Development of an UPLC-MS/MS Method for Quantitative Analysis of Clotrimazole in Human Plasma Samples

Abstract

An ultra-performance liquid chromatography-tandem mass spectrometry method was developed for the quantification of clotrimazole (CTZ) plasma levels after intravaginal administration of the drug given at approved dosages. Plasma samples were extracted by liquid–liquid extraction and a single chromatographic run could be completed within about 2 min. The method was linear over the investigated range (0.488–250 ng/mL) with all the correlation coefficients, R², greater than 0.9903. All data were in the range of ±15.0% with respect to the nominal concentration for high QC and medium QC, and in the range ±20% with respect to the nominal concentration for low QC. This rapid and sensitive method was validated and could be applied to human plasma samples from a healthy volunteer, showing that the assay is able to detect plasma concentrations of CTZ in the range of those found after the administration of the drug at approved dosages in the clinical setting.

1. Introduction

Clotrimazole (CTZ) is a well-known imidazole derivative primarily used for local treatment of vaginal and skin infections due to yeasts and dermatophytes, especially candida spp. [1]. CTZ was initially tested for systemic use in candidal septicemia, urinary and pulmonary candidiasis or in other types of serious fungal infections, including pulmonary aspergillosis, where the drug was given orally. This use was abandoned, mostly because of the high incidence of gastro-intestinal disturbances and neurological reactions [1]. CTZ is currently used in skin infections caused by Candida or dermatophytes. CTZ cream showed similar efficacy compared to tolnaftate in the treatment of dermatophytoses, and was as effective as nystatin in cutaneous candidiasis [1]. CTZ absorption through the skin is thought to be minimal, with peak serum concentrations below the detection limit of 0.001 µg/mL [2]. In the treatment of vaginal candidiasis, CTZ vaginal tablets and cream obtained cure rates comparable with those of nystatin [1]. Likewise, the absorption of CTZ after vaginal application is estimated to be very low, ranging between 3 and 10% of the dose administered [3].

A well-established medicinal product, CTZ has long been out of patent; therefore, the active ingredient is suitable for the development of generic drugs. This fact normally prompts the development of good-laboratory-practice (GLP)-level analytical methods supporting the bioequivalence (BE) studies required for generic drug approval. This did not seem to be the case with CTZ, most probably because BE studies are not required for locally applied and locally acting products [4].

In fact, most recent reports of analytical methods developed to measure plasma CTZ levels rely on the high-performance liquid chromatography (HPLC) approach for CTZ detection, and the detection limit reported is not lower than 50 ng/mL [5,6]. Conversely, peak CTZ plasma levels are reported to be 30 and 10 ng/mL, respectively, 24 h after the intravaginal administration of a 100 mg tablet or a cream containing 50 mg of the drug [7]. Thus, based on the above data, the issue of CTZ determination in biological fluids emerges as a somewhat neglected area of bioanalytical research.

With this is in mind, in this work we developed a fast, inexpensive ultra-performance liquid chromatography (UPLC)-tandem mass spectrometry method for the quantification of CTZ in human plasma. The important novelty of our rapid method is given by the possibility of dosing in the plasma of patients who have received CTZ up to 500 pg/mL of the drug, thus measuring very low concentrations that can derive from partial systemic absorption after vaginal or cutaneous administration.

To date, the need of a highly sensitive assay method for CTZ (a drug out of patent and therefore suitable for the development of generic drug) assessment has been limited, because the bioequivalence (BE) studies required for generic drug approval are not required for locally applied and locally acting products. However, it might be foreseen that the regulatory scenario will change for BE studies on CTZ.

2. Materials and Methods

2.1. Drugs and Administration

The powder of CTZ used for calibration standard and quality control samples was purchased by SIGMA; CTZ for healthy volunteer administration was Bayer 2% clotrimazole cream (Gyno-Canesten^® batch #BXPJSK2 and #GP01W1N). One healthy volunteer (a woman of 39 years old) received a 5 g intravaginal dose of 2% clotrimazole cream (Gyno-Canesten^®), corresponding to 100 mg of CTZ. The volunteer gave her informed consent. The volunteer self-administered the drug twice: on day 0 and after 21 days (day 21) from the first administration. The day after administration, blood was collected in the EDTA tube. All subjects gave their informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the Ethics Committee of Il Comitato Etico (N. 0190157/2020).

2.2. Preparation of Stock Solution, Calibration Standard and Quality Control Samples

Stock solutions of CTZ were prepared by dissolving accurately weighed amounts of the drug in MeOH to obtain a final concentration of 0.1 mg/mL. Stock solutions were stored at 4 °C. Calibration standards were freshly prepared the day of the assay by diluting stock solutions of CTZ in drug-free human plasma to yield CTZ concentrations of 250, 125, 62.5, 31.25, 15.635, 7.813, 3.906, 1.953, 0.977, 0.488 ng/mL. Three quality control (QC) samples or spiked samples were obtained by dilution of the stock solutions of CTZ in blank plasma at the high, medium, and low concentrations of CTZ, i.e., 250, 100 and 25 ng/mL, respectively. Aliquots of spiked samples were kept at 4 or −20 °C and thawed on the day of analysis.

2.3. Clotrimazole Liquid/Liquid Extraction from Plasma Samples

Liquid/liquid extraction was used for the purification and concentration of CTZ from plasma samples. In the method used, briefly, a 100-μL aliquot of plasma was added to 50 μL of H₂O/AcN (50:50, v/v) and then to 200 μL of ACN. After a rapid (2 min) vortex mixing, the mixture was centrifuged at 3000 rpm for 10 min at room temperature. The upper organic layer (about 250 μL) was separated and evaporated to dryness at 40 °C (normally 80 min). The residue was then reconstituted in 70 μL of MEOH. A 5 μL aliquot of each sample was injected into the UPLC-MS/MS system for analysis.

2.4. Chromatographic and Mass-Spectrometric Conditions

The chromatographic separation was performed on an AQUITY UPLC system (Waters Corp., Milford, MA, USA) with cooled auto-sampler and column oven for temperature control. An AQUITY UPLC BEH C18 column (1.7 µm; 2.1 × 50 mm; Waters Corp., Milford, MA, USA) was employed, and the column temperature was maintained at 40 °C. The elution was performed at a flow rate of 0.1 mL/min with a run time of 2 min and then a flow rate of 0.7 mL/min for another 1 min. Mobile phases were constituted by a mixture of 18:82 of: Phase A (H₂O+ Ammonium Acetate 0.2% + HCOOH 0.1%) and Phase B (MeOH). The UPLC was connected to a triple quadrupole tandem mass detector (TQD) (Waters Corp., Milford, MA, USA) with an electrospray ionization (ESI) source for the mass spectrometric detection. The ESI source was set in positive ion mode and the quantification was performed using multi-reaction monitoring (MRM) mode for the most suitable mass transitions. The quantitative transition was from 277.1 to 165.2 m/z at collision energy set to 27 V and the confirmatory transition was from 277.1 to 242.2 m/z at collision energy set to 28 V [8]. The optimal MS parameters are showed in

Table 1. The optimal MS parameters for plasma determination of clotrimazole (CTZ).

Source (ESI+) and Analyzer (SI+) and	Settings
Capillary voltage (Kv)	4.0
Cone voltage (V)	40.0
Extractor (V)	3.0
Source temperature (°C)	150
Desolvation temperature (°C)	250
Cone gas flow (L/h)	1
Desolvation gas flow (L/h)	500
Collision energy (eV)	27.0

. Data were processed using MassLynx software with a TargetLynx program version 4.1 (Waters Corp., Milford, MA, USA).

3. Results

3.1. UPLC/MS-MS Chromatograms

Under the above-described chromatographic conditions, the retention time for CTZ was 2.07 min. Figure 1 shows representative chromatograms of two different ion transition m/z 277.1 to 165.1 and m/z 277.1 to 242.2 obtained from the high-concentration QC (250 ng/mL CTZ).

Figure 2 shows a chromatogram obtained from a blank plasma. CTZ was well separated from the other detectable components at the selected wavelength. Comparing the mean areas of post-extraction spiked plasma samples with the neat standard solution at the same concentration, no significant matrix effect was observed. The last point of calibration curve, shown in Figure 3, was 0.488 ng/mL.

3.2. Validation

Calibration curves of CTZ appeared linear over the studied concentration range of 250–0.49 ng/mL, which covers the expected plasma concentrations commonly found in plasma [5], with a medium correlation coefficient R² of 0.9903 (Figure 4).

Table 2. Validation parameters.

Intraday CV	7.80%
Inter-day CV	2.88%
LOD	0.135 ng/mL
LOQ	0.450 ng/mL
Range of linearity	0.488–250 ng/mL
Equation	Y = 0.9436 * X + 1.537
R2	0.9903
CV intra-subject	11.34%

shows all the major parameters studied for the validation of the method. LOD was calculated as three times the standard deviation of plasma blank, while LOQ was 10 times the standard deviation of plasma blank.

In

Table 3. The results of three different measures of spiked samples.

Time of Spiked Samples Measure	Nominal Concentration [ng/mL]	[ng/mL]	Mean [ng/mL] ± SD (N)		% Deviation Respect the Nominal Concentration	Mean % Deviation
After extraction	250	220.2	222.9 ±	4.0 (3)	−11.9	−10.8
		221.1			−11.6
		227.5			−9
	100	104.4	105.0 ±	4.5 (3)	4.4	5.5
		101.7			1.7
		110.4			10.4
	25	27.7	28.5 ±	0.8 (3)	10.7	13.8
		28.5			14.1
		29.2			16.7
After keeping at 4 °C	250	200.6	205.5 ±	7.3 (3)	−19.8	−17.8
		213.8			−14.5
		202.0			−19.2
	100	99.1	105.8 ±	5.9 (3)	−0.9	5.6
		110.5			10.5
		107.1			7.1
	25	30.9	30.1 ±	0.7 (3)	23.7	20.4
		29.7			18.8
		29.7			18.7
After keeping at −20 °C	250	276.1	259.1 ± 15.8 (3)		10.4	3.6
		256.6			2.6
		244.7			−2.1
	100	103.1	98.9 ±	6.4 (3)	3.1	−1.4
		101.3			1.3
		91.3			−8.7
	25	32.9	29.1 ±	3.4 (3)	31.8	16.3
		27.5			9.9
		26.8			7.2

, the results of three different measures of spiked samples were reported. In particular, the samples were measured after extraction, after keeping them for a month at 4 °C and after keeping them for a month at −20 °C. All observed data were in the range of ±15.0% with respect to the nominal concentration for high and medium spiked samples, and in the range ±20% with respect to the nominal concentration for the low spiked sample. Therefore, as established by the FDA guideline for Bioanalytical Method Validation [9], and fully discussed in the paper of Kaza and collaborators [10], this method achieved a degree of reproducibility and accuracy high enough for the determination of CTZ.

In addition, the differences between the fresh and stored spiked samples are also in the range of ±20%. In particular, the differences between freshly prepared spiked samples and 4 °C spiked samples were +7.83% at 250 ng/mL, −0.06% at 100 ng/mL, −5.72% at 25 ng/mL. The differences between freshly prepared spiked samples and −20 °C QCs were −16.23% at 250 ng/mL, +6.56% at 100 ng/mL, −2.11% at 25 ng/mL.

3.3. In Vivo Testing

One healthy volunteer (a woman of 39 years old) received a 5-g intravaginal dose of 2% clotrimazole cream (Gyno-Canesten^®), corresponding to 100 mg of CTZ, at Day-0. After 24 h (at the time of peak plasma levels [5]), blood was collected, and CTZ plasma levels were measured. We found 28.7 ± 4.5 ng/mL of plasma (the mean ± SD of six replicates). Drug administration, at the same dose as above, was repeated at Day-21, and a blood sample was collected 24 h later. CTZ plasma levels from the repeated dosing were 24.4 ± 2.2 ng/mL of plasma (the mean ± SD of six replicates). Figure 5 shows a representative peak from healthy volunteer. The intra-subject coefficient of variations were 11.34%.

4. Discussion

Here, we describe an UPLC-MS/MS-based analytical method to determine the plasma levels of CTZ. With a detection limit ≈500 pg/mL and linear calibration curves in the range of 250–0.49 ng/mL, this assay is able to detect plasma concentrations of CTZ in the range of those found after the administration of the drug at approved dosages in the clinical setting [7]. To our knowledge, this is the first published method achieving such a low level of performance. In fact, two recently reported methods based on the HPLC approach were able to detect CTZ in the concentration range 0.05–5 µg/mL [5], or in the range 0.1–8 µg/mL [6]. Another less recent method reported a detection limit of 0.1 µMol/L, corresponding to about 33.4 µg/L [11]. In addition, there are other published methods measuring CTZ in different solutions [12] or monitoring the degradation pathway of CTZ [13], but the measure of drug concentration is in the microgram range.

Our UPLC-MS/MS method involves non-expensive liquid/liquid extraction. The choice of conditions comes from a thorough study of the literature. In particular, a readjustment of the CTZ and HZ08 extraction conditions of Yan F and collaborators was implemented [14,15]. In the methods of Yan F, CTZ was used as an internal standard [14].

According to other HPLC methods [16,17], our method uses a column temperature of 40 °C. In addition, according to the stability study of Patricia Garcia Ferreira group [18], the sample of CTZ was dried at 40 °C.

Apart from HPLC-based methods, CTZ in plasma and other biological fluids was also measured by quantitative thin-layer chromatography, allowing to detect fungicidal CTZ concentrations in vaginal fluids, in contrast to CTZ plasma levels lower than 0.01 µg/mL [3]. By comparing the detection limits of these methods with the range of plasma concentration expected after the intravaginal administration of CTZ given according to SmPC dosages, it emerges that previous methods would fall short when assessing CTZ plasma levels under these conditions.

In addition, the method underway in MRM mode can measure different analytes and, with an RT of 2.07, CTZ measurement takes place in a very short time.

The need of a highly sensitive and rapid assay method for CTZ assessment has been limited to date, because of the reasons discussed in the Introduction section. However, it might be foreseen that the regulatory scenario will change for BE studies on CTZ. In fact, the new EMA guideline on the quality and equivalence of topical products, which is currently in its draft version and has not come into force, in Section 5.3.1, introduces the possibility of performing pharmacokinetic BE studies for these products [19]. In this regard, the draft states that “human bioequivalence studies are appropriate when the active substance has quantifiable systemic bioavailability” [19].