Chromatography Research InternationalVolume 2012 (2012), Article ID 458153, 6 pagesdoi:10.1155/2012/458153

Research Article

Selectivity of Brij-35 in Micellar Liquid Chromatographic Separation of Positional Isomers

Najma Memon, Huma I. Shaikh, and Amber R. Solangi

National Centre of Excellence in Analytical Chemistry, University of Sindh, Jamshoro, Sindh 78060, Pakistan

Received 19 September 2011; Revised 31 October 2011; Accepted 14 November 2011

Academic Editor: Maria Jose Ruiz-Angel

Copyright © 2012 Najma Memon et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Implementation of Brij-35, a nonionic surfactant, as a mobile phase for separation of positional isomers is investigated. Chromolith C-18 SpeedROD is used as a stationary phase. The effect of surfactant and organic modifier (propanol) concentration on the separation of some selected isomers is studied and evaluated in terms of linear solvation energy relationship (LSER). Shape selectivity is assessed by α value of sorbic and benzoic acid, which is found to be 1.339 by using mobile phase composed of 0.5% aqueous solutions of Brij-35 and propanol in 9 : 1. Isomers of parabens, nitroanilines, nitrophenols, and quinolinols are successfully separated using mobile phases composed of various percentages of surfactant and propanol. System constants for nonionic MLC using LSER analysis show that hydrogen bond basicity and dipolarity may be major contributors to selectivity, while excess molar refraction helps fine-tuning the separation which also imparts unique selectivity to nonionic surfactants as compared to ionic ones.

1. Introduction

Use of surfactants as mobile phases in HPLC above critical micellar concentration (cmc) gave birth to a new branch of chromatography, now known as micellar liquid chromatography (MLC) [1]. Since its first use for separation of PAHs in 1980 [2], a number of publications, books, and monographs appeared in the literature covering the applications and characterization of MLC systems [3–5].

The most commonly used surfactant in liquid chromatography and in overall analytical chemistry is sodium dodecylsulfate (SDS) [6], an anionic surfactant as compared to other cationic and nonionic surfactants [7]. In nonionic surfactants, Brij-35 (polyoxyethylene dodecyl ether) has found applications in liquid chromatography as it is non-UV absorbing, which is a drawback of other nonionic surfactants having aromatic ring into their structure.

Brij-35 is reported as mobile phase for the separation of a number of compounds [7]. In a previous report [8] by our group, we reported that isomers of propyl-parabens could be better separated by Brij-35 as compared to SDS. Takayanagi et al. [9, 10] have also reported the separation of various positional isomers using Brij-35 as a surfactant in capillary electrophoresis. Vlasenko et al. [11] have studied the dissociation constants of hydroxybenzoic acids and parabens and found that addition of Brij-35 alters the dissociation of these compounds. Inspite of the number of publications on MLC using non-ionic surfactants as mobile phases, none of them is specifically focused on separation of isomers.

Separation of positional isomers is of importance from pharmaceutical perspective, due to differences in their complexation, toxicity, and reactivity in biological systems. Positional isomers cannot normally be separated through reverse phase HPLC with ODS columns commonly available in the laboratories with methanol/water or acetonitrile/water as mobile phases [12]. The objective of current study is to evaluate if Brij-35 could be used as mobile phase for separation of positional isomers and to find out the interaction responsible for selectivity in MLC using Brij-35. Here, we have investigated nonionic surfactants as mobile phase for separation of positional isomers using Chromolith C-18 column. The organic modifier (propanol) and surfactant (Brij-35) concentration on separation of some positional isomers is studied. The findings are discussed and selectivity is accessed by using benzoic acid/sorbic acid selectivity ratio and reported in terms of LSER parameters, which then are correlated to understand the system selectivity.

2. Experimental

2.1. Instrumentation

A Hitachi 6010 liquid chromatograph fitted with a Hitachi L-4200 variable wavelength UV-Vis detector, a Rheodyne 7125 injector, and a Chromolith performance RP-18 e, 100 mm × 4.6 mm i.d. column (E. Merck, Darmstadt, Germany) was used. CSW32 software (Data Apex) was used for data acquisition and integration. The 220 nm (quinolinols), 254 nm (Methazones, parabens, cresols, and nitrophenols), and 320 nm (nitroanilines) were set, and flow rate was 1.0 mL/min for all experiments except nitrophenols and quinolinols, which is 2.0 mL/min.

2.2. Materials and Reagents

Brij-35 was purchased from Sumito Corporation, Tokyo, Japan, prepared in Millipore water and used without degassing and filtration; propanol (Fluka, Sigma-Aldrich, Buchs, St.Gallen, Switzerland) was mixed within system depending on percentage required. Benzoic acid, quinolinols, nitroanilines, parabens (Fluka, Sigma-Aldrich, Buchs, St.Gallen, Switzerland), sorbic acid (Merck, Frankfurt, Germany), beta-and dexamethasone (Glaxo SmithKline, Dungarvan, Ireland) and cresol (Riedel-Hansen, Sigma-Aldrich, Seelze, Lower Saxony, Germany) were used as received their stock solutions were prepared in propanol, and working solutions were diluted with running mobile phase. HPLC grade methanol was purchased from Fisher Scientific, Loughborough, UK.

3. Results and Discussion

3.1. Separation of Isomers

Table 1 shows the retention time and resolution data for various isomers including benzoic acid and sorbic acid for hydro-organic and hybrid non-ionic micellar mobile phase. It could be clearly observed that same mobile phase is not optimum for all separations and for most solutes studied here; separation is also possible with hydro-organic mobile phases but micellar mobile phase offers better resolution.

Table 1: Retention time and resolution data for various positional isomers using hydro-organic and hybrid surfactant mobile phase composition.

Analyte
Solvent composition
* (R)
Solvent composition
* (R)

2-nitroaniline

2.87
88 : 12
4.57

3-nitroaniline
1 : 1 MeOH/water
2.28 (1.99)
Brij35 (2% aq. soln.)/propanol
3.7 (2.56)

4-nitroaniline

1.99 (1.14)
3.43 (0.92)

2-quinolinol
1 : 1MeOH/water
2.2
99 : 1
2.53

4-quinolinol
1.67 (1.53)
Brij-35 (1.5% aq. soln.)/propanol
1.78 (1.629)

o-cresol

2.03
90 : 10
1.69

p-cresol
7 : 3 MeOH/water
1.96
Brij35 (1.75% aq. soln.)/propanol
1.65

m-cresol

1.96
1.65

m-nitrophenol
7 : 3 MeOH/water
2.27
88 : 12
1.83

p-nitrophenol
2.07 (0.453)
Brij-35 (2% aq. soln.)/propanol
1.62 (1.35)

Dexamethazone
7 : 3 MeOH/water
2.49
99 : 1
4.24

Betamethasone
2.52
Brij-35 (1.5% aq. soln.)/propanol
4.04

Propylparaben
7 : 3 MeOH/water
2.3
96 : 4
7.33

iso-propylparaben

2.21 (0.32)
Brij-35 (1.75% aq. soln.)/propanol
6.47 (0.809)

Bezoic acid
4 : 6 MeOH/water
1.78
90 : 10
4.92

Sorbic acid
2.24 (0.64)
Brij-35 (1.5% aq. soln.)/propanol
3.88 (1.73)

* is retention time in minutes; in parenthesis “R” is resolution.

These separations were studied with mobile phase composed of aqueous solution of surfactant with concentration (1-2%) and modifier in the ratio 1–20% to the surfactant at pH 3 (adjusted with phosphoric acid). All the solutes were studied for 1.25, 1.5, 1.75, and 2% Brij-35 aqueous solution prepared in millipore water with various percentages of propanol. It was found that the increase in surfactant concentration can reduce the retention time but does not affect separation appreciably. So, for all pair of analytes, surfactant that provides better resolution was selected. Addition of organic modifier (1-propanol) imparts interesting changes in retention times and resolution. Figure 1 shows the effect of propanol concentration on retention times of isomers of nitroanilines, quinolinols, and parabens.

(a)

(b)

(c)

(d)

Figure 1: Effect of propanol concentration on retention of isomers of (a) quinolinol (Brij-35 1.5% aq. Soln.), (b) nitroanilines (Brij-35 1.75% aq. Soln.), (c) parabenes (Brij-35 1.5% aq. Soln.), and (d) parabens (Brij-35 1.75% aq. Soln.).

Propanol decreases the retention times in all cases, and more difference in retention time is seen at small organic modifier content but resolution is better at higher concentrations. The decrease in retention is linear for quinolinols (Figure 1(a)) and nitroanilines (Figure 1(b)) though for nitroanilines not as good as for quinolinols. For parabens, a visible shift in retention time trend at 6% propanol (Figures 1(c) and 1(d)) is seen which is also observed with nitroanilines (visible when Figure 1(b) is expanded) and other compounds (data not shown). These findings are different in the previously reported data [7] that up to 20% propanol concentration micelles exist which may still be valid that this trend may be due to stripping of adsorbed surfactant from stationary phase at increasing propanol concentration. This study indicates that retention behaviour in MLC changes at 6% propanol with non-ionic Brij-35 surfactant when hybrid micellar mobile phase in HPLC with C-18 columns is used.

Better separation of isomers is observed at higher propanol concentration in most cases studied here as relatively sharp peaks appeared as compared to those at low propanol content (Figure 2). This may be due to decreased amount of adsorbed surfactant on C-18 stationary phase, which helps better mass transfer between stationary and mobile phase hence reduce diffusion of analyte.

Figure 2: Effect of propanol concentration on sharpness of peaks of isomers of nitroanilines. Ratio of Brij-35 (2% aq. Soln.) to propanol (1) 88 : 12, (2) 90 : 10, (3) 92 : 08, (4) 94 : 06, (5) 96 : 04.

It is also interesting to observe that o- and m-nitroanilines are better resolved with methanol/water while m- and p-nitroanilines with hybrid surfactant system. Cresols could not be separated with either system; for rest of the studied isomers, better separations are obvious using hybrid surfactant mobile phases.

Selectivity of system was assessed by calculating value of benzoic acid/sorbic acid . Highest value of 1.40 was observed with Brij35 (1.5% aqueous solution)/propanol in the ratio of 90 : 10, while with 40 : 60 methanol/water the factor was 0.74. Also the elution order was reversed; with surfactant containing mobile phase sorbic acid elutes first, while with hydro-organic benzoic acid appears first.

3.2. Interactions Responsible for Separation of Isomers

In traditional hydro-organic chromatography, selectivity for separation of isomers is correlated with molecular order within stationary phase. Selectivity is enhanced with increasing hydrocarbon stationary phase, increased chain length, and decreased temperature [17]. Unique selectivity is observed with micellar liquid chromatography as compared to hydro-organic chromatography, that is, retention factor has linear relationship with homologous series in MLC in contrast to LC which is logarithmic. The phenomenon is explained on the basis of absence of free energy change in MLC for the formation of cavity in mobile phase for incorporation of solute with increasing hydrophobicity [18]. The linear increase in “” is also ascribed for larger number of compounds eluted per unit time [14, 18].

In MLC, not only mobile phase contributes to the separation but surfactant modified stationary phase also plays a role. It is obvious in early reports on MLC that surfactants adsorb on stationary phases consequently modify their properties. Ionic surfactants adsorb on ODS surfaces and reaches plateau when surfactant-modified mobile phases are run. For nonionic surfactants, no plateau is observed and adsorption of surfactant is continuous with micellar mobile even above the cmc [19]. Quiñons-Torrelo et al. [20] have reported that nonionic surfactant impart interesting changes in polarity of stationary phase and termed the type of chromatography as Micellar Biopartitioning Chromatography (MBC). The same author further reported that this cannot afford separation of enantiomers, while in our work we can partially separate enantiomers of steroids; this shows that statement is valid for MBC only.

Linear solvation energy relation (LSER) is used to understand the types and relative strengths of chemical interactions that control retention and selectivity in various separation techniques [21]. LSER equation as proposed by Abraham is , where is retention factor, is constant, , , , , and are solute descriptors independent of mobile and stationary phase used. is solute excess molar refraction, is dipolarity/polarizability, and are acidity and basicity and is MsGowan’s characteristic molecular volume. The lower case letters , , , , , and are the system constant reflecting the difference in solute interactions between mobile and stationary phase [22].

LSER has also been applied to MLC [13], where additional solute descriptors are added in the equation to explain the behaviour of ionic surfactants. In a recent review by Ruiz-Ángel [14], it is demonstrated that hydrophobicity coefficient “” varies in narrow range with change in micellar mobile phase composition hence hydrophobic interactions are scarcely affected. LSER studies of MBC has shown to have pronounce effect by hydrophobicity as given by high coefficients for “” [20]. This type of effect can also be observed in a report by Mutelet et al. [15], where values for Brij-35 (0.08 M), SDS (0.1 M), and CTAB (0.01 M), with 15% isopropanol as additive are , and , respectively.

Nonetheless, characterization of separation of isomers is explained on the basis of hydrophobicity value since most of the positional isomers have identical value for example, 2-, 3-, 4-nitroaniline. Berthod et al. [22] have discussed the utility of Abraham’s LSER model to characterize chiral recognition behaviour of teicoplanin aglycon chiral phases. Appreciably different patterns were found for chiral phases as compared to others, while it is worth noting in the report that and parameters besides and also play a role in fine tuning of separation mechanism.

The system constants using LSER approach are system specific, that is, applicable to given stationary and mobile phase. As for non-ionic liquid chromatography, system constants are already reported so to understand the isomer recognition mechanism of MLC Linear Solvation Energy Relationship parameters for various systems reported in the literature gathered (Table 2).

Table 2: LSER system constants for various stationary and mobile phases reported in the literature.

Column
Mobile phase

System parameters
Ref.

e
s
a
b

ODS
50% ACN
0.181

1.492
[13]

Polar Endcapped
50% ACN
0.173
−0.444
−0.396
−1.261
1.323

Polar embedded
50% ACN
0.146
−0.339
−0.079
−1.581
1.320

TAG
20% ACN
0.345
−0.001
−0.315
−1.202
1.349
[14]

TAG
25% MeOH
0.478
0.267
−0.493

1.496

Monolith C-18
50% ACN
0.07

−0.52
−1.55
1.49
[15]

Monolith C-18
50% MeOH
0.30

−0.41
−1.77
2.10

Monolith C-18
10% MeOH
0
−0.51
−0.26
−2.18
3.83

Monolith C-18
0.04 M Brij-35*
−0.165
−0.087
−0.191
−1.284
1.080
[16]

*Mobile phase is 0.04 M Brij-35 with 0.01 M sodium dihydrogen phosphate at pH 7.4 adjusted with NaOH at 40°C.

Systems listed in Table 2 are included here on the basis of columns and mobile phases used; ODS column is most commonly used while polar-endcapped and polar embedded columns were included bearing in the mind that non-ionic surfactants that modify the surface of ODS column may have any similarity. TAG columns are chiral selectors with multiple interactions which also could provide clue, and monolith column is the part of current study and is most relevant. The LSER parameter; “” is maximum for TAG phases with MeOH as mobile phase, 0 with monolithic columns with 10% MeOH and negative for Brij-35, “” is negative for all systems except TAG phases with MeOH, while “” and “” are negative and “” is positive throughout. Table 2 shows that excess molar refraction “e” is a discriminating factor for non-ionic micellar liquid chromatography, which is negatively related to log k value. Such types of interactions are also reported by Quina et al. [16] while characterizing incorporation of non-ionic solutes in aqueous micelles using LSER analysis [23–25] and Altomare et al. [26] for estimating partitioning parameters of non-ionic surfactants. The “e” value for Brij-35 surfactant is 1.63 as compared to 0.76 for CTAB and 0.32 for SDS. The author has attributed this to polyoxyethylene head groups in Brij-35 that contribute to the polarizability of the micellar solubilization sites. Also the hydrogen bond basicity of micellar solubilization site is enhanced by the presence of ether oxygen of the polyoxyethylene headgroup. Jason et al. [23] have highlighted similar finding for other non-ionic surfactants, where molar excess refraction and basicity are major contributors to partitioning as compared to previous work on other systems. To check if similar factors contribute here, available molecular descriptors for some of the isomers are compiled in Table 3. It could be observed from Table 3 that dipolarizability is a major contributor while molar excess refraction also varies for three isomers. For cresols, no appreciable separation was observed. Only, o-cresol was little separated and this separation may be attributed to the combined effect of “” and “”. For p- and m-dinitrophenols, “” and “” are major contributors.

Table 3: Abraham’s LSER molecular descriptors for some of the isomers included in current study.

Analyte
A (acidity)
B (basicity)
S (dipolarity/dipolarizability)
E (excess molar refraction)

4-nitroaniline
0.46
0.35
1.93
1.22

3-nitroaniline
0.4
0.36
1.71
1.2

2-nitroaniline
0.3
0.36
1.37
1.18

o-cresol
0.52
0.30
0.86
0.84

m-cresol
0.57
0.34
0.88
0.82

p-cresol
0.57
0.31
0.87
0.82

p-nitrophenol
0.82
0.26
1.72
1.07

m-nitrophenol
0.79
0.23
1.57
1.05

4. Conclusions

Non-ionic micellar liquid chromatography offers different mode of interaction than hydro-organic or ionic micellar liquid chromatography. Better separation of positional isomers is possible with Brij-35/propanol hybrid mobile phase. Besides basicity, dipolarizability and excess molar refraction are responsible for fine-tuning of separation. This new face of non-ionic MLC opens field for many applications in separation of positional isomers.

Acknowledgment

Corresponding author is thankful to Professor Dr. Willie L. Hinze of Department of Chemistry, Wake Forest University, Winston, Salem, NC, USA, for his suggestions and discussion in using LSER for characterization of molecular interactions.

References

A. Berthod and C. GarcÃa-Ãlvarez-Coque, Micellar Liquid Chromatography, Marcel Dekker, New York, NY, USA, 2000.

D. W. Armstrong and S. J. Henry, “Use of an aqueous micellar mobile phase for separation of phenols and polynuclear aromatic hydrocarbons via HPLC,” Journal of Liquid Chromatography, vol. 3, no. 5, pp. 657–662, 1980.

A. Detroyer, S. Stokbroekx, H. Bohets et al., “Fast monolithic micellar liquid chromatography: an alternative drug permeability assessing method for high-throughput screening,” Analytical Chemistry, vol. 76, no. 24, pp. 7304–7309, 2004.

R. Izquierdo-Hornillos, R. Gonzalo-Lumbreras, and A. Santos-Montes, “Method development for cortisol and cortisone by micellar liquid chromatography using sodium dodecyl sulphate: application to urine samples of rugby players,” Journal of Chromatographic Science, vol. 43, no. 5, pp. 235–240, 2005.

N. Memon and M. I. Bhanger, “Micellar liquid chromatographic determination of aluminum using 8-hydroxyquinoline-5-sulphonic acid,” Acta Chromatographica, vol. 14, pp. 172–179, 2004.

M. Gil-Agustí, J. Esteve-Romero, and M. H. Abraham, “Solute-solvent interactions in micellar liquid chromatography. Characterization of hybrid micellar systems of sodium dodecyl sulfate-pentanol,” Journal of Chromatography A, vol. 1117, no. 1, pp. 47–55, 2006.

M. J. Ruiz-Ángel, M. C. Garcia-Álvarez-Coque, and A. Berthod, “New insights and recent developments in micellar liquid chromatography,” Separation and Purification Reviews, vol. 38, no. 1, pp. 45–96, 2009.

N. Memon, M. I. Bhanger, and M. Y. Khuhawer, “Determination of preservatives in cosmetics and food samples by micellar liquid chromatography,” Journal of Separation Science, vol. 28, no. 7, pp. 635–638, 2005.

T. Takayanagi and S. Motomizu, “Equilibrium analysis of reactions between aromatic anions and nonionic surfactant micelles by capillary zone electrophoresis,” Journal of Chromatography A, vol. 853, no. 1-2, pp. 55–61, 1999.

T. Takayanagi, K. Fushimi, and S. Motomizu, “Separation of various positional isomers of aromatic anions by nonionic micellar electrokinetic chromatography coupled with ion association distribution,” Journal of Microcolumn Separations, vol. 12, no. 2, pp. 107–112, 2000.

A. S. Vlasenko, L. P. Loginova, and E. L. Iwashchenko, “Dissociation constants and micelle-water partition coefficients of hydroxybenzoic acids and parabens in surfactant micellar solutions,” Journal of Molecular Liquids, vol. 145, no. 3, pp. 182–187, 2009.

T. Chasse, R. Wenslow, and Y. Bereznitski, “Chromatographic selectivity study of 4-fluorophenylacetic acid positional isomers separation,” Journal of Chromatography A, vol. 1156, no. 1-2, pp. 25–34, 2007.

J. R. Torres-Lapasió, M. J. Ruiz-Ángel, M. C. García-Álvarez-Coque, and M. H. Abraham, “Micellar versus hydro-organic reversed-phase liquid chromatography: a solvation parameter-based perspective,” Journal of Chromatography A, vol. 1182, no. 2, pp. 176–196, 2008.

M. J. Ruiz-Ángel, S. Carda-Broch, J. R. Torres-Lapasió, and M. C. García-Álvarez-Coque, “Retention mechanisms in micellar liquid chromatography,” Journal of Chromatography A, vol. 1216, no. 10, pp. 1798–1814, 2009.

F. Mutelet, M. Rogalski, and M. H. Guermouche, “Micellar liquid chromatography of polyaromatic hydrocarbons using anionic, cationic, and nonionic surfactants: armstrong model, LSER interpretation,” Chromatographia, vol. 57, no. 9-10, pp. 605–610, 2003.

F. H. Quina, E. O. Alonso, and J. P. S. Farah, “Incorporation of nonionic solutes into aqueous micelles: a linear solvation free energy relationship analysis,” Journal of Physical Chemistry, vol. 99, no. 30, pp. 11708–11714, 1995.

C. A. Rimmer and L. C. Sander, “Shape selectivity in embedded polar group stationary phases for liquid chromatography,” Analytical and Bioanalytical Chemistry, vol. 394, no. 1, pp. 285–291, 2009.

M. F. Borgerding, F. H. Quina, W. L. Hinze, J. Bowermaster, and H. M. McNair, “Investigation of the retention mechanism in nonionic micellar liquid chromatography using an alkylbenzene homologous series,” Analytical Chemistry, vol. 60, no. 22, pp. 2520–2527, 1988.

M. F. Borgerding and W. L. Hinze, “Characterization and evaluation of the use of nonionic polyoxyethylene (23) dodecanol micellar mobile phases in reversed-phase high-performance liquid chromatography,” Analytical Chemistry, vol. 57, no. 12, pp. 2183–2190, 1985.

C. Quiñones-Torrelo, Y. Martin-Biosca, J. J. Martínez-Pla, S. Sagrado, R. M. Villanueva-Camañas, and M. J. Medina-Hernández, “QRAR models for central nervous system drugs using biopartitioning micellar chromatography,” Mini Reviews in Medicinal Chemistry, vol. 2, no. 2, pp. 145–161, 2002.

M. Vitha and P. W. Carr, “The chemical interpretation and practice of linear solvation energy relationships in chromatography,” Journal of Chromatography A, vol. 1126, no. 1-2, pp. 143–194, 2006.

A. Berthod, C. R. Mitchell, and D. W. Armstrong, “Could linear solvation energy relationships give insights into chiral recognition mechanisms?. 1. π-π and charge interaction in the reversed versus the normal phase mode,” Journal of Chromatography A, vol. 1166, no. 1-2, pp. 61–69, 2007.

W. C. Jason, “Comparison of retention on traditional alkyl, Polar endcapped, and Polar embedded group stationary phases,” Journal of Separation Science, vol. 31, no. 10, pp. 1712–1718, 2008.

Y. Chu and C. F. Poole, “System maps for retention of neutral organic compounds under isocratic conditions on a reversed-phase monolithic column,” Journal of Chromatography A, vol. 1003, no. 1-2, pp. 113–121, 2003.

R. Lu, J. Sun, Y. Wang et al., “Characterization of biopartitioning micellar chromatography system using monolithic column by linear solvation energy relationship and application to predict blood-brain barrier penetration,” Journal of Chromatography A, vol. 1216, no. 27, pp. 5190–5198, 2009.

C. Altomare, A. Carotti, G. Trapani, and G. Liso, “Estimation of partitioning parameters of nonionic surfactans using calculated descriptors of molecular size, polarity, and hydrogen bonding,” Journal of Pharmaceutical Sciences, vol. 86, no. 12, pp. 1417–1425, 1997.