For correspondence:-  Hany Darwish   Email: hdarwish75@yahoo.com

Received: 10 June 2016        Accepted: 8 October 2016        Published: 29 November 2016

Citation: Darwish HW, Attwa MW, Kadi AA. Rapid validated liquid chromatographic method coupled with Tandem mass spectrometry for quantification of nintedanib in human plasma. Trop J Pharm Res 2016; 15(11):2467-2473 doi: 10.4314/tjpr.v15i11.23

© 2016 The authors.
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Accordingly, this study was devoted for quantification of NTB in spiked human plasma in presence of cyclobenzaprine (CBP; IS, (b)) in a very short run time (2 min), which permits the analysis of a lot of clinical samples containing NTB in a reasonable time. Additionally, the current procedure was fully validated following the EMA guidelines for validation of the bioanalytical method [10].

Chemicals and reagents

Ninetedanib (NTB) reference powder was obtained from LC Laboratories (Woburn, MA, USA). Cyclobenzaprine (CBP; IS) reference powder, ammonium formate, HPLC-grade acetonitrile (ACN) and formic acid were procured from Sigma-Aldrich and VWR International (West Chester, PA, USA). Purified water was obtained from Milli-Q plus purification system, Millipore, Waters (Millipore, Bedford, MA, USA). Human plasma was kindly supplied by King Khaled University Hospital (Riyadh, KSA), after approved permissions from donners and it was kept frozen at -70 °C until use.

Instrumentation and conditions

Chromatographic separation was conducted on an Agilent 1200 series system consisting of G1311A binary pump, G1322A degasser, G1367B HIP-ALS autosampler, G1316 thermostatted column compartment (column temperature was kept constant at 21 ± 2 ºC), G1315 DAD detector and an Agilent 6410 QqQ LC/MS (Agilent Technologies, Palo Alto, CA, USA).  Chromatographic separation was performed on Luna® PFP column (50 × 2 mm, 3 μm) (Phenomenex, Torrance, CA, USA). The flow rate was 0.4 mLmin^-1 with a mobile phase composed of 40 % water containing 0.01 Molar ammonium formate buffer (pH~ 4.2) and 60 % acetonitrile (ACN).  Sample injection volume was five microliter with a total run time of 2 min. QqQ MS detector was utilized for detection of the analytes and operated with an ESI interface in the positive ionization mode. Nitrogen gas was utilized for desolvation (flow rate of 12 L/min) while nitrogen gas of high purity was utilized as collision gas (pressure = 55 psi). ESI source temperature was kept at 350 ^oC, capillary voltage at 4 kV, and dwell time for each ion was 200 ms.  For quantification purposes, multiple reaction monitoring (MRM) was adopted for the transitions 540.3→113 for NTB, 276→231 and 276→84 for CBP (IS). Fragmentor voltage was set to 135 and 140 V with collision energy of 25 and 20 V for NTB and CBP, respectively. Data manipulation and acquisition was achieved by Agilent MassHunter software.

Preparation of standard solutions

NTB stock standard solution (1.0 mgmL^-1) was prepared in DMSO. This stock solution was further diluted to prepare a working standard solution of 1 µgmL^-1. For preparation of CBP (IS) stock solution, reference CBP powder was solubilized in DMSO to produce a concentration of 0.1 mgmL^-1. One hundred µL of this stock solution was diluted to 10 mL with mobile phase producing a working solution of 1 µgmL^-1.

Sample preparation procedure and construction of calibration curve

Fifty microliter of CBP working standard solution (1 µgmL^-1) was added to different  aliquots of NTB working standard solution (1 µgmL^-1) and diluted to 1 mL with human plasma to prepare ten NTB concentrations: 2, 4, 6 (low quality control; LQC), 10, 30, 50 (medium quality control; MQC), 80, 100 and 120 (high quality control; HQC), and 150 ng mL^-1.

For extraction of NTB and CBP from plasma matrix, one mL of 0.1 M NaOH/glycine buffer (pH∼9) was added to 1 mL spiked human plasma and the samples were shaken for 60 seconds.  Three mL of ACN was then added for protein precipitation. Precipitated proteins were removed by centrifugation at 14000 rpm for 12 min at 4 ^oC. Supernatants was filtered through a Millex-GP, 0.22 µm syringe filter (Millipore, Billerica, MA, USA). The filtered supernatants were then loaded in the auto-sampler tray and volume of 5 µL were injected into LC-MS/MS. Blank was prepared similarly by processing of blank human plasma with same procedure but using mobile phase instead of NTB aliquots, then tested to ensure the absence of interference from any endogenous compounds with NTB and CBP peaks.  Calibration curve (2, 4, 6, 10, 30, 50, 80, 100, 120, and 150 ngmL^-1) were generated for spiked human plasma samples by drawing the peak area ratio of NTB to CBP (y axis) versus NTB nominal concentrations (x axis).  Calibration samples’ analysis at each concentration was attained in triplicates.  Various parameters including intercept, determination coefficient (r²) and slope were utilized as tools for expressing linear regression.  NTB concentrations in spiked plasma samples were calculated utilizing the corresponding linear regression equation.

Under the previously mentioned chromatographic conditions, NTB and CBP were well separated, and carryover effect was minimal in either blank matrix or blank samples containing CBP alone. showed overlaid chromatograms of calibration standard solutions of NTB in addition to CBP (IS) in plasma matrix samples.

NTB and CBP mass spectra were composed mainly of a single ion peaks at m/z 540.3 and 276.1, respectively. These ions were correspondent to the protonated parent ion.  Isolation of m/z 540.3(NTB) and 276.1(CBP) took place in the first mass analyzer (Q1) followed by fragmentation (q2) in the collision cell. By scanning of the fragments in the second analyzer, m/z 113 was detected for NTB while m/z 231 and 84 were detected for CPB as shown in .  For the quantification of NTB and CBP, m/z 113 and 231 were selected respectively as daughter peak in MRM mode because they gave the highest signal intensity. While m/z 84 was utilized as a qualifier for CBP.

Validation results

Specificity

The current procedure showed high specificity for NTB determination as no interference was observed from expected components of plasma matrix at the retention time of NTB and/or CBP. The mass detector showed no carry over effect from samples. NTB and CBP were well separated under the optimized chromatographic conditions with retention times of 0.92 and 1.65 min, respectively.

Linearity and sensitivity

The linear regression analysis for the results was carried out using the least-square method. The results of six calibration curves showed linearity in the range of 2-150 ngmL^-1 for NTB, with a determination coefficient (r²) ≥ 0.9991.  The mean calibration curve of NTB standard solutions in plasma had the regression equation of y = 2.5773x + 1.31. The limit of quantitation (LOD) and limit of quantification (LOQ) were found to be 0.32 and 0.97 ngmL^-1 in plasma. The standard deviation values of each concentration point (six replicates) did not exceed 2.91 %. Calibration and quality control samples of NTB in human plasma (ten points) were back-calculated to ensure optimum performance of the proposed method. The precision and accuracy for NTB in plasma samples were found in the range of 0.85 to 5.39 % and -3.86 to 2.34 %, respectively ().

Precision and accuracy

The current chromatographic procedure was confirmed to be precise and accurate using intra- and inter-day precision and accuracy values of NTB QC samples. Percentage relative error (% RE) and percentage relative standard deviation (% RSD) were used for evaluating accuracy and precision, respectively.  The values for accuracy and precision lied into the suitable range following EMA guidelines [10] as displayed in .

Stability

Stability studies were performed on QC samples under various conditions as stated in . The deviation of the results from the mean value of the samples was less than 3.15 % for human plasma. Stability results displayed in approved that plasma samples containing NTB can be kept under laboratory conditions with no observed decrease in NTB concentration.

Numerous experiments were tried for achieving maximum resolution and better separation for both NTB and CBP. The selection of the composition of the mobile phase was the corner stone of these trials; various percentages of ACN and water were tried.  Addition of ammonium formate (pH ~ 4.2) to the mobile phase allowed easy ionization of NTB and CBP in addition to a better separation of the two peaks. Accordingly, the proportion of 40 % of aqueous solution containing 0.01 Molar ammonium formate buffer (pH ~ 4.2) and  60 % ACN was  utilized isocratically for good separation of the both analytes (retention times of 0.92 and 1.65 minutes for NTB and CBP, respectively), using the optimized LC-MS/MS condition.  Run time for each run was not more than two min.

In addition to the optimization of chromatographic conditions, mass spectrometric parameters were also adjusted for achieving consistent behaviour of the parent ions and the major product ions of NTB and CBP.  From different modes afforded by tanden mass spectrometry, multiple reaction monitoring (MRM) mode is advantageous when compared to selected ion monitoring (SIM) in decreasing matrix effect of plasma as well as increasing sensitivity to the analyte of interest. Additionally the sensitivity and selectivity were enhanced by operating the ionization source (ESI) in positive ion mode.

For quantification of NTB and CBP, m/z 113 and 231 were selected as daughter peaks in MRM mode because they gave the highest signal intensity. While m/z 84 was utilized as a qualifier for CBP.

After method development, validation took place in terms of sensitivity, linearity, stability, selectivity, accuracy, intra-day and inter-day precision, and system suitability.  The method validation was developed based on the criteria established by the recommendations of the European Medicines Agency (EMA) [10].

The limit of quantitation (LOQ) is the lowest concentration of the standard curve which can be measured with acceptable accuracy and precision for the analyte from human plasma. The limit of detection (LOD) and the limit of quantitation (LOQ) were calculated based on Eq 1. 

LOQ OR LOD=(k υ)⁄M …………………… (1)

where k equal to 10 and 3.3 for LOQ and LOD respectively, υ is the standard deviation of the intercept of regression line and M is the slope of regression line of the calibration curve.

Intra-day accuracy and precision were evaluated by repeated analysis of NTB in human plasma.  The run consisted of a calibration curve plus twelve replicates of each low, medium and high quality control (QC) samples (6, 50, 120 ngmL^-1). Inter-day accuracy and precision were assessed by analysis of samples consisting of a calibration curve and six replicates of low, medium, and high quality control samples for NTB on three successive days.  The overall precision of the method expressed as relative standard deviation and accuracy of the method expressed in term of % error which is calculated according to Eq 2.

% Error = [(A-B)/B] x 100 …….………….. (2)

where A is mean measured concentration, B is nominal concentration of NTB.

For assessing of NTB stability in plasma matrix, six replicates of QC samples were analyzed utilizing various storage conditions. Calculation of accuracy and precision values were carried out using freshly prepared calibration curves in plasma matrix. Estimation of NTB bench-top stability was done after 8 h of storing NTB QC samples at room temperature. Three freeze–thaw cycles were achieved to estimate NTB stability of spiked QC samples after freezing and thawing samples at -80 ^oC and room temperature respectively. Moreover, evaluation of NTB stability was performed by analyzing the spiked QC samples after one day of storing them at 4 o C and after one month of their storage at -20 ^oC.

A rapid and validated LC-MS/MS method has been developed for the quantification of NTB in human plasma with good linearity. The assay procedure is simple for sample preparation with a short run time.  Its elution is eco-friendly with regard to reduced consumption of organic solvent and low-cost.  The developed method should be useful for therapeutic drug monitoring of NTB in plasma and thus for further pharmacokinetic studies of NTB.