Transdermal delivery of resveratrol loaded solid lipid nanoparticle as a microneedle patch: a novel approach for the treatment of Parkinson's disease.

IF 5.7 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Drug Delivery and Translational Research Pub Date : 2025-03-01 Epub Date: 2024-06-29 DOI:10.1007/s13346-024-01656-0
Akshay Bandiwadekar, Jobin Jose, Gopika Gopan, Varsha Augustin, Harsha Ashtekar, Kartik Bhairu Khot
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Abstract

Parkinson's disease (PD), affecting millions of people worldwide and expected to impact 10 million by 2030, manifests a spectrum of motor and non-motor symptoms linked to the decline of dopaminergic neurons. Current therapies manage PD symptoms but lack efficacy in slowing disease progression, emphasizing the urgency for more effective treatments. Resveratrol (RSV), recognized for its neuroprotective and antioxidative properties, encounters challenges in clinical use for PD due to limited bioavailability. Researchers have investigated lipid-based nanoformulations, specifically solid lipid nanoparticles (SLNs), to enhance RSV stability. Oral drug delivery via SLNs faces obstacles, prompting exploration into transdermal delivery using SLNs integrated with microneedles (MNs) for improved patient compliance. In this study, an RSV-loaded SLNs (RSV -SLNs) incorporated into the MN patch was developed for transdermal RSV delivery to improve its stability and patient compliance. Characterization studies demonstrated favorable physical properties of SLNs with a sustained drug release profile of 78.36 ± 0.74%. The developed MNs exhibited mechanical robustness and skin penetration capabilities. Ex vivo permeation studies displayed substantial drug permeation of 68.39 ± 1.4% through the skin. In an in vivo pharmacokinetic study, the RSV-SLNs delivered through MNs exhibited a significant increase in Cmax, Tmax, and AUC0 - t values, alongside a reduced elimination rate in blood plasma in contrast to the administration of pure RSV via MNs. Moreover, an in vivo study showcased enhanced behavioral functioning and increased brain antioxidant levels in the treated animals. In-vivo skin irritation study revealed no signs of irritation till 24 h which permits long-term MNs application. Histopathological analysis showed notable changes in the brain regions of the rat, specifically the striatum and substantia nigra, after the completion of the treatment. Based on these findings, the development of an RSV-SLN loaded MNs (RSVSNLMP) patch presents a novel approach, with the potential to enhance the drug's efficiency, patient compliance, and therapeutic outcomes for PD, offering a promising avenue for advanced PD therapy.

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以微针贴片形式透皮给药白藜芦醇固体脂质纳米粒子:治疗帕金森病的新方法。
帕金森病(Parkinson's disease,PD)影响着全球数百万人,预计到 2030 年将有 1,000 万人受到影响,它表现出一系列运动和非运动症状,与多巴胺能神经元的衰退有关。目前的疗法可以控制帕金森氏症的症状,但在延缓疾病进展方面缺乏疗效,因此迫切需要更有效的治疗方法。白藜芦醇(Resveratrol,RSV)具有公认的神经保护和抗氧化特性,但由于生物利用度有限,在临床上用于治疗帕金森氏症时遇到了挑战。研究人员研究了基于脂质的纳米制剂,特别是固体脂质纳米颗粒(SLNs),以提高白藜芦醇的稳定性。通过固体脂质纳米颗粒口服给药面临障碍,这促使人们探索使用与微针(MN)集成的固体脂质纳米颗粒进行透皮给药,以提高患者的依从性。本研究开发了一种将 RSV 装载在 SLNs(RSV -SLNs)中的微针贴片,用于透皮给药 RSV,以提高其稳定性和患者依从性。表征研究表明,SLNs 具有良好的物理性质,药物持续释放率为 78.36 ± 0.74%。所开发的 MNs 具有机械坚固性和皮肤渗透能力。体内外渗透研究显示,药物通过皮肤的渗透率高达 68.39 ± 1.4%。在体内药代动力学研究中,与通过 MNs 给药的纯 RSV 相比,通过 MNs 给药的 RSV-SLNs 的 Cmax、Tmax 和 AUC0 - t 值显著增加,血浆中的消除率也有所降低。此外,一项体内研究显示,接受治疗的动物行为功能增强,脑部抗氧化剂水平提高。体内皮肤刺激性研究表明,在 24 小时内没有出现刺激迹象,因此可以长期使用 MNs。组织病理学分析表明,治疗结束后,大鼠大脑区域(尤其是纹状体和黑质)发生了显著变化。基于这些发现,RSV-SLN 负载 MNs(RSVSNLMP)贴片的开发是一种新方法,有可能提高药物的效率、患者的依从性和对帕金森病的治疗效果,为先进的帕金森病治疗提供了一个前景广阔的途径。
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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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