Application of validated LC-MS/MS method development to quantify pexidartinib in biological media: In-vivo bioavailability studies in healthy rabbits

Reagents and chemicals

Ledipasvir (IS) was acquired from MSN Labs, Ahmedabad, India. Pexidartinib was procured from Sreeni Labs Pvt Ltd., Hyderabad. Water used was collected from water purification systems (MilliQ, USA) mounted in the lab. Formic acid of analytical grade and acetonitrile of liquid chromatography (LC) grade were provided by JT Baker, Hyderabad, India. The study was approved by the Institutional Ethical Committee with no. 1292/ac/09/CPCSEA/17-49/A.

Apparatus and software

A modular LC system (Shimadzu, Japan) comprising an LC 20AD pump, DGU-30A4 solvent degasser, efficiency SIL-HTC autosampler, and CTO-AS-column thermostat was utilized for the work. A triple quadrupole mass spectrometer (API-4000) was furnished with a turbo ion–spray interface. Analyst 1.5 software was utilized for data monitoring.

Calibration standards

A stock solution of 1 mg/ml of pexidartinib was processed freshly by solubilizing 10 mg of the drug in 10 ml methanol of 70% v/v. Eight different calibration standards were processed by spiking blank plasma with the pexidartinib standard solution to get concentration levels of 72.45, 150.0, 325.0, 650.0, 1,020.0, 1,420.0, 1,780.0, and 2,173.5 ng/ml.

Quality control standards

These solutions were prepared at three different levels of lowest quality control (LQC), medium quality control (MQC), and high quality control (HQC) standards. These quality control (QC) solutions were processed according to calibration standards to get concentrations of 150, 1,449, and 2,173.5 ng/ml for LQC, MQC, and HQC, respectively. Prepared solutions were store at −20°C until the samples were analyzed.

Chromatography parameters

Isocratic LC elution was achieved on a ZorbaxSB-C₁₈ column (250 × 4.6 mm × 5 μm) with formic acid (0.1% v/v) and acetonitrile in the proportion of 20:80 as mobile phase. The LC system was operated at 0.90 ml/minutes flow rate with a single runtime of 6.5 minutes. The column and autosampler temperatures were monitored at 40.0°C and 5.0°C, respectively, with a 0.9 ml/minutes infusion flow rate.

Mass system parameters

The mass instrument was operated in the positive ionization mode. The specific optimized mass instrument settings for pexidartinib and IS were curtain gas 25 psi, ion source gas 1 (ISG) 50 psi, ISG2 50 psi, ion spray voltage 4,500 V, and turbo spray temperature 550°C. Quantitative analysis was carried out by multiple reaction monitoring of the pairs of transitions m/z 418.10→242.02 for pexidartinib and 889.4→130.0 for ledipasvir, with 100 ms per transition as well as time. Pexidartinib and IS precursor ions were formed by declustering potential of 150 and 155 V, respectively, and precursor ions of pexidartinib and IS were converted into fragments at collision energies of 20 and 20 eV with nitrogen (N₂) gas at a pressure of 5 arbitrary units (Chen and Hsu, 2013; Patel et al., 2017; Shaha et al., 2017)

Sample preparation method

The sample solution was prepared by transferring 250 μl of plasma and 50 μl of ledipasvir (1 μg/ml) into a polypropylene tube and vortexed for 2 minutes. Pexidartinib and IS were extracted with 4 ml of ethyl acetate as solvent and were subjected to centrifugation at 5,000 rpm for 25 minutes at 5.0°C. After centrifugation, the organic phase was separated and it was dried using lyophilizer. The resulting product was made to solubilize in 250 μl of the mobile phase and then it was transferred into pre-labeled vials. The vials were kept in an autosampler and infused into the LC system.

Validation

The developed technique was subjected to validation for specificity, selectivity, linearity, stability, matrix effect, carryover effect, recovery, precision, and accuracy (ICH, 2005; US FDA, 2001).

Selectivity and specificity

The interfering endogenous components with analytes were identified by close analysis of six batches of blank human plasma samples from variable sources. Blank and lower limit of quantification (LLOQ) (72.45 ng/ml) samples were prepared from each batch and infused into the LC–MS/MS system and results were analyzed. To measure the interference between IS and analytes, blank samples were spiked with analyte and IS separately and the results were evaluated. The peak response of interfering compound should less than 20% in the response of LLOQQC (Rana et al., 2008).

Linearity

Calibration standards (non-zero) of eight different concentrations of 72.45, 150.0, 325.0, 650.0, 1,020.0, 1,420.0, 1,780.0, and 2,173.5 ng/ml were freshly prepared and quantified in three separate runs. Calibration curves (peak area ratio of analyte and IS peaks vs. nominal concentration) were plotted by least squares linear regression and reciprocal of the squared concentration (1/x²) used as a weighting factor. Deviation should be within ± 20% for LLOQ and +15% for remaining concentrations (Patel et al., 2017).

Recovery studies

Recovery of pexidartinib was assessed by equating the average peak response of extracted samples against the unextracted samples at the concentration level of LQC, MQC, and HQC standards. The overall mean percentage recovery was calculated from percentage recovery at each concentration level (Shaha et al., 2017).

% Recovery of analyte = Mean analyte peak response in extracted samples / Mean analyte peak response in unextracted sample × 100

Accuracy and precision

These parameters were measured in terms of intraday and interday. Intraday accuracy and precision were assessed by injecting QC samples (150, 1,449, and 2,173.5 ng/ml) and LLOQ (72.45 ng/ml) in five duplicates a day arbitrarily. Interday accuracy and precision were measured from the examination of every QC standard (150, 1,449, and 2,173.5 ng/ml) solutions and LLOQ QC standard (72.45 ng/ml) once a day for five dissimilar days.

Matrix effect

Prepare one sample each of LQC and HQC after extraction in six different blank matrix lots (postextraction spiked samples). Simultaneously, prepare six replicates of equivalent aqueous / neat QC samples and analyze. Evaluate the matrix factor for analyte and IS in each lot using the following formula:

Matrix Factor = Peak response in presence of matrix ions / Average peak response in aqueous samples

Carryover test

Carryover test was assessed by infusing a solution at upper limit of quantification (ULQC) (2,898 ng/ml) and two blank plasma samples immediately after ULQC infusion. The peak response of the initial blank sample at retention time (RT) of pexidartinib should be <20% of the peak response of an LLOQ sample.

Stability studies

Three sets of samples were processed without the presence of any residue extracted from blank plasma by directly spiking the analyte into the reconstitution sample. In the post-preparative stability study, three aliquot HQC and LQC samples were kept at 10.0°C in an autosampler for 24 hours and examined; the resulting data were equated with those original findings. Three aliquot samples of every HQC and LQC were stored in a deep freezer (at −70.0°C) for 36 days. The solutions were assessed and the resulting concentrations were equated with the actual values of control standard sample solutions to estimate the long-term stability of analytes. Three aliquot sample solutions each of HQC and LQC levels were monitored at 25°C for 19 hours in order to found the short-term stability of the analyte. The freeze and thaw stability of analytes was estimated after three freeze–thaw cycles at LQC and HQC samples. During the freeze cycle, the samples were kept at −70°C for 24 hours and during the thaw cycle, the samples were kept at room temperature. After three freeze–thaw levels, the concentration of standard samples was determined. Separate standard working solutions containing pexidartinib and IS were prepared and kept at 25°C and 2~8°C for 20 hours and 17 days (Titier et al., 1997; Yen and Kuang, 2013).

In-vivo bioavailability studies

Six male rabbits of about 2–3 kg were opted for pharmacokinetics. Rabbits were fasted 12 hours before drug administration till 48 hours post-dosing. Water was provided for animals during the examination. A dose of 25 mg of drugs was administered to rabbits and 0.60 ml blood samples were taken through the ear vein of animals earlier to drug administration and during the time being of 0.50, 1.00, 1.50, 2.00, 2.50, 3.00, 4.00, 5.00, 6.00, 8.00, 12.00, 16.00, 24.00, 36.00, and 48.00 hours. Consequential solutions were kept in a centrifuge to operate at 5,000 rpm for 20 minutes and the separated plasma samples were relocated into a polypropylene prelabeled tubes at −20°C (Patel et al., 2011; Shashidhar et al., 2011; Wozniakiewicz et al., 2014). The in-vivo animal bioavailability protocol was accepted by the institutional animal ethical committee with reference no. 1292/ac/09/CPCSEA/17-49/A.

Specificity

From the typical chromatograms shown in Figures 2 and 3, no interference peaks from matrix components were detected at the retaining times of drug samples and IS. The RT of pexidartinib and IS were 5.12 and 3.31 minutes. The total elution time for pexidartinib was 6.5 minutes.

Linearity

The calibration graphs are plotted between the 72.45 and 2,173.5 ng/ml concentration range with eight calibration standards for the analysis of linear regression. The linear regression line equation was found to be y = 0.994x + 2.662 with r² = 0.999. The coefficient of variance (%CV) measured for the calibration graph was found to be ≤3.73 for pexidartinib. The results are presented in Table 1.

Recovery and matrix effect

The average percentage recovery of pexidartinib at LQC, MQC, and HQC samples was found to be 90.70%, 86.49%, and 85.86%, respectively, and the results are tabulated in Table 2. This parameter was calculated by determining the %CV values for HQC and LQC samples and was found to be 1.64% and 0.70%, respectively. The findings are shown in Table 3.

Figure 2. Chromatograms of blank plasma (A) and LLOQ (B) samples. [Click here to view]

Figure 3. Chromatograms of pexidartinib at the LQC level. [Click here to view]

Figure 4. Chromatograms of pexidartinib at the MQC level. [Click here to view]

Figure 5. Chromatograms of pexidartinib at the HQC level. [Click here to view]

Figure 6. Plasma concentration time profile curves of six rabbits. [Click here to view]

Table 1. Linearity of pexidartinib. [Click here to view]

Table 2. %Mean Recovery of pexidartinib. [Click here to view]

Table 3. Matrix effect results for pexidartinib. [Click here to view]

Accuracy and precision

Accuracy and precision were assessed by determining the average intraday and interday precisions of the analytical technique at the QC samples. All the findings were within the acceptance limit of precision, i.e., 15%. The findings for precision and accuracy are presented in Table 4.

Stability studies

From the result of stability studies, there was no degradation of analyte that occurred during the chromatographic technique; extraction and sample storage of pexidertinib occurred during the chromatographic technique and extraction and also sample storage of pexidartinib plasma samples at different storage conditions. Results of the stability data are presented in Table 5.

Application of pharmacokinetic study

The pharmacokinetic parameters of pexidartinib were calculated from the graph obtained by taking time on X-axis and plasma sample concentrations on Y-axis using PKSolver software. In this study, trapezoidal rule was considered for the calculation of area under the curve from 0 to 48 hours (AUC_0-48). Pexidartinib showed a T_max of 3.09 ± 0.14; and mean C_max and AUC_0→last for test formulation were 211.63 ± 11.045 and 4,448.8 ± 257.892, respectively. The findings are shown in Tables 5, and 6 and Figure 6.

Table 4. Intraday and interday QC samples for pexidartinib. [Click here to view]

Table 5. Stability of pexidartinib in human plasma. [Click here to view]

Table 6. Plasma concentrations at different timings. [Click here to view]

Table 7. Test animals pk parameters’ mean values. [Click here to view]