Simultaneous determination of lopinavir, saquinavir and ritonavirin human plasma using liquid chromatography – ion trap mass spectrometry
Lopinavir, saquinavir, and ritonavir are viral protease inhibitors (PIs) developed for and widely used in the therapy of human immunodeficiency virus (HIV)-related disease. These compounds are also active in vitro against the pathogens causing tuberculosis, malaria and coronavirus infections. PIs have been regarded as a platform for the design of inhibitors targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-encoded proteases. This study aimed to develop a liquid chromatography/mass spectrometry (LC/MS) procedure for accurate simultaneous determination of concentrations of these three PIs in the plasma.
Samples of human plasma were protein precipitated with 0.3 M zinc sulfate in a water/methanol solution (30:70, v/v). The extracts were analyzed with reversed-phase chromatography coupled with the electrospray ionization (ESI) source of the ion trap mass detector operating in mEass spectrometry (MS) and tandem mass spectrometry (MS/MS) modes.
Calibration curves demonstrated good linearity from 0.01 to 10 µg/mL and acceptable reproducibilities and recoveries.
Conclusions: The described procedure proves that a very basic ion-trap LC/MS system could be applied for selective, rapid, and precise determination of antiviral protease inhibitors.
Keywordsantiviral therapyy, lopinaviry, saquinaviry, ritonaviry, LC/MS
- ESI – electrospray ionization,
- HAART – highly active antiretroviral therapy,
- HIV – human immunodeficiency virus,
- LC/MS – liquid chromatography/mass spectrometry,
- MS/MS – tandem mass spectrometry,
- PIs – protease inhibitors,
- SARS-CoV-2 – severe acute respiratory syndrome coronavirus 2,
- TMD – therapeutic drug monitoring
Lopinavir, saquinavir, and ritonavir are peptidomimetic inhibitors of human immunodeficiency (HIV) protease and belong to the protease inhibitors (PIs) group of drugs. They were developed to treat HIV/AIDS (acquired immunodeficiency syndrome) and are currently used in clinical practice in combinations with nucleoside inhibitors of HIV reverse transcriptase in the highly active antiretroviral therapy (HAART)[1-2]. Lopinavir and saquinavir (or other new generation PIs) are routinely combined with ritonavir in the so-called boosted protease inhibitor regimens because ritonavir administered in low doses can additionally block the cytochrome P450 (CYP3A4), thus increasing the bioavailability of the two first compounds .
In addition to its anti-retroviral properties, PIs exert anti-malarial activity targeting aspartyl proteases in the Plasmodium species and may be associated with a reduced incidence of malaria in HAART receivers [4-5]. Saquinavir has also appeared as a potential agent for tuberculosis, based on an in vitro study of a Mycobacterium tuberculosis infection model .
The policy of repurposing existing drugs has brought the three PIs to light as strong candidates for anti-coronavirus disease 2019 (COVID-19) drugs, specifically as potential inhibitors of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-encoded proteases. Saquinavir could block the proteolytic activity of SARS-CoV-2 3CLpro protease in vitro and the in silico predictions demonstrated its ability to bind the dimeric SARS-CoV-2 Mpro protease [7-8]. Lopinavir/ritonavir was previously demonstrated to have in vitro activity against both severe acquired respiratory syndrome coronavirus 1 (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV), with some efficacy in animal and clinical studies [9-10]. Despite the poor performance of PIs, when compared to the standard of care, in clinical studies with COVID-19 patients, these drugs can be still regarded as a platform to design new and more potent inhibitors of SARS-CoV proteases [8, 11-12].
In addition, the clinical data from HIV-infected patients indicate individual variations in responses to treatment, with some non-responders that demonstrate no phenotype- or genotype-related resistance . This insufficient response could result from specific pharmacokinetics in the individual subjects and the extent to which the patients follow the prescribed therapy. Information about the drug kinetics profiles of patients can be very important in clinical practice [3, 13]. An optimal way to address it is to evaluate the PIs concentrations in the patient’s plasma and to perform therapeutic drug monitoring. This study aimed to develop a liquid chromatography/mass spectrometry (LC/ MS) procedure for accurate simultaneous determination of concentrations of these three PIs in the plasma.
Materials and methods
Preparation of standards and a calibration curve
The standards of lopinavir, saquinavir, and ritonavir (Fig. 1) were provided by Roche (Basel, Switzerland). Diazepam for use as an internal standard (IS) was from WZF Polfa (Warsaw, Poland). Stock solutions of drug standards were prepared at 1 mg/mL concentration by dissolving 5 mg of ritonavir in 5 mL of methanol, 5 mg of saquinavir in 5 mL methanol/water (50:50, v/v), and 5 mg lopinavir in 5 mL of methanol/water (50:50, v/v). To assess the linearity of the assay, seven-point calibration curves were obtained by diluting the stock solutions in acetonitrile/water solution (AcN/W, 4:6, v/v), obtaining finally 0.01, 0.03, 0.1, 0.3, 1, 3, 10 µg/mL of each drug in 200 µl. Diazepam was added to the solutions as an internal standard (IS) at the final concentration of 5 µg/mL.
Figure 1. Chemical structures of three drugs: A. lopinavir, B. saquinavir, C. ritonavir.
Plasma sample preparation
0.3 M zinc sulfate (Sigma/Merck, Darmstadt, Germany) in water/methanol (30:70, v/v) was used as an extracting solution for protein precipitation. Diazepam was added to the solutions on the day of extraction as an internal standard (IS) at the final concentration of 5 µg/mL. To extract drugs from the plasma, 200 μL of human plasma samples were mixed with 600 μl of the extracting solution. Sample tubes were vortexed for 5 min and centrifuged at 13000 rpm for 3 min. Supernatants were transferred into autosampler injection vials and analyzed with LC/MS.
The system applied for the analysis was the LCQ Advantage ion trap mass detector equipped with the electrospray ionization (ESI) source connected to the Surveyor autosampler and the Surveyor quaternary gradient pump (Thermo-Finnigan, San Jose, USA). Separation was carried out on a BDS Hypersil 5 μm column (2 mm/50 mm) protected with a 2x2 mm C18 Security Guard cartridge (Phenomenex, Torrance, USA). Buffer A was 10 mM ammonium acetate, whereas buffer B was acetonitrile. Starting conditions were 60% A/40% B which changed linearly to 1% A/99% B within 3 min. 1%A/99% B was maintained for 3 min and conditions returned to the initial values within the next 0.5 min. The total injection cycle was 6 min. The flow was maintained at 0.25 mL/min. The column temperature was maintained at 25ºC. The injection volume was 20 μL. The mass detector was operated in a positive ionization mode. Ion source parameters were optimized during direct drug infusion into the detector. The sheath gas flow rate was 35 arb. (instrument arbitrary units) and the spray voltage was 5.4 kV. The capillary temperature was set at 300ºC. Direct infusion allowed also to establish a fragmentation pattern of all three drugs and to optimize the collision energy for analysis in a fragmentation (tandem mass spectrometry, MS/MS) mode. Under those conditions, saquinavir formed a parent ion at m/z = 671.6 with some sodium adduct at m/z = 693.6, at quantities below 10%. The isolated ion 671.6 when subjected to a collision energy of 45% resulted in the formation of a major fragment at m/z = 570.2 which was used for detection. Ritonavir formed an ion at m/z = 721.3 with about 30% of sodium adduct (m/z = 743.3). Isolated ion 721.3 when subjected to a collision energy of 25% resulted in the formation of two major fragments at m/z = 295.1 and 426.1 which were used for detection. Lopinavir formed a parent ion at m/z = 629.1. The isolated ion 629.1 when subjected to a collision energy of 28% resulted in the formation of a major fragment at m/z = 447.1 which was used for detection. During chromatographic separation, MS detector was set to operate in alternate full MS (100-1000 m/z)/selective ion or reaction monitoring modes (m/z: 286, 671.6 > 570.2 (45%), 721.3 > 295.2 & 426.1 (25%), and 629.1 > 447.1 (28%)).
Determination of reproducibility and recovery
To determine reproducibility and recovery, we continued analyses on separate days with five injections of calibration standards and a quality control sample each day. Fresh samples were prepared each day. The data is presented in Table 1. We also used a negative control subject (treated with neither of the target compounds) to determine recovery at three different concentrations of each drug (3, 0.3, and 0.03 µg/mL).
Table 1: Reproducibility and recovery data from patients plasma extracts analysis at three different concentrations of each drug (3, 0.3, and 0.03 µg/mL). Av: average, SD: standard deviation, CV: coefficient of variation, Rec: percentage of the recovery
Results and Discussion
As demonstrated in the chromatograms/LC reports in Figure 2, the internal standard (diazepam), lopinavir, saquinavir and ritonavir separated well chromatographically as standards, although with the possibility of construction of separate chromatograms for selected ions such a separation is not an absolute requirement. However, the problem with carryover occurred during several primary injections of the standards. We confirmed the presence of traces of analyzed compounds in compound-free samples following injections of higher concentrations of the standards. We solved this problem, using acetonitrile/water as a wash solution. The response of chromatographic peak areas for chromatograms extracted for selected ions was linear within the concentration range (between 0.01 and 10 µg/mL) for ritonavir, saquinavir, and lopinavir. Recoveries of drug standards added to the4 plasma were > 90% (Table 1). The chromatograms/reports for the calibration curve are attached to demonstrate the signal-to-noise ratio (Fig. 2). Figure 3 represents chromatograms obtained in the analysis of the control plasma extract from an individual non-treated with the analyzed therapeutics, for comparison. Figure 4 with representative chromatograms/reports from the analyses of the treated patients' plasma extracts demonstrates that the analyzed drugs, if present, form clear peaks.
Figure 2. LC/MS chromatograms for standards of protease inhibitors in MS/MS mode: A. Total Ion Current. B. lopinavir, C. saquinavir, D. ritonavir
Figure 3. LC/MS chromatograms for the plasma extract of a control subject. Ion chromatograms for: A. lopinavir, B. saquinavir, and C. ritonavir. Each chromatogram consists of: Total Ion Current, Internal standard, Full MS mode, and MS/MS mode
Figure 4. LC/MS chromatograms for plasma extract from a patient treated with: A. lopinavir, B. saquinavir, and C. ritonavir. Each chromatogram consists of: Total Ion Current, Internal standard, Full MS mode, and MS/MS mode
Our method, although applied for monitoring of just three compounds, can be suitable for monitoring other drugs in the same sample. Low sensitivity preliminary data could be obtained from a full MS trace of already recorded chromatograms, while more accurate determination would require extending the selective ion monitoring/fragmentation mode and re-run of the separation.
Several previously described analytical methods using high-performance liquid chromatography (HPLC) for evaluation of the plasma levels of antiretroviral drugs have been established only for individual compounds  or for more than one, but with different extraction procedures and chromatographic conditions for each compound. That type of analytical procedure is expensive and time-consuming [15-17]. Some other methods used liquid chromatography but with different detection modes [18-20]. Our procedure seems to be much less expensive due to the implementation of the ion trap detector type which provides considerably lower operating costs than other mass detector types. While most of the procedures employ solid-phase extraction for material preparation, we used a simple precipitation procedure with methanol/zinc sulfate for the drug determination. Finally, the total run time of 6 minutes is significantly shorter than in many others assays. Then, the established method can be suitable for routine analyses of a large number of samples in a very short time.
Although viral protease inhibitors described in this study take their origin from HIV treatment, their future use in the therapies of other diseases (e.g. malaria) is possible. There is still an urgent need for repurposed or new anti-SARS-CoV-2 therapeutics with sufficient clinical outcomes. So far four COVID-19 vaccines have been conditionally approved by the European Medicines Agency: 2 are based on the mRNA technology (Moderna and Pfizer/BioNTech) and 2 use the adenovirus platforms (AstraZeneca and Janssen/Johnson and Johnson)  and the number of vaccinated individuals has been increasing. However, fast-acting and efficient antiviral therapy based on the clinically well-defined compounds seems to be a necessary approach for the still recorded severely-ill COVID-19 patients, particularly in the parts of the world where the progress in vaccination is limited. The plasma drug concentrations of lopinavir/ritonavir administered in typical doses do not reach the levels that may be needed to inhibit SARS-CoV-2 proteases  and their use for COVID-19 treatment is currently not recommended. However, the data predicting saquinavir activity have appeared only recently [7- 8], therefore if this drug is used in clinical tests, a method to control the concentration of this drug in the plasma with an inexpensive LC/MS system could be very useful for optimization and monitoring of such treatment.
We developed an LC/MS procedure employing basic and most commonly accessible ion-trap LC/MS system and demonstrated that it could be used for simultaneous selective, rapid, and precise determination of the plasma concentrations three antiviral PIs. The described method can be adapted for high-throughput analyses in routine therapeutic drug monitoring.
The experiments conducted in this study were funded by the Polish National Science Centre (NCN) Harmonia grant no: 2016/22/M/NZ4/00678.
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About the article
Submission: 15 May 2021
Acceptance: 02 July 2021
Online publication: 02 December 2021
Issue publication: 02 December 2021