Pharmaceutical Technology, University of Basel, Klingelbergstrasse. 50, 4056 Basel, Switzerland.
Fundamental Research, Omya International AG, 4665 Oftringen, Switzerland.
Eur J Pharm Biopharm. 2018 Jan;122:96-103. doi: 10.1016/j.ejpb.2017.10.012. Epub 2017 Oct 17.
The recently introduced functionalized calcium carbonate (FCC), a porous microparticle with a nano-structured, lamellar surface, shows promising properties in the field of oral drug delivery. In this work, FCC was loaded with biomolecules e.g. lysozyme (Lys) and bovine serum albumin (BSA) in order to investigate its suitability to deliver protein based drugs. Loading efficiency for our model proteins was >90% and enzyme activity was preserved as demonstrated by Michaelis-Menten enzyme kinetic experiments. Circular dichroism analysis confirmed, that neither the structure of both model substances, nor the activity of Lys was affected by the loading process or the interaction with the surface of FCC. Electron microscopy (SEM) and mercury porosimetry were indicative of protein deposition on the particle surface as well as within the particle pores. Release properties were investigated in a customized flow cell, which simulates the conditions in the oral cavity. Depending on the isoelectric point of the investigated proteins, complete release was obtained within 1.5h. This work shows, that FCC is a suitable pharmaceutical excipient for delivery of proteins.
最近引入的功能化碳酸钙(FCC)是一种具有纳米结构层状表面的多孔微颗粒,在口服药物输送领域显示出有前景的性质。在这项工作中,FCC 被加载生物分子,例如溶菌酶(Lys)和牛血清白蛋白(BSA),以研究其适合输送基于蛋白质的药物。我们模型蛋白的加载效率>90%,并且通过 Michaelis-Menten 酶动力学实验证明了酶活性得以保留。圆二色性分析证实,无论是这两种模型物质的结构,还是 Lys 的活性,都不受加载过程或与 FCC 表面相互作用的影响。电子显微镜(SEM)和汞孔隙率分析表明蛋白质沉积在颗粒表面以及颗粒孔内。在定制的流动池(其模拟口腔中的条件)中研究了释放特性。根据所研究蛋白质的等电点,在 1.5 小时内即可完全释放。这项工作表明,FCC 是一种适合蛋白质输送的药物赋形剂。