The Validation and Determination of Empagliflozin Concentration in the Presence of Grapefruit Juice Using HPLC for Pharmacokinetic Applications

Author:

Abu Dayyih Wael1ORCID,Zakaraya Zainab2ORCID,Hailat Mohammad3ORCID,Al-Tawarah Nafe M.4,Alkharabsheh Sahem4ORCID,Nadher Haya Khalid5,Hailat Zeyad6,Alarman Samia M.1,Khaleel Anas5ORCID,Awad Riad5

Affiliation:

1. Faculty of Pharmacy, Mutah University, Al-Karak 61710, Jordan

2. Faculty of Pharmacy, Al-Ahliyya Amman University, Amman 19328, Jordan

3. Faculty of Pharmacy, Al-Zaytoonah University of Jordan, Amman 11733, Jordan

4. Faculty of Allied Medical Sciences, Medical Laboratory Sciences, Mutah University, Al-Karak 61710, Jordan

5. Faculty of Pharmacy and Medical Sciences, University of Petra, Amman 11196, Jordan

6. Department of Information Systems, Yarmouk University, Irbid 21163, Jordan

Abstract

Type 2 diabetes mellitus is a multifactorial disorder whose primary manifestation usually initiates with elevated blood sugar levels. Several antidiabetic agents are used to manage type 2 diabetes mellitus, of which empagliflozin is an oral sodium-glucose co-transporter (SGLT-2) inhibitor in the kidney. This research aims to develop and validate a simple analytical method for determining empagliflozin levels in biological fluid and to further evaluate grapefruit juice’s impact on empagliflozin pharmacokinetics in rats. High-Performance Liquid Chromatography (HPLC) was used to establish a simple, rapid, and accurate method for determining empagliflozin levels in rat plasma, in the presence of grapefruit juice. Four groups of rats (n = 10 rats in each) were used in the preclinical study. Group A (healthy rats) received empagliflozin alone; Group B (healthy rats) received empagliflozin with grapefruit; Group C (diabetic rats) received empagliflozin with grapefruit; and Group D (healthy, negative control) received no medication. The rats (n = 10) were given grapefruit juice instead of water for seven days before receiving the empagliflozin dose (0.16 mg/kg). Some pharmacokinetic parameters for each group were determined. The maximum plasma concentration (Cmax) and area under the curve (AUC) of empagliflozin in Group A without grapefruit intake were 730 ng/mL and 9264.6 ng × h/mL, respectively, with Tmax (2 h). In Group B, Cmax was 1907 ng/mL and AUC was 10,290.75 ng × h/mL in the presence of grapefruit, with Tmax (1 h); whereas, in Group C, the Cmax was 2936 ng/mL and AUC was 18657 ng × h/mL, with Tmax (2 h). In conclusion, our results showed that the co-administration of grapefruit with empagliflozin should be cautiously monitored and avoided, in which grapefruit elevates the plasma level of empagliflozin. This may be attributed to the inhibition of the uridine enzyme in the grapefruit by hesperidin, naringin, and flavonoid.

Publisher

MDPI AG

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