Development and Evaluation of Nano-Vesicular Emulsion-Based Gel as a Promising Approach for Dermal Atorvastatin Delivery Against Inflammation.

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY International Journal of Nanomedicine Pub Date : 2024-11-07 eCollection Date: 2024-01-01 DOI:10.2147/IJN.S477001
Marwa H Abdallah, Seham Shawky, Mona M Shahien, Hemat El-Sayed El-Horany, Enas Haridy Ahmed, Shaimaa El-Housiny
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Abstract

Introduction: Atorvastatin (ATV), a medication used to reduce cholesterol levels, possesses properties that can counteract the damaging effects of free radicals and reduce inflammation. However, the administration of ATV orally is associated with low systemic bioavailability due to its limited capacity to dissolve in water and significant first-pass effect. This study aimed to assess the appropriateness of employing nano-vesicles for transdermal administration of ATV in order to enhance its anti-inflammatory effects.

Methods: ATV-loaded transethosomes (ATV-TEs) were optimized using the 33 Box-Behnken design. The ATV-TEs that were created were evaluated for their vesicle size, encapsulation efficiency (% EE), and percent release of drug. The optimum formulation was integrated into a hydroxypropyl methylcellulose (HPMC) emulsion-based gel (ATV-TEs emulgel) using jojoba oil. ATV-TEs emulgel was examined for its physical characteristics, ex vivo permeability, histological, and anti-inflammatory effect in a rat model of inflamed paw edema.

Results: The optimized transethosomes exhibited a vesicle size of 158.00 nm and an encapsulation efficiency of 80.14 ± 1.42%. Furthermore, the use of transethosomal vesicles effectively prolonged the release of ATV for a duration of 24 hours, in contrast to the pure drug suspension. In addition, the transethosomal emulgel loaded with ATV exhibited a 3.8-fold increase in the transdermal flow of ATV, in comparison to the pure drug suspension. ATV-TEs emulgel demonstrated a strong anti-inflammatory impact in the carrageenan-induced paw edema model.

Discussion: This was evident from the significant reduction in paw edema, which was equivalent to the effect of the standard anti-inflammatory medicine, Diclofenac sodium.

Conclusion: In summary, transethosomes, as a whole, might potentially serve as an effective method for delivering drugs via the skin. This could improve the ability of ATV to reduce inflammation by increasing its absorption through the skin.

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开发和评估基于纳米囊状乳液的凝胶,作为皮肤阿托伐他汀给药抗炎的有效方法
简介阿托伐他汀(ATV)是一种用于降低胆固醇水平的药物,具有抵消自由基的破坏作用和减少炎症的特性。然而,由于阿托伐他汀在水中的溶解能力有限,且具有明显的首过效应,因此口服阿托伐他汀的全身生物利用度较低。本研究旨在评估采用纳米微粒经皮给药亚视以增强其抗炎效果的适宜性:方法:采用 33 Box-Behnken 设计优化了负载 ATV 的透硫体(ATV-TEs)。对所制成的 ATV-TEs 的囊泡大小、封装效率(EE%)和药物释放率进行了评估。使用荷荷巴油将最佳配方整合到羟丙基甲基纤维素(HPMC)乳液凝胶(ATV-TEs emulgel)中。对 ATV-TEs 凝胶的物理特性、体内渗透性、组织学以及在大鼠炎性爪水肿模型中的抗炎效果进行了检测:结果:优化后的反式硫糖体的囊泡大小为 158.00 nm,封装效率为 80.14 ± 1.42%。此外,与纯药物悬浮液相比,使用转乙体囊泡可有效延长亚视释放时间达 24 小时。此外,与纯药物悬浮液相比,负载了亚视酸的透硫体软胶囊的亚视酸透皮流量增加了 3.8 倍。在角叉菜胶诱导的爪水肿模型中,ATV-TEs 润肤剂表现出了很强的抗炎作用:讨论:在角叉菜胶诱导的爪水肿模型中,ATV-TEs emulgel 表现出了很强的抗炎作用,爪水肿明显减轻,与标准抗炎药双氯芬酸钠的效果相当:总之,反式硫体作为一个整体,有可能成为通过皮肤给药的有效方法。这可以通过增加皮肤对 ATV 的吸收来提高 ATV 的消炎能力。
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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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