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Journal of Chemistry
Volume 2014 (2014), Article ID 354618, 8 pages
http://dx.doi.org/10.1155/2014/354618
Research Article

Pharmacokinetic Comparison of Isoalantolactone and Alantolactone in Rats after Administration Separately by Optimization of an UPLC-MS2 Method

School of Pharmacy, Shanghai Jiao Tong University, No. 800 Dongchuan Road, Minhang District, Shanghai 200240, China

Received 2 September 2014; Accepted 4 November 2014; Published 20 November 2014

Academic Editor: Patricia Valentao

Copyright © 2014 Renjie Xu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Isoalantolactone and alantolactone are two major active ingredients that are present in many medicinal plants. In this study, a sensitive and rapid ultraperformance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was developed for determination of the two compounds in rat plasma, separately. In this method, an electrospray ionization source was applied and operated in positive ion mode; multiple reaction monitoring (MRM) was selected for quantification using target fragment ions 233.2187.1 for isoalantolactone (alantolactone) and 245.1189.1 for internal standard (IS). Retention time of the lactones and IS was within 3.0 min. Further calibration suggested a linear regression can be calculated within 2.5–500 ng/mL for isoalantolactone and 4–500 ng/mL for alantolactone. This method was used to compare the pharmacokinetic characteristics of isoalantolactone and alantolactone at a single dose of 5 mg/kg into male Sprague-Dawley rats by intravenous administration separately. The levels of , Kel, CL, , and AUC were significantly increased in the alantolactone group compared to isoalantolactone. These results suggested that isoalantolactone was distributed and eliminated more rapidly than alantolactone in rats when administered, respectively.

1. Introduction

Isoalantolactone and alantolactone were first isolated from Inula helenium [1] and have been found in many Inula plants such as I. royleana [2] and I. japonica [3]; also they have been isolated from Aucklandia lappa [4] and Chinese medicine preparation called Liuwei Anxiao San [5]. Isoalantolactone and alantolactone have a wide range of activities both in vivo and in vitro, including antimicrobial [6, 7], anti-inflammatory, and antitrypanosomal activities [8], and protect against Staphylococcus aureus pneumonia [9]. Moreover, isoalantolactone was reported to reduce significantly the mitochondrial potential (ΔΨm) in pancreatic carcinoma PANC-1 cells [10]. The effects of alantolactone on the intrinsic pathway of apoptosis have been examined in many cell lines, including human leukemia K562 [11] and glioblastoma U87 cells [12]. These studies suggest that alantolactone and isoalantolactone are potential promising anticancer candidates but in various applications. First of all is to develop a method for determination of isoalantolactone and alantolactone in plasma in preclinical studies and subsequent investigations. However, despite being critical preclinical parameter [13], the pharmacokinetics of these compounds were rarely studied to this date and we found the concentrations of isoalantolactone and alantolactone were too low to be determined by UV scan after intravenous injection due to the end of absorption of the lactones (210 nm). LC coupled with tandem mass spectrometer (LC-MS/MS) techniques frequently provided specific, selective, and sensitive quantitative results and reduced sample preparation and analysis time compared with the other common used techniques [14].

A simultaneous determination of isoalantolactone and alantolactone in rat plasma via intravenous injection was reported in a recent study [15], and it turned out that the pharmacokinetic parameters of the two lactones were analogous. Unfortunately, alantolactone was found to induce detoxifying enzymes such as quinone reductase (QR) and glutathione S-transferase (GST) activity [16], suggesting that the pharmacokinetic parameters by simultaneous administration might not be accurate because of the drug interactions in metabolism in vivo. Furthermore, total analysis time of this method is too long by HPLC for almost 19 min and the retention time of IS and lactones was so different (6.4 min versus 12.4 min).

In present study, we developed a novel customized UPLC-MS/MS method to determine isoalantolactone and alantolactone in rat plasma with a shorter retention time (less than 3 min) and lower LLOQ by optimized MS conditions. Osthole was selected as the internal standard (IS) since its retention time was similar to the two lactones. This method was validated and applied to the pharmacokinetic studies of isoalantolactone and alantolactone separately via intravenous injection in rats models with a longer sample collection time than the study before [15] (10 h to 50 min) which made the pharmacokinetic parameters more accurate. At the end, we found the pharmacokinetic parameters of isoalantolactone were so different from those of alantolactone after administration separately.

2. Experimental

2.1. Chemicals and Reagents

Osthole (purity > 98.0%, Figure 1(c)) as internal standard (IS) was obtained from the National Institute for the Control of Pharmaceutical and Biological Products (Beijing, China). HPLC-grade acetonitrile was purchased from Merck Company (Darmstadt, Germany). Ultrapure water for the LC mobile phase was prepared in-house using a Milli-Q system (Millipore, Bedford, MA, USA). All other chemicals were of analytical grade and were used without further purification.

fig1
Figure 1: Structures of isoalantolactone (a), alantolactone (b), and osthole ((c), IS).
2.2. Instrumentation and Analytical Conditions

All analysis was performed with The UPLC-MS/MS system that consisted of a Waters UPLC system with an Applied Biosystem 5500 QTRAP hybrid triple-quadrupole mass spectrometer (Applied Biosystems/MDS Sciex, Foster City, CA, USA), equipped with a turbo ion spray source. Chromatographic separation was performed on a ZORBAX Eclipse Plus C18 (50 mm × 2.1 mm, 1.8 μm). The mobile phase consisted of (A) deionized water and (B) acetonitrile, and the flow rate was 0.4 mL/min. The following gradient elutions were used: 0.0–3.0 min, 30.074.0% B; 3.0-3.1 min, 74.095.0% B; 3.1–4.6 min 95% B; 4.6-4.7 min, 95.030% B; and 4.7–7.0 min, 30% B. The column was maintained at 50°C and the autosampler tray at 20°C.

Nitrogen was used as the nebulizer (GS1), heater (GS2), curtain (CUR) gas, and the collision activation dissociation (CAD) gas. Tandem MS analyses were performed in the MRM acquisition mode for simultaneous detection of all the targeted analytes, with two precursor-to-product ion transitions monitored for the two compounds. The source settings and instrument parameters for each MRM transition were optimized to maximize the generation of protonated analyte molecule ([M+H]+) of each targeted compound, as well as efficiently produce its characteristic fragments/product ions. The ion spray needle voltage was set at 5500 V and the source temperature was 550°C. Following optimization of the setting parameters, the ESI source was operated with the CUR, GS1, and GS2 set at 40, 35, and 35 psi, respectively. The compound-dependent instrumental parameters of two individual precursor-to-product ion transitions specific for each analyte including precursor ion, two product ions, declustering potential (DP), entrance potential (EP), collision energy (CE), and collision cell exit potentials (CXP) were optimized. The parameters are 50 V, 19 eV, 10 V, and 12 successively for both lactones and IS. The transition from precursor ion [M+H]+ at 233.2 to product ion at 187.1 was monitored; to detect osthole, the transition from the precursor at 245.1 to the product at 189.1 was monitored. The dwell time was set at 550 ms.

2.3. Preparation of Isoalantolactone and Alantolactone

Inula helenium (1 kg) was refluxed two times with 95% ethanol at 100°C for 2 h. The extraction solutions were combined, and ethanol was removed under reduced pressure. The residue was suspended in water and extracted with chloroform. The resulting solution was evaporated under reduced pressure and offered a brown residue that contained isoalantolactone and alantolactone. The two lactones were separated by repeated silica column chromatography (contained 10% AgNO3) and eluted with petroleum ether and acetone (100 : 2). Isoalantolactone (48 mg) and alantolactone (36 mg) were collected, respectively (Figures 1(a) and 1(b)).

2.4. Preparation of Stock and Working Solutions

Primary stock solutions of two lactones for preparation of standard and quality control (QC) samples were prepared from separate weighing. Stock solutions (1.0 mg/mL) of both lactones and IS were prepared in acetonitrile. The isoalantolactone (alantolactone) stock solution was diluted with acetonitrile to generate working solutions with concentrations ranging from 25 ng/mL to 5000 ng/mL (concentrations 40, 50, 100, 200, 500, 1000, and 5000 ng/mL) and alantolactone from 40 ng/mL to 5000 ng/mL (concentrations 25, 50, 100, 200, 500, 1000, and 5000 ng/mL) for calibration curves; IS working solutions were prepared with acetonitrile at 5 ng/mL.

2.5. Calibration Standards and Quality Control Samples

Calibration samples were prepared by spiking 90 μL of control rat plasma with the appropriate 10 μL of working solutions of the analytes on the day of analysis. All solutions were stored at 4°C and brought to room temperature before use. Quality control (QC) samples were prepared in the same way as the calibration standards, with three plasma concentrations at 5, 50, and 400 ng/mL. The analytical standards and QC samples were stored at −80°C.

2.6. Sample Preparation

Before analysis, the plasma samples were thawed to room temperature. In a 1.5 mL centrifuge tube, an aliquot of 10 μL of the internal standard working solution (5 ng/mL) was added to 100 μL of collected plasma sample followed by the supplementary addition of 390 μL of acetonitrile (4 : 1, v/v). The tubes were vortex-mixed for 1 min and centrifuged at 14,000 rpm for 10 min. The supernatant (2 μL) was injected into the UPLC-MS/MS system for analysis directly.

2.7. Method Validation

The method was validated for selectivity, linearity, accuracy, precision, recovery, and stability according to the literatures for validation of bioanalytical methods (Food and Drug Administration 2001). Validations were conducted on three consecutive days. Each validation consisted of six replicates of QC plasma samples.

2.7.1. Specificity and Selectivity

The selectivity of the method was evaluated by analyzing blank rat plasma and blank plasma spiked with lactones and IS as well as a rat plasma sample. The selectivity and specificity validations were carried out by analyzing six different blank plasma samples from rats to demonstrate the lack of chromatographic interference from endogenous plasma at the retention time of the analytes and IS.

2.7.2. LOD, LOQ, and Linearity

The lower limit of determination (LOD) had to fulfill the requirement that the signal-to-noise ratio was at least 3 : 1 and the accuracy did not deviate by more than 20%. The lower limit of quantification (LLOQ), defined as the lowest concentration on the calibration curve, had to fulfill the requirement that the signal-to-noise ratio was at least 10 : 1 and the accuracy did not deviate by more than 20%. Calibration curves were constructed by assaying calibration standards spiked with seven nominal lactones concentrations as in Section 2.5 mentioned and then processed as in Section 2.6.

2.7.3. Precision and Accuracy

The precision of the method was determined by calculating RSD for QCs at three concentration levels over three validation days. The accuracy of the method was determined by calculating RE at each QC level.

2.7.4. Recovery and Matrix Effect

By determining the absolute peak areas of lactones at all the three QC levels in six samples, the matrix effect and recovery of the method were evaluated, including standards, standards spiked prior to the extraction, and standards spiked after extraction in six samples. Matrix effect was calculated by dividing the peak area of isoalantolactone and alantolactone in samples spiked postextraction by that of the acetonitrile dissolved samples. The extraction recovery was calculated by dividing the peak area of standards spiked prior to the extraction by that of the isoalantolactone and alantolactone spiked postextraction sample.

2.7.5. Stability

The stability of QC samples was investigated at 5, 50, and 400 ng/mL. The stability investigation included stability in conditions after three freeze-thaw cycles, room temperature for 4 h, autosampler stability of analysis in the room temperature for 24 h, and stability in the stock solution for 20 days at −80°C.

2.7.6. Application of the Method to Pharmacokinetic Study

An ideal chromatographic separation was achieved on a reversed phase Zorbax Eclipse Plus- (2.1 × 50 mm, 1.8 μm) column within 7 min. An electrospray ionization source was applied and operated in positive ion mode; MRM was used for quantification using target fragment ions 233.2→187.1 for isoalantolactone (alantolactone) and 245.1→189.1 for the osthole. Twelve male Sprague-Dawley rats (200–220 g) about 6 weeks were obtained from the Laboratory Animal Centre of Shanghai Jiao Tong University (Shanghai, China). Before the experiments, rats were housed in a temperature (°C) and moisture (%) controlled room, exposed to a controlled 12 h light/dark cycle, and allowed unrestricted access to food and water ad libitum. The animal experimentation was approved by the Shanghai Jiao Tong University Animal Ethics Committee (Shanghai, China).

Accurately weighed isoalantolactone was suspended in 5% PEG-400 deionized water and the same operation for alantolactone. For the pharmacokinetic study, isoalantolactone and alantolactone at 5 mg/kg were injected intravenously into the tail vein in six rats separately. Blood samples were collected from the orbital sinus before and after dosing between 0.083 and 10 h and immediately centrifuged at 5000 rpm for 10 min to obtain plasma samples, which were stored at −80°C until LC-MS/MS analysis.

Drug and Statistics Software Kenitica 4.4.1 was used to analyze plasma isoalantolactone concentration over time in each experimental rat. Mass processing software version was MultiQuant 2.1.1.

3. Investigations Results and Discussion

3.1. Optimization of Mass Spectroscopy Conditions

Quadrupole full scans were carried out in both positive and negative ion detection mode using a 100 ng/mL tuning solution in methanol. A good response was achieved in positive ionization mode for isoalantolactone, alantolactone, and IS. The protonated molecular ions for isoalantolactone, alantolactone, and IS revealed peaks at 233.2, 233.2, and 245.1, respectively, and [M+H]+ ions were found using a direct infusion experiment. The most abundant ions produced by the target protonated molecular ions are 187.1 for the two isomers. A similar situation occurred during the analysis of IS as previously reported [17].

The mobile phase, as well as types of chromatography columns and column temperatures, was tested to optimize the chromatographic conditions. An acetonitrile-water mobile phase system from 30% to 95% acetonitrile without any acid in 3.10 min was proven to strengthen the mass spectrum response of isoalantolactone and alantolactone. Zorbax Eclipse Plus-C18 (2.1 × 50 mm, 1.8 μm) analytical column was selected to give the most satisfactory chromatography from other commercially available C18 columns such as Poroshell 120EC-C18 (3.0 × 50 mm, 2.7 μm), Zorbax Eclipse Plus-C18 (2.1 × 50 mm, 1.8 μm), and Acquity UPLC BEH C18 column (2.1 × 50 mm, 1.7 μm). Three column temperatures (30°C, 40°C, and 50°C) were tested and 50°C was selected due to the shortest retention time. Based on the above analysis, isoalantolactone and alantolactone were eluted at retention time 2.83 and 2.90 min and IS was at 2.60 min. UPLC-MS/MS was performed in MRM mode with target ions at 233.2187.1 for isoalantolactone (alantolactone) and 245.1189.1 for the osthole.

3.2. Sample Pretreatment Method

To minimize potential interferences of rat plasma matrix to UPLC-MS/MS system, a simple, rapid protein precipitation pretreatment was performed as previously reported [18]. Over 99.7% of proteins in plasma samples were precipitated using four acetonitrile volumes. The solid phase extraction column C18 was also tried. The samples were purified by water and eluted with 100% methanol, and then the eluent was dried, reconstituted in 100 μL of mobile phase, vortex-mixed for 30 s, and centrifuged at 14,000 rpm for 5 min. Finally, 2 μL of supernatant was injected into the UPLC-MS/MS system for analysis. It was found to be inapplicable due to large standard deviation and the cumbersome steps.

3.3. Method Validation
3.3.1. Specificity and Selectivity

Both lactones and IS were well extracted and separated from the blank matrix as shown in Figure 2. All the peaks of the analytes and IS were detected with excellent resolution as well as peak shapes. Both lactones and IS were eluted within 3.10 min, with retention time for lactones and IS between 2.63 min and 3.10 min. There was no cross-reaction from plasma in the chromatogram.

fig2
Figure 2: Representative multiple reaction monitoring chromatograms of (a) a blank plasma sample of rats, (b) a blank rat plasma sample spiked with IS (0.1 ng/mL), (c) a blank rat plasma sample spiked with lactones ((c1) for isoalantolactone at 2.5 ng/mL and (c2) for alantolactone at 4 ng/mL), (d) acetonitrile spiked with IS and lactones ((d1) for isoalantolactone and (d2) for alantolactone), and (e) a rat plasma sample obtained 2 h after intravenous injection of 5 mg/kg isoalantolactone (e1) and 4 h of alantolactone (e2).
3.3.2. LOD, LOQ, and Linearity

The limit of detection (LOD) of isoalantolactone and alantolactone was 0.8 and 1 ng/mL, and the lower LOQ was 2.5 and 4 ng/mL (Figure 2). The calibration curves, constructed using linear least squares regression, suggested good linearity in rat plasma. A typical calibration curve equation for isoalantolactone and alantolactone was    and   , where represents the ratio of the isoalantolactone or alantolactone peak area to the osthole peak area ( is the concentration of isoalantolactone or alantolactone in rat plasma and is about the correlation coefficient).

3.3.3. Precision and Accuracy

Precision and accuracy of this assay were determined by analysis of quality control (QC) samples in the blank rat plasma. Intraday precision was 7.06% or less and the interday precision was 9.57% or less at each QC level. The accuracy of intraday and interday performances of validation QC at concentrations of 5, 50, and 400 ng/mL is listed in Table 1. The assay values on both the occasions (intra- and interday) were within the accepted variable limits.

tab1
Table 1: Precision and accuracy of QC samples in rat plasma ().
3.3.4. Recovery and Matrix Effect

Data on absolute recovery and matrix effect are shown in Table 2. In all samples, the average extraction recovery rates of the two lactones were obtained by analyzing six QC samples at low, medium, and high concentrations, respectively. The low concentration should be slightly above but close to LLOQ and the high concentration should be lower but close to the highest concentration on the standard curve. The matrix effect for two lactones ranged from 100.84% to 109.44% and it was 101.76% for osthole. These near 100% results suggested that the matrix exerted minimal effects on the method in response to analytes. The results were within the assay variability limits during the entire process.

tab2
Table 2: Extraction recovery and matrix effect of the method ().
3.3.5. Stability

The extracted quality control samples of the lactones were found to be stable in autosampler, room temperature (20°C), freeze-thaw and long-term (20 days) storage, suggesting that the established method was suitable for the pharmacokinetic study (Table 3).

tab3
Table 3: Stability of samples under different storage conditions ().
3.3.6. Sample Analysis of the Pharmacokinetic Study

The method was applied to a pharmacokinetic study of isoalantolactone and alantolactone separately in rats. The average concentration-time profiles of six rats after intravenous injection of 5 mg/kg and its data on mean plasma concentration of the two lactones over time were given in Tables 4 and 5. The concentration-time curves were shown in Figure 3. Our results indicated that isoalantolactone and alantolactone were distributed and eliminated rapidly possibly due to its low-polarity characteristic and isoalantolactone was eliminated faster than alantolactone in rat plasma after intravenous injection of 5 mg/kg. A large apparent volume of distribution ( and  L) suggests that the lactones may accumulate in certain organs with high concentration after intravenous injection. The plasma concentration profiles of the both two lactones in rats fitted to two-compartment models after administration separately. The level of , Kel, CL, , and AUC was significantly increased in the alantolactone group compared to isoalantolactone group. These results were so different from the previous report in which simultaneous administration was applied [15]. It seemed like the effect of drug-drug interactions in metabolism in vivo can be avoided in a separating administration study. However, further research is required to identify the effect of the two sesquiterpene lactones on drug-metabolizing enzymes.

tab4
Table 4: Mean plasma concentrations of the lactones (, ng/mL) over time.
tab5
Table 5: Pharmacokinetic parameters of the lactones in ratsa,b.
354618.fig.003
Figure 3: Mean ± SD plasma concentration-time profiles of isoalantolactone and alantolactone in rat plasma following i.v. administration at 5 mg/kg dose, respectively.

Disclosure

Renjie Xu was the first author.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work was supported by the Important National Science & Technology Specific Projects funded by the Chinese Government (2012ZX09103201-038). The authors thank SJTULAB for their research support.

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