Self-Nanoemulsifying Drug Delivery System of Morin: A New Approach for Combating Acute Alcohol Intoxication.

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY International Journal of Nanomedicine Pub Date : 2024-10-18 eCollection Date: 2024-01-01 DOI:10.2147/IJN.S472287
Jiamin Mao, Xiaoyuan Liu, Lie Zhang, Yu Chen, Shiyu Zhou, Yujiao Liu, Jing Ye, Xiaohong Xu, Quan Zhang
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Abstract

Purpose: Acute alcohol intoxication (AAI) is a life-threatening medical condition resulting from excessive alcohol consumption. Our research revealed the potential of morin (MOR) in treating AAI. However, MOR's effectiveness against AAI was hindered by its poor solubility in water and low bioavailability. In this study, our aim was to develop a self-nanoemulsifying drug delivery system (SNEDDS) to enhance MOR's solubility and bioavailability, evaluate its anti-AAI effects, and investigate the underlying mechanism.

Methods: The composition of MOR-loaded self-nanoemulsifying drug delivery system (MOR-SNEDDS) was determined by constructing pseudo-ternary phase diagrams, and its formulation proportion was optimized using the Box-Behnken design. Following characterization of MOR-SNEDDS, we investigated its pharmacokinetics and biodistribution in healthy animals. Additionally, we assessed the anti-AAI effects and gastric mucosal protection of MOR-SNEDDS in an AAI mice model, exploring potential mechanisms.

Results: After breaking down into tiny droplets, the optimized mixture of MOR-SNEDDS showed small droplet size on average, even distribution, strong stability, and permeability. Pharmacokinetic studies indicated that MOR-SNEDDS, compared to a MOR suspension, increased the area under the plasma concentration-time curve (AUC0-t) by 10.43 times. Additionally, studies on how drugs move and are distributed in the body showed that MOR-SNEDDS had an advantage in passively targeting the liver. Moreover, in a mouse model for alcohol addiction, MOR not only decreased alcohol levels by boosting the activity of alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) in the stomach and liver, which counteracted the loss of righting reflex (LORR), but also reduced alcohol-induced damage to the stomach lining by lowering malondialdehyde (MDA) levels and increasing superoxide dismutase (SOD) levels. Furthermore, MOR-SNEDDS notably amplified these effects.

Conclusion: MOR exhibits significant potential as a new medication for treating AAI, and utilizing MOR-SNEDDS with high oral bioavailability represents a promising new strategy in combating AAI.

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莫林自纳米乳化给药系统:对抗急性酒精中毒的新方法。
目的:急性酒精中毒(AAI)是一种因过量饮酒而导致的危及生命的病症。我们的研究揭示了吗啉(MOR)治疗 AAI 的潜力。然而,MOR 在水中的溶解度较低,生物利用度较低,这阻碍了其对 AAI 的疗效。本研究旨在开发一种自纳米乳化给药系统(SNEDDS),以提高 MOR 的溶解度和生物利用度,评估其抗 AAI 的效果,并研究其潜在机制:方法:通过构建伪三元相图确定了MOR负载型自纳米乳化给药系统(MOR-SNEDDS)的组成,并采用Box-Behnken设计法对其配方比例进行了优化。在确定 MOR-SNEDDS 的特性后,我们研究了它在健康动物体内的药代动力学和生物分布。此外,我们还在 AAI 小鼠模型中评估了 MOR-SNEDDS 的抗 AAI 作用和胃黏膜保护作用,探索其潜在机制:结果:MOR-SNEDDS 的优化混合物在分解成微小液滴后,显示出平均液滴体积小、分布均匀、稳定性强、渗透性好等特点。药代动力学研究表明,与 MOR 悬浮液相比,MOR-SNEDDS 的血浆浓度-时间曲线下面积(AUC0-t)增加了 10.43 倍。此外,对药物如何在体内移动和分布的研究表明,MOR-SNEDDS 在被动靶向肝脏方面具有优势。此外,在酒精成瘾的小鼠模型中,MOR 不仅通过提高胃部和肝脏中酒精脱氢酶(ADH)和醛脱氢酶(ALDH)的活性来降低酒精含量,从而抵消右旋反射(LORR)的丧失,还通过降低丙二醛(MDA)水平和提高超氧化物歧化酶(SOD)水平来减少酒精对胃黏膜的损伤。此外,MOR-SNEDDS 还显著增强了这些效果:MOR 作为一种治疗 AAI 的新药具有很大的潜力,利用口服生物利用度高的 MOR-SNEDDS 是一种很有前景的防治 AAI 的新策略。
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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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