Palakurthi Sushesh Srivatsa, Shah Brijesh, Kapre Sumedha, Charbe Nitin, Immanuel Susan, Pasham Sindhura, Thalla Maharshi, Jain Ankit, Palakurthi Srinath
Department of Pharmaceutical Sciences, Irma Lerma Rangel College of Pharmacy, Texas A&M University Kingsville TX 78363 USA
Nanoscale Adv. 2024 Oct 29;6(23):5803-26. doi: 10.1039/d4na00501e.
Exosomes or so-called natural nanoparticles have recently shown enormous potential for targeted drug delivery systems. Several studies have reported that exosomes as advanced drug delivery platforms offer efficient targeting of chemotherapeutics compared to individual polymeric nanoparticles or liposomes. Taking structural constituents of exosomes, , proteins, nucleic acids, and lipids, into consideration, exosomes are the most promising carriers as genetic messengers and for treating genetic deficiencies or tumor progression. Unfortunately, very little attention has been paid to the factors like source, scalability, stability, and validation that contribute to the quality attributes of exosome-based drug products. Some studies suggested that exosomes were stable at around -80 °C, which is impractical for storing pharmaceutical products. Currently, no reports on the shelf-life and stability of exosome formulations are available. Exosomes are quickly cleared from blood circulation, and their distribution depends on the source. Considering these challenges, further studies are necessary to address major limitations such as poor drug loading, reduced stability, a need for robust, economical, and scalable production methods, , which may unlock the potential of exosomes in clinical applications. A few reports based on hybrid exosomes involving hybridization between different cell/tumor/macrophage-derived exosomes with synthetic liposomes through membrane fusion have shown to overcome some limitations associated with natural or synthetic exosomes. Yet, sufficient evidence is indispensable to prove their stability and clinical efficacy.
外泌体或所谓的天然纳米颗粒最近在靶向给药系统中显示出巨大潜力。多项研究报告称,与单个聚合物纳米颗粒或脂质体相比,外泌体作为先进的给药平台能有效靶向递送化疗药物。考虑到外泌体的结构成分,如蛋白质、核酸和脂质,外泌体作为遗传信使以及用于治疗基因缺陷或肿瘤进展是最有前景的载体。不幸的是,对于影响基于外泌体的药物产品质量属性的来源、可扩展性、稳定性和验证等因素,人们关注甚少。一些研究表明,外泌体在约-80°C时稳定,这对于储存药品来说不切实际。目前,尚无关于外泌体制剂保质期和稳定性的报道。外泌体在血液循环中会迅速被清除,其分布取决于来源。考虑到这些挑战,有必要进一步开展研究以解决诸如药物负载量低、稳定性降低、需要强大、经济且可扩展的生产方法等主要限制因素,这可能会释放外泌体在临床应用中的潜力。一些基于杂交外泌体的报告显示,通过膜融合将不同细胞/肿瘤/巨噬细胞来源的外泌体与合成脂质体进行杂交,可克服与天然或合成外泌体相关的一些限制。然而,要证明它们的稳定性和临床疗效,充分的证据必不可少。