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基于神经酰胺的纳米载体在药物传递中的应用:概述。

Application of sphingolipid-based nanocarriers in drug delivery: an overview.

机构信息

Formulation Research & Development-Non-Orals, Sun Pharmaceutical Industries Ltd, Vadodara, 390012, Gujarat, India.

Faculty of Pharmacy, The Maharaja Sayajirao University of Baroda, Vadodara, Gujarat, 390001, India.

出版信息

Ther Deliv. 2024;15(8):619-637. doi: 10.1080/20415990.2024.2377066. Epub 2024 Jul 29.

Abstract

Sphingolipids (SL) are well recognized for their cell signaling through extracellular and intracellular pathways. Based on chemistry different types of SL are biosynthesized in mammalian cells and have specific function in cellular activity. SL has an ampiphilic structure with have hydrophobic body attached to the polar head enables their use as a drug delivery agent in the form of nanocarriers. SL-based liposomes can improve the solubility of lipophilic drugs through host and drug complexes and are more stable than conventional liposomal formulations. Preclinical studies of SL nanocarriers are reported on topical delivery, oral delivery, ocular delivery, chemotherapeutic delivery, cardiovascular delivery and Alzheimer's disease. The commercial challenges and patents related to SL nanoformulations are highlighted in this article.

摘要

鞘脂类(SL)通过细胞外和细胞内途径的细胞信号传递而广为人知。根据化学性质的不同,哺乳动物细胞中生物合成不同类型的 SL,并在细胞活动中具有特定的功能。SL 具有两亲性结构,其疏水体附着在极性头部上,使其能够用作纳米载体的药物递送剂。基于 SL 的脂质体可以通过主体和药物复合物提高亲脂性药物的溶解度,并且比常规脂质体制剂更稳定。已报道 SL 纳米载体的临床前研究用于局部递药、口服递药、眼部递药、化疗药物递药、心血管递药和阿尔茨海默病。本文强调了与 SL 纳米制剂相关的商业挑战和专利。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d0f/11412150/1546dd604707/ITDE_A_2377066_UF0001_C.jpg

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