Barba Anna Angela, Bochicchio Sabrina, Dalmoro Annalisa, Lamberti Gaetano
Eng4Life Srl, Spin-off Accademico, Via Fiorentino, 32, 83100 Avellino, Italy.
Dipartimento di Farmacia; Università degli Studi di Salerno, via Giovanni Paolo II, 132 84084 Fisciano (SA), Italy.
Pharmaceutics. 2019 Jul 24;11(8):360. doi: 10.3390/pharmaceutics11080360.
In the last years the rapid development of Nucleic Acid Based Drugs (NABDs) to be used in gene therapy has had a great impact in the medical field, holding enormous promise, becoming "the latest generation medicine" with the first ever siRNA-lipid based formulation approved by the United States Food and Drug Administration (FDA) for human use, and currently on the market under the trade name Onpattro™. The growth of such powerful biologic therapeutics has gone hand in hand with the progress in delivery systems technology, which is absolutely required to improve their safety and effectiveness. Lipid carrier systems, particularly liposomes, have been proven to be the most suitable vehicles meeting NABDs requirements in the medical healthcare framework, limiting their toxicity, and ensuring their delivery and expression into the target tissues. In this review, after a description of the several kinds of liposomes structures and formulations used for in vitro or in vivo NABDs delivery, the broad range of siRNA-liposomes production techniques are discussed in the light of the latest technological progresses. Then, the current status of siRNA-lipid delivery systems in clinical trials is addressed, offering an updated overview on the clinical goals and the next challenges of this new class of therapeutics which will soon replace traditional drugs.
在过去几年中,用于基因治疗的核酸类药物(NABDs)迅速发展,对医学领域产生了重大影响,具有巨大的前景,随着首款基于小干扰RNA(siRNA)-脂质的制剂被美国食品药品监督管理局(FDA)批准用于人类,并以Onpattro™的商品名上市,这类药物成为了“新一代药物”。这类强大的生物疗法的发展与递送系统技术的进步齐头并进,而递送系统技术对于提高其安全性和有效性是绝对必要的。脂质载体系统,尤其是脂质体,已被证明是在医疗保健框架中满足NABDs要求的最合适载体,可限制其毒性,并确保其递送至靶组织并在其中表达。在本综述中,在描述了用于体外或体内NABDs递送的几种脂质体结构和制剂后,根据最新技术进展讨论了广泛的siRNA-脂质体制备技术。然后,阐述了siRNA-脂质递送系统在临床试验中的现状,提供了关于这一新型疗法的临床目标和未来挑战的最新概述,这类疗法将很快取代传统药物。