Tailoring the multi-functional properties of phospholipids for simple to complex self-assemblies

IF 11.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Tejashree Waghule , Ranendra Narayan Saha , Amit Alexander , Gautam Singhvi
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引用次数: 10

Abstract

The unique interfacial properties, huge diversity, and biocompatible nature of phospholipids make them an attractive pharmaceutical excipient. The amphiphilic nature of these molecules offers them the property to self-assemble into distinct structures. The solubility, chemical and structural properties, surface charge, and critical packing parameters of phospholipids play an essential role during formulation design. This review focuses on the relationship between the structural features of a phospholipid molecule and the formation of different lipid-based nanocarrier drug delivery systems. This provides a rationale and guideline for the selection of appropriate phospholipids while designing a drug delivery system. Finally, we refer to relevant recent case studies covering different types of phospholipid-based systems including simple to complex assemblies. Different carriers in the size range of 50 nm to a few microns can be prepared using phospholipids. The carriers can be delivered through oral, intravenous, nasal, dermal, transmucosal, and subcutaneous routes. A wide range of applicability can be achieved by incorporating various hydrophilic and lipophilic additives in the phospholipid bilayer. Advanced research has led to the discovery of phospholipid complexes and cell membrane mimicking lipids. Overall, phospholipids remain a versatile pharmaceutical excipient for drug delivery. They play multiple roles as solubilizer, emulsifier, surfactant, permeation enhancer, coating agent, release modifier, and liposome former.

Abstract Image

裁剪磷脂的多功能特性,从简单到复杂的自组装
磷脂独特的界面特性、丰富的多样性和生物相容性使其成为具有吸引力的药用辅料。这些分子的两亲性使它们具有自组装成不同结构的特性。磷脂的溶解度、化学和结构性质、表面电荷和关键包装参数在配方设计中起着至关重要的作用。本文综述了磷脂分子的结构特征与不同脂基纳米载药系统的形成之间的关系。这为设计给药系统时选择合适的磷脂提供了理论依据和指导。最后,我们参考了最近的相关案例研究,涵盖了不同类型的基于磷脂的系统,包括简单到复杂的组装。利用磷脂可以制备50nm到几微米大小的不同载体。载体可通过口服、静脉注射、鼻腔、真皮、经黏膜和皮下途径给药。通过在磷脂双分子层中掺入各种亲水性和亲脂性添加剂,可以实现广泛的适用性。先进的研究导致发现磷脂复合物和细胞膜模拟脂质。总的来说,磷脂仍然是一种多功能的药物赋形剂。它们具有增溶剂、乳化剂、表面活性剂、渗透增强剂、包衣剂、脱模剂、脂质体成形剂等多种作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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