined according to resolution, efficiency and analysis time. As demonstrated in Figure 5, when a 20-mM concentration was used, the Rs values for the peak pairs carprofen-ketoprofen and flurbiprofen-ibuprofen were 1.3 and 1.2, respectively. Concentrations above 30 mM provided baseline separations with Rs values higher than 1.5. In addition, the total analysis time, in the cases of 20, 30 and 40 mM L-AlaC4Lac, was not altered (~ 9.5 min), while, from 50 to 70 mM, it was increased to ~ 12 min. Efficiency was determined by calculating the number of theoretical plates (N) for all peaks. It was observed that at a concentration of 40 mM, N for all peaks was very high, in comparison to the ones obtained when the other concentrations were applied (Figure 6). Another important observation involved the elution order of NSAIDs, which was different from the elution order observed when the SDS was added in the BGE, probably due to the different types of interactions between the additive and the analytes. In the case of SDS, the interactions are based on hydrophobicity, while in the case of the additive L-AlaC4Lac, the separation is based on electrostatic interactions.
pH is another important parameter that is necessary to be optimized because, firstly, alterations in pH can affect the analyte charge and, secondly, the primary amine group of the cation of the AAIL can be positively charged or neutral in several pHs. An increase in pH from 8.0 to 8.5, the resolution decreased from 2.9 to 1.5 for peaks carprofen-ketoprofen and from 1.7 to 1.3 for peaks flurbiprofen-ibuprofen. A further increase in pH (9.0 and 9.5) resulted in two coelutions and shorter migration times due to fewer electrostatic interactions between the AAIL and the negatively charged analyte, since the amount of the positively charged amino group is decreased. In addition, at high pH values, the AAIL may undergo ester hydrolysis, which results in the lack of the
The reproducibilities were also evaluated and compared by calculating the relative standard deviation (RSD) values of the electroosmotic flow (EOF) and the migration times of all the analyte peaks. In particular, in both SDS and L-AlaC4Lac cases, the run-to-run RSD values were obtained from 10 consecutive electrophoresis runs. In the case of SDS, the RSD of the EOF was 2.1%, and the RSD values of the analytes ranged from 2.8% to 11.7%. In the case of L-AlaC4Lac, the RSD of the EOF was 0.4% and the RSDs of the NSAIDs ranged from 1.2% to 1.3% (Table 1). In the same table, a comparison between the two additives in regard to efficiency is also demonstrated. The efficiency of all analyte peaks was above 102,000 for L-AlaC4Lac, in comparison to SDS, which provided efficiency values between 47,000 and 76,000 theoretical plates.
A last consideration for this study involved the effect of the addition of both SDS and L-AlaC4Lac into the BGE on the separation of NSAIDs. A concentration of 10 mM SDS and different concentrations of L-AlaC4Lac were added into the BGE (1-40 mM). An increase in the concentration of L-AlaC4Lac resulted in a more effective separation of NSAIDs, in regard to efficiency and resolution, probably due to the synergistic effect of the SDS/L-AlaC4Lac system. However, the elution order and analysis time (~ 23 min) were similar to the ones obtained when the SDS was used as the sole additive. Therefore, it was clear from this study that the additive L-AlaC4Lac is considered an effective alternative to SDS for a reproducible, baseline, high efficient and fast separation of NSAIDs.
3. AAILs as chiral selectors
Although numerous studies reported the use of AAILs in electrophoretic enantiomeric separation, only one study was performed by using AAILs both as co-electrolytes and chiral selectors . However, other CILs, that are not amino-acid based, have been added into the BGE and used as sole chiral selectors for the enantioseparation of a number of analytes [28-31]. Yuan
In another study by Tran and Mejac , the CIL
In 2013, Yu
As mentioned earlier, the use of AAILs as sole chiral selectors has only been reported once by Stavrou
The optimum separation conditions were established by altering different important parameters, such as the alkyl ester group, the anion, the configuration and the concentration of the AAIL. In their first study, the influence of steric hindrance on the enantiomeric separation of BNP was examined by applying separately as sole chiral selectors the AAILs L-AlaC1Lac, L-AlaC2Lac and L-AlaC4Lac at concentrations of 60 mM and 100 mM. It was observed that as the length and the bulkiness of the ester group increased, the resolution of BNP increased. In particular, the first AAIL did not demonstrate any enantioselectivity, while the second one was able to provide partial enantioseparation (RS: 1.09). However, when L-AlaC4Lac was used at both concentrations, a baseline separation was achieved with RS values of 1.94 and 2.43 (Table 2). It is, therefore, concluded that the enantioseparation of BNP is favored in the presence of
Two very important considerations in this study involved the effect of the anion and the configuration of the cation on resolution. Two different anions were used (Lac and NTf2), which provided baseline separation (Table 2). In particular, the resolution obtained by use of L-AlaC4NTf2 was slightly lower (RS=1.72) than the one obtained with L-AlaC4Lac (RS=1.94), possibly due to the low solubility of the first in water, which provides fewer free cations and less interaction with the analyte molecules. In addition, the results obtained with NTf2 were not reproducible and provided an unstable baseline. As far as the cation configuration is concerned, the D-and L-AlaC4Lac were used at a concentration of 60 mM in order to compare their enantioseparation ability. It was observed that the
In another study for the optimization of the BNP enantioseparation, the effect of the concentration of L-AlaC4Lac on resolution was investigated. As demonstrated in Figure 7, resolution increased significantly from ~ 0.4 to 2.43 with increasing the concentration from 20 to 100 mM. It was also observed that an increase in the AAIL concentration resulted in a decrease in the electroosmotic flow mobility, probably due to the coating of the AAIL cations onto the capillary wall Figure 8. The electrophoretic mobility,
The last parameter examined was the BGE pH, which was important, since the cation of the CILs used seems to be pH depended. Resolution decreased from 1.94 to 1.29, upon increasing the pH from 8 to 8.5, while at higher pHs (9 and 10), no enantioseparation was observed. As mentioned in Section 2.2, an increase in the pH decreases the amount of the positively charged amino group, which consequently reduces the electrostatic interactions between the AAIL and the negatively charged analyte. In addition, at high pH values, and particularly pH 9 and 10, the AAIL may undergo ester hydrolysis. This results in the lack of the
4. Concluding remarks
In this chapter, the suitability of the AAILs in chiral and achiral CE analysis was evaluated. These new AAILs, which can be easily synthesized from commercially available reagents, proved to be efficient chiral additives for the enantioseparation of different analytes. Even though only a limited number of studies have, so far, applied AAILs as BGE additives and chiral selectors, it is easy to conclude from the data demonstrated in this chapter that the future of AAILs in separation science has a great deal of potential, and it is expected to expand significantly. Further research though is required in order to understand the chiral recognition mechanisms between the AAILs, the common chiral selectors and the enantiomers. This will, in turn, help us design even more effective AAILs for applications in chiral electrophoretic and chromatographic recognition.
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