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Article

Effect of Rumex Acetosa Extract, a Herbal Drug, on the Absorption of Fexofenadine

by
Jung Hwan Ahn
†,
Junhyeong Kim
†,
Naveed Ur Rehman
,
Hye-Jin Kim
,
Mi-Jeong Ahn
and
Hye Jin Chung
*
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 52828, Korea
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Pharmaceutics 2020, 12(6), 547; https://doi.org/10.3390/pharmaceutics12060547
Submission received: 29 April 2020 / Revised: 6 June 2020 / Accepted: 10 June 2020 / Published: 12 June 2020
(This article belongs to the Special Issue Drug–Drug Interactions)
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Abstract

:
Herbal drugs are widely used for the auxiliary treatment of diseases. The pharmacokinetics of a drug may be altered when it is coadministered with herbal drugs that can affect drug absorption. The effects of herbal drugs on absorption must be evaluated. In this study, we investigated the effects of Rumex acetosa (R. acetosa) extract on fexofenadine absorption. Fexofenadine was selected as a model drug that is a substrate of P-glycoprotein (P-gp) and organic anion transporting polypeptide 1A2 (OATP1A2). Emodine—the major component of R. acetosa extract—showed P-gp inhibition in vitro and in vivo. Uptake of fexofenadine via OATP1A2 was inhibited by R. acetosa extract in OATP1A2 transfected cells. A pharmacokinetic study showed that the area under the plasma concentration–time curve (AUC) of fexofenadine was smaller in the R. acetosa extract coadministered group than in the control group. R. acetosa extract also decreased aqueous solubility of fexofenadine HCl. The results of this study suggest that R. acetosa extract could inhibit the absorption of certain drugs via intervention in the aqueous solubility and the drug transporters. Therefore, R. acetosa extract may cause drug interactions when coadministered with substrates of drug transporters and poorly water-soluble drugs, although further clinical studies are needed.

Graphical Abstract

1. Introduction

Oral drug administration is a preferred route, offering the advantages of convenience and safety. Many drug interactions with foods and other drugs occur via alteration of drug absorption. There are absorptive transporters, such as organic anion transporting polypeptide (OATP) and secretory transporters, including P-glycoprotein (P-gp), associated with drug absorption. To improve drug therapy, it is necessary to investigate possible interactions mediated by transporters that could alter systemic exposure of drugs.
P-gp, belonging to the ATP binding cassette superfamily, is an ATP-dependent efflux protein that excretes drugs out of cells [1,2,3]. P-gp is an important factor limiting the absorption of drugs and plays a key role in drug distribution and resistance [3,4]. For example, P-gp overexpression induced by a hypoxic environment in many cancers decreases the effects of chemotherapy [5,6]. Furthermore, drug–drug interactions may occur when substrates of P-gp (e.g., cimetidine, digoxin, doxorubicin, fexofenadine, and vinblastine) are coadministered with inhibitors of P-gp (e.g., atorvastatin, ketoconazole and quinidine) or inducers of P-gp (e.g., rifampin and clotrimazole) [7,8]. The OATP family is also an important transporter for drug disposition. The OATP members of the solute carrier (SLC) family, contributes to the uptake of substrates, including endogenous compounds and drugs [9,10]. Drug–drug interactions and food–drug interactions mediated by these two active transporters—P-gp and OATP—have been reported. In addition, a study on medication use patterns revealed that 50% of 2590 study participants had taken at least one prescription drug during the week prior to the study, and 16% of them had taken one or more herbals/supplements [11,12]. Given that St. John’s wort was found to increase P-gp expression [13], it is necessary to evaluate the effects of herbal supplements on these transporters. Despite the widespread use of herbal drugs in combination with drugs, there has been little research on the interactions between drugs and herbal medicines.
This study investigated the effects of Rumex acetosa (R. acetosa) extract on P-gp and OATP1A2 in vitro and on fexofenadine absorption in vivo. R. acetosa, used in folk remedies for skin diseases, has been singled out as a natural herbal medicine for its potential to be used in combination with fexofenadine [14]. R. acetosa is widely distributed in eastern Asia and decoction of this plant has been used for the treatment of several health disorders such as fever, gastro-intestinal problems, inflammatory diseases. It is belonging in the Polygonaceae family, known to produce many biologic metabolites [15]. Particularly, R. acetosa is rich in anthraquinones and flavonoids that have anti-inflammatory and antiproliferative effects [16,17]. Emodin, a major anthraquinone component of R. acetosa extract, is reported that has the potential for P-gp mediated drug interaction [18] and has various pharmacological effects, such as antidiabetic [19] and anticancer activities [20].
Fexofenadine, a selective histamine H1 receptor antagonist, is widely used for seasonal allergic rhinitis and chronic idiopathic urticarial treatment [21]. There is no evidence for cardiotoxicity associated with fexofenadine, the active metabolite of terfenadine, even though terfenadine is not used anymore due to the risk of cardiac arrhythmia. Fexofenadine was selected as a model drug that is a marker substrate of P-gp [22] and OATP1A2 [23]. Fexofenadine is considered a good model drug, because only around 5% of its dose is metabolized and most of the dose is excreted into urine (11%) and feces (80%) as the unchanged form [24,25], which means that metabolism can be excluded in interpreting the pharmacokinetics of fexofenadine.
To date, there have been many drug interaction studies involving P-gp or OATP. However, there have been few studies concerning drug interactions with herbal medicines involving both P-gp and OATP1A2. Furthermore, it has been reported that the emodin acts on P-gp as an inducer [26] or an inhibitor [18]. Our results clarify the inhibitory effect of emodin on the P-gp through in vitro and in vivo study. In addition, our findings include the fact that R. acetosa extract could affect drug absorption via intervention in the OATP-mediated influx and the aqueous solubility. These results indicate that the effects of herbal medicines such as plant extracts, on drug absorption must be considered in terms of not only efflux through P-gp, but also OATP-mediated influx and the aqueous solubility.

2. Materials and Methods

2.1. Chemicals and Reagents

Fexofenadine hydrochloride and emodin were purchased from Tokyo Chemical Industry (Tokyo, Japan). Dimethyl sulfoxide (DMSO), terfenadine, verapamil, Dulbecco’s modified Eagle’s medium (DMEM) with high glucose, MEM non-essential amino acid solution (NEAA) and glutamine were purchased from Sigma-Aldrich (St. Louis, MO, USA). HPLC grade acetonitrile and water were purchased from Fisher Scientific Korea (Seoul, Korea). Emodin, emodin-8-O-β-d-glucoside, chrysophanol, chrysophanol-8-O-β-d-glucoside, physcion and physcion-8-O-β-d-glucoside isolated from R. acetosa were obtained from the pharmacognosy laboratory of the College of Pharmacy at Gyeongsang National University (Jinju, Korea) [27]. Fetal bovine serum (FBS), N-2-hydroxyethylpiperazine–N′-2-ethanesulfonic acid (HEPES) and Hanks’ balanced salt solution (HBSS) were purchased from Corning (Manassas, VA, USA). Penicillin–streptomycin, Opti-MEM and 0.25% (w/v) trypsin–EDTA were purchased from Gibco (Carlsbad, CA, USA). Phosphate buffered saline (PBS) was purchased from Welgene (Gyeongsan, Korea). An MDR assay kit (fluorometric) was purchased from Abcam (Cambridge, UK).

2.2. R. acetosa Extract

The R. acetosa extract was prepared by previously reported procedure [27]. Briefly, the dried whole part of R. acetosa was extracted with 70% ethanol. The extraction was performed by the Soxhlet extractor for 3 h at 80 °C. The extract was filtered and lyophilized.
The total phenol content and total flavonoid content of R. acetosa extract were 74.5 mg GAE (gallic acid equivalent)/g of dry weight and 180.3 μg QAE (quercetin equivalent)/g of dry weight, respectively. The contents of anthraquinones in R. acetosa extract were determined by HPLC. The contents of emodin, emodin-8-O-β-d-glucoside, chrysophanol, chrysophanol-8-O-β-d-glucoside, physcion and physcion-8-O-β-d-glucoside in R. acetosa extract were 0.94 ± 0.15%, 1.29 ± 0.06%, 0.68 ± 0.09%, 0.77 ± 0.12%, 0.17 ± 0.02% and 0.41% ± 0.05% (w/w), respectively. The values were expressed as mean ± standard deviation.

2.3. Cell Culture

The Caco-2 (HTB-37™) cells were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). OATP1A2/SLCO1A2 transfected HEK293 cells were purchased from Corning (New York, NY, USA). The Caco-2 cells were cultured in high glucose added DMEM with 10% FBS, 1% NEAA, 10-mM HEPES, 4-mM glutamine, 100 U/mL of penicillin and 100 μg/mL of streptomycin, and maintained in humidified 5% CO2 at 37 °C. The medium of the Caco-2 cells was replaced 2–3 times per week.
The transfected HEK293 cells were cultured in high glucose added DMEM with 10% FBS and 1% NEAA, and maintained in 8% CO2 with low humidity at 37 °C for 4 h. After incubation for 4 h, the medium of the transfected HEK293 cells was replaced with high glucose added DMEM with 10% FBS, 1% NEAA and 2-mM sodium butyrate, and incubated for 24 h.

2.4. Cytotoxicity Assay

The cytotoxicity of R. acetosa extract on Caco-2 cells and HEK293 cells was measured using an EZ-Cytox cell viability assay kit (Daeil Lab Service, Seoul, Korea). The cells were cultured in DMEM containing 10% FBS, 1% NEAA, 10-mM HEPES, 100 U/mL of penicillin and 100-μg/mL streptomycin without phenol red. The seeding density was 3 × 104 cells/well for Caco-2 cells and 2.5 × 104 cell/well for HEK293 cells, respectively. The Caco-2 cells were incubated for 7 days and the HEK 293 cells were incubated for 24 h after seeding. The medium was replaced with 50 μL of new medium containing R. acetosa extract at the concentrations of 1, 2, 5, 10, 20, 50 and 100 μg/mL achieved the 0.5% of DMSO content. After 15 min of incubation, 5 μL of EZ-Cytox reagent (water-soluble tetrazolium) was added to the cells, and the cells were incubated for 3 h. Cell viability was calculated as a percentage of the absorbance at 450 nm compared to untreated cells.

2.5. P-gp Inhibition Test of Anthraquinones and R. acetosa Extract

The P-gp inhibition effect of anthraquinones from R. acetosa was evaluated via MDR assay kit using Caco-2 cells. It was reported that verapamil has concentration-dependent inhibition effects on absorptive and secretory transporters. Accordingly, 100-μM verapamil was used as a positive control [28]. Caco-2 cells were cultured in 96-well plates at a density of 5 × 105 cells/mL and incubated in humidified 5% CO2 at 37 °C for 24 h. They were treated with 6 test compounds (10 μM) [18] or R. acetosa extract in HBSS and incubated for 15 min. The concentration levels of R. acetosa extract were 5, 10, 25 and 50 μg/mL. The MDR dye-loading solution was added at a volume of 100 μL and incubated. Fluorescence intensity was detected with a microplate reader Synerge H1 (Biotek, Winooski, VT, USA) at a wavelength of 490 nm for the excitation and 525 nm for the emission.

2.6. Fexofenadine Uptake Test Using OATP1A2/SLCO1A2 Transfected HEK293 Cells

The seeding density of the OATP1A2 overexpressed HEK293 cells was 105 cells/well. Verapamil was used as a positive control with a concentration of 100 μM [28]. The cultured cells were washed twice with warmed HBSS with 5-mM MES after removing the medium, then 15-μM fexofenadine was treated with R. acetosa extract of 10, 20 and 50 μg/mL. After 15 min of incubation in 8% CO2 with low humidity at 37 °C, they were washed twice with cold HBSS. They were gently shaken after adding 120 μL of 50-ng/mL terfenadine in 80% acetonitrile. Terfenadine was used as an internal standard. After centrifugation at 10,000× g for 5 min, 50 μL of supernatant was mixed with 50 μL of 5-mM ammonium formate (pH 4). The liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to quantify the fexofenadine uptake amount [28,29].

2.7. LC-MS/MS Analysis

The chromatographic analysis was performed using an Agilent 1260 series (Agilent, Germany) HPLC system. Chromatographic separation was achieved from the Phoroshell® column (C18, 3.0 × 50 mm, 2.7 µm). The mobile phase consisted of 5-mM ammonium formate (pH 4) in water (A) and acetonitrile (B). A gradient method was applied at a flow rate of 0.3 mL/min and, kept on the column temperature at 25 °C. The injection volume was 2 μL. An Agilent 6460 triple-quadruple mass spectrometer (Agilent Technologies, Singapore) with an electrospray ionization (ESI) source was used to detect the signal. It was operated in positive ion mode on multiple reaction monitoring (MRM). The monitored ions of fexofenadine and internal standard (terfenadine) were m/z 502→466 and m/z 472→436 [30,31], respectively. The collision energy and fragmentor of the ions were 25 V and 175 V for fexofenadine, and 25 V and 130 V for terfenadine, respectively. The data were acquired and processed using Mass Hunter Workstation B.06.00 software (Agilent Technologies, Singapore).

2.8. Animal Study

2.8.1. Animals

Male Sprague‒Dawley rats (9 weeks, weighing 300 ± 50 g) were purchased from Koatech (Pyeongtaek, Korea). The rats were acclimated in the Animal Laboratory (Gyeongsang National University) under controlled condition of temperature (between 20 and 23 °C) and humidity (50% ± 5%) and allowed free access to food and water for 7 days. All rats were allowed to recover for 1 day after cannulation into the carotid artery. The rats were fasted for 12 h with free access to water, before the pharmacokinetic experiments.

2.8.2. Pharmacokinetic Study

The pharmacokinetic study was performed on a rat model. The dose of R. acetosa extract evaluated was 2 g/kg, the maximum dose without the toxicity in rats (unpublished data). The selected oral dose of emodin was 11 mg/kg that inhibited P-gp mediated efflux in rats from the reported study [32]. All test compounds—including 11 mg/kg of emodin and 2 g/kg of R. acetosa extract suspended in 0.5% carboxy methyl cellulose (CMC)—were administered orally to rats. Same volume of 0.5% CMC was administered to the vehicle control group rats. After 30 min, a single dose of 10 mg/kg of fexofenadine in 10% ethanol was orally administered to each group of rats [33]. Blood samples of 120 μL were collected from the carotid artery at each time point (0, 0.25, 0.5, 0.75, 1, 1.5, 2, 4, 6, 8, 12 and 24 h) after oral administration of fexofenadine. The samples were then immediately centrifuged at 10,000× g and 4 °C for 10 min. All plasma samples were stored at −20 °C. The plasma concentrations of fexofenadine were determined by LC-MS/MS. All experimental procedures of the animal study were approved (GNU-170705-R0030, 5 July 2017) by the Animal Care and Use Committee of Gyeongsang National University, Korea.

2.8.3. Sample Preparation

The method of sample preparation was a modified method of Isleyen et al. [34] for determination of fexofenadine plasma concentration. In summary, 50 μL of 50-ng/mL terfenadine in acetonitrile solution was added to a 50-μL aliquot of plasma, then 20 μL of aqueous 13-μM formic acid solution was added. After vortexing, 50 μL of extraction solvent (a mixture of dichloromethane, ethyl acetate, diethyl ether at the ratio of 30:40:30, v/v/v) was added. The sample was then vortexed for 40 s. The protein precipitation was performed via centrifugation at 10,000× g and 4 °C for 5 min. The supernatant was cooled at −80 °C for 10 min. The upper fraction of the supernatant was transferred to a polypropylene tube and evaporated with N2 gas. After being reconstituted with 200 μL of the mobile phase initial composition [5-mM ammonium formate (at a pH of 4): acetonitrile = 60:40], an aliquot of 2 μL was injected into LC-MS/MS.

2.9. Physicochemical Interaction Study

To investigate the possible physicochemical interactions between drug and R. acetosa extract, Fourier transform infrared (FT-IR) spectrum measurement and solubility test were carried out.
FT-IR spectra of fexofenadine HCl, R. acetosa extract and mixture of fexofenadine-extract (1:1) were measured by Nicolet iS 50 FT-IR spectrometer (Thermo Scientific, Waltham, MA, USA) with attenuated total reflectance (ATR) mode.
The change on the solubility of fexofenadine after mixing with R. acetosa extract was tested. The method was modified previously reported method [35,36]. Briefly, 200 μg of fexofenadine and R. acetosa extract were placed in the tube after centrifugal vacuum evaporation of solvent. The control group has fexofenadine only, and the mixed group has both fexofenadine and the extract. A 200-μL aliquot of the simulated intestinal fluid (SIF, pH 6.8) without enzyme [37] was added to each tube. The tubes were then incubated in a shaking water bath at 37 °C for 12 h. The concentration of fexofenadine was 1 mg/mL, corresponding to the orally administered concentration to the rats (10 mg/5 mL/kg-fexofenadine with 5-mL/kg extract, total 10 mL). After the incubation, the tubes were centrifuged at 10,000× g for 10 min. The supernatant was filtered, diluted with mobile phase, and analyzed by LC-MS/MS.

2.10. Statistical Analysis

The statistical analysis was performed using one-way analysis of variance (ANOVA) followed by a Dunnett’s multiple comparison test. A p-value of less than 0.05 was considered statistically significant.

3. Results

3.1. Cytotoxicity Assay

Cell viability was expressed as a percentage of the absorbance value obtained from the media only treated control group (Figure 1). Even though there were statistically significant differences in Caco-2 cell viability between control and R. acetosa treated groups at concentrations of 20, 10, 2 and 1 μg/mL, the cell viability values were high enough to study (96.4% ± 1.3%, 95.0% ± 2.1%, 95.0% ± 1.2% and 95.5% ± 2.1% at concentrations of 20, 10, 2 and 1 μg/mL, respectively). It is suggested that there is a negligible cytotoxic effect of R. acetosa on the Caco-2 cells at the concentration range of 1 to 100 μg/mL.
There was no significant difference on the cell viability on HEK293 cells at the concentration ranges of 1 to 50 μg/mL. The cytotoxic effect of R. acetosa was only detected on HEK293 cells at a concentration of 100 μg/mL with the value of 80.9% ± 11.7%. This result suggests a dose window of R. acetosa extract for the experiment using HEK293 cells. It also indicates that the inhibitory effect of R. acetosa on fexofenadine uptake discussed in Section 3.2 was not due to the cytotoxic effects of R. acetosa on HEK293 cells at the concentration range tested.

3.2. P-gp Inhibition Test of Anthraquinones and R. acetosa Extract

To determine inhibitory effect of anthraquinones on P-gp, an MDR kit was used. The accumulated amount of fluorescent dye in the cells represented the P-gp inhibition activity. The measured fluorescence intensity is expressed as a percentage of the fluorescence intensity in the control group and is shown in Figure 2. The verapamil, chrysophanol-8-O-β-d-glucoside and emodin treated groups displayed significantly different fluorescence intensities in comparison to those of the control group. However, the chrysophanol-8-O-β-d-glucoside and emodin treated groups showed significantly higher fluorescence intensities than the control group, with average values of 121.4% ± 2.3% and 147.2% ± 12.4%, respectively (mean ± standard deviation). This result suggests that chrysophanol-8-O-β-d-glucoside and emodin affect the efflux of fluorescent dye from Caco-2 cells through P-gp inhibition. This is consistent with previous findings that emodin inhibits P-gp [18]. It is thus reasonable to suggest that herbal drug containing chrysophanol-8-O-β-d-glucoside and emodin may also inhibit P-gp.
The effects of R. acetosa extract on the P-gp were also assessed using an MDR kit. The measured fluorescence intensity is expressed as a percentage of the fluorescence intensity in the control group and is shown in Figure 3. There was no significant difference in fluorescence intensity between the control and the R. acetosa extract treated group. The significant inhibitory effect at the 95% confidence interval was only detected in the verapamil group used as a positive control. Although R. acetosa extract contains chrysophanol-8-O-β-d-glucoside and emodin at concentrations of 0.77% ± 0.12% and 0.94% ± 0.15% (w/w), respectively [27], inhibitory effects on P-gp could not be detected from R. acetosa extract at the concentrations tested in this assay. The concentrations of emodin and chrysophanol-8-O-β-d-glucoside in R. acetosa extract may not be high enough to inhibit P-gp in Caco-2 cells.

3.3. Fexofenadine Uptake Test with OATP1A2/SLCO1A2 Transfected HEK293 Cells

The decreased fexofenadine uptake in the OATP1A2/SLCO1A2 transfected HEK293 cells represented the inhibitory effects on OATP1A2. The accumulated amount of fexofenadine in the OATP/SLCO1A2 transfected cells (the control group) was higher than that of untransfected cells (untransfected control group), which means that the OATP1A2 gene was transfected and expressed sufficiently in the control group. In addition, the fexofenadine uptake was lower in the verapamil cotreated group than in the transfected control group. In the R. acetosa extract co-treated group, the uptake amounts of fexofenadine in the OATP1A2 transfected HEK293 cells were significantly lower than that in the control group (Figure 4). This result suggests that R. acetosa extract could affect the absorption of fexofenadine through the inhibition of OATP1A2.

3.4. Pharmacokinetic Study

The mean arterial plasma concentration–time profiles of fexofenadine after the pharmacokinetic study of fexofenadine in a rat drug interaction model, are shown in Figure 5. The pharmacokinetic parameters of fexofenadine after oral coadministration of vehicle, emodin and R. acetosa extract are shown in Table 1. The area under the plasma concentration–time curve (AUC) values of fexofenadine were 222.0 ± 85.5 ng∙h/mL in the control group and 411.9 ± 189.1 ng∙h/mL in the emodin coadministered group. In the emodin group, the absorption of fexofenadine was significantly higher, with a larger fexofenadine AUC and no difference in Tmax. However, the fexofenadine AUC was lower, with a value of 132.0 ± 50.5 ng∙h/mL, in the 2 g/kg R. acetosa extract coadministered group. Because fexofenadine is characterized by limited metabolism, it is probable that the lower fexofenadine AUC is due to the inhibitory effect of R. acetosa extract on absorption. Consequently, R. acetosa extract could inhibit the absorption of fexofenadine. Together with the results of the in vitro assay, this suggests that R. acetosa extract inhibits the intracellular uptake of fexofenadine via an intervention in OATP1A2.

3.5. Physicochemical Interaction Study

To evaluate the possible physicochemical interactions between R. acetosa extract and fexofenadine, FT-IR spectra of extract, fexofenadine and mixture were measured and are shown in Figure 6. The FT-IR spectrum of fexofenadine HCl showed the characteristic absorption bands at 3291.03 (OH stretching), 2936.14 (CH stretching), 2639.82 (OH of carboxylate), 1698.68 (CO stretching), 1448.00, 1403.11 (C=C stretching of aromatic ring), 1167.57 (CO stretching of tertiary alcohol) and 1067.94 (CO stretching of secondary alcohol) [38,39]. According to Figure 6, the mixture of R. acetosa extract and fexofenadine HCl showed the same bands compared to the pure fexofenadine HCl. It suggests that there is no significant physical interaction between fexofenadine molecule and R. acetosa extract component on fexofenadine functional groups.
However, there was significant difference on the solubility of fexofenadine after incubation with the extract (Table 2). The average solubilities of fexofenadine in SIF were 1.03 ± 0.04 mg/mL and 0.83 ± 0.10 mg/mL without and with R. acetosa extract, respectively. This result indicates that R. acetosa extract could alter the solubility of fexofenadine and lead to precipitation in gastro-intestinal tract.

4. Discussion

Pharmacokinetic drug interactions involving drug absorption should be considered for optimum drug therapy, apart from the drug interactions attributed to the oxidative metabolism via the CYP-450 system of different isozymes [40]. Ostensibly harmless natural products—such as juices, fruits, vegetables and herbal products in the form of ayurvedic medicine—have been reported in several studies to potentially cause many drug interactions affecting drug absorption mediated by transporters [41,42]. For example, emodin—a potential antineoplastic drug and a major component of the Rhamnus, Rumex, Aloe, Rheum and Cassia species—has been reported to be a possible P-gp inducer [26] or an inhibitor [18].
This study evaluated the effects of R. acetosa extract on the drug transporters discussed above, as well as its potential for drug interactions, while presenting a clear view of the interactions of emodin with the transporter P-gp. The major six anthraquinones present in R. acetosa were shown in our previous study [27]. A prior cytotoxicity assay was performed to establish the working range for the extract suitable for optimal viability of the cells during the experiment. Afterwards, the effects of these six anthraquinones on P-gp were demonstrated individually with an MDR assay kit using Caco-2 cells. Verapamil, being an inhibitor of P-gp, served as a positive control. Only groups treated with chrysophanol-8-O-β-d-glucoside and emodin showed higher fluorescence intensity than the control group, with average values of 121.4% ± 2.3% and 147.2% ± 12.4%, respectively, suggesting P-gp inhibition. This result is consistent with those obtained in a study by Min et al. [18], in which emodin was shown to inhibit P-gp. On the other hand, the results from the P-gp inhibition test of R. acetosa extract suggest no significant inhibition of the efflux transporter, as opposed to the emodin and chrysophanol-8-O-β-d-glucoside, which in contrast showed significant inhibition of the P-gp transporter when treated individually. A possible explanation is that the emodin content may not be high enough to exert its inhibitory effect in the extract. Chemical contents of herbal plant extracts can vary depending on various factors such as climate, harvesting seasons and extraction solvent. The probability of inhibition of P-gp by R. acetosa extract cannot be ruled out.
OATP1A2—the uptake transporter used in our in vitro test—is widely expressed in the intestines and serves as a major uptake mechanism for fexofenadine [43,44]. Sometimes, a substrate of P-gp—such as this study’s selected model drug, fexofenadine—can also be a substrate for the OATP uptake transporter [43,44], making it necessary to differentiate between the contributions of P-gp and OATP to potential drug interactions and those of other simultaneously administered drugs that could affect these transporters. Therefore, our in vitro studies were also performed with HEK293 cells transfected with the polypeptide transporter OATP1A2. R. acetosa extract was found to inhibit the uptake of fexofenadine through in vitro studies. In other words, the uptake of fexofenadine by OATP1A2 into cells declined when R. acetosa extract was used as a co-treatment. This result suggests that R. acetosa extract can affect the absorption of fexofenadine through the inhibition of OATP1A2.
A pharmacokinetic study was designed to verify the results of our in vitro study in view of the observed herbal extract’s drug interactions at the uptake transporter for fexofenadine in rats. Rat model is considered unsuitable to predict metabolic drug interaction in human [45]. However, there is a correlation in drug intestinal permeability with both carrier-mediated absorption and passive diffusion mechanisms between rat and human [46]. Because the property of our selected model drug, fexofenadine, has little metabolism, it is reasonable to use the rat model for predicting the intervention of extract on absorption. All rats were divided into 3 groups: an emodin administration group, an R. acetosa administration group and a control group. Eleven milligrams per kilogram of emodin, 2 g/kg of R. acetosa extract and 0.5% CMC as a control was administered orally to each group. Fexofenadine at the dose of 10 mg/kg was given orally to each group after 30 min. The results showed a smaller AUC of fexofenadine (132.1 ± 50.3 ng∙h/mL) in the R. acetosa group in comparison to that of the control group, in which the AUC was 222.0 ± 92.1 ng∙h/mL. These results suggest decreased absorption of fexofenadine in the rats treated with R. acetosa extract. In other words, the gut uptake transporter OATP1A2, which is responsible for fexofenadine absorption, was inhibited, as predicted by the in vitro results. Moreover, the alteration on the solubility of fexofenadine was also observed by R. acetosa extract through the physicochemical interaction study. The FT-IR spectra results suggest that there is no functional group interaction between fexofenadine and the component of R. acetosa extract. The fexofenadine solubility in SIF changed from 1.03 ± 0.04 mg/mL to 0.83 ± 0.10 mg/mL after mixing with the extract. It means that the solubility alteration could also be the reason for the decreased fexofenadine AUC by R. acetosa extract because fexofenadine HCl is Biopharmaceutics Classification System (BCS) class 3 drug with high solubility and low permeability. Drug interactions due to changes in solubility can be avoided by adjusting the administration time. R. acetosa extract contains many kinds of compounds, not only anthraquinones, but also flavonoids and polysaccharides [15]. They have also the possibility of interference with the drug absorption through the intervention to the transporters [47,48]. Particularly, one of the flavonoids of R. acetosa extract, epicatechin-3-O-gallate [49], also has an inhibitory effect on the OATP1A2 [50]. Moreover, there was the possibility that R. acetosa extract may change the gastric emptying time [51,52] and the pH in the gastro-intestinal tract when coadministered with the fexofenadine. The effects of anthraquinones on OATP have been rarely reported. Further studies are needed to elucidate the components in R. acetosa extract responsible for inhibition of fexofenadine absorption. Meanwhile, emodin increased the AUC for fexofenadine, possibly via the inhibitory effect on an efflux transporter of fexofenadine, P-gp [32], the effect of which on the uptake transporter of fexofenadine has yet to be fully understood.
Given the evidence from both in vitro and in vivo studies, R. acetosa extract should be used with caution when substrates of the drug transporters or poorly water-soluble drugs are prescribed.

5. Conclusions

The present study evaluated the effects of R. acetosa extract on 2 active transporters, P-gp and OATP1A2 and the resulting effects on fexofenadine absorption through in vitro and in vivo studies. The findings suggest that emodin can enhance fexofenadine absorption via an inhibitory effect on P-gp. In addition, R. acetosa extract could decrease the absorption of fexofenadine via intervention in the aqueous solubility and the drug transporters.

Author Contributions

Conceptualization, H.J.C.; methodology, H.J.C.; validation, J.K. and N.U.R.; formal analysis, J.K.; investigation, J.H.A., J.K. and H.-J.K.; resources, M.-J.A. and H.J.C.; data curation, J.H.A., J.K. and H.J.C.; writing—original draft preparation, J.K. and N.U.R.; writing—review and editing, H.J.C.; visualization, J.K.; supervision, H.J.C. and M.-J.A.; project administration, H.J.C.; funding acquisition, H.J.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIP; Ministry of Science & ICT), Grant Number 2017R1C1B5017343.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Dean, M.; Hamon, Y.; Chimini, G. The human ATP-binding cassette (ABC) transporter superfamily. J. Lipid Res. 2001, 42, 1007–1017. [Google Scholar] [CrossRef] [PubMed]
  2. Anderle, P.; Niederer, E.; Rubas, W.; Hilgendorf, C.; Spahn-Langguth, H.; Wunderli-Allenspach, H.; Merkle, H.P.; Langguth, P. P-Glycoprotein (P-gp) mediated efflux in Caco-2 cell monolayers: The influence of culturing conditions and drug exposure on P-gp expression levels. J. Pharm. Sci. 1998, 87, 757–762. [Google Scholar] [CrossRef] [PubMed]
  3. Fardel, O.; Lecureur, V.; Guillouzo, A. The P-glycoprotein multidrug transporter. Gen. Pharm. 1996, 27, 1283–1291. [Google Scholar] [CrossRef]
  4. Chan, L.M.; Lowes, S.; Hirst, B.H. The ABCs of drug transport in intestine and liver: Efflux proteins limiting drug absorption and bioavailability. Eur. J. Pharm. Sci. 2004, 21, 25–51. [Google Scholar] [CrossRef]
  5. Talks, K.L.; Turley, H.; Gatter, K.C.; Maxwell, P.H.; Pugh, C.W.; Ratcliffe, P.J.; Harris, A.L. The expression and distribution of the hypoxia-inducible factors HIF-1alpha and HIF-2alpha in normal human tissues, cancers, and tumor-associated macrophages. Am. J. Pathol 2000, 157, 411–421. [Google Scholar] [CrossRef]
  6. Comerford, K.M.; Wallace, T.J.; Karhausen, J.; Louis, N.A.; Montalto, M.C.; Colgan, S.P. Hypoxia-inducible factor-1-dependent regulation of the multidrug resistance (MDR1) gene. Cancer Res. 2002, 62, 3387–3394. [Google Scholar]
  7. Kim, R.B. Drugs as P-glycoprotein substrates, inhibitors, and inducers. Drug Metab. Rev. 2002, 34, 47–54. [Google Scholar] [CrossRef]
  8. Palmeira, A.; Sousa, E.; Vasconcelos, M.H.; Pinto, M.M. Three decades of P-gp: Skimming through several generations and scaffolds. Curr. Med. Che 2012, 19, 1946–2025. [Google Scholar] [CrossRef]
  9. Shitara, Y.; Maeda, K.; Ikejiri, K.; Yoshida, K.; Horie, T.; Sugiyama, Y. Clinical significance of organic anion transporting polypeptides (OATPs) in drug disposition: Their roles in hepatic clearance and intestinal absorption. Biopharm. Drug Dispos. 2013, 34, 45–78. [Google Scholar] [CrossRef]
  10. Yu, J.; Zhou, Z.; Tay-Sontheimer, J.; Levy, R.H.; Ragueneau-Majlessi, I. Intestinal drug interactions mediated by OATPs: A systematic review of preclinical and clinical findings. J. Pharm. Sci. 2017, 106, 2312–2325. [Google Scholar] [CrossRef] [Green Version]
  11. Agbabiaka, T.B.; Spencer, N.H.; Khanom, S.; Goodman, C. Prevalence of drug-herb and drug-supplement interactions in older adults: A cross-sectional survey. Br. J. Gen. Pr. 2018, 68, e711–e717. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Kaufman, D.W.; Kelly, J.P.; Rosenberg, L.; Anderson, T.E.; Mitchell, A.A. Recent patterns of medication use in the ambulatory adult population of the United States: The Slone survey. JAMA 2002, 287, 337–344. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Durr, D.; Stieger, B.; Kullak-Ublick, G.A.; Rentsch, K.M.; Steinert, H.C.; Meier, P.J.; Fattinger, K. St John’s Wort induces intestinal P-glycoprotein/MDR1 and intestinal and hepatic CYP3A4. Clin. Pharm. 2000, 68, 598–604. [Google Scholar] [CrossRef] [PubMed]
  14. Gescher, K.; Hensel, A.; Hafezi, W.; Derksen, A.; Kuhn, J. Oligomeric proanthocyanidins from Rumex acetosa L. inhibit the attachment of herpes simplex virus type-1. Antivir. Res. 2011, 89, 9–18. [Google Scholar] [CrossRef] [PubMed]
  15. Vasas, A.; Orban-Gyapai, O.; Hohmann, J. The genus Rumex: Review of traditional uses, phytochemistry and pharmacology. J. Ethnopharmacol. 2015, 175, 198–228. [Google Scholar] [CrossRef] [PubMed]
  16. Kucekova, Z.; Mlcek, J.; Humpolicek, P.; Rop, O.; Valasek, P.; Saha, P. Phenolic compounds from Allium schoenoprasum, Tragopogon pratensis and Rumex acetosa and their antiproliferative effects. Molecules 2011, 16, 9207–9217. [Google Scholar] [CrossRef]
  17. Bae, J.Y.; Lee, Y.S.; Han, S.Y.; Jeong, E.J.; Lee, M.K.; Kong, J.Y.; Lee, D.H.; Cho, K.J.; Lee, H.S.; Ahn, M.J. A comparison between water and ethanol extracts of Rumex acetosa for protective effects on gastric ulcers in mice. Biomol. Ther. (Seoul) 2012, 20, 425–430. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Min, H.; Niu, M.; Zhang, W.; Yan, J.; Li, J.; Tan, X.; Li, B.; Su, M.; Di, B.; Yan, F. Emodin reverses leukemia multidrug resistance by competitive inhibition and downregulation of P-glycoprotein. PLoS ONE 2017, 12, e0187971. [Google Scholar] [CrossRef] [Green Version]
  19. Feng, Y.; Huang, S.L.; Dou, W.; Zhang, S.; Chen, J.H.; Shen, Y.; Shen, J.H.; Leng, Y. Emodin, a natural product, selectively inhibits 11beta-hydroxysteroid dehydrogenase type 1 and ameliorates metabolic disorder in diet-induced obese mice. Br. J. Pharm. 2010, 161, 113–126. [Google Scholar] [CrossRef] [Green Version]
  20. Hsu, S.C.; Chung, J.G. Anticancer potential of emodin. BioMedicine (Taipei) 2012, 2, 108–116. [Google Scholar] [CrossRef]
  21. Simpson, K.; Jarvis, B. Fexofenadine: A review of its use in the management of seasonal allergic rhinitis and chronic idiopathic urticaria. Drugs 2000, 59, 301–321. [Google Scholar] [CrossRef] [PubMed]
  22. Tahara, H.; Kusuhara, H.; Fuse, E.; Sugiyama, Y. P-glycoprotein plays a major role in the efflux of fexofenadine in the small intestine and blood-brain barrier, but only a limited role in its biliary excretion. Drug Metab. Dispos. 2005, 33, 963–968. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Shimizu, M.; Fuse, K.; Okudaira, K.; Nishigaki, R.; Maeda, K.; Kusuhara, H.; Sugiyama, Y. Contribution of OATP (organic anion-transporting polypeptide) family transporters to the hepatic uptake of fexofenadine in humans. Drug Metab. Dispos. 2005, 33, 1477–1481. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Molimard, M.; Diquet, B.; Benedetti, M.S. Comparison of pharmacokinetics and metabolism of desloratadine, fexofenadine, levocetirizine and mizolastine in humans. Fundam. Clin. Pharm. 2004, 18, 399–411. [Google Scholar] [CrossRef] [PubMed]
  25. Prescribing Information for Allegra® (fexofenadine hydrochloride). Available online: https://www.accessdata.fda.gov/drugsatfda_docs/label/2003/20872se8-003,20625se8-010_allegra_lbl.pdf (accessed on 16 March 2020).
  26. Huang, J.; Guo, L.; Tan, R.; Wei, M.; Zhang, J.; Zhao, Y.; Gong, L.; Huang, Z.; Qiu, X. Interactions between emodin and efflux transporters on rat enterocyte by a validated ussing chamber technique. Front. Pharm. 2018, 9, 646. [Google Scholar] [CrossRef]
  27. Ullah, H.M.A.; Kim, J.; Rehman, N.U.; Kim, H.J.; Ahn, M.J.; Chung, H.J. A simple and sensitive liquid chromatography with tandem mass spectrometric method for the simultaneous determination of anthraquinone glycosides and their aglycones in rat plasma: Application to a pharmacokinetic study of Rumex acetosa extract. Pharmaceutics 2018, 10, 100. [Google Scholar] [CrossRef] [Green Version]
  28. Petri, N.; Tannergren, C.; Rungstad, D.; Lennernas, H. Transport characteristics of fexofenadine in the Caco-2 cell model. Pharm. Res. 2004, 21, 1398–1404. [Google Scholar] [CrossRef]
  29. Rebello, S.; Zhao, S.; Hariry, S.; Dahlke, M.; Alexander, N.; Vapurcuyan, A.; Hanna, I.; Jarugula, V. Intestinal OATP1A2 inhibition as a potential mechanism for the effect of grapefruit juice on aliskiren pharmacokinetics in healthy subjects. Eur. J. Clin. Pharm. 2012, 68, 697–708. [Google Scholar] [CrossRef]
  30. Yamane, N.; Tozuka, Z.; Sugiyama, Y.; Tanimoto, T.; Yamazaki, A.; Kumagai, Y. Microdose clinical trial: Quantitative determination of fexofenadine in human plasma using liquid chromatography/electrospray ionization tandem mass spectrometry. J. Chromatogr B Anal. Technol Biomed. Life Sci 2007, 858, 118–128. [Google Scholar] [CrossRef]
  31. Bharathi, V.D.; Radharani, K.; Jagadeesh, B.; Ramulu, G.; Bhushan, I.; Naidu, A.; Mullangi, R. LC–MS–MS assay for simultaneous quantification of fexofenadine and pseudoephedrine in human plasma. Chromatographia 2008, 67, 461–466. [Google Scholar] [CrossRef]
  32. Li, X.; Hu, J.; Wang, B.; Sheng, L.; Liu, Z.; Yang, S.; Li, Y. Inhibitory effects of herbal constituents on P-glycoprotein in vitro and in vivo: Herb-drug interactions mediated via P-gp. Toxicol. Appl. Pharm. 2014, 275, 163–175. [Google Scholar] [CrossRef] [PubMed]
  33. Kamath, A.V.; Yao, M.; Zhang, Y.; Chong, S. Effect of fruit juices on the oral bioavailability of fexofenadine in rats. J. Pharm. Sci. 2005, 94, 233–239. [Google Scholar] [CrossRef] [PubMed]
  34. İşleyen, E.A.Ö.; Özden, T.; Özilhan, S.; Toptan, S. Quantitative determination of fexofenadine in human plasma by HPLC-MS. Chromatographia 2007, 66, 109–113. [Google Scholar] [CrossRef]
  35. Dai, W.G. In vitro methods to assess drug precipitation. Int. J. Pharm. 2010, 393, 1–16. [Google Scholar] [CrossRef] [PubMed]
  36. Saito, Y.; Usami, T.; Katoh, M.; Nadai, M. Effects of thylakoid-rich spinach extract on the pharmacokinetics of drugs in rats. Biol. Pharm. Bull. 2019, 42, 103–109. [Google Scholar] [CrossRef] [PubMed]
  37. Stippler, E.; Kopp, S.; Dressman, J.B. Comparison of US pharmacopeia simulated intestinal fluid TS (without pancreatin) and phosphate standard buffer pH 6.8, TS of the international pharmacopoeia with respect to their use in in vitro dissolution testing. Dissolution Technol. 2004, 11, 6–10. [Google Scholar] [CrossRef]
  38. Singh, B.; Saini, G.; Vyas, M.; Verma, S.; Thakur, S. Optimized chronomodulated dual release bilayer tablets of fexofenadine and montelukast: Quality by design, development, and in vitro evaluation. Future J. Pharm. Sci. 2019, 5, 5. [Google Scholar] [CrossRef] [Green Version]
  39. Arefin, P.; Hasan, I.; Reza, M.S. Design, characterization and in vitro evaluation of HPMC K100 M CR loaded fexofenadine HCl microspheres. Springerplus 2016, 5, 691. [Google Scholar] [CrossRef] [Green Version]
  40. Hansten, P.D.; Levy, R.H. Role of P-glycoprotein and organic anion transporting polypeptides in drug absorption and distribution. Clin. Drug Investig. 2001, 21, 587–596. [Google Scholar] [CrossRef]
  41. Mallhi, T.H.; Sarriff, A.; Adnan, A.S.; Khan, Y.H.; Qadir, M.I.; Hamzah, A.A.; Khan, A.H. Effect of fruit/vegetable-drug interactions on CYP450, OATP and p-glycoprotein: A systematic review. Trop. J. Pharm. Res. 2015, 14, 1927–1935. [Google Scholar] [CrossRef]
  42. Bailey, D.G. Fruit juice inhibition of uptake transport: A new type of food-drug interaction. Br. J. Clin. Pharm. 2010, 70, 645–655. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Cvetkovic, M.; Leake, B.; Fromm, M.F.; Wilkinson, G.R.; Kim, R.B. OATP and P-glycoprotein transporters mediate the cellular uptake and excretion of fexofenadine. Drug Metab. Dispos. 1999, 27, 866–871. [Google Scholar] [PubMed]
  44. Niemi, M.; Kivisto, K.T.; Hofmann, U.; Schwab, M.; Eichelbaum, M.; Fromm, M.F. Fexofenadine pharmacokinetics are associated with a polymorphism of the SLCO1B1 gene (encoding OATP1B1). Br. J. Clin. Pharm. 2005, 59, 602–604. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Jaiswal, S.; Sharma, A.; Shukla, M.; Vaghasiya, K.; Rangaraj, N.; Lal, J. Novel pre-clinical methodologies for pharmacokinetic drug-drug interaction studies: Spotlight on "humanized" animal models. Drug Metab. Rev. 2014, 46, 475–493. [Google Scholar] [CrossRef] [PubMed]
  46. Cao, X.; Gibbs, S.T.; Fang, L.; Miller, H.A.; Landowski, C.P.; Shin, H.C.; Lennernas, H.; Zhong, Y.; Amidon, G.L.; Yu, L.X.; et al. Why is it challenging to predict intestinal drug absorption and oral bioavailability in human using rat model. Pharm. Res. 2006, 23, 1675–1686. [Google Scholar] [CrossRef]
  47. Mandery, K.; Bujok, K.; Schmidt, I.; Keiser, M.; Siegmund, W.; Balk, B.; Konig, J.; Fromm, M.F.; Glaeser, H. Influence of the flavonoids apigenin, kaempferol, and quercetin on the function of organic anion transporting polypeptides 1A2 and 2B1. Biochem. Pharm. 2010, 80, 1746–1753. [Google Scholar] [CrossRef] [Green Version]
  48. Masumoto, K.; Quan, Z.; Ishiuchi, K.i.; Matsumoto, T.; Watanabe, J.; Makino, T. Drug interaction between shoseiryuto extract or catechins and fexofenadine through organic-anion-transporting polypeptide 1A2 in vitro. Pharmacogn. Mag. 2019, 15, 304–308. [Google Scholar] [CrossRef]
  49. Bicker, J.; Petereit, F.; Hensel, A. Proanthocyanidins and a phloroglucinol derivative from Rumex acetosa L. Fitoterapia 2009, 80, 483–495. [Google Scholar] [CrossRef]
  50. Roth, M.; Timmermann, B.N.; Hagenbuch, B. Interactions of green tea catechins with organic anion-transporting polypeptides. Drug Metab. Dispos. 2011, 39, 920–926. [Google Scholar] [CrossRef] [Green Version]
  51. Bajad, S.; Bedi, K.L.; Singla, A.K.; Johri, R.K. Piperine inhibits gastric emptying and gastrointestinal transit in rats and mice. Planta Med. 2001, 67, 176–179. [Google Scholar] [CrossRef]
  52. Hu, M.L.; Rayner, C.K.; Wu, K.L.; Chuah, S.K.; Tai, W.C.; Chou, Y.P.; Chiu, Y.C.; Chiu, K.W.; Hu, T.H. Effect of ginger on gastric motility and symptoms of functional dyspepsia. World J. Gastroenter. 2011, 17, 105–110. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Cytotoxicity of R. acetosa extract in (A) Caco-2 cells and (B) HEK293 cells (n = 6). Con—media only treated control; Veh—vehicle treated group; *—p < 0.05 compared to media only treated control group.
Figure 1. Cytotoxicity of R. acetosa extract in (A) Caco-2 cells and (B) HEK293 cells (n = 6). Con—media only treated control; Veh—vehicle treated group; *—p < 0.05 compared to media only treated control group.
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Figure 2. P-gp inhibitory effect of anthraquinones in Caco-2 cells. Cells were treated with 10-μM anthraquinones or 100-μM verapamil (n = 3). Con—vehicle treated control; Ver—verapamil; 1—chrysophanol; 2—chrysophanol-8-O-β-d-glucoside; 3—emodin; 4—emodin-8-O-β-d-glucoside; 5—physcion; 6—physcion-8-O-β-d-glucoside; *—p < 0.05 compared to control group.
Figure 2. P-gp inhibitory effect of anthraquinones in Caco-2 cells. Cells were treated with 10-μM anthraquinones or 100-μM verapamil (n = 3). Con—vehicle treated control; Ver—verapamil; 1—chrysophanol; 2—chrysophanol-8-O-β-d-glucoside; 3—emodin; 4—emodin-8-O-β-d-glucoside; 5—physcion; 6—physcion-8-O-β-d-glucoside; *—p < 0.05 compared to control group.
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Figure 3. P-gp inhibition test of R. acetosa extract using an MDR kit in Caco-2 cells (n = 6). Con—vehicle treated control; Ver—100-μM verapamil; *—p < 0.05 compared to control group.
Figure 3. P-gp inhibition test of R. acetosa extract using an MDR kit in Caco-2 cells (n = 6). Con—vehicle treated control; Ver—100-μM verapamil; *—p < 0.05 compared to control group.
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Figure 4. Inhibitory effect of R. acetosa extract on fexofenadine uptake in OATP1A2/SLCO1A2 transfected HEK293 cells (n = 6). Con—OATP1A2/SLCO1A2 transfected control; Nov—untransfected control; Ver—100-μM verapamil; *—p < 0.05 compared to control group.
Figure 4. Inhibitory effect of R. acetosa extract on fexofenadine uptake in OATP1A2/SLCO1A2 transfected HEK293 cells (n = 6). Con—OATP1A2/SLCO1A2 transfected control; Nov—untransfected control; Ver—100-μM verapamil; *—p < 0.05 compared to control group.
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Figure 5. Mean plasma concentration–time profiles of fexofenadine (ng/mL) after oral coadministration of fexofenadine (10 mg/kg) with vehicle (●; n = 6), emodin (11 mg/ kg, ○; n = 6) and R. acetosa extract (2 g/kg, ▼; n = 6) to rats. Bars represent standard deviations.
Figure 5. Mean plasma concentration–time profiles of fexofenadine (ng/mL) after oral coadministration of fexofenadine (10 mg/kg) with vehicle (●; n = 6), emodin (11 mg/ kg, ○; n = 6) and R. acetosa extract (2 g/kg, ▼; n = 6) to rats. Bars represent standard deviations.
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Figure 6. FT-IR spectra of (A) fexofenadine, (B) a mixture of fexofenadine and R. acetosa extract and (C) R. acetosa extract.
Figure 6. FT-IR spectra of (A) fexofenadine, (B) a mixture of fexofenadine and R. acetosa extract and (C) R. acetosa extract.
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Table
Table 1. Pharmacokinetic parameters of fexofenadine after oral coadministration of fexofenadine (10 mg/kg) with vehicle (control), emodin and R. acetosa extract to rats. Values represent means ± standard deviations for AUC0-24 h and Cmax (ng/mL), median (range) for Tmax.
Table 1. Pharmacokinetic parameters of fexofenadine after oral coadministration of fexofenadine (10 mg/kg) with vehicle (control), emodin and R. acetosa extract to rats. Values represent means ± standard deviations for AUC0-24 h and Cmax (ng/mL), median (range) for Tmax.
ParametersControl
(n = 6)		Emodin
11 mg/kg
(n = 6)		R. acetosa Extract
2 g/kg
(n = 6)
AUC0-24 h (ng∙h/mL)222.0 ± 85.5411.9 ± 189.1 *132.0 ± 50.5
Cmax (ng/mL)36.4 ± 22.853.4 ± 33.932.9 ± 28.5
Tmax (h)0.75 (0.5–1)0.75 (0.5–1)0.75 (0.25–8)
AUC0-24 h, total area under the plasma concentration–time curve from time zero to 24 h; Cmax—maximum plasma concentration; Tmax—time to reach Cmax; *—p < 0.05 compared to vehicle only control group.
Table
Table 2. The solubility of fexofenadine HCl in simulated intestinal fluid (SIF) with and without R. acetosa extract.
Table 2. The solubility of fexofenadine HCl in simulated intestinal fluid (SIF) with and without R. acetosa extract.
SolubilityWithout R. acetosa Extract(n = 3)With R. acetosa Extract(n = 3)
Fexofenadine HCl concentration (mg/mL)1.03 ± 0.040.83 ± 0.10 *
*—p < 0.05 compared to without R. acetosa extract.

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Ahn, J.H.; Kim, J.; Rehman, N.U.; Kim, H.-J.; Ahn, M.-J.; Chung, H.J. Effect of Rumex Acetosa Extract, a Herbal Drug, on the Absorption of Fexofenadine. Pharmaceutics 2020, 12, 547. https://doi.org/10.3390/pharmaceutics12060547

AMA Style

Ahn JH, Kim J, Rehman NU, Kim H-J, Ahn M-J, Chung HJ. Effect of Rumex Acetosa Extract, a Herbal Drug, on the Absorption of Fexofenadine. Pharmaceutics. 2020; 12(6):547. https://doi.org/10.3390/pharmaceutics12060547

Chicago/Turabian Style

Ahn, Jung Hwan, Junhyeong Kim, Naveed Ur Rehman, Hye-Jin Kim, Mi-Jeong Ahn, and Hye Jin Chung. 2020. "Effect of Rumex Acetosa Extract, a Herbal Drug, on the Absorption of Fexofenadine" Pharmaceutics 12, no. 6: 547. https://doi.org/10.3390/pharmaceutics12060547

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