# Assessment of sub-chronic toxicity and anti-aging effects of a solid self-microemulsifying drug delivery system of Kaempferia parviflora extract in a D-galactose-induced rat model

**Authors:** Somsuda Somintara, Waraporn Sakaew, Sarunya Tuntiyasawasdikul, Peera Tabboon, Catheleeya Mekjaruskul, Jenjiralai Phanphak, Choowadee Pariwatthanakun, Bungorn Sripanidkulchai, Tawut Rudtanatip

PMC · DOI: 10.1080/13880209.2025.2606956 · 2026-01-05

## TL;DR

A new drug delivery system for Kaempferia parviflora extract was found to be safe and effective in reducing aging-related damage in rats.

## Contribution

Developed and tested a solid SMEDDS formulation of K. parviflora extract for improved safety and anti-aging efficacy.

## Key findings

- KPS-SMEDDS showed no toxicity in sub-chronic testing with no adverse effects on health parameters.
- KPS-SMEDDS reduced oxidative stress and improved testicular health in D-galactose-induced aging rats.
- KPS-SMEDDS modulated key aging and inflammation-related proteins and cytokines.

## Abstract

The pharmacological effects of Kaempferia parviflora have been extensively documented. A solid self-microemulsifying drug delivery system (SMEDDS) has been developed to address limitations such as poor water solubility and low bioavailability.

This study evaluated the safety and anti-aging efficacy of the solid SMEDDS containing K. parviflora extract (KPS-SMEDDS) in rats.

A sub-chronic toxicity study was performed to assess the safety of KPS-SMEDDS. Healthy rats (n = 10/group) received oral doses of 125, 250, or 500 mg/kg body weight daily for 90 days. Clinical signs, body weight, hematological and biochemical parameters, and major organ histopathology were evaluated. Separately, the anti-aging effects of KPS-SMEDDS were investigated in a different cohort of rats (n = 9/group) with D-galactose-induced aging. Rats received intraperitoneal D-galactose (50 mg/kg/day) and oral KPS-SMEDDS at the same doses for 60 days. Oxidative stress markers, hormone levels, histopathology, and the expression of proteins related to aging, apoptosis, and inflammation were assessed.

No significant changes were observed in clinical signs, body weight, organ weights, hematological or biochemical parameters, or histopathology in KPS-SMEDDS-treated rats, indicating its safety. KPS-SMEDDS treatment significantly improved testicular weight, reduced malondialdehyde levels, normalized hormone levels, and restored testicular structure in rats with D-galactose-induced aging. Additionally, it upregulated SIRT-1 and Bcl-2, downregulated SA-β-gal, p53, and caspase-3, and modulated inflammatory cytokines (TNF-α, IL-6, and IL-10).

KPS-SMEDDS was well-tolerated in rats and exerted protective effects against D-galactose-induced aging. These findings support its potential as a safe, natural anti-aging agent and highlight the value of formulation enhancement in traditional herbal medicine.

## Linked entities

- **Proteins:** SIRT1 (sirtuin 1), BCL2 (BCL2 apoptosis regulator), TP53 (tumor protein p53), Casp3 (caspase 3), TNF (tumor necrosis factor), IL6 (interleukin 6), IL10 (interleukin 10)
- **Chemicals:** D-galactose (PubChem CID 206), malondialdehyde (PubChem CID 10964)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** p53-ps (Wistar clone pR53P1 p53 pseudogene) [NCBI Gene 301300], Sirt1 (sirtuin 1) [NCBI Gene 309757] {aka Sir2}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, Casp3 (caspase 3) [NCBI Gene 25402] {aka CPP32-beta, Lice, Yama}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, Bcl2 (BCL2, apoptosis regulator) [NCBI Gene 24224] {aka Bcl-2}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}
- **Diseases:** inflammation (MESH:D007249), toxicity (MESH:D064420)
- **Chemicals:** K. parviflora extract (-), D-galactose (MESH:D005690), malondialdehyde (MESH:D008315), water (MESH:D014867)
- **Species:** Kaempferia parviflora (species) [taxon 97751], Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12777754/full.md

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Source: https://tomesphere.com/paper/PMC12777754