含黄豆素结冷胶的离子激活原位凝胶用于帕金森病鼻给药。

Khushboo Lavania, Anuj Garg
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引用次数: 0

摘要

本研究的重点是为帕金森病(PD)创造一种创新的治疗方法,帕金森病是一种进行性神经退行性疾病,其特征是大脑中特定神经元的丧失。目的:制备含大黄素-羟丙基-β-环糊精(HP-β-CD)复合物的结冷胶鼻用凝胶,以提高药物的溶解度和稳定性。方法:以黏度和粘接强度为主要因素,采用中心复合设计(CCD)对结冷胶和HPMC E5的浓度进行优化。优化后的原位凝胶由0.7% w/v的结冷胶和0.6% w/v的HPMC E5组成,在溶胶和凝胶状态下都表现出理想的粘度水平,以及强大的粘接性能。对配制的凝胶进行综合评价,包括凝胶性、药物含量、体外药物释放、体外渗透和组织病理学评估。结果:原位凝胶的释药效果优于单独的白菊花素。体外研究表明,药物可通过鼻黏膜有效渗透而无损伤。此外,对暴露于氧化应激(H2O2诱导)的神经细胞的实验显示,菊花素及其配方具有显著的神经保护作用。与对照组相比,这些治疗明显增强了细胞活力,减少了细胞凋亡和坏死的发生。该配方通过清除自由基和恢复抗氧化酶活性等机制减轻氧化损伤,显示出神经保护特性。结论:这种原位凝胶制剂是一种很有前景的PD治疗鼻腔给药系统。通过解决与药物特性和给药途径相关的挑战,它具有增强治疗效果和改善帕金森病患者生活质量的潜力。
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Ion-activated In Situ Gel of Gellan Gum Containing Chrysin for Nasal Administration in Parkinson's Disease.

Introduction: This study focused on creating an innovative treatment approach for Parkinson's disease (PD), a progressive neurodegenerative condition characterized by the loss of specific neurons in the brain.

Aim: The research aimed to develop a nasal gel using gellan gum containing a complex of chrysin with hydroxypropyl-β-cyclodextrin (HP-β-CD) to enhance the drug's solubility and stability.

Method: The formulation process involved utilizing central composite design (CCD) to optimize the concentrations of gellan gum and HPMC E5, with viscosity and mucoadhesive strength as key factors. The resulting optimized In Situ gel comprised 0.7% w/v gellan gum and 0.6% w/v HPMC E5, exhibiting desirable viscosity levels for both sol and gel states, along with robust mucoadhesive properties. The formulated gel underwent comprehensive evaluation, including assessments for gelation, drug content, in vitro drug release, ex vivo permeation, and histopathology.

Result: The findings demonstrated superior drug release from the In Situ gel compared to standalone chrysin. Ex vivo studies revealed effective drug permeation through nasal mucosa without causing harm. Moreover, experiments on neuronal cells exposed to oxidative stress (H2O2- induced) showcased significant neuroprotection conferred by chrysin and its formulations. These treatments exhibited notable enhancements in cell viability and reduced instances of apoptosis and necrosis, compared to the control group. The formulations exhibited neuroprotective properties by mitigating oxidative damage through mechanisms, like free radical scavenging and restoration of antioxidant enzyme activity.

Conclusion: In conclusion, this developed In situ gel formulation presents a promising novel nasal delivery system for PD therapy. By addressing challenges related to drug properties and administration route, it holds the potential to enhance treatment outcomes and improve the quality of life for individuals with Parkinson's disease.

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