Mundada Veenu, Patel Mitali, Sawant Krutika
The M.S.University of Baroda, Vadodara, Gujarat, India.
Crit Rev Ther Drug Carrier Syst. 2016;33(3):265-308. doi: 10.1615/CritRevTherDrugCarrierSyst.2016017218.
A "submicron emulsion" is an isotropic mixture of drug, lipids, and surfactants, usually with hydrophilic cosolvents and with droplet diameters ranging from 10 to 500 nm. Submicron emulsions are of increasing interest in medicine due to their kinetic stability, high solubilizing capacity, and tiny globule size. Because of these properties, they have been applied in various fields, such as personal care, cosmetics, health care, pharmaceuticals, and agrochemicals. Submicron emulsions are by far the most advanced nanoparticulate systems for the systemic delivery of biologically active agents for controlled drug delivery and targeting. They are designed mainly for pharmaceutical formulations suitable for various routes of administration like parenteral, ocular, transdermal, and oral. This review article describes the marked potential of submicron emulsions for oral drug delivery owing to their numerous advantages like reduced first pass metabolism, inhibition of P-glycoprotein efflux system, and enhanced absorption via intestinal lymphatic pathway. To overcome the limitations of liquid dosage forms, submicron emulsions can be formulated into solid dosage forms such as solid self-emulsifying systems. This article covers various types of submicron emulsions like microemulsion, nanoemulsion, and self-emulsifying drug delivery system (SEDDS), and their potential pharmaceutical applications in oral delivery with emphasis on their advantages, limitations, and advancements.
“亚微乳剂”是药物、脂质和表面活性剂的各向同性混合物,通常含有亲水性助溶剂,液滴直径范围为10至500纳米。亚微乳剂因其动力学稳定性、高增溶能力和微小的液滴尺寸而在医学领域越来越受关注。由于这些特性,它们已被应用于各个领域,如个人护理、化妆品、保健、制药和农用化学品。亚微乳剂是迄今为止用于生物活性剂全身递送以实现控释给药和靶向给药的最先进的纳米颗粒系统。它们主要设计用于适用于各种给药途径(如肠胃外、眼部、透皮和口服)的药物制剂。这篇综述文章描述了亚微乳剂用于口服给药的显著潜力,这归因于它们的众多优点,如减少首过代谢、抑制P-糖蛋白外排系统以及通过肠道淋巴途径增强吸收。为了克服液体制剂的局限性,亚微乳剂可以制成固体剂型,如固体自乳化系统。本文涵盖了各种类型的亚微乳剂,如微乳、纳米乳和自乳化给药系统(SEDDS),以及它们在口服给药中的潜在药物应用,重点介绍了它们的优点、局限性和进展。