One-stop sharing facility center for future drug discoveries, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Department of Bioanalytical Chemistry, School of Pharmacy, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan.
J Chromatogr A. 2018 Aug 24;1564:224-227. doi: 10.1016/j.chroma.2018.06.011. Epub 2018 Jun 5.
Silicate is an excellent adsorbent because of its large surface area and amenability to surface modification. In this study, the representative liposome nanomedicines DOXIL and AmBisome were enriched using a silica monolith disc (diameter 4.2 mm, length 1.5 mm) with bimodal pores. Although the nanoparticles passed through the disc without retention when water was used as the preactivation solution, they were strongly retained by the disc when a 1 M bivalent metal (such as Mg, Ca, and Ni) solution was used. Notably, strong affinity was observed to DOXIL, a pegylated liposomal nanoparticle, by the disc composed of 5 μm and 10 nm through- and meso pores, respectively, and nearly 100% of DOXIL was recovered from a 40× diluted solution. Overall, the results demonstrate that monolithic discs are effective for the enrichment of liposomal nanomedicines.
由于具有较大的表面积和易于进行表面修饰,硅酸盐是一种优良的吸附剂。在这项研究中,使用具有双模态孔的二氧化硅整体柱(直径 4.2mm,长度 1.5mm)来富集代表性的脂质体纳米药物 DOXIL 和 AmBisome。尽管当水用作预激活溶液时,纳米颗粒在通过整体柱时没有被保留,但当使用 1M 二价金属(如 Mg、Ca 和 Ni)溶液时,纳米颗粒被整体柱强烈保留。值得注意的是,由分别具有 5μm 和 10nm 贯穿孔和中孔的整体柱对 DOXIL(一种聚乙二醇化的脂质体纳米颗粒)表现出很强的亲和力,并且从 40 倍稀释溶液中几乎可以回收 100%的 DOXIL。总的来说,这些结果表明整体柱对于脂质体纳米药物的富集是有效的。