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Article

Adsorption/Desorption Characteristics and Simultaneous Enrichment of Orientin, Isoorientin, Vitexin and Isovitexin from Hydrolyzed Oil Palm Leaf Extract Using Macroporous Resins

by
Mohamad Shazeli Che Zain
1,
Soo Yee Lee
1,
Chian Ying Teo
2,* and
Khozirah Shaari
1,*
1
Natural Medicines and Products Research Laboratory (NaturMeds), Institute of Bioscience, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia
2
Department of Pharmaceutical Chemistry, School of Pharmacy, International Medical University, Bukit Jalil 57000, Kuala Lumpur, Malaysia
*
Authors to whom correspondence should be addressed.
Processes 2021, 9(4), 659; https://doi.org/10.3390/pr9040659
Submission received: 12 March 2021 / Revised: 31 March 2021 / Accepted: 7 April 2021 / Published: 9 April 2021
(This article belongs to the Special Issue Extraction and Purification of Bioactive Compounds)
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Abstract

:
Oil palm leaves (OPL) containing flavonoid C-glycosides are abundantly generated as oil palm byproducts. The performances of three macroporous resins with different physical and chemical properties for the enrichment of isoorientin, orientin, vitexin, and isovitexin from acid-hydrolyzed OPL (OPLAH) extract were screened. The XAD7HP resin exhibited the best sorption capacities for the targeted flavonoid C-glycosides and was thus selected for further evaluation. Static adsorption using the XAD7HP resin under optimal conditions (extract adjusted to pH 5, shaken at 298 K for 24 h) gave adsorption kinetics that fit well with a pseudo-second-order kinetic model. The adsorption of isoorientin and orientin was well described by Langmuir isotherms, while vitexin and isovitexin fit well with the Freundlich isotherms. Dynamic sorption trials using the column-packed XAD7HP resin produced 55–60-fold enrichment of isovitexin and between 11 and 25-fold enrichment of isoorientin, vitexin, and orientin using aqueous ethanol. The total flavonoid C-glycoside-enriched fractions (enriched OPLAH) with isoorientin (247.28–284.18 µg/mg), orientin (104.88–136.19 µg/mg), vitexin (1197.61–1726.11 µg/mg), and isovitexin (13.03–14.61 µg/mg) showed excellent antioxidant free radical scavenging activities compared with their crude extracts, with IC50 values of 6.90–70.63 µg/mL and 44.58–200.00 µg/mL, respectively. Hence, this rapid and efficient procedure for the preliminary enrichment of flavonoid C-glycosides by using macroporous resin may have practical value in OPL biomass waste utilization programs to produce high value-added products, particularly in the nutraceuticals, cosmeceuticals, pharmaceuticals, and fine chemicals industries.

Graphical Abstract

1. Introduction

The oil palm (Elaeis guineensis Jacq.) tree was introduced into Malaysia in 1875, with the first oil palm tree plantation established at Tennamaran Estate in Kuala Selangor [1]. Fueled by full support from Malaysian government agricultural diversification initiatives, palm oil plantations expanded tremendously and now cover a large acreage of agricultural land areas [2]. Currently, Malaysia is the second-largest oil palm producer in the world after Indonesia [3]. In fact, the latest statistics show that Malaysia was reaching 20 million tons of crude palm oil production in 2020 [4]. However, in the wake of this massive cultivation, a huge amount of oil palm biomass is generated as agricultural waste. Apart from mesocarp fibers (MF), empty fruit bunches (EFB), and palm kernel shells (PKS) from downstream processing in oil palm mills, in parallel, oil palm trunks (OPT), oil palm fronds (OPF), and oil palm leaves (OPL) were also generated, presenting a huge environmental problem if left unutilized [5].
Like many other species in the plant kingdom, OPL byproduct is an excellent source of phytochemicals which could be used for some applications. OPL have in fact been reported to contain bioactive compounds that are responsible for various medicinal properties, such as treating kidney diseases, cancer, cardiovascular diseases, and wounds [6]. A previous study on OPL revealed the presence of both flavonoid O- and C-glycosides [7]. In general, flavonoid C-glycosides are not widely present in plants, and due to this, they have received less attention in comparison with their O-glycosyl counterparts. Nevertheless, several recent biological and pharmacological studies have shown that flavonoid C-glycosides also possess a wide spectrum of biological properties, which include anticancer, hepatoprotective, antioxidant, and antidiabetic properties [8]. Flavonoid C-glycosides differ from flavonoid O-glycosides in that they are more resistant to hydrolysis, since the aglycone is linked to the anomeric carbon of the sugar moiety via an acid-resistant C-C bond. Figure 1 shows the structures of four flavonoid C-glycosides of OPL, which include orientin, isoorientin, vitexin, and isovitexin. These flavonoid C-glycosides were present in considerable amounts in comparison with other luteolin and apigenin derivatives in OPL [7,9,10,11,12]. It is worth noting that the global demand for flavonoids, including flavonoid C-glycosides, is forecasted to reach USD 1.2 billion by 2024 [13]. Therefore, their presence in a widely available and abundant biomass material warrants further investigation into the development of efficient methods for the preparative purification for downstream purposes and applications.
Utilization of macroporous resins (MARs) in separating and purifying the flavonoid C-glycosides present in plant extracts has been practiced in recent years. It offers an alternative to conventional methods, which often start with solid-liquid extraction, followed by liquid-liquid extraction and eventually column chromatography [14]. These conventional approaches are not only time-consuming and inefficient, but they also require high consumption of solvents and energy [15,16]. The chemical nature of MARs allows them to selectively adsorb through hydrogen bonding and Van der Waals interactions with benzene rings and hydrogen groups present in the molecular structure of the targeted flavonoids [17]. The entrapment of these flavonoids on MARs is due to similarity in their physical and chemical characteristics, such as the appropriate surface area, average pore diameter, and polarity of both the MARs and the targeted flavonoids [18,19,20]. The high flavonoid sorption capacities made MARs a useful and practical adsorbent to enrich and purify flavonoid C-glycosides from various plants such as Cajanus cajan (L.) Millsp. (pegionpea) [19], Ficus microcarpa L.f leaves [20], Abrus mollis (Jigucao) [18], and many others. Additionally, compared with silica gel, which is commonly used as the adsorbent of choice for compound separation, MARs are reusable, fast, simple, and efficient in trapping compounds of interest, particularly flavonoids from various plant materials [18,19,20].
Previously, we reported the adsorption behavior of the total flavonoids of OPL extract on different macroporous resins [9]. As an extension of this study, we further examine the adsorption and desorption properties of flavonoid C-glycosides, specifically (1) orientin, (2) vitexin, (3) isoorientin, and (4) isovitexin on a selection of MARs. The MARs with the best sorption properties for the target compounds were then used to develop a rapid and efficient method for the enrichment and purification of C-glycosyl flavonoids from acid-hydrolyzed OPL (OPLAH) extract. Factors affecting the sorption properties of the individual flavonoids C-glycoside were optimized, and their kinetics and isotherms were simultaneously evaluated. The method developed in this study presents an improved process for converting OPL biomass into fine chemicals at a high purity for potential applications.

2. Materials and Methods

2.1. Chemicals and Reagents

For the selected macroporous resins (MARs), n-(1-naphthyl) ethylenediamine dihydrochloride; quercetin; sodium acetate; sulphanilamide; 1,1-diphenyl-2-picrylhydrazyl (DPPH); and phosphoric acid were purchased from Sigma-Aldrich (St. Louis, MO, USA). Hydrochloric acid (HCl), dimethyl sulfoxide (DMSO), sodium hydroxide (NaOH), formic acid, acetonitrile, and ammonium formate were acquired from Merck (Darmstadt, Germany). Sodium nitroprusside was obtained from Bendosen Laboratory Chemicals (Bendosen, Norway), methanol (MeOH) and ethanol (EtOH) were acquired from R&R Chemicals (Essex, UK), and aluminum chloride was procured from HmbG Chemicals (Hamburg, Germany). With purities greater than 98.0%, isoorientin, orientin, vitexin, and isovitexin were obtained from Wuhan ChemFaces Biochemical Co., Ltd. (Wuhan, China). Milli-Q ultrapure water (Millipore Lab, Bedford, MA, USA) was used in all experiments.

2.2. Pretreatment of MARs

The chemical and physical properties of the selected MARs (XAD7HP, DAX-8, and XAD4) are summarized in Table 1. All MARs were pretreated prior to use to remove residual monomers and porogenic agents, which could be trapped in the pores of the resins during manufacturing. The MARs were soaked in 95% EtOH at a 1:20 ratio and washed with deionized water. The resins were then immersed in 1 mol/L NaOH and washed several times with deionized water to remove the base. Subsequently, the resins were subjected to a second immersion in 1 mol/L HCl and then washed thoroughly with deionized water to remove the acid. For each stage of the pretreatment, the resins were allowed to soak for 24 h before washing. The washed resins were then dried in a drying oven (model 100–800, Memmert, Schwabach, Germany) at 60 °C until reaching a constant weight.

2.3. Preparation of Crude and Acid-Hydrolyzed Extracts

Mature OPL were harvested from oil palm trees growing in the University Agricultural Park at the Universiti Putra Malaysia (UPM). A voucher specimen (SK 3332/18) was placed in the mini herbarium of the Institute of Bioscience (IBS) at UPM after the species was authenticated by an appointed botanist. The optimized procedures of preparing crude and acid-hydrolyzed OPL extract were described in our recent publication [10]. Briefly, the powdered OPL was mixed with aqueous MeOH (4:1 MeOH:water, v:v) and vortex-mixed for 0.5 min at 3000 g/min. The mixture was ultrasonicated at a frequency of 40 Hz for 30 min at 25 °C.
Subsequently, the crude OPL extract was mixed with distilled water and 6 mol/L HCl in a ratio of 1:10:10 (w:v:v). The mixture was incubated for 45 min at 95 °C. At 25 °C, 40 mL MeOH was added. After centrifuging at 4000 g/min for 15 min, the supernatant was separated, vacuum-evaporated to dryness, and then freeze-dried at 0.064 mbar and −50 °C using a Labconco® FreeZone Freeze Drier System (Kansas, MO, USA) to yield acid-hydrolyzed OPL extract (OPLAH).

2.4. UHPLC Analysis of Orientin, Isoorientin, Vitexin, and Isovitexin

Chromatographic separation was carried out with an ultra-high performance liquid chromatography (UHPLC) system consisting of an Ultimate 3000 LC system (Thermo ScientificTM DionexTM (Sunnyvale, CA, USA) equipped with a photodiode array detector (PDA-3000) scanning from 200 nm to 600 nm, a thermostatted column compartment, and an autosampler (ExactiveTM, Thermo Fisher Scientific, Waltham, MA, USA). An Acquity UPLC® BEH C18 column (2.1 × 100 mm, 1.7 µm) (Waters, Manchester, UK) was used for analysis. The mobile phase was comprised of solvent A (water containing 0.1% formic acid and 0.063% ammonium formate) and solvent B (acetonitrile containing 0.1% formic acid) flowing at 0.30 mL/min.
The gradient program employed was performed according to the previously reported method [9,12]. Briefly, the program was started with 10% solvent B for 0.6 min, gradually increased to 11.3% until 1.5 min, maintained isocratically until 5.5 min, and slightly increased to 11.4% until 8.0 min and 11.8% until 8.2 min. Solvent B was further increased to 12% until 12.0 min and then decreased to 10% for 1.0 min and maintained until 25 min. The column temperature was maintained at 25 °C, and the UV detector was set to a wavelength of 340 nm. Peak identification was based on the retention time and comparison of UV spectra with the respective reference standards. For sample analysis, 5 mg/mL of each sample solution was prepared and filtered through a 0.22 µm membrane filter. A 2 µL sample injection volume was used for all sample analysis.
The quantification method was developed and validated based on the following characteristics: specificity, linearity, limit of detection (LOD) and quantification (LOQ), accuracy, repeatability, intermediate precision, and robustness, according to the International Conference on Harmonization (ICH) guidelines [21]. The full information with regard to method validation has been recently published [22]. Briefly, the developed method displayed good calibration curves with linearity (R2 = 0.999) in the ranges of 16–500 µg/mL for isoorientin, 31–800 µg/mL for orientin, 47–1500 µg/mL for vitexin, and 16–500 µg/mL for isovitexin. In addition, the LODs for isoorientin, orientin, vitexin and isovitexin were 17.99, 30.22, 80.63, and 17.69 µg/mL, respectively while the LOQs for these compounds were 54.52, 91.58, 244.35, and 53.61 µg/mL, respectively. The recovery percentages were between 95% and 105% for all tested compounds, while for the inter- and intraday precisions, the relative standard deviation (RSD) values were found to be below 5%. For robustness, the chromatographic conditions, such as the detected changes in wavelength, column temperature, and sample stability showed insignificant changes, as indicated by t-test results (p > 0.05).

2.5. Preliminary Selection Macroporous Resin as an Effective Adsorbent

The static adsorption capacities of the resins were first screened to select the best resin for flavonoid enrichment. An accurately weighed amount (0.1 g) of each of the pretreated resins was transferred into 15 mL centrifuge tubes. A 5 mL aliquot of OPLAH was then added into the tubes. These centrifuge tubes were capped, placed horizontally, and taped tightly in an orbital shaker (Wisube WIG-10RL Precise Shaking Incubator, Wisd Laboratory Instruments, Wertheim, Germany). The mixture was shaken for 24 h at 298 K with an agitation speed of 150 g/min to reach adsorption equilibrium. The filtrates were then analyzed by UHPLC. To desorb the flavonoid C-glycosides from the resins, 5 mL of 95% EtOH was added into each tube, and the mixing was repeated using the same conditions, followed by filtering and the filtrates being analyzed by UHPLC. Three individual experiments were performed. Selection of the optimal MAR for use in subsequent studies was made based on the adsorption and desorption capacities of each MAR.

2.6. Optimization of Sorption Conditions Using Batch Adsorption Tests

In the present study, the four main operating parameters of temperature, pH, equilibrium time point, and initial concentration were optimized. The optimum conditions for the adsorption of flavonoid C-glycosides from OPLAH were performed using batch adsorption tests, where the 15 mL OPLAH solution was mixed with a selected adsorbent (0.3 g) and subjected to continuous agitation using an orbital shaker with a agitation speed of 150 g/min. All experiments were carried out in triplicate. The optimal conditions were selected based on the quantification of orientin, isoorientin, vitexin, and isovitexin using a developed and validated UHPLC-UV/PDA method. Simultaneously, sorption behaviors such as the kinetics and isotherm were assessed.
To select a suitable sorption temperature, the adsorption and desorption were performed at different oscillation temperatures (298 K, 308 K, and 318 K). The OPLAH solution was adjusted to a pH of 5, and the mixture was then agitated for 24 h. EtOH (95%) was used as a desorbing solvent.
To optimize the pH solution of the OPLAH, three different pHs (5, 7, and 9) were adjusted with 1 mol/L HCl or 1 mol/L NaOH. Concurrently, the equilibrium time point was monitored by withdrawing an aliquot of supernatant at 0, 15, 30, 60, 120, 180, 240, 300, 360, 480, and 1440 min. The adsorption kinetics curves for the target flavonoid C-glycosides on the XAD7HP resin were constructed. The kinetic data were subjected to two common kinetic models—pseudo-first-order [23] and pseudo-second-order models [24]—and one particle diffusion kinetic model [25].
To optimize the suitable initial concentration, different OPLAH concentrations with a known amount of target flavonoid C-glycosides were prepared, whereby the concentrations of isoorientin, orientin, vitexin, and isovitexin, were in ranges of 1.62–45.12 µg/mL, 12.64–89.76 µg/mL, 66.76–863.22 µg/mL and 1.00–12.06 µg/mL, respectively. The OPLAH solution was adjusted to the optimized pH and temperature. Simultaneously, the isotherm data was subjected to two well-known theoretical isotherm models: the Langmuir [26] and Freundlich models [27]. The RL is a dimensionless constant that was applied to signify the important equilibrium parameter of the Langmuir isotherm [28].

2.7. Dynamic Sorption Experiments on the Chromatography Column

The dynamic sorption procedure was carried out according to our recent publication [9] with modifications. By using a 2.5 cm × 46 cm glass column wet-packed with 4.4 g of dried XAD7HP resin, the dynamic adsorption and desorption experiments were performed. The resin bed volume (BV) was kept at 200 mL. The 750 mg of OPLAH was mixed with 150 mL of deionized water to form a 5 mg/mL solution. The pH of the filtered solution was adjusted to pH 5, applied to the glass column, and allowed to elute at a flow rate of 0.3 mL/min. The eluates were collected every 10 mL for UHPLC analysis. The 5% breakthrough and 95% saturation points were set based on the final to the initial concentration ratio (C/Co) of each flavonoid C-glycoside. After reaching the saturation point, the desorption process proceeded by first washing the column with 30 mL of deionized water to remove the residue and eluting with EtOH, which acted as desorbing solvent, at a flow rate of 0.3 min/mL. The eluates were collected every 10 mL for UHPLC analysis. All dynamic sorption experiments were carried out in triplicate and at an optimized temperature. The breakthrough and desorption curves were plotted to determine the breakthrough and saturation points.
To select a suitable ethanol concentration for optimal desorption, both the isocratic and gradient elution modes were performed. For the isocratic mode, upon reaching equilibrium, 20% EtOH was loaded to elute the adsorbed flavonoids. The experiment was repeated by using different EtOH concentrations (40%, 60%, 80%, and 95%). For the gradient elution mode, a separate set of experiments was performed by eluting the adsorbed flavonoids using different EtOH concentrations of 20%, 40%, 60%, 80%, and 95%. The collected fractions for both modes were concentrated using a rotary evaporator, freeze-dried, weighed, and subjected to UHPLC analysis.

2.8. Adsorption and Desorption Capacity, Kinetics, and Isotherm Model Equations

Adsorption capacity:
q e = C o − C e W × V
Desorption capacity:
q d = C d V d   W
Pseudo-first-order:
l n ( q e   −   q t   ) = − k 1 t + l n q e
Pseudo-second-order:
t q t = 1 k 2 q e 2 + t q e
Intraparticle diffusion:
q t   =   k p   ·   t 1 2 + C
Langmuir:
C e q e = K L q m + C e q m
Freundlich:
q e = K f C e 1 n
RL:
R L = 1 1 + K L C o
where qe, qd, qm, and qt are the adsorption capacity, desorption capacity, maximum adsorption capacity, and adsorption capacity at different contact times (t, min), respectively, which are stated as mg/g of dry resin; Co and Ce, are the initial and equilibrium sample concentrations, respectively, while Cd is the sample concentration in the desorption solution (these concentrations are measured in mg/mL); V, W, and C are the volume of the initial sample solution (mL), weight of the resin (g), and the constant representing the boundary layer diffusion effects (mg/g), respectively; k1, k2, and kp are the pseudo-first-order rate constant (1/min), pseudo-second-order rate constant (g/mg.min), and particle diffusion rate constant (mg/g.min1/2), respectively; KL is the Langmuir constant (mg/mL), and Kf and 1/n are the Freundlich constant ((mg/g)(mL/mg)1/n).

2.9. Determination of the Total Flavonoid Content and Antioxidant Free Radical Scavenging Activities

Evaluation of the total flavonoid content (TFC) was conducted using an aluminum chloride complex colorimetric assay [9]. Briefly, a 125 µL aliquot of 0.1 mg/mL OPL extract was transferred into a 2 mL microcentrifuge tube. Subsequently, 375 µL of 95% EtOH, 25 µL of a 10% aluminum chloride solution, 25 µL of a 1 mol/L sodium acetate solution, and 700 µL of distilled water were added, and the mixture was vortex-mixed (Vortex IKA MS 3 Basic, Selangor, Malaysia). A 200 µL aliquot of the mixture was then transferred into 96 well plates and incubated for 40 min at 25 °C, and the absorbance was recorded at 415 nm on a Tecan Infinite F200 Pro plate reader (Tecan Group Ltd., Männedorf, Switzerland). All tests were performed in triplicate. The TFC values were expressed in milligrams of quercetin equivalents per gram of extract (mg QCE/g extract).
The antioxidant assays, such as 1,1-diphenyl-2-picrylhydrazyl (DPPH), and nitric oxide (NO)-free radical scavenging activities were carried out according to the previous report [9]. The samples were prepared at 1000 µg/mL as a stock solution and serially diluted. For the DPPH assay, aliquots of 50 µL of the sample working solution were pipetted into a microtiter well plate, and each was added with 100 µL of a 59 µg/mL DPPH solution. The reaction mixtures were mixed well and incubated in the dark for 30 min, after which their absorbances were recorded at 515 nm. Similarly, for the NO assay, aliquots of 60 µL of the test concentrations were pipetted into the microtiter well plate, and each was added with 60 µL of a sodium nitroprusside solution. The reaction mixtures were mixed well and incubated for 150 min at 25 °C. Griess reagent (60 µL) was then added to each well, and the absorbance was measured at 550 nm. The scavenging activity (SA) was assessed as SA% = [(Ao − As)/Ao] × 100%, where Ao and As are the absorbances of the blank and test sample, respectively. In this experiment, quercetin was used as a positive control. The experiment was carried out in triplicate, and the results were expressed as IC50 values in µg/mL.

2.10. Statistical Analysis

The InStat V2.02 statistical package (GraphPad Software, San Diego, CA, USA) and Minitab statistical software (Version 16, Minitab Inc., State College, PA, USA) were employed for all data analyses. For analysis of significance differences, one-way analysis of variance (ANOVA) done by Tukey’s test was employed. The significant level was determined at p < 0.05. All data are shown as the mean of three replicates (n = 3).

3. Results and Discussion

3.1. Adsorption and Desorption Capacities of Selected MARs

The sorption capacities of the three MARs (XAD7HP, DAX-8, and XAD4) for the four flavonoid C-glycosides in OPLAH are shown in Figure 2. The adsorption capacity of the XAD7HP resin was 7.62 mg/g, which was considerably higher than those of DAX-8 and XAD4 at 7.41 mg/g and 0.92 mg/g, respectively. With a value of 6.73 mg/g, the desorption capacity of the XAD7HP resin was also higher than that of DAX-8 at 4.89 mg/g. Meanwhile, no desorption of flavonoid C-glycosides was observed for XAD4. Referring to these data, the XAD7HP resin had the best sorption capacities, demonstrating that an acrylic matrix, moderately polar resin, medium surface area, and large average pore diameter are the most suitable characteristics of MARs for the adsorption and desorption of the major OPLAH flavonoid C-glycosides. The findings are consistent with the previous findings, which reported high sorption capacities of the XAD7HP resin and low sorption capacities for XAD4 for grapefruit polyphenols [29] and oleuropein from olive (Olea europaea) leaves [30]. Therefore, the XAD7HP resin was selected for further evaluation.

3.2. Effect of Oscillation Temperatures on the Sorption Capacities

The oscillation temperature is crucial for the optimum sorption properties of the resins, as the intermolecular forces between the adsorbates and adsorbents could be altered by subjection to a suitable temperature. According to the results shown in Figure 3, there was no significant difference in the adsorption capacity of flavonoid C-glycosides at the three different oscillation temperatures. However, the results were different for the desorption capacity, which decreased with an increase in the oscillation temperature. Similar results were reported in a study using MARs to enrich C-glycosyl flavonoids found in trolliflowers and Abrus mollis [18,31]. Within the evaluated temperature range, the sorption process is thermopositive [32]. Hence, the optimal oscillation temperature selected was 298 K, due to it demonstrating the highest adsorption and desorption capacities for flavonoid C-glycosides.

3.3. Adsorption Kinetics of the XAD7HP Resin

The pH is a factor affecting the ionization capability of certain compounds in the solvent, which ultimately influences their adsorption affinity. Hence, it is vital to perform the sorption at the right pH [33]. Figure 4 shows that the adsorption capacities (qe) of the XAD7HP resin for isoorientin, orientin, vitexin, and isovitexin were higher at a pH of 5 than at pHs of 7 and 9. The qe values for isoorientin, orientin, vitexin, and isovitexin decreased linearly as the pH increased. Based on the observations, hydrogen bonding was deemed to play a significant role in the sorption of the XAD7HP resins. The reduction in adsorption capacity at higher pH values may have been due to the decrease of hydrogen bonding interactions, caused by the deprotonation of hydroxyl groups in the flavonoid C-glycosides and the formation of their corresponding anions [19]. On the other hand, a low pH led to an abundance of hydronium ions at the surface of the resins, which may have enhanced the hydrogen bonding between hydroxyl groups present in the flavonoid C-glycosides with the XAD7HP resin, subsequently enhancing the adsorption capacity. The better adsorption capacity of flavonoid C-glycosides in acidic rather than basic conditions has been reported previously [18,19].
The kinetics of adsorption, which explains the solute uptake rate governing the contact time of the sorption reaction, is an important characteristic that defines the sorption efficiency [34]. Hence, the adsorption behavior of the XAD7HP resins could be comprehended by accessing the adsorption kinetics of the flavonoid C-glycosides. Figure 4D presents the adsorption capacity qt versus contact time (t, min) curves for the XAD7HP resin at different pH levels at 298 K. Overall, the qt values were enhanced with an increase in time before achieving equilibrium [34]. The equilibrium time for the flavonoid C-glycosides was up to 24 h on the XAD7HP resin.
There are three commonly suggested kinetics models for adsorption: pseudo-first-order, pseudo-second-order, and intraparticle diffusion kinetic models [24,25]. Overall, the correlation coefficient (R2) values revealed that the adsorption of flavonoid C-glycosides on the XAD7HP resin fit better to a pseudo-second order kinetic model compared with a pseudo-first-order model. In addition, Table 2 also reveals the multilinear characteristics of adsorption of the flavonoid C-glycosides on the XAD7HP resin, based on the R2 values of the intraparticle diffusion kinetics model. The intraparticle diffusion curves of the XAD7HP resin show poor linear curves over time. By taking a pH of 5 as an example, the whole process was divided into three major phases: boundary layer diffusion (0–30 min), where the adsorption took place rapidly; a gradual adsorption phase (30–240 min), where the adsorption happened slowly; and finally, the equilibrium phase (240–1440 min), where the adsorption reached equilibrium. Similar results were reported in previous studies that showed intraparticle diffusion took place in the adsorption phase [35]. In the present study, the whole adsorption phase could not be represented by the particle diffusion kinetic models due to weak R2 values. Nevertheless, it could still explain the adsorption mechanism up to a certain phase [36]. However, it is important to note that different flavonoids, including isoorientin, orientin, vitexin, and isovitexin, will have different ratios of their molecular status to ionic status in various pH environments. This will probably result in a more complex adsorption mechanism and kinetics, which will require more extensive future studies for greater insights into the mechanisms involved.

3.4. Adsorption Isotherms on the XAD7HP Resin

The adsorption isotherms of flavonoid C-glycosides on XAD7HP resins was performed at room temperature (298 K) after taking into consideration several factors, including the practicality and energy conservation. Figure S1 shows the isotherm curves for the individual flavonoid C-glycosides in OPLAH. The adsorption behaviors of flavonoid C-glycosides on the XAD7HP resin were further assessed by using two adsorption isotherm equations, namely Langmuir and Freundlich equations. The equations revealed the interaction between the compounds and the resin [37].
The Langmuir and Freundlich parameters are listed in Table 3. The R2 values of the two models were relatively higher for isoorientin, orientin, and vitexin. With R2 values of 0.9977 and 0.9519, the adsorption behavior of isoorientin and orientin, respectively, on the XAD7HP resin followed the Langmuir equation. The results indicated that these two compounds displayed monolayer adsorption on the resin, suggesting that orientin and its isomer were in contact with the surface layer of the XAD7HP resin. Meanwhile, vitexin and isovitexin followed the Freundlich equation with R2 = 0.9700 and 0.8418, respectively, indicating the adsorption of these isomeric compounds followed a multilayer process wherein the XAD7HP resin accommodated more than one layer for the adsorption of vitexin and its pair to take place. This situation could be related to the molecular structures of vitexin/isovitexin and orientin/isoorientin [38]. As shown in Figure 1A, the molecular sizes of the vitexin and isovitexin structures were relatively smaller compared with orientin and isoorientin, due to the lack of one hydroxyl group (-OH). This could have reduced the steric hindrance in the interaction between vitexin/isovitexin and the XAD7HP resin, thus favoring a multilayer adsorption process. In the Freundlich equation, the value of RL indicates the isotherm shape, which is either unfavorable (RL > 1), linear (RL = 1), favorable (0 < RL <1), or irreversible (RL = 0) [39]. Hence, the present findings showed that the adsorption of the flavonoid C-glycosides on the XAD7HP resin was favorable. The 1/n value is a measure of the adsorption intensity [38]. A value of 1/n above 2 indicates that adsorption is unlikely to happen [40]. In this study, the 1/n values of the flavonoid C-glycosides were all above 2, suggesting that the XAD7HP resin was a suitable resin to use for absorbing the flavonoid C-glycosides from OPLAH.

3.5. Dynamic Sorption Properties of the XAD7HP Resin

On an open column, information of the breakthrough volume is important in estimating the optimum volume of sample-containing compounds of interest that can be loaded onto the column. The breakthrough point was set at 5% of the inlet concentration [9]. As shown in Figure 5A, the dynamic breakthrough curves on the XAD7HP resin were attained for isoorientin, orientin, vitexin, and isovitexin. The breakthrough volume of isoorientin on the XAD7HP resin was 100 mL, while that of orientin, vitexin, and isovitexin was 30 mL. Meanwhile, the saturation point was defined, at which the exit solute concentration reached 95% of the inlet concentration [9]. The saturation volume of isoorientin and isovitexin was 150 mL, while that of orientin and vitexin was 130 mL. The dynamic desorption curves for isoorientin, orientin, vitexin, and isovitexin on the XAD7HP resin are shown in Figure 5B,C. The results indicate that at 150 mL, the flavonoids could be sufficiently desorbed and eluted off of the XAD7HP resin column.

3.6. Comparison between Isocratic and Gradient Elution Modes for Optimal Flavonoid C-Glycoside Enrichment

Enrichment of the OPLAH flavonoid C-glycosides was carried out via isocratic and gradient elution modes by using EtOH as a desorbing solvent after considering its low cost, ease of removal, and low toxicity [41]. Previous studies have also used EtOH to desorb flavonoid C-glycosides from other various MARs [20,31,42]. The desorbed fractions from the XAD7HP resin were analyzed qualitatively and quantitatively and compared to the original OPLAH. For the isocratic elution mode, a single desorbing solvent system was applied. As shown in Figure 6A, the amount of desorbed flavonoid C-glycosides increased with an increase in the EtOH concentration (from 20% to 95%). Orientin and vitexin were enriched the most when 80% EtOH was used as a single desorbing solvent system, as a further increment to 95% EtOH gave insignificant changes. Their respective isomers, isoorientin, and isovitexin were found in the highest fold at 95% EtOH. Meanwhile, a multiple desorbing solvent system was employed in the gradient elution mode. Figure 6B shows that orientin, isoorientin, vitexin, and isovitexin started to desorb rapidly from 20% to 40% EtOH concentrations and started to decrease as the EtOH concentration increased from 60% to 95%. Thus, the results revealed that the flavonoid C-glycosides found in the OPLAH solution could be desorbed optimally at 95% and 40% for the isocratic and gradient desorption techniques, respectively. The desorption of flavonoid C-glycosides from the XAD7HP resin into the solvent was attributed to the competition between the interaction of intermolecular forces and dissolution into the solvent used [9,42].
The UHPLC chromatograms of the OPLAH and enriched fractions obtained from the isocratic desorption (95% EtOH) and gradient desorption modes (40% EtOH) are shown in Figure S2A. Comparing the chromatogram of the enriched fractions and OPLAH, it could be observed that some impurities present in the original extract were eliminated, while the relative peak areas of the four major flavonoid C-glycosides were increased by different degrees. The compounds assigned to peaks 1–4 were confirmed by commercial standards and characterized by liquid chromatography tandem mass spectrometry (LC-MS/MS) (Figure S2B) [10]. The rest of the unassigned peaks have been comprehensively discussed in our previous publications [7,9,12].
Table 4 summarized the quantitative information of the OPLAH and the enriched fractions obtained through the isocratic (with 95% EtOH) and gradient elution modes (with 40% EtOH). The XAD7HP resin was able to increase the TFC from 88.98 mg QCE/g up to 284.18 mg QCE/g dried extract by 3.2-fold. Among the four flavonoid C-glycosides, at the optimum EtOH concentrations, isovitexin was enriched the most, followed by isoorientin, vitexin, and orientin. As illustrated by Figure 6A for the isocratic elution mode, with 95% EtOH, isovitexin was enriched almost 55-fold while isoorientin, vitexin, and orientin were enriched by 11- to 20-fold. A similar trend was also observed in the gradient elution mode, where at 40% EtOH, isovitexin was enriched by 60-fold, isoorientin by 25-fold, vitexin by 20-fold, and orientin by 15-fold (Figure 6B).

3.7. Antioxidant DPPH and NO Free Radical Scavenging Activities

The antioxidant activities of OPLAH, enriched fractions, and the individual flavonoid C-glycosides were tested using DPPH and NO free radical scavenging assays, and the results are shown in Table 4. The DPPH results revealed that the total flavonoid C-glycoside enriched fractions, obtained using the isocratic and gradient desorption methods, exhibited stronger antioxidant activity, with IC50 values of 69.19 and 70.63 µg/mL, respectively. In comparison with the original OPLAH extract, the IC50 value was much lower (200 µg/mL). The results for the NO free radical scavenging assay were also similar, as the enriched fractions exhibited significantly improved activity compared with the original extract. This increase in antioxidant activity indicated the substantial contribution of the enriched flavonoid C-glycoside contents to the overall activity. The results highlighted that both the DPPH and NO free radical scavenging assays were in good agreement for evaluating the antioxidant activities in both the original and enriched fractions. Previous studies have also reported the positive correlation between the free radical scavenging activity and the presence of high amounts of phenolic constituents [43,44].
The single flavonoid C-glycoside was also assayed for the free radical scavenging activities. Isoorientin with an IC50 value of 14.70 µg/mg exhibited superior DPPH free radical scavenging activity. Its isomer, orientin, was moderately active, with an IC50 value of 57.60 µg/mg, while isovitexin and vitexin were weakly active in comparison. The results are in agreement with previous studies that reported vitexin and isovitexin were poor DPPH free radical scavengers [45,46]. The structural differences of these flavonoid C-glycosides, such as the position of glycosidic linkages and the number or position of hydroxyl groups at play, will have a significant effect on the bioactivity. For example, the presence of a single hydroxyl group on the B ring of both vitexin and isovitexin may be the reason for their lower activity, in comparison with isoorientin and orientin, which have two hydroxyl groups on the same ring (Figure 1A). Additionally, the weaker activity of isovitexin could be due to steric hindrance associated with glycosylation on C-6, as compared with on C-8 for its isomer, vitexin [47].
Meanwhile, the NO free radical scavenging activity was quite different from the DPPH free radical scavenging activity. All tested apigenin and luteolin C-glycosides had good antioxidant activity by showing a great ability to inhibit nitric oxide and superoxide anion at low concentrations. In contrast to the DPPH assay results, isovitexin and vitexin exhibited strong NO scavenging activity, with IC50 values of 0.73 and 4.31 µg/mg, respectively, whereas orientin and isoorientin exhibited weaker values. These results reflect the superiority of isovitexin and vitexin in scavenging nitric oxide and superoxide radicals, which have also been similarly reported in the study of Trigonella foenum graecum L. (fenugreek seeds) [47].

3.8. Adsorption Mechanisms

The efficiency of the adsorption and desorption processes primarily relies on the polarity of the MARs. In this experiment, the tested MARs comprised both nonpolar (XAD4) and moderately polar (XAD7HP and DAX-8) resins. The data obtained showed that moderately polar resins were more appropriate to entrap and release flavonoid C-glycosides from OPL extract. The polarity matching between the extract and resin was related to the multiple interactions between the targeted metabolites and the surface chemistry of the resin [9,19,29,48]. Being a nonpolar resin, XAD4, with its smaller pore size, has low wettability and thus is not well-dispersed in an aqueous solution, which explains the low adsorption and no desorption of polar compounds (flavonoid C-glycosides (29)). Figure 7 displays the possible interactions between the isoorientin, orientin, vitexin, and isovitexin and the moderately polar XAD7HP resin under acidic conditions. The early part of the study indicated that isovitexin showed the highest adsorption and desorption capacities, followed by vitexin, orientin, and isorientin, suggesting multiple interactions, such as electrostatic interaction, intramolecular and intermolecular hydrogen bonding, ion-dipole interactions, cation-ᴫ interaction, and Van der Waals forces of the adsorbent. The XAD7HP resin was more favorable in isovitexin compared with the other compounds (Figure 7). More specifically, the hydroxyl groups at C-4′, C-5, or C-7 of the flavones have been reported to be more acidic than the hydroxyl groups attached at other positions [49]. Thus, it is highly likely that the electrostatic interactions of the flavonoids on the surface of the resins could have resulted from the attraction of protons dissociated from the hydroxyl groups at these positions. The hydroxyl groups of the flavonoid C-glycosides can also interact with the resin through the formation of intramolecular and intermolecular hydrogen bonds [50]. Furthermore, polar adsorbates can cause ion-dipole interactions with the polar segment of the moderately polar resin. Other than that, adsorption can also be facilitated by cation-ᴫ interaction [29], which can occur between hydronium ions (H3O+) surrounding the XAD7HP resin and the benzene ring from flavonoids. Lastly, the main driving force for the sorption process on polymeric XAD7HP resin is the existence of Van der Waals forces in an aqueous solvent system. Therefore, based on the high sorption capacities obtained in the study, the efficient simultaneous sorption of isoorientin, orientin, vitexin, and isovitexin was suggested to be substantially contributed by multiple interactions [9,42].
The findings from both the isocratic and gradient elution experiments showed that isovitexin was enriched between 55- and 60-fold, while isoorientin, vitexin, and orientin were enriched by 20–25, 15–20 and 11–15-fold, respectively. This phenomenon could be due to strong hydrogen bonding interactions between the hydroxyl groups attached to the aglycones and the surface of the cross-linked polymeric resins [9,19]. The studied flavonoid C-glycosides shared similar flavone aglycone with differences in the sugar moiety position, as shown in Figure 1A. It was previously reported that a flavonoid molecule with sugar moiety attached to it could reach approximately 2.0 nm in size [50], and with additional hydroxyl groups contributed by glucosides, this collectively enhanced the sorption process to the large pore size and moderately polar resin XAD7HP.
Moreover, in between isomeric compounds, isovitexin/vitexin had higher enrichment than isoorientin/orientin. This could be explained by the steric hindrance [48,51,52]. Referring to Figure 1A, vitexin isomers have one hydroxyl group bonded at C-4′ (para position) of ring B, whereas orientin isomers have two hydroxyl groups attached at C-3′ (meta position) and C-4′ (para position) of the same ring. Since the hydroxyl group is one of the para directing groups, attachment of these hydroxyl groups onto the para position lessened the steric hindrance, resulting in less repulsion between the groups and lastly assisting the interaction of these groups with the resin through hydrogen bonds. However, the addition of one hydroxyl group onto the C-3′ position of the orientin isomers increased the steric hindrance, as the hydroxyl group was larger than the hydrogen atom, causing congestion that may have slowed down the interaction of the atom with the surface of resins.

4. Conclusions

The present study provides experimental data on the enrichment of the total flavonoid C-glycosides content via a process combining acid hydrolysis and adsorption and desorption on MARs. The XAD7HP resin showed the best sorption capacities. The enrichment of the flavonoid C-glycosides content of OPL extract was conducted at optimal conditions, where the leaf extract, prehydrolyzed with acid and adjusted to a pH of 5, was shaken at 298 K for a period of 24 h for static adsorption. The adsorption process of the target flavonoids on the XAD7HP resin could be well-described with the pseudo-second-order kinetic model. The equilibrium experimental data of the adsorption of isoorientin and orientin on the XAD7HP resin at 298 K were well fitted to the Langmuir isotherm model, while those of vitexin and isovitexin were well described by the Freundlich isotherm model. The enriched fractions recovered using the isocratic (with 95% EtOH) and gradient elution modes (with 40% EtOH) produced up to 60-fold flavonoid enrichment with excellent antioxidant free radical scavenging activities. The enriched OPLAH contained isoorientin (247.28–284.18 µg/mg), orientin (104.88–136.19 µg/mg), vitexin (1197.61–1726.11 µg/mg), and isovitexin (13.03–14.61 µg/mg), as compared to OPLAH with isoorientin (2.34 µg/mg), orientin (9.35 µg/mg), vitexin (84.11 µg/mg), and isovitexin (0.25 µg/mg). Additionally, the enriched OPLAH also showed excellent antioxidant free radical scavenging activities compared with OPLAH, with IC50 values of 6.90–70.63 µg/mL and 44.58–200.00 µg/mL, respectively. Strong hydrogen bonding may explain the efficient enrichment of the target flavonoid C-glycosides. The results indicated the combination of acid treatment and MARs could selectively and effectively enrich flavonoid C-glycosides from OPL. This study presents a simple, rapid, and efficient method for enriching the flavonoid C-glycoside content of oil palm leaf extract, a major type of agriculture waste, which has been underutilized. This method provides several potential applications, such as for further purification of major flavonoid C-glycosides as fine chemicals or pharmaceuticals or the use of the enriched fraction as bioactive ingredients in nutraceutical, cosmeceutical, and other healthcare or personal care products.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/pr9040659/s1. Figure S1: Adsorption isotherms of isoorientin (A), orientin (B), vitexin (C) and isovitexin (D) present in OPLAH at 298 K on XAD7HP resin; Figure S2: (A) UHPLC chromatograms (340 nm) of OPLAH and OPLAH-enriched fractions obtained via isocratic and gradient elution desorption modes. (B) Compound confirmation using UHPLC-MS/MS analysis.

Author Contributions

K.S. and M.S.C.Z. conceptualized and designed the experiments; K.S. provided the research materials; M.S.C.Z. performed the experiments and wrote the manuscript; K.S. and M.S.C.Z. analyzed the data; K.S. and C.Y.T. validated the data; K.S. and S.Y.L. edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The first author would like to thank Universiti Putra Malaysia for granting him a graduate research fellowship (GRF) scheme.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. (A) Structures of C-glycosyl flavonoids identified in oil palm leaves (OPL): orientin (1), vitexin (2), isoorientin (3), isovitexin (4). (B) Structure of the XAD7HP resin. R = polyfunctional aliphatic residue.
Figure 1. (A) Structures of C-glycosyl flavonoids identified in oil palm leaves (OPL): orientin (1), vitexin (2), isoorientin (3), isovitexin (4). (B) Structure of the XAD7HP resin. R = polyfunctional aliphatic residue.
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Figure 2. Adsorption (A) and desorption (B) capacities of three different macroporous resins (MARs) for major flavonoid C-glycosides in acid-hydrolized oil palm leaves (OPLAH). Each value is the average reading from three replicates (n = 3).
Figure 2. Adsorption (A) and desorption (B) capacities of three different macroporous resins (MARs) for major flavonoid C-glycosides in acid-hydrolized oil palm leaves (OPLAH). Each value is the average reading from three replicates (n = 3).
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Figure 3. Adsorption (A) and desorption (B) capacities of XAD7HP resin for major flavonoid C-glycosides in OPLAH at three different temperatures. Each value is the average reading from three replicates (n = 3).
Figure 3. Adsorption (A) and desorption (B) capacities of XAD7HP resin for major flavonoid C-glycosides in OPLAH at three different temperatures. Each value is the average reading from three replicates (n = 3).
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Figure 4. Adsorption kinetic curves of C-glycosyl flavonoids on the XAD7HP resin at pH levels of 5 (A), 7 (B), and 9 (C), and the total of four C-glycosyl flavonoids present in the OPLAH at different pH levels (D). Each value is the average reading from three replicates (n = 3).
Figure 4. Adsorption kinetic curves of C-glycosyl flavonoids on the XAD7HP resin at pH levels of 5 (A), 7 (B), and 9 (C), and the total of four C-glycosyl flavonoids present in the OPLAH at different pH levels (D). Each value is the average reading from three replicates (n = 3).
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Figure 5. Dynamic breakthrough curves for flavonoid C-glycosides (A) and dynamic desorption curves for isoorientin, orientin, and isovitexin (B) and vitexin (C) in OPLAH on XAD7HP resin. Each value is the average reading from three replicates (n = 3).
Figure 5. Dynamic breakthrough curves for flavonoid C-glycosides (A) and dynamic desorption curves for isoorientin, orientin, and isovitexin (B) and vitexin (C) in OPLAH on XAD7HP resin. Each value is the average reading from three replicates (n = 3).
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Figure 6. Enrichment of flavonoid C-glycosides from OPLAH by the isocratic elution mode (A) and gradient elution mode (B) on the XAD7HP resin. Each value is the average reading from three replicates (n = 3).
Figure 6. Enrichment of flavonoid C-glycosides from OPLAH by the isocratic elution mode (A) and gradient elution mode (B) on the XAD7HP resin. Each value is the average reading from three replicates (n = 3).
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Figure 7. Schematic representation of the postulated interactions between targeted flavonoid C-glycosides for orientin (a), isoorientin (b), isovitexin (c), and vitexin (d) and the XAD7HP resin under acidic conditions.
Figure 7. Schematic representation of the postulated interactions between targeted flavonoid C-glycosides for orientin (a), isoorientin (b), isovitexin (c), and vitexin (d) and the XAD7HP resin under acidic conditions.
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Table
Table 1. Chemical and physical properties of different macroporous resins (MARs).
Table 1. Chemical and physical properties of different macroporous resins (MARs).
XAD7HPDAX-8XAD4
Functional groupAcrylicAcrylic esterStyrene-divinylbenzene
Particle diameter (mm)0.250–0.8410.250–0.4200.250–0.841
Surface area (m2/g)380140750
Pore size (Å)300–400225100
PolarityModerateModeratePolar
Table
Table 2. Pseudo-first-order and pseudo-second-order kinetic equations and the intraparticle diffusion equation for the major C-glycosyl flavonoids in the OPLAH extract on the XAD7HP resin.
Table 2. Pseudo-first-order and pseudo-second-order kinetic equations and the intraparticle diffusion equation for the major C-glycosyl flavonoids in the OPLAH extract on the XAD7HP resin.
CompoundpHqe (exp) (mg/g)Pseudo-First OrderPseudo-Second OrderIntraParticle Diffusion
R2qe (mg/g)k1 (1/min)R2qe (mg/g)k2 (g/mg.min)R2C (mg/g)kp (mg/g.min1/2)
Isoorientin52.5668 Aa0.7935 Aa2.0738 Aa0.0063 Aa0.9995 Aa2.5813 Aa0.0416 Aa0.5133 Aa1.6715 Aa0.0485 Aa
70.5916 Ba0.8134 Ba3.1817 Ba0.0050 Ba0.9971 Ba0.6007 Ba0.0403 Ba0.8506 Ba0.1468 Ba0.0218 Ba
90.1866 Ca0.9322 Ca8.6789 Ca0.0048 Ba0.9640 Ca0.1851 Ca0.1102 Ca0.9196 Ca0.0701 Ca0.0048 Ca
Orientin55.2571 Ab0.8178 Ab1.2216 Aa0.0085 Ab0.9995 Aa5.3362 Ab0.0238 Ab0.5008 Ab3.5373 Ab0.0978 Ab
71.8269 Bb0.7892 Bb1.3399 Bb0.0059 Ba0.9980 Bb1.8643 Bb0.0195 Bb0.7597 Bb0.6503 Bb0.0613 Bb
90.2947 Cb0.8829 Cb4.9644 Cb0.0014 Cb0.9641 Ca0.2024 Cb0.0881 Cb0.8223 Cb0.0703 Ca0.0054 Ca
Vitexin51.6622 Ac0.9158 Ac3.7371 Ac0.0090 Ab0.9999 Aa1.6793 Ac0.0967 Ac0.5653 Ac1.2447 Ac0.0233 Ac
70.8356 Bc0.8718 Bc5.0799 Bc0.0075 Bb0.9999 Ac0.8457 Bc0.1137 Bc0.8157 Bc0.3242 Bc0.0235 Ac
90.2481 Cc0.9252 Cc6.8244 Cc0.0064 Cc0.9959 Bb0.2683 Cc0.0703 Cc0.8229 Cb0.0518 Cb0.0101 Bb
Isovitexin59.5296 Ad0.8763 Ad1.9927 Ad0.0072 Ac0.9998 Aa9.5877 Ad0.0120 Ad0.6099 Ad6.4869 Ad0.1639 Ad
72.5159 Bd0.8952 Ad1.1389 Bd0.0078 Ab0.9983 Bb2.6185 Bd0.0143 Bd0.7582 Bb1.0526 Bd0.0772 Bd
91.4779 Cd0.9261 Bc1.0830 Cd0.0101 Bd0.9974 Cc1.5564 Cd0.0195 Cd0.8568 Cc0.5758 Cc0.0464 Cc
Values marked with different uppercase letters (A–C) indicate a comparison between pH levels for the same compound. Values marked with different lowercase letters (a–d) indicate a comparison between different compounds for the same pH. Each value is the average reading from three replicates (n = 3).
Table
Table 3. Langmuir and Freundlich models for the adsorption of OPLAH flavonoid C-glycosides on XAD7HP resin.
Table 3. Langmuir and Freundlich models for the adsorption of OPLAH flavonoid C-glycosides on XAD7HP resin.
CompoundLangmuir EquationFreundlich Equation
qm (mg/g)R12KL (mg/mL)RL1/nKf ((mg/g) (mL/mg)1/n)R22
Isoorientin476.1905 a0.9977 a0.2381 a0.2929 a0.3754 a366.090 a0.9260 a
Orientin2000.000 b0.9519 b0.6000 b0.0480 b0.3757 a1075.70 b0.9247 a
Vitexin50000.00 c0.9624 c30.000 c0.0001 c0.9538 b1422.10 c0.9700 b
Isovitexin204.0816 d0.5187 d0.2653 d0.5120 d0.4149 c138.930 d0.8418 c
Values marked with different letters (a–d) indicate a comparison between compounds in each tested parameter. Each value is the average reading from three replicates (n = 3).
Table
Table 4. Quantification and free radical scavenging activities of flavonoid C-glycosides in OPLAH, enriched OPLAH fractions and individual compounds.
Table 4. Quantification and free radical scavenging activities of flavonoid C-glycosides in OPLAH, enriched OPLAH fractions and individual compounds.
Extract or CompoundTFC (mg QCE/g)Flavonoid C-Glycosides (µg/mg)Antioxidant Activities (IC50, µg/mL)
IsoorientinOrientinVitexinIsovitexinDPPHNO
OPLAH88.98 a2.34 a9.35 a84.11 a0.25 a200.00 a44.58 a
Enriched OPLAH (Isocratic)247.28 b46.27 b104.88 b1197.61 b13.03 b69.16 b6.90 b
Enriched OPLAH (Gradient)284.18 c55.98 c136.19 c1726.11 c14.61 b70.63 b7.32 b
Isoorientin 14.70 c68.19 c
Orientin 57.60 d42.72 a
Isovitexin >1000 e0.73 d
Vitexin >1000 e4.31 e
Values marked with different letters (a–e) indicate a comparison between OPLAH, enriched OPLAH and individual compounds for each flavonoid content and antioxidant activities. Each value is the average reading from three replicates (n = 3).
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Che Zain, M.S.; Lee, S.Y.; Teo, C.Y.; Shaari, K. Adsorption/Desorption Characteristics and Simultaneous Enrichment of Orientin, Isoorientin, Vitexin and Isovitexin from Hydrolyzed Oil Palm Leaf Extract Using Macroporous Resins. Processes 2021, 9, 659. https://doi.org/10.3390/pr9040659

AMA Style

Che Zain MS, Lee SY, Teo CY, Shaari K. Adsorption/Desorption Characteristics and Simultaneous Enrichment of Orientin, Isoorientin, Vitexin and Isovitexin from Hydrolyzed Oil Palm Leaf Extract Using Macroporous Resins. Processes. 2021; 9(4):659. https://doi.org/10.3390/pr9040659

Chicago/Turabian Style

Che Zain, Mohamad Shazeli, Soo Yee Lee, Chian Ying Teo, and Khozirah Shaari. 2021. "Adsorption/Desorption Characteristics and Simultaneous Enrichment of Orientin, Isoorientin, Vitexin and Isovitexin from Hydrolyzed Oil Palm Leaf Extract Using Macroporous Resins" Processes 9, no. 4: 659. https://doi.org/10.3390/pr9040659

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