用于治疗牛皮癣样皮肤炎症的白桦脂素-NLC-水凝胶:白桦脂-NLC-水凝胶用于治疗牛皮癣样皮肤炎症:优化、表征、体外和体内评估

Dev Prakash, Anjali Chaudhary, Amit Chaudhary
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引用次数: 0

摘要

目的:牛皮癣是一种慢性炎症性皮肤病,给有效和靶向给药带来了巨大挑战。白桦脂等生物活性物质在治疗这些疾病方面显示出巨大的效用;然而,由于其物理化学特性,它们的效用有限。在此,我们旨在开发一种治疗银屑病的新型外用剂型,利用将白桦脂载入水凝胶基质的固体脂质纳米颗粒(NLCs):方法:采用实验设计方法对制剂进行了细致的优化,并对其各种理化属性进行了深入研究。对 NLC-水凝胶中白桦脂的体外释放模式进行了评估,结果表明该配方具有稳定、可调节的药物释放特性。此外,通过使用弗朗兹扩散细胞进行体外皮肤渗透实验,确定了该制剂具有更好的皮肤渗透能力,并使用咪喹莫特诱导的银屑病样皮肤炎症模型对 BALB/c 雌性小鼠进行体内实验,评估了白桦脂-NLC-水凝胶的治疗效果:NLCs的pH值为5.67±0.86,粒径为148.16±12.66 nm,zeta电位为-22.84±2.37 mV,确保了其稳定性和局部使用的适宜性。该凝胶的 pH 值为 6.05±0.43,粘度为 17550±120 cPs,具有增强皮肤水合作用和脂质修复作用。药物释放研究表明,NLCs 和凝胶的释放速度较慢,从而提高了皮肤的保留率。稳定性测试表明,制剂在室温下稳定,但在高温下不稳定。制剂的体外安全性研究表明,对 HaCaT 细胞系没有明显的不良影响。NLC 凝胶具有显著的抗银屑病活性,可降低炎症和细胞因子水平:白桦脂-NLC-水凝胶配方在局部治疗银屑病方面表现出良好的特性,具有优化的药物输送、持续释放和显著的疗效。这项研究的结果为这种创新的局部剂型在临床上的潜在应用奠定了基础,从而改善了银屑病的治疗效果。
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Betulin-NLC-hydrogel for the Treatment of Psoriasis-like Skin Inflammation: Optimization, Characterisation, and In vitro and In vivo Evaluation.

Purpose: Psoriasis is a chronic inflammatory skin disorder that poses significant challenges regarding effective and targeted drug delivery. Bioactive substances like betulin have shown tremendous utility in treating these conditions; however, they pose limited utility owing to their physicochemical characteristics. Here, we aimed to develop a novel topical dosage form for treating psoriasis, utilising betulin-loaded solid lipid nanoparticles (NLCs) incorporated into a hydrogel matrix.

Methods: The optimization of the formulation was meticulously conducted using a design of experiments methodology, and its diverse physicochemical attributes were thoroughly examined. Evaluating betulin's in vitro release pattern from the NLC-hydrogel demonstrated consistent and regulated drug release properties. Additionally, the formulation demonstrated improved skin penetration abilities as determined by in vitro skin permeation experiments employing Franz diffusion cells- furthermore, the therapeutic effectiveness of the betulin-NLC-hydrogel was assessed by an in vivo experiment carried out using an imiquimod-induced psoriasis-like skin inflammation model in BALB/c female mice.

Results: The NLCs exhibited a pH of 5.67±0.86, particle size of 148.16±12.66 nm, and zeta potential of -22.84±2.37 mV, ensuring stability and suitability for topical use. The gel, with a pH of 6.05±0.43 and viscosity of 17550±120 cPs, showed enhanced skin hydration and lipid restoration. Drug release studies indicated a slower release from NLCs and gel, improving skin retention. Stability tests revealed that the formulations were stable at room temperature but not at elevated temperatures. The in vitro safety profile of the formulation revealed no significant adverse effects on HaCaT cell lines. The NLC gel demonstrated significant anti-psoriatic activity, reducing inflammation and cytokine levels.

Conclusion: The betulin-NLC-hydrogel formulation exhibited promising characteristics for the topical treatment of psoriasis, showcasing optimised drug delivery, sustained release, and notable therapeutic efficacy. The findings from this study provide a foundation for the potential clinical translation of this innovative topical dosage form for improved psoriasis management.

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