NANO-VAC Research Group, Department of Pharmaceutical Sciences, School of Pharmacy and Nutrition, University of Navarra, 31008, Pamplona, Spain.
Department of Chemistry, University of Navarra, 31008, Pamplona, Spain.
Drug Deliv Transl Res. 2024 May;14(5):1189-1205. doi: 10.1007/s13346-023-01454-0. Epub 2023 Oct 26.
The oral administration of therapeutic proteins copes with important challenges (mainly degradation and poor absorption) making their potential therapeutic application extremely difficult. The aim of this study was to design and evaluate the potential of the combination between mucus-permeating nanoparticles and permeation enhancers as a carrier for the oral delivery of the monoclonal antibody bevacizumab, used as a model of therapeutic protein. For this purpose, bevacizumab was encapsulated in PEG-coated albumin nanoparticles as a hydrophobic ion-pairing complex with either sodium deoxycholate (DS) or sodium docusate (DOCU). In both cases, complex formation efficiencies close to 90% were found. The incorporation of either DS or DOCU in PEG-coated nanoparticles significantly increased their mean size, particularly when DOCU was used. Moreover, the diffusion in mucus of DOCU-loaded nanoparticles was significantly reduced, compared with DS ones. In a C. elegans model, DS or DOCU (free or nanoencapsulated) disrupted the intestinal epithelial integrity, but the overall survival of the worms was not affected. In rats, the relative oral bioavailability of bevacizumab incorporated in PEG-coated nanoparticles as a complex with DS (B-DS-NP-P) was 3.7%, a 1000-fold increase compared to free bevacizumab encapsulated in nanoparticles (B-NP-P). This important effect of DS may be explained not only by its capability to transiently disrupt tight junctions but also to their ability to increase the fluidity of membranes and to inhibit cytosolic and brush border enzymes. In summary, the current strategy may be useful to allow the therapeutic use of orally administered proteins, including monoclonal antibodies.
口服给予治疗性蛋白可解决重要的挑战(主要是降解和吸收不良),这使得它们的潜在治疗应用变得极其困难。本研究的目的是设计并评估将黏液穿透纳米颗粒与渗透增强剂结合作为载体用于口服递送单克隆抗体贝伐单抗(用作治疗性蛋白的模型)的潜力。为此,将贝伐单抗包封在聚乙二醇(PEG)包覆的白蛋白纳米颗粒中,作为与脱氧胆酸钠(DS)或十二烷基硫酸钠(DOCU)的疏水离子对复合物。在这两种情况下,均发现复合物形成效率接近 90%。DS 或 DOCU 的掺入均显著增加了纳米颗粒的平均粒径,尤其是当使用 DOCU 时。此外,与 DS 相比,DOCU 负载的纳米颗粒在黏液中的扩散明显减少。在秀丽隐杆线虫模型中,DS 或 DOCU(游离或纳米封装)破坏了肠道上皮的完整性,但对蠕虫的总体存活率没有影响。在大鼠中,作为与 DS 形成复合物的聚乙二醇包覆纳米颗粒包封的贝伐单抗(B-DS-NP-P)的相对口服生物利用度为 3.7%,与游离贝伐单抗相比增加了 1000 倍纳米颗粒包封(B-NP-P)。DS 的这种重要作用可能不仅与其暂时破坏紧密连接的能力有关,而且与其增加膜流动性和抑制细胞溶质和刷状缘酶的能力有关。总之,该策略可能有助于允许口服给予的蛋白质(包括单克隆抗体)的治疗用途。