油酸囊泡综述:药物输送的新方法。

Q2 Pharmacology, Toxicology and Pharmaceutics
Sandhya S, Jayatheertha S Lokapur, Prakash S Goudanavar
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引用次数: 0

摘要

近年来,多种创新给药技术的应用使药物分配更有针对性和可控性。如今,囊泡给药系统确定了药物的分布速度和作用部位,以改善药物的作用并提高患者的依从性;新开发的囊泡给药系统种类繁多,包括转移体、niosomes、aquasomes、ufasomes、pharmicosomes 和 phytosomes。Ufasomes 是不饱和脂肪酸囊泡,pH 值范围限定在 7 到 9 之间。它们是由脂肪酸及其离子种类组成的封闭脂质双分子层悬浮液。脂肪酸分子的烃尾朝向膜的内核,其羧基与水接触。ufasomes制造过程中最常用的两种脂肪酸是油酸和亚油酸。通过薄膜水合工艺生产脂肪酸囊泡是一种常见的做法。制造稳定的ufasomes主要取决于脂肪酸的选择、胆固醇的用量、pH值范围、缓冲剂等。本文将详细介绍不饱和脂肪酸的特性、优点和缺点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comprehensive Review on Oleic Acid Vesicles: A Novel Approach to Drug Delivery.

The implementation of several innovative drug delivery technologies has made medication distribution more focused and managed in recent years. These days, a vesicular drug delivery system defines the rate of distribution and the site of action in order to improve the action and increase patient compliance; there are various kinds of newly developed vesicular drug delivery systems, including transferosomes, niosomes, aquasomes, ufasomes, pharmacosomes, and phytosomes. Ufasomes are unsaturated fatty acid vesicles with a limited pH range of 7 to 9. They are a suspension of closed lipid bilayers made of fatty acids and their ionized species. The hydrocarbon tails of fatty acid molecules are oriented toward the membrane's inner core, and their carboxyl groups are in contact with water. The two fatty acids that are most frequently employed in the ufasomes' manufacturing process are oleic and linoleic acids. It is a common practice to produce fatty acid vesicles via the thin film hydration process. The manufacture of stable ufasomes is mostly dependent on the choice of fatty acids, amount of cholesterol, pH range, buffer, etc. This article goes into additional detail regarding unsaturated fatty acids' characteristics, benefits, and drawbacks.

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来源期刊
Pharmaceutical nanotechnology
Pharmaceutical nanotechnology Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.20
自引率
0.00%
发文量
46
期刊介绍: Pharmaceutical Nanotechnology publishes original manuscripts, full-length/mini reviews, thematic issues, rapid technical notes and commentaries that provide insights into the synthesis, characterisation and pharmaceutical (or diagnostic) application of materials at the nanoscale. The nanoscale is defined as a size range of below 1 µm. Scientific findings related to micro and macro systems with functionality residing within features defined at the nanoscale are also within the scope of the journal. Manuscripts detailing the synthesis, exhaustive characterisation, biological evaluation, clinical testing and/ or toxicological assessment of nanomaterials are of particular interest to the journal’s readership. Articles should be self contained, centred around a well founded hypothesis and should aim to showcase the pharmaceutical/ diagnostic implications of the nanotechnology approach. Manuscripts should aim, wherever possible, to demonstrate the in vivo impact of any nanotechnological intervention. As reducing a material to the nanoscale is capable of fundamentally altering the material’s properties, the journal’s readership is particularly interested in new characterisation techniques and the advanced properties that originate from this size reduction. Both bottom up and top down approaches to the realisation of nanomaterials lie within the scope of the journal.
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