脂质体
小泡
纳米技术
药物输送
磷脂
纳米医学
两亲分子
化学
生物物理学
材料科学
生物
生物化学
两亲性
纳米颗粒
膜
有机化学
聚合物
共聚物
作者
Abolfazl Akbarzadeh,Rogaie Rezaei-Sadabady,Soodabeh Davaran,Sang Woo Joo,Nosratollah Zarghami,Younes Hanifehpour,Mohammad Samiei,Mohammad Kouhi,Kazem Nejati‐Koshki
标识
DOI:10.1186/1556-276x-8-102
摘要
Liposomes, sphere-shaped vesicles consisting of one or more phospholipid bilayers, were first described in the mid-60s. Today, they are a very useful reproduction, reagent, and tool in various scientific disciplines, including mathematics and theoretical physics, biophysics, chemistry, colloid science, biochemistry, and biology. Since then, liposomes have made their way to the market. Among several talented new drug delivery systems, liposomes characterize an advanced technology to deliver active molecules to the site of action, and at present, several formulations are in clinical use. Research on liposome technology has progressed from conventional vesicles to ‘second-generation liposomes’, in which long-circulating liposomes are obtained by modulating the lipid composition, size, and charge of the vesicle. Liposomes with modified surfaces have also been developed using several molecules, such as glycolipids or sialic acid. This paper summarizes exclusively scalable techniques and focuses on strengths, respectively, limitations in respect to industrial applicability and regulatory requirements concerning liposomal drug formulations based on FDA and EMEA documents.
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