Ian Wark Research Institute, University of South Australia, Mawson Lakes Campus, Mawson Lakes, SA 5095, Australia.
Ian Wark Research Institute, University of South Australia, Mawson Lakes Campus, Mawson Lakes, SA 5095, Australia,.
J Control Release. 2014 Nov 10;193:174-87. doi: 10.1016/j.jconrel.2014.05.013. Epub 2014 May 20.
Cardiovascular diseases (CVDs) remain the major cause of morbidity and mortality globally. Despite the large number of cardiovascular drugs available for pharmacological therapies, factors limiting the efficient oral use are identified, including low water solubility, pre-systemic metabolism, food intake effects and short half-life. Numerous in vivo proof-of-concepts studies are presented to highlight the viability of lipid-based delivery to optimize the oral delivery of cardiovascular drugs. In particular, the key performance enhancement roles of oral lipid-based drug delivery systems (LBDDSs) are identified, which include i) improving the oral bioavailability, ii) sustaining/controlling drug release, iii) improving drug stability, iv) reducing food intake effect, v) targeting to injured sites, and vi) potential for combination therapy. Mechanisms involved in achieving these features, range of applicability, and limits of available systems are detailed. Future research and development efforts to address these issues are discussed, which is of significant value in directing future research work in fostering translation of lipid-based formulations into clinical applications to reduce the prevalence of CVDs.
心血管疾病(CVDs)仍然是全球发病率和死亡率的主要原因。尽管有大量的心血管药物可用于药物治疗,但仍存在一些限制其有效口服使用的因素,包括低水溶性、前体药物代谢、食物摄入效应和半衰期短。本文介绍了大量体内概念验证研究,以强调基于脂质的递送来优化心血管药物口服递送的可行性。特别是,确定了口服基于脂质的药物递送系统(LBDDS)的关键性能增强作用,包括 i)提高口服生物利用度,ii)持续/控制药物释放,iii)提高药物稳定性,iv)减少食物摄入效应,v)靶向损伤部位,以及 vi)潜在的联合治疗。详细讨论了实现这些特性的机制、适用范围和现有系统的局限性。讨论了未来解决这些问题的研究和开发工作,这对于指导未来的研究工作,将基于脂质的制剂转化为临床应用,以降低 CVDs 的患病率具有重要价值。