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用于增强局部抗炎作用和递送的本贾库尔微乳剂配方的开发与优化。

Development and optimization of Benjakul microemulsion formulations for enhancing topical anti-inflammatory effect and delivery.

作者信息

Kuropakornpong Pranporn, Itharat Arunporn, Ooraikul Buncha, Loebenberg Raimar, Davies Neal M

机构信息

Graduate School, Faculty of Medicine, Thammasat University, 12120, Pathumthani, Thailand.

Department of Applied Thai Traditional Medicine, Faculty of Medicine, Thammasat University, 12120, Pathumthani, Thailand.

出版信息

Res Pharm Sci. 2022 Jan 15;17(2):111-122. doi: 10.4103/1735-5362.335170. eCollection 2022 Apr.

Abstract

BACKGROUND AND PURPOSE

Benjakul (BJK) is a combination of five botanical herbal constituents widely used in Thai traditional medicine as an anti-inflammatory remedy. This study aimed to develop a novel topical microemulsion containing BJK for clinical use.

EXPERIMENTAL APPROACH

The microemulsions were produced by a phase inversion temperature (PIT) methodology. Physicochemical properties and stability were evaluated to determine an optimal formula. The stable BJK-loaded microemulsion formulas were then subjected to studies for their anti-inflammatory activity, skin cell toxicity, drug permeation, and stability.

FINDING/RESULTS: Two novel formulations containing isopropyl myristate (ME1-BJK and ME2-BJK) passed the compendial stability test. BJK constituents were completely dissolved in the oil phase and incorporated into the microemulsion base Transcutol® and Labrasol® avoiding the use of alcohol, both microemulsion formulations demonstrated high anti-inflammatory activity with IC values of 3.41 ± 0.36 and 3.95 ± 1.73 μg/mL, respectively. However, dissolution of ME1-BJK showed a superior release profile through both lipophilic and hydrophilic membranes with the highest accumulated amount at 4 h of 25.13% and 38.06%, respectively. All tested formulations of BJK extract demonstrated no apparent skin cell toxicity at concentrations up to 50 μg/mL. After six-month storage under accelerated conditions, there were no significant changes in anti-inflammatory activity.

CONCLUSIONS AND IMPLICATIONS

A novel and stable BJK-loaded microemulsion formulation was successfully developed with excellent release and stability properties. Further clinical research to evaluate pain reduction, edema, and skin irritation using this formulation in animal models is ongoing.

摘要

背景与目的

Benjakul(BJK)是五种植物草药成分的组合,在泰国传统医学中广泛用作抗炎药物。本研究旨在开发一种含BJK的新型外用微乳剂以供临床使用。

实验方法

采用相转变温度(PIT)法制备微乳剂。评估其物理化学性质和稳定性以确定最佳配方。然后对稳定的载BJK微乳剂配方进行抗炎活性、皮肤细胞毒性、药物渗透和稳定性研究。

研究结果

两种含肉豆蔻酸异丙酯的新型制剂(ME1-BJK和ME2-BJK)通过了药典稳定性试验。BJK成分完全溶解于油相中,并被纳入微乳基质Transcutol®和Labrasol®中,避免使用酒精。两种微乳剂配方均显示出高抗炎活性,IC值分别为3.41±0.36和3.95±1.73μg/mL。然而,ME1-BJK的溶解通过亲脂性和亲水性膜均显示出优异的释放曲线,在4小时时的最高累积量分别为25.13%和38.06%。所有测试的BJK提取物制剂在浓度高达50μg/mL时均未表现出明显的皮肤细胞毒性。在加速条件下储存六个月后,抗炎活性没有显著变化。

结论与意义

成功开发出一种新型且稳定的载BJK微乳剂配方,具有优异的释放和稳定性。目前正在进行进一步的临床研究,以评估在动物模型中使用该配方减轻疼痛、水肿和皮肤刺激的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0262/8860110/16be13540c1a/RPS-17-111-g002.jpg

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