Tomsen-Melero Judit, Merlo-Mas Josep, Carreño Aida, Sala Santi, Córdoba Alba, Veciana Jaume, González-Mira Elisabet, Ventosa Nora
Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus UAB, 08193 Bellaterra, Spain; Centro de Investigación Biomédica en Red - Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Spain.
Nanomol Technologies SL, 08193 Cerdanyola del Vallès, Spain.
Adv Drug Deliv Rev. 2022 Nov;190:114531. doi: 10.1016/j.addr.2022.114531. Epub 2022 Sep 8.
Lysosomal storage disorders (LSD) are a group of rare life-threatening diseases caused by a lysosomal dysfunction, usually due to the lack of a single enzyme required for the metabolism of macromolecules, which leads to a lysosomal accumulation of specific substrates, resulting in severe disease manifestations and early death. There is currently no definitive cure for LSD, and despite the approval of certain therapies, their effectiveness is limited. Therefore, an appropriate nanocarrier could help improve the efficacy of some of these therapies. Liposomes show excellent properties as drug carriers, because they can entrap active therapeutic compounds offering protection, biocompatibility, and selectivity. Here, we discuss the potential of liposomes for LSD treatment and conduct a detailed analysis of promising liposomal formulations still in the preclinical development stage from various perspectives, including treatment strategy, manufacturing, characterization, and future directions for implementing liposomal formulations for LSD.
溶酶体贮积症(LSD)是一组由溶酶体功能障碍引起的罕见的危及生命的疾病,通常是由于缺乏大分子代谢所需的单一酶,这导致特定底物在溶酶体中积累,从而产生严重的疾病表现并导致早期死亡。目前尚无针对LSD的确切治愈方法,尽管某些疗法已获批准,但其疗效有限。因此,合适的纳米载体有助于提高其中一些疗法的疗效。脂质体作为药物载体具有优异的特性,因为它们可以包裹活性治疗化合物,提供保护、生物相容性和选择性。在此,我们讨论脂质体用于LSD治疗的潜力,并从治疗策略、制造、表征以及将脂质体制剂应用于LSD的未来方向等各个角度,对仍处于临床前开发阶段的有前景的脂质体制剂进行详细分析。