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用于治疗外周动脉疾病的前体脂质体纳米颗粒

Proniosomes Nanoparticle for the Treatment of Peripheral Arterial Disease.

作者信息

Panchal Preyash A, Patel Shruti, Patel Asha, Ahlawat Priyanka

机构信息

Department of Pharmaceutics, Parul Institute of Pharmacy, Parul University, Vadodara, Gujarat, 391760, India.

出版信息

Pharm Nanotechnol. 2024;12(5):428-437. doi: 10.2174/2211738511666230912160729.

DOI:10.2174/2211738511666230912160729
PMID:37702235
Abstract

BACKGROUND

The common symptom of systemic atherosclerosis is peripheral arterial disease (PAD), which occurs when the artery lumen in the lower extremities gradually becomes blocked by atherosclerotic plaque. The most frequent symptom of lower extremity PAD, called "vascular claudication," which is pain experienced when walking. Partial or total blockage of the peripheral arteries in the upper and lower limbs is called PAD. The danger of death from concurrent coronary artery and cerebrovascular atherosclerosis outweighs the risk of amputation.

OBJECTIVES

However, niosomes have issues with fusion, aggregation, leakage, vesicle sedimentation, and difficulty in sterilizing. A more recent strategy known as pro-vesicular carriers was used to solve these issues. The formulations in Proniosomes are dry and anhydrous, protected with a non-ionic surfactant that serves as a carrier when combined with water.

MATERIALS AND METHODS

Formulation prepared by organic solvent, surfactant, cholesterol, other components and hydration medium. Coacervation Phase separation Technique used for proniosome Nanoparticle. Box Bhenken Design is used for optimization batches.

RESULTS

In this context, we shall discuss the development of Proniosome for the treatment of peripheral arterial diseases. From here, we know that proniosome nanoparticles is pro vesicular system good characteristics and effectiveness for treating peripheral arterial diseases.

CONCLUSION

Proniosomes may be created using various techniques, which may impact how they develop along with the drug's characteristics. They increase the drug's stability while being delivered while being entrapped. They don't need particular conditions for handling, protection, storage, or industrial manufacturing.

摘要

背景

系统性动脉粥样硬化的常见症状是外周动脉疾病(PAD),当下肢动脉管腔逐渐被动脉粥样硬化斑块阻塞时就会发生。下肢PAD最常见的症状称为“血管性间歇性跛行”,即行走时出现的疼痛。上肢和下肢外周动脉的部分或完全阻塞称为PAD。冠状动脉和脑血管动脉粥样硬化并发导致的死亡风险超过截肢风险。

目的

然而,脂质体存在融合、聚集、渗漏、囊泡沉降以及灭菌困难等问题。一种称为前体囊泡载体的最新策略被用于解决这些问题。前体脂质体中的制剂是干燥无水的,用非离子表面活性剂保护,当与水混合时该表面活性剂作为载体。

材料与方法

由有机溶剂、表面活性剂、胆固醇、其他成分和水合介质制备制剂。采用凝聚相分离技术制备前体脂质体纳米颗粒。使用Box - Behnken设计优化批次。

结果

在这种情况下,我们将讨论用于治疗外周动脉疾病的前体脂质体的开发。由此我们知道,前体脂质体纳米颗粒是一种前体囊泡系统,在治疗外周动脉疾病方面具有良好的特性和有效性。

结论

前体脂质体可以使用各种技术制备,这可能会影响它们的发展以及药物的特性。它们在包裹药物递送时提高了药物的稳定性。它们在处理、保护、储存或工业生产方面不需要特殊条件。

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本文引用的文献

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Enhancement in antinociceptive and anti-inflammatory effects of tramadol by transdermal proniosome gel.透皮前体脂质体凝胶增强曲马多的抗伤害感受和抗炎作用。
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Proniosomal gel-mediated topical delivery of fluconazole: Development, characterization, and microbiological evaluation.
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Advances of Non-Ionic Surfactant Vesicles (Niosomes) and Their Application in Drug Delivery.非离子表面活性剂囊泡(Niosomes)的研究进展及其在药物递送中的应用
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Elucidation of the Diagnosis and Treatment of Peripheral Arterial Disease.外周动脉疾病的诊断与治疗阐释
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Technology overview and drug delivery application of proniosome.前体脂质体的技术概述及其药物递送应用
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Novel non-ionic surfactant proniosomes for transdermal delivery of lacidipine: optimization using 2(3) factorial design and in vivo evaluation in rabbits.新型非离子表面活性剂 proniosomes 经皮传递拉西地平:采用 2(3) 因子设计优化和兔体内评价。
Drug Deliv. 2016 Jun;23(5):1608-22. doi: 10.3109/10717544.2015.1132797. Epub 2016 Jan 13.
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Proniosomes in transdermal drug delivery.经皮给药中的前体脂质体
Curr Pharm Des. 2015;21(20):2883-91. doi: 10.2174/1381612821666150428145940.
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A review on proniosomal drug delivery system for targeted drug action.关于用于靶向药物作用的前体脂质体给药系统的综述。
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Proniosomes as drug carriers.作为药物载体的前体脂质体
Pak J Pharm Sci. 2010 Jan;23(1):103-7.