用于治疗阿尔茨海默病的透皮治疗系统:专利审查。

Letícia Basso, Silvia Cristina Fagundes, Tatiana Staudt, Karini da Rosa, Elizane Langaro, Hamid Omidian, Charise Dallazem Bertol
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引用次数: 0

摘要

背景:两类药物用于治疗阿尔茨海默病(AD);多奈哌齐、加兰他敏和利瓦斯汀是乙酰胆碱酯酶抑制剂,美金刚是n-甲基- d -天冬氨酸受体的非竞争性拮抗剂。虽然这些药物通常口服,但也有经皮治疗系统(tss)市售,用于治疗利瓦斯丁胺和多奈哌齐。由于易于使用、减少副作用和提高治疗依从性,透皮途径对监护人/护理人员更可取。目的:利用Espacenet平台了解这些药物的性质,并检索TTS治疗AD的相关专利。方法:2015年1月至2022年1月,检索词为“利瓦司丁与透皮给药和阿尔茨海默氏症”,药物名称为“美金刚”、“多奈哌齐”、“加兰他明”。采用标题和摘要选择专利。结果:由于皮肤生理和分子大小的限制,tss在吸收方面存在一些限制因素,并具有确定的经皮渗透极限(分子质量为500 g/mol, log P为5)。我们分别发现了加兰他明、利瓦司汀、多奈哌齐和美金刚的1、4、4和2项专利。加兰他明TTS的分子质量为287.35 g/mol, logP为1.8,因此更具挑战性。吸收渗透剂是必要的。美金刚、利瓦司汀和多奈哌齐的logP分别为3.28、2.3和4.27,分子量分别为179.30、250.34和415.96 g/mol。结论:tss主要对小分子药物输送有效。使用吸收增强剂和刺激缓解剂可以是必要的,以提高性能。这些技术的发展对患者和护理人员的便利至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transdermal Therapeutic Systems for the Treatment of Alzheimer's Disease: A Patent Review.

Background: Two classes of medications are used to treat Alzheimer's disease (AD); donepezil, galantamine, and rivastigmine are acetylcholinesterase inhibitors, and memantine is a non-competitive antagonist of the N-methyl-D-aspartate receptor. Although these are typically taken orally, there are transdermal therapeutic systems (TTSs) commercially available for rivastigmine and donepezil. The transdermal route has been preferable for guardians/caregivers due to ease of use, reduced side effects, and improved adherence to therapy.

Objective: The study aimed to obtain knowledge of the properties of these drugs and to search for patents relating to the TTS for AD using the Espacenet platform.

Methods: The search terms were "rivastigmine AND transdermal AND skin delivery AND Alzheimer's", changing the drugs "memantine", "donepezil", and "galantamine", between January 2015 and January 2022. Title and abstract were used to choose patents.

Results: TTSs present some limit factors in terms of absorption due to skin physiology and the size of the molecules with established limits of percutaneous penetration (molecular mass of 500 g/mol and log P of 5). We found 1, 4, 4, and 2 patents for galantamine, rivastigmine, donepezil, and memantine, respectively. Galantamine TTS seems to be more challenging due to the molecular mass of 287.35 g/mol and logP of 1.8. The permeator of absorption is necessary. Memantine, rivastigmine, and donepezil present logP of 3.28, 2.3, and 4.27 and molecular weights of 179.30, 250.34, and 415.96 g/mol, respectively.

Conclusion: TTSs are primarily effective for delivering small molecules. The use of absorption enhancers and irritation mitigators can be necessary to enhance the performance. The development of these technologies is essential for the convenience of patients and caregivers.

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