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用于银屑病局部治疗的载甲氨蝶呤纳米乳剂制剂的研发与评价

Development and evaluation of methotrexate-loaded nanoemulsion formulation for topical treatment of psoriasis.

作者信息

Rashid Sheikh Abdur, Naseem Faiza, Shah Pervaiz Akhtar, Hashmi Hamna Batool, Mazher Mudassar, Mubarak Mohammad S, Sharifi-Rad Javad, Badar Muhammad

机构信息

Gomal Center of Pharmaceutical Sciences, Faculty of Pharmacy, Gomal University, 29050, Dera Ismail Khan, Pakistan.

Punjab University College of Pharmacy, University of the Punjab Lahore, Lahore, Pakistan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb;398(2):1765-1783. doi: 10.1007/s00210-024-03364-5. Epub 2024 Aug 23.

Abstract

Psoriasis is a chronic inflammatory disease that is becoming widespread and is associated with many kinds of additional severe diseases. The present study aimed to develop a methotrexate-loaded almond oil-based nanoemulsion formulation (MTX NE) for topical administration. The drug-loaded nanoemulsion formulation was prepared by high shear homogenization technique. The formulation's stability, as well as other physical and chemical characteristics, including entrapment effectiveness, drug release kinetics, skin permeability, skin irritation, and in vivo evaluation of the optimized formulation, was assessed. Additionally, imiquimod-induced psoriasis in rats was employed to investigate the efficacy of MTX NE against skin disorders. The MTX NE formulation was developed with a particle size of 18.74 ± 9.748 nm, a polydispersity index (PDI) of 0.198 ± 0.01, and an average entrapment efficiency of 79.65 ± 3.84%. The release kinetics model estimates 81.08% drug release at pH 5.5 after 24 h. The major layers of the skin, the epidermis, and dermis were successfully fluidized by the optimized MTX NE formulation, as shown by FTIR results, most likely enhancing drug retention and permeability. However, since Tween 80 and PEG 400 are well-known penetration enhancers, their application greatly accelerates these effects. Permeation data indicate that after 24 h, methotrexate was released from the nano-emulsion at 76.83 ± 4.98 g/cm with a flux rate of 2.385 ± 0.61 µg/cm/h. The in vivo study conducted on rabbit skin showed that the enhanced skin penetration of the prepared MTX-loaded nanoemulsion formulation does not cause any structural modifications in the inter-cellular lipid layers of the stratum corneum. Rabbits used in the in vivo anti-psoriatic investigation demonstrated that MTX NE produced a 95% reduction in PASI. The pharmacokinetic profile revealed that the C, T, and t values were 8.63 µg/mL, 12.5 h, and 17.77 ± 2.21 h, respectively. These findings suggest that the formulation MTX NE is effective in treating psoriasis and may reduce psoriasis symptoms.

摘要

银屑病是一种慢性炎症性疾病,正在变得普遍,并且与多种其他严重疾病相关。本研究旨在开发一种用于局部给药的载有甲氨蝶呤的杏仁油基纳米乳剂制剂(MTX NE)。通过高剪切均质技术制备载药纳米乳剂制剂。评估了该制剂的稳定性以及其他物理和化学特性,包括包封率、药物释放动力学、皮肤渗透性、皮肤刺激性以及对优化制剂的体内评估。此外,采用咪喹莫特诱导的大鼠银屑病来研究MTX NE对皮肤疾病的疗效。所开发的MTX NE制剂的粒径为18.74±9.748 nm,多分散指数(PDI)为0.198±0.01,平均包封率为79.65±3.84%。释放动力学模型估计在pH 5.5条件下24小时后药物释放率为81.08%。傅里叶变换红外光谱(FTIR)结果表明,优化后的MTX NE制剂成功地使皮肤的主要层,即表皮和真皮流化,这很可能增强了药物保留和渗透性。然而,由于吐温80和聚乙二醇400是众所周知的渗透促进剂,它们的应用极大地加速了这些作用。渗透数据表明,24小时后,甲氨蝶呤从纳米乳剂中的释放量为76.83±4.98 μg/cm,通量率为2.385±0.61 μg/cm/h。对兔皮肤进行的体内研究表明,所制备的载有MTX的纳米乳剂制剂增强的皮肤渗透性不会对角质层的细胞间脂质层造成任何结构改变。在体内抗银屑病研究中使用的兔子表明,MTX NE使银屑病面积和严重程度指数(PASI)降低了95%。药代动力学曲线显示,Cmax、Tmax和t1/2值分别为8.63 μg/mL、12.5小时和17.77±2.21小时。这些发现表明制剂MTX NE在治疗银屑病方面有效,并且可能减轻银屑病症状。

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