Division of Molecular Therapeutics and Formulation, School of Pharmacy, University of Nottingham, NG7 2RD, UK; Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Pharmaceutical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Int J Pharm. 2024 Sep 30;663:124545. doi: 10.1016/j.ijpharm.2024.124545. Epub 2024 Aug 2.
Cancers are increasing in prevalence and many challenges remain for their treatment, such as chemoresistance and toxicity. In this context, siRNA-based therapeutics have many potential advantages for cancer therapies as a result of their ability to reduce or prevent expression of specific cancer-related genes. However, the direct delivery of naked siRNA is hindered by issues like enzymatic degradation, insufficient cellular uptake, and poor pharmacokinetics. Hence, the discovery of a safe and efficient delivery vehicle is essential. This review explores various lipid and polymer-based delivery systems for siRNA in cancer treatment. Both polymers and lipids have garnered considerable attention as carriers for siRNA delivery. While all of these systems protect siRNA and enhance transfection efficacy, each exhibits its unique strengths. Lipid-based delivery systems, for instance, demonstrate high entrapment efficacy and utilize cost-effective materials. Conversely, polymeric-based delivery systems offer advantages through chemical modifications. Nonetheless, certain drawbacks still limit their usage. To address these limitations, combining different materials in formulations (lipid, polymer, or targeting agent) could enhance pharmaceutical properties, boost transfection efficacy, and reduce side effects. Furthermore, co-delivery of siRNA with other therapeutic agents presents a promising strategy to overcome cancer resistance. Lipid-based delivery systems have been demonstrated to encapsulate many therapeutic agents and with high efficiency, but most are limited in terms of the functionalities they display. In contrast, polymeric-based delivery systems can be chemically modified by a wide variety of routes to include multiple components, such as release or targeting elements, from the same materials backbone. Accordingly, by incorporating multiple materials such as lipids, polymers, and/or targeting agents in RNA formulations it is possible to improve the pharmaceutical properties and therapeutic efficacy while reducing side effects. This review focuses on strategies to improve siRNA cancer treatments and discusses future prospects in this important field.
癌症的发病率正在上升,其治疗仍然存在许多挑战,如化疗耐药性和毒性。在这种情况下,siRNA 疗法作为一种减少或预防特定癌症相关基因表达的治疗方法具有许多潜在优势。然而,由于裸 siRNA 的直接递送受到酶降解、细胞摄取不足和差的药代动力学等问题的阻碍。因此,发现安全有效的递送载体至关重要。本文探讨了用于癌症治疗的各种基于脂质和聚合物的 siRNA 递送系统。聚合物和脂质都作为 siRNA 递送载体引起了相当大的关注。虽然所有这些系统都可以保护 siRNA 并增强转染效率,但每种系统都有其独特的优势。例如,基于脂质的递送系统表现出高包封效率并利用具有成本效益的材料。相反,基于聚合物的递送系统通过化学修饰提供优势。然而,某些缺点仍然限制了它们的使用。为了解决这些限制,可以在制剂中组合不同的材料(脂质、聚合物或靶向剂),以增强药物特性、提高转染效率并降低副作用。此外,与其他治疗剂共递送 siRNA 是克服癌症耐药性的一种很有前途的策略。已经证明,基于脂质的递送系统可以高效地封装许多治疗剂,但大多数在它们所显示的功能方面受到限制。相比之下,基于聚合物的递送系统可以通过广泛的途径进行化学修饰,以包含相同材料主链上的多个组件,如释放或靶向元件。因此,通过将脂质、聚合物和/或靶向剂等多种材料纳入 RNA 制剂中,可以改善药物特性和治疗效果,同时降低副作用。本综述重点讨论了改善 siRNA 癌症治疗的策略,并讨论了该重要领域的未来前景。