# Pharmacokinetic assessment of tacrolimus in combination with deoxyschizandrin in rats

**Authors:** Jianguo Sun, Zhipeng Wang, Na Liu, Zhijun Liu, Lili Cui, Xia Tao, Wansheng Chen, Shouhong Gao, Zhijun Wu

PMC · DOI: 10.3389/fphar.2024.1344369 · 2024-05-23

## TL;DR

This study examines how deoxyschizandrin affects the pharmacokinetics of tacrolimus in rats, showing improved drug exposure and stability.

## Contribution

A validated UHPLC-MS/MS method was developed to assess the combined pharmacokinetics of tacrolimus and deoxyschizandrin.

## Key findings

- Deoxyschizandrin increased tacrolimus' Cmax and AUC0–t in a dose-dependent manner.
- Deoxyschizandrin improved tacrolimus' pharmacokinetic stability compared to Wuzhi capsule.
- The UHPLC-MS/MS method enabled rapid and accurate quantification of both compounds.

## Abstract

Tacrolimus (Tac) is commonly used for postoperative immunosuppressive therapy in transplant patients. However, problems, for example, low bioavailability and unstable plasma concentration, persist for a long time, Studies have reported that the deoxyschizandrin could effectively improve these problems, but the pharmacokinetic parameters (PKs) of Tac combined with deoxyschizandrin are still unknown.

In this study, an UHPLC-MS/MS method has been established for simultaneous quantitation of Tac and deoxyschizandrin. The PKs of Tac influenced by different doses of deoxyschizandrin after single and multiple administrations were analyzed, and the different impact of deoxyschizandrin and Wuzhi capsule on PKs of Tac were compared.

The modified UHPLC-MS/MS method could rapid quantification of Tac and deoxyschizandrin within 2 min using bifendatatum as the internal standard (IS). All items were successfully validated. The C
max of deoxyschizandrin increased from 148.27 ± 23.20 to 229.13 ± 54.77 ng/mL in rats after multiple administrations for 12 days. After co-administration of 150 mg/mL deoxyschizandrin, Tac had an earlier T
max and greater C
max and AUC0–t, and the C
max and AUC0–t of Tac increased from 14.26 ± 4.73 to 54.48 ± 14.37 ng/mL and from 95.10 ± 32.61 to 315.23 ± 92.22 h/ng/mL, respectively; this relationship was positively proportional to the dosage of deoxyschizandrin. In addition, compared with Wuzhi capsule, the same dose of deoxyschizandrin has a better effective on Tac along with more stable overall PKs.

An UHPLC-MS/MS method was established and validated for simultaneous detection of deoxyschizandrin and Tac. Deoxyschizandrin could improve the in vivo exposure level and stability of Tac, besides, this effect is better than Wuzhi capsule in same dose.

## Linked entities

- **Chemicals:** tacrolimus (PubChem CID 445643), deoxyschizandrin (PubChem CID 43595), bifendatatum (PubChem CID 108213)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11188489/full.md

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Source: https://tomesphere.com/paper/PMC11188489