Development and Validation of a High-Performance Liquid Chromatography–Tandem Mass Spectrometry Method to Determine Promethazine and Its Metabolites in Edible Tissues of Swine

This study aimed to determine promethazine (PMZ) and its metabolites, promethazine sulfoxide (PMZSO) and monodesmethyl-promethazine (Nor1PMZ), in swine muscle, liver, kidney, and fat. A sample preparation method and high-performance liquid chromatography–tandem mass spectrometry (LC–MS/MS) analysis were established and validated. The samples were extracted using 0.1% formic acid–acetonitrile and purified with acetonitrile-saturated n-hexane. After concentration by rotary evaporation, the extract was re-dissolved in a mixture of 0.1% formic acid-water and acetonitrile (80:20, v/v). Analysis was performed using a Waters Symmetry C18 column (100 mm × 2.1 mm i.d., 3.5 μm) with 0.1% formic acid–water and acetonitrile as the mobile phase. The target compounds were determined using positive ion scan and multiple reaction monitoring. PMZ and Nor1PMZ were quantified with deuterated promethazine (PMZ-d6) as the internal standard, while PMZSO was quantified using the external standard method. In spiked muscle, liver, and kidney samples, the limits of detection (LOD) and limits of quantification (LOQ) for PMZ and PMZSO were 0.05 μg/kg and 0.1 μg/kg, respectively, while for Nor1PMZ, these values were 0.1 μg/kg and 0.5 μg/kg, respectively. For spiked fat samples, the LOD and LOQ for all three analytes were found to be 0.05 μg/kg and 0.1 μg/kg, respectively. The sensitivity of this proposed method reaches or exceeds that presented in previous reports. The analytes PMZ and PMZSO exhibited good linearity within the range of 0.1 μg/kg to 50 μg/kg, while Nor1PMZ showed good linearity within the range of 0.5 μg/kg to 50 μg/kg, with correlation coefficients (r) greater than 0.99. The average recoveries of the target analytes in the samples varied from 77% to 111%, with the precision fluctuating between 1.8% and 11%. This study developed, for the first time, an HPLC–MS/MS method for the determination of PMZ, PMZSO, and Nor1PMZ in four swine edible tissues, comprehensively covering the target tissues of monitoring object. The method is applicable for monitoring veterinary drug residues in animal-derived foods, ensuring food safety.


Introduction
Promethazine (PMZ) is a first-generation antihistamine drug known for its anti-allergic properties. It exhibits additional central inhibitory effects on the subcortical regions of the brain, resulting in significant central sedation, hypnotic, antiemetic, and antipyretic effects, making it commonly used for sedation and sleep [1][2][3]. In China, PMZ is approved for treating allergic reactions in animals such as sheep and pigs, including urticaria and serum "Guiding Principles for Veterinary Drug Residue Elimination Tests" and the "Technical Guiding Principles for Quantitative Analysis Method Validation of Biological Samples", released on 20 June 2022. In these technical guiding principles, experimental approaches, standards, parameters, and reference threshold values for detection method comply with the current international norms, such as COMMISSION IMPLEMENTING REGULATION (EU) 2021/808 of 22 March 2021. According to previous reports, PMZ is primarily metabolized by CYP450 enzymes in animals [10][11][12]. Studies on PMZ metabolism in pig tissues seem to be scarce; no literature on PMZ metabolism in pigs was found. However, from the existing literature (see Table S1), PMZ metabolizes into five to eight metabolites, including PMZSO and Nor 1 PMZ in humans, rats, and mice. PMZSO and Nor 1 PMZ appear to be stable when present and account for a high proportion of metabolites which can be found in humans, rats, and mice. If drugs metabolize in mammals through CYP450 enzymes, there is a certain similarity in the metabolic pathways. Hence, we initially attempted to establish an LC-MS/MS analytical method for PMZ, PMZSO, and Nor 1 PMZ in pig plasma and tissues, then carried out a dosing trial in three experimental pigs. After a single intramuscular injection of PMZ, PMZ and its metabolites PMZSO and Nor 1 PMZ were found in the plasma of all three pigs. Ten days after the injection, PMZ, PMZSO, and Nor 1 PMZ were still present in plasma and tissue above the limit of quantification. Therefore, we eventually chose PMZ and its metabolites PMZSO and Nor 1 PMZ as the target analytes. Nor 1 PMZ was chosen as a target compound of analysis on drug residues in edible tissues for the first time in this study.

Standards and Reagents
A 99.5% pure Promethazine Hydrochloride standard was procured from the China National Institute for Food and Drug Control, China. A Promethazine-d6 Hydrochloride standard with 98% chemical purity and 99.5% isotopic purity, a Promethazine Sulfoxide (PMZSO) standard with 96% purity, and a Monodesmethyl-Promethazine Hydrochloride standard with 97% purity were all sourced from Toronto Research Chemicals, Canada.
HPLC-grade acetonitrile (ACN) and methanol (MeOH) were obtained from Thermo Fisher Scientific, Waltham, MA, USA. HPLC-grade formic acid was bought from Shanghai Macklin Biochemical Co., Ltd., Shanghai, China. Analytical grade n-hexane was purchased from Tianjin Damao Chemical Reagent Factory, Tianjin, China. Ultrapure water was acquired from a Milli-Q water purification system (Millipore, Billerica, MA, USA).

Instruments and Equipment
Experiments utilized a high-performance liquid chromatography-tandem mass spectrometer (LC-30AD 220V liquid chromatograph, Shimadzu Corporation, Kyoto, Japan), equipped with an ESI5500 tandem quadrupole mass spectrometer and a Turbo Ionspray electrospray interface, as well as an Analyst 1.6.3 software workstation (Applied Biosystems, ABI, Corporation, MA, USA).

Preparation of Solution
Standard stock solution: Promethazine hydrochloride standard (calculated as PMZ, C 17 H 20 N 2 S), PMZSO standard (PMZSO, C 17 H 20 N 2 OS), and Monodesmethyl-Promethazine hydrochloride standard (calculated as Nor 1 PMZ, C 16 H 18 N 2 S) were accurately weighed and separately dissolved in HPLC-grade ACN in 50 mL volumetric flasks to achieve a concentration of 1000 µg/mL. These solutions were stored at −22 • C.
PMZ-d6 standard stock solution: A mass of 10 mg of promethazine-d6 hydrochloride standard (C 17 H 15 D 6 ClN 2 S) was transferred to a 10 mL volumetric flask, dissolved in HPLCgrade MeOH to achieve a concentration of 1000 µg/mL, sealed, and stored at −22 • C.
PMZ-d6 working solution: An appropriate amount of PMZ-d6 standard stock solution was diluted with HPLC-grade ACN to obtain an internal standard solution to a final concentration of 1.0 µg/mL, sealed, and kept at 4 • C.
Acetonitrile saturated n-hexane: An appropriate amount of analytical grade n-hexane was added to an appropriate amount of ACN, mixed well, and allowed to stand until layered.
Formic Acid Solution (0.1%) in Water: A volume of 1.00 mL of HPLC-grade formic acid was transferred, diluted to 1 L volume with ultrapure water, and mixed well.
Formic Acid (0.1%) in Acetonitrile: A volume of 1.00 mL of HPLC-grade formic acid was transferred, and ACN was added to form a volume of 1 L. Formic Acid Solution (0.1%) in Water-Acetonitrile (80:20, v/v): A volume of 200 mL of HPLC-grade ACN was transferred to a 1 L volumetric cylinder, approximately 800 mL of 0.1% formic acid solution in water was added, and the combination was mixed well.

Chromatography and Mass Spectrometry Parameters
A Symmetry C 18 (100 mm × 2.1 mm i.d., 3.5 µm) was used. The mobile phases were composed of phase A (0.1% formic acid solution in water) and phase B (acetonitrile, ACN). A flow rate of 0.3 mL/min was maintained with a gradient elution procedure, as presented in Table 1. The mass spectrometer was operated in positive ion mode (ESI+), utilizing a multiple reaction monitoring (MRM) scan mode. The primary operating parameters are presented in Table 2. The standard stock solution from Section 2.3 was diluted to 1 µg/mL with ACN and injected directly into the spectrometer for mass spectrometric optimization. Molecular ion peaks of the target analytes and the internal standard were identified by full-scan mass spectrometry in positive ion mode: m/z was 285.2 for PMZ, 301.3 for PMZSO, 271.3 for Nor 1 PMZ, and 291.3 for PMZ-d6. Each precursor ion underwent MS/MS scanning to determine and evaluate monitored ions for each analyte as a quantitative ion and a qualitative ion. The operation parameters for each ion were optimized using the mass spectrometric scan mode of multiple reaction monitoring (MRM). Consequently, the m/z of 86.2 and 198.1 were established as the quantitative and qualitative ions for PMZ, 198.2 and 239.1 for PMZSO, 197.9 and 240.3 for Nor 1 PMZ, and 92 and 240.3 for PMZ-d6. The quantitative and qualitative ion pairs, declustering potential, and collision energy for each target compound are listed in Table 3. For quantification, PMZ and Nor 1 PMZ utilized PMZ-d6 as the internal standard, while PMZSO employed an external standard method.

Sample Preparation
The blank matrix used in this study came from the muscles, liver, kidneys, and fat of several different pigs and was not mixed during the processing.
Approximately 500 g of muscle, liver, and kidney samples had connective tissue, blood vessels, and fat removed before being chopped into a uniform slurry using a homogenizer. About 5.0 g ± 0.1 g of this slurry was weighed into a 50 mL centrifuge tube, mixed with 100 µL of PMZ-d6 internal standard working solution (1 µg/mL), vortexed for 30 s, and left to stand for 30 min. After adding 10 mL of 0.1% formic acid in acetonitrile, the mixture was vortexed for 1 min and shaken for 10 min at 100% speed on a platform shaker before being centrifuged at 10,000 rpm for 10 min. The supernatant was transferred to a pear-shaped bottle. Another 10 mL of 0.1% formic acid acetonitrile was added to the residue in the centrifuge tube, and the above steps were repeated for a second extraction. Both extraction liquids were collected in a pear-shaped bottle for purification and concentration. Around 500 g of subcutaneous fat from pig, free from muscle and connective tissue, was homogenized to produce a uniform slurry. About 5.0 ± 0.1 g of this fat slurry was weighed into a 50 mL centrifuge tube, into which 100 µL of PMZ-d6 internal standard working solution (1 µg/mL) were added, before being vortexed for 30 s and left to stand for 30 min. Then, 10 mL of acetonitrile saturated n-hexane was added, vortexed until the fat was completely dissolved, and left to stand for 30 min. After adding 10 mL of 0.1% formic acid in acetonitrile, the fat mixture was vortexed for 1 min and shaken for 10 min at 100% speed on a platform shaker, before being centrifuged at 10,000 rpm for 10 min. The upper hexane layer was discarded, and the lower extraction liquid was transferred to a new 50 mL centrifuge tube for purification.
The extraction liquids of muscle, liver, kidney, and fat were added to 10 mL of acetonitrile-saturated n-hexane and vortexed for about 30 s to mix. After settling, the upper hexane layer was discarded and the lower extraction liquid was added to 10 mL of anhydrous ethanol. This was then reduced in volume by using a rotary evaporator at 45 • C, then 5 mL of 0.1% formic acid water-acetonitrile was added and vortexed for 30 s to dissolve the residue completely. After this, 5 mL of n-hexane-saturated acetonitrile was added to the solution and vortexed to mix, then left to stand for layering. Approximately 1 mL of the lower solution was transferred to a 1.5 mL centrifuge tube and centrifuged at 14,000 r/min, 0 • C, for 10 min. The clarified middle liquid was filtered using 0.22 µm nylon syringe filters, sealed in an autosampler vial, and stored at 4 • C for analysis.

Limit of Detection and Limit of Quantification
To establish the limit of detection (LOD) and limit of quantification (LOQ), a blank tissue sample homogenate (5 ± 0.1 g) was spiked with 100 µL of PMZ-d6 internal standard working solution (1 µg/mL) and 100 µL of mixed standard working solution. Thus, spiked samples at varying concentrations of 0.05 µg/kg, 0.1 µg/kg, 0.5 µg/kg, and 1 µg/kg were prepared. These samples were processed and analyzed by the method described in Sections 2.4 and 2.5. The concentration of the sample with a signal-to-noise ratio (S/N) ≥ 3 was considered the LOD, and the concentration with an S/N ≥ 10 was regarded as the LOQ.

Calibration Curve and Linearity
Blank tissue sample slurries (5 ± 0.1 g) were spiked with a 1 µg/mL PMZ-d6 internal standard working solution (100 µL) and a mixed standard working solution (100 µL) to achieve varying concentrations-for PMZ and PMZSO, ranging from 0.1 µg/kg to 50 µg/kg; for Nor 1 PMZ, ranging from 0.5 µg/kg to 50 µg/kg. These samples were processed and analyzed by the method described in Sections 2.4 and 2.5. The calibration curve and correlation coefficient (r) were determined using a weighted least-squares method with the ratio of the concentration of PMZ, Nor 1 PMZ, and PMZ-d6 as the abscissa and the peak area ratio of the quantitative ion pairs of PMZ, Nor 1 PMZ, and PMZ-d6 as the ordinate, with the weight chosen as 1/X 2 . The calibration curve and correlation coefficient of PMZSO were obtained using a weighted least-squares method with the concentration of PMZSO as the abscissa and the peak area of the PMZSO quantitative ion pair as the ordinate, with the weight chosen as 1/X 2 . The experiment was repeated in triplicate.

Recovery and Precision
To assess recovery and precision, blank tissue samples slurry (5 ± 0.1 g) were spiked with mixed standard working solutions of low, medium, and high concentration. These spiked samples at concentrations of 0.5 µg/kg, 5 µg/kg, and 50 µg/kg were processed and analyzed. The recovery and relative standard deviation (RSD) of the sample determination values were calculated, with RSD serving as an indicator of precision. The experiment was repeated for three batches to test inter-day precision.

Investigation of Matrix Effects
A homogenized blank tissue sample of 5 g ± 0.1 g, processed as delineated in Section 2.5, was utilized to generate a sample matrix solution. The mixed standard working solution from Section 2.3, amounting to 100 µL, was separately integrated into the sample matrix solution, thus forming matrix-matched samples at concentrations of 0.1 µg/kg, 0.5 µg/kg, 1 µg/kg, 5 µg/kg, 10 µg/kg, 20 µg/kg, and 50 µg/kg. These samples were analyzed by the method described in Section 2.4, and the matrix-matched sample curve was subsequently plotted. This experiment was conducted thrice.
The mixed standard working solution, described in Section 2.3, was diluted with methanol, resulting in concentrations of 0.1 µg/L, 0.5 µg/L, 1 µg/L, 5 µg/L, 10 µg/L, 20 µg/L, and 50 µg/L. The analysis was conducted as per the conditions specified in Section 2.4, enabling the derivation of the standard working solution curve.
The matrix effect, which refers to the extent of the sample matrix's influence on target compound determination, was evaluated by comparing the slope of the matrix-matched sample curve with the standard working solution of equivalent concentration. Matrix enhancement is indicated by ME > 0, while ME < 0 signifies matrix suppression. Low signal interference from the matrix, which can be overlooked, occurs when 0 ≤ |ME| ≤ 20%. Moderate matrix interference is signaled by 20% < |ME| < 50%, and strong matrix interference is inferred when |ME| ≥ 50%.
Matrix effect is calculated using the following formula:

Stability Test
A homogenized blank tissue sample (5 ± 0.1 g), combined with a low or high concentration of the mixed standard working solution, was used to yield a quality control (QC) sample. QC samples, boasting target drug concentrations of 0.5 µg/kg and 50 µg/kg, were processed in accordance with the method delineated in Section 2.5. The stability of these samples was assessed at different situations: after 30 days of storage at −22 • C, after a week's storage at 4 • C, after three freeze-thaw cycles, and after exposure to room temperature and light for 24 h. Each concentration was replicated thrice. The actual measured concentration was compared with the theoretical added concentration. The deviation between each concentration's mean value and the theoretical concentration was calculated, with the relative standard deviation (RSD) aimed to be within 15%.

Optimization of HPLC-MS/MS Conditions
The Symmetry C 18 column (100 mm × 2.1 mm i.d., 3.5 µm), supplied by Waters, USA, was chosen for separation in this study. Several mobile phase combinations were tested, including 0.1% formic acid water-acetonitrile, 0.1% acetic acid water-acetonitrile, 0.2% formic acid water-acetonitrile, and a blend of 0.1% formic acid and 0.1% acetonitrile. The results indicated that the 0.1% formic acid water-acetonitrile mobile phase system provided the optimum response value and retention time. Figure 1 depicts the characteristic ion mass spectrometry of a mixed standard working solution of 0.005 µg/mL, with mobile phase of 0.1% formic acid in water and acetonitrile.
samples was assessed at different situations: after 30 days of storage at −22 °C, after a week's storage at 4 °C, after three freeze-thaw cycles, and after exposure to room temperature and light for 24 h. Each concentration was replicated thrice. The actual measured concentration was compared with the theoretical added concentration. The deviation between each concentration's mean value and the theoretical concentration was calculated, with the relative standard deviation (RSD) aimed to be within 15%.

Optimization of HPLC-MS/MS Conditions
The Symmetry C18 column (100 mm × 2.1 mm i.d., 3.5 µm), supplied by Waters, USA, was chosen for separation in this study. Several mobile phase combinations were tested, including 0.1% formic acid water-acetonitrile, 0.1% acetic acid water-acetonitrile, 0.2% formic acid water-acetonitrile, and a blend of 0.1% formic acid and 0.1% acetonitrile. The results indicated that the 0.1% formic acid water-acetonitrile mobile phase system provided the optimum response value and retention time. Figure 1 depicts the characteristic ion mass spectrometry of a mixed standard working solution of 0.005 µg/mL, with mobile phase of 0.1% formic acid in water and acetonitrile.

Selection of Extraction Reagents
The actual absolute recoveries of four analytes in muscle, liver, kidney, and fat tissue were compared using four extraction reagents: acetonitrile, 0.1% formic acid in acetonitrile, a blend of ethyl acetate and acetonitrile (20/80, v/v), and 1% ammoniated acetonitrile, as depicted in Figure 3. In Figure 3, the bar represents the average absolute recovery rate of each analyte in four types of tissues, extracted using different extraction reagents, and the error bar represents the standard deviation. The extraction efficiency of 0.1% formic acid in acetonitrile was superior to the others. Consequently, it was chosen as the extraction reagent for the four analytes.

Selection of Extraction Reagents
The actual absolute recoveries of four analytes in muscle, liver, kidney, and fat tissue were compared using four extraction reagents: acetonitrile, 0.1% formic acid in acetonitrile, a blend of ethyl acetate and acetonitrile (20/80, v/v), and 1% ammoniated acetonitrile, as depicted in Figure 3. In Figure 3, the bar represents the average absolute recovery rate of each analyte in four types of tissues, extracted using different extraction reagents, and the error bar represents the standard deviation. The extraction efficiency of 0.1% formic acid in acetonitrile was superior to the others. Consequently, it was chosen as the extraction reagent for the four analytes.

Methodological Validation
Selectivity was evaluated by comparing the chromatograms derived from spiked tissue samples and blank tissue samples, processed and detected following the method outlined in Sections 2.4 and 2.5. It was demonstrated that no endogenous peaks from blank samples were present, and no interfering signals were observed at the retention times of each monitored ion of the analytes. As such, the method developed in this study allowed for accurate qualitative and quantitative analysis of PMZ and its metabolites, PMZSO and

Methodological Validation
Selectivity was evaluated by comparing the chromatograms derived from spiked tissue samples and blank tissue samples, processed and detected following the method outlined in Sections 2.4 and 2.5. It was demonstrated that no endogenous peaks from blank samples were present, and no interfering signals were observed at the retention times of each monitored ion of the analytes. As such, the method developed in this study allowed for accurate qualitative and quantitative analysis of PMZ and its metabolites, PMZSO and Nor 1 PMZ.
The limit of detection (LOD), limit of quantification (LOQ), linear range, and linearity were assessed using spiked samples. After processing and detecting the samples in accordance with Section 2.6, the LOD and LOQ for PMZ and PMZSO were determined to be 0.05 µg/kg and 0.1 µg/kg, respectively, in muscle, liver, and kidney samples; for Nor 1 PMZ, the LOD and LOQ were 0.1 µg/kg and 0.5 µg/kg, respectively. For spiked fat samples, the LOD and LOQ for all three analytes were found to be 0.05 µg/kg and 0.1 µg/kg, respectively. Employing the method described in Section 2.7, PMZ and PMZSO displayed good linear relationships in the range of 0.1 µg/kg to 50 µg/kg across the four tissue types. Nor 1 PMZ also exhibited a strong linear relationship in the range of 0.5 µg/kg to 50 µg/kg, with correlation coefficients (r) exceeding 0.99. Refer to Table 4 for additional details. Table 4. Linear equations, correlation coefficient (r), limit of detection (LOD), and limit of quantification (LOQ) of PMZ and its two metabolites. Recovery and precision were evaluated using spiked samples, following the methodology presented in Section 2.8. As can be seen in Table 5 (original data are shown in Table S2), average recoveries for PMZ, PMZSO, and Nor 1 PMZ in muscle, liver, kidney and fat ranged from 77% to 111%. The intra-day and inter-day precision for all tissues remained less than 15%, thereby meeting the Ministry of Agriculture and Rural Affairs of China's technical guiding principles for residue analysis methods.

Tissues
After processing and analyzing the samples as described in Section 2.9, the matrix effects were determined, as presented in Table 6. The matrix effects for the four types of tissue were predominantly negative, signifying a suppression effect on the signal of the compounds. The matrix effect on the three target compounds in pig fat tissue suggested weak matrix interference. In contrast, the matrix effect on the three target compounds in pig muscle and kidney tissues indicated moderate matrix interference. In pig liver tissue, the matrix effect on the three target compounds signified strong matrix interference. These findings underscore the necessity for thoughtful consideration of tissue matrix types when analyzing analytes, as varying matrices can influence the accuracy of the results. The stability of the samples was assessed following the methodology outlined in Section 2.10. As detailed in Table 7, the relative standard deviations (RSDs) for each analyte concentration within tissue samples, subjected to conditions such as ambient temperature and light exposure for 24 h, refrigeration at 4 • C for 48 h, a three-cycle freeze-thaw process, and prolonged storage for a month, typically hovered around ±15%. Hence, the structural and compositional stability of PMZ, PMZSO, and Nor 1 PMZ in tissue samples proved to be fairly robust under a range of conditions.

Discussion
Thiophene compounds encompass amino groups, which, when dissociated in water, exhibit alkalinity. These compounds may be adsorbed by residual silicon hydroxyl groups present on the surface of the stationary phase of a chromatographic column. To address this issue, the selection of fully end-capped C 18 , phenyl, and C 8 chromatographic columns is recommended. The Symmetry C 18 column (100 mm × 2.1 mm i.d., 3.5 µm, Waters, Milford, MA, USA) was utilized for separation in this investigation. In LC-MS/MS analysis, the ESI+ mode is favorable for alkaline PMZ and its metabolites, while acidic mobile phase systems tend to form [M + H] + ions. Acetonitrile and water, which are frequently used as mobile phases, can be proportioned according to specific requirements. Formic acid or acetic acid serve as typical protonation reagents in the LC-MS mobile phase. This study examined the effects of introducing different ratios of formic acid or acetic acid into the mobile phase. It was discovered that acetic acid increased the baseline of the Nor 1 PMZ representative ion chromatogram, rendering it unsuitable. The most optimal retention time and representative ion chromatograms for the analytes were achieved by adding 0.1% (by volume) formic acid to the aqueous phase.
Matrix effects from animal tissue samples can interfere with the accuracy of drug content analysis in tissues. The internal standard method is routinely employed to mitigate matrix effects and significantly enhance the accuracy and precision of the analysis. Numerous studies have reported the use of the internal standard method in determining PMZ and its metabolite content. Metronidazole served as the internal standard for estimating PMZ and PMZSO in rat plasma and various tissues [36]. PMZ-d6 and PMZSO-d6 were utilized as internal standards to detect the content of PMZ and PMZSO in pig muscle, liver, and kidney [43]. Donepezil was used to detect drugs, include PMZ, in human plasma and urine [31]. Haloperidol was reported to be used as internal standard to quantify chlorpromazine and PMZ in pig kidneys [21], and loratadine was used as internal standard when studying PMZ and ephedrine mixture [38]. The PMZ-d6, a deuterated isotope of PMZ, was employed as the internal standard for quantification in this study.
In the research work, it was found that PMZ, PMZSO, Nor 1 -PMZ, and PMZ-d6 stock solutions and working solutions were stable long-term at −20 • C and 4 • C, and were stable at room temperature and during the sample preparation process. However, after evaporating the solvent of PMZ-d6 working solution, the response value of PMZ-d6 detected by LC-MS/MS significantly decreased after one week at room temperature and exposed to the air. Therefore, we sealed and stored the solution containing PMZ-d6 in the refrigerator. After the solvent of the sample solution containing PMZ-d6 is evaporated by a rotary evaporator, it should be immediately re-dissolved, sealed, and stored at 4 • C.
It was found that the recovery of PMZSO was generally significantly high (>120%) while quantified by PMZ-d6 with internal standard method, though the recovery of PMZ and Nor 1 PMZ was in the range of 80-120%. After investigations, it was found that, in spiked samples, the actual extraction recovery of PMZ, PMZ-d6, and Nor 1 PMZ were all between 60% and 70%, which were very close. However, the actual extraction recovery of PMZSO was above 85%, which was significantly different from the internal standard and other analytes, as shown in Figure 3. As such, PMZ-d6 is unsuitable for quantification analysis of PMZSO. As a metabolite, PMZSO shows stronger polarity than PMZ, with its chemical properties differing from those of PMZ, PMZ-d6, and Nor 1 PMZ. Finally, the internal standard method was used for quantifying PMZ and Nor 1 PMZ, and the external standard method was used for quantifying PMZSO.
Based on the physicochemical characteristics of the target analytes in this study, along with evidence from previous studies [33,41,46], several extraction solvents, including ACN, 0.1% formic acid in ACN, ethyl acetate-ACN (20:80, v/v), and 1% ammoniated ACN, were investigated for their extraction recovery efficacy in pig tissues. Results indicated that formic acid-acetonitrile combination exhibited the most efficient extraction recovery across all analytes, as depicted in Figure 3. Considering the efficiency of extraction for PMZ, PMZSO, Nor 1 PMZ, and PMZ-d6 across four tissue samples, 0.1% formic acid in ACN was utilized as the extraction solvent for this study. It was observed that the extraction efficiency could be boosted by adding a slight amount of acid. However, with an increasing increment in formic acid volume, the extraction liquid for liver and kidney became darker, harboring more impurities, and, thus, posing interference in instrument detection. Consequently, an optimal extractant ratio of 0.1% formic acid in ACN was established.
Fat tissue is a significant animal source food and one of the target tissues for monitoring drug residues. However, fat samples pose challenges in sample preparation and detection procedures due to their high lipophilic impurity content. The extraction recovery of analytes in fat is generally low. In this study, various procedures were explored to enhance extraction and purification efficacy in fat samples. It was determined that complete dissolution of the fat sample slurry in n-hexane prior to analyte extraction improved extraction recovery. During the sample concentration and purification process, the lipid-rich impurity content in the sample solvent could be discarded through extraction with n-hexane, both before and after the extraction solvent was removed using a rotary evaporator. Centrifuging the sample solution at 0 • C or lower facilitated the upward migration of lipid-interfering substances. Finally, the parameters of the fat tissue detection method complied with the requirements of technical guiding principles.

Conclusions
We have, for the first time, developed and validated an LC-MS/MS method for the determination of promethazine and its two metabolites across all edible tissues of swine, in accordance with the Ministry of Agriculture and Rural Affairs of China's technical guiding principles. In this method, 0.1% formic acid in acetonitrile served as the extraction solvent, and LC-MS/MS was used for analyte detection. The limit of quantification ranged between 0.1 µg/kg and 0.5 µg/kg, demonstrating a sensitivity equal to or surpassing previous reports. This study included swine fat as a research subject for the first time and Nor 1 -PMZ as one of the target analytes, thereby presenting an accurate and reliable detection method for monitoring PMZ residues and its metabolites in swine edible tissues.