Rehman Mubashar, Tahir Nayab, Sohail Muhammad Farhan, Qadri Muhammad Usman, Duarte Sofia O D, Brandão Pedro, Esteves Teresa, Javed Ibrahim, Fonte Pedro
Department of Pharmacy, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad 45320, Pakistan.
College of Pharmacy, University of Sargodha, Sargodha 40100, Pakistan.
Pharmaceutics. 2024 Oct 26;16(11):1376. doi: 10.3390/pharmaceutics16111376.
Oils and lipids help make water-insoluble drugs soluble by dispersing them in an aqueous medium with the help of a surfactant and enabling their absorption across the gut barrier. The emergence of microemulsions (thermodynamically stable), nanoemulsions (kinetically stable), and self-emulsifying drug delivery systems added unique characteristics that make them suitable for prolonged storage and controlled release. In the 1990s, solid-phase lipids were introduced to reduce drug leakage from nanoparticles and prolong drug release. Manipulating the structure of emulsions and solid lipid nanoparticles has enabled multifunctional nanoparticles and the loading of therapeutic macromolecules such as proteins, nucleic acid, vaccines, etc. Phospholipids and surfactants with a well-defined polar head and carbon chain have been used to prepare bilayer vesicles known as liposomes and niosomes, respectively. The increasing knowledge of targeting ligands and external factors to gain control over pharmacokinetics and the ever-increasing number of synthetic lipids are expected to make lipid nanoparticles and vesicular systems a preferred choice for the encapsulation and targeted delivery of therapeutic agents. This review discusses different lipids and oil-based nanoparticulate systems for the delivery of water-insoluble drugs. The salient features of each system are highlighted, and special emphasis is given to studies that compare them.
油脂通过在表面活性剂的帮助下将水不溶性药物分散于水介质中,使其具有溶解性,并促进其穿过肠道屏障被吸收。微乳剂(热力学稳定)、纳米乳剂(动力学稳定)和自乳化药物递送系统的出现赋予了独特的特性,使其适合长期储存和控释。在20世纪90年代,引入了固相脂质以减少药物从纳米颗粒中的泄漏并延长药物释放。对乳剂和固体脂质纳米颗粒结构的操控使得多功能纳米颗粒以及蛋白质、核酸、疫苗等治疗性大分子的负载成为可能。具有明确极性头部和碳链的磷脂和表面活性剂已分别用于制备称为脂质体和非离子表面活性剂泡囊的双层囊泡。对靶向配体和外部因素的了解不断增加,以实现对药代动力学的控制,以及合成脂质数量的不断增加,预计将使脂质纳米颗粒和囊泡系统成为治疗剂包封和靶向递送的首选。本文综述讨论了用于递送水不溶性药物的不同脂质和油基纳米颗粒系统。突出了每个系统的显著特征,并特别强调了比较它们的研究。