Laboratory of Pharmaceutical Technology, Department of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Department of Materials Science, University of Patras, Patras, Greece.
Pharm Dev Technol. 2020 Apr;25(4):517-523. doi: 10.1080/10837450.2019.1711396. Epub 2020 Jan 8.
To this day, the oral delivery of biomacromolecules remains a major developmentally-oriented challenge. A combinatorial approach was followed at this study, to formulate an efficient carrier for the delivery of a model macromolecule, fluorescein isothiocyanate-dextran 4 kDa (FD4). The model macromolecule was formulated in a self-assembling peptide hydrogel (ac-(RADA)-CONH), prior to deposition in a hydroxypropyl methylcellulose-phthalate (HPMCP)-based 3D-printed capsule. Loading of FD4 was investigated for potential alterations on the structural (AFM) and gelling properties of the peptide carrier. Thermal analysis and morphological properties of the 3D-printed capsules were assessed by TGA, DSC and microscopy studies. For the peptide hydrogel, similar release profiles of FD4 were recorded in simulated gastric fluid pH 1.2 and phosphate buffer saline pH 7.4, indicating the need for a structural barrier, to protect the peptide carrier from the acidic environment of the stomach. The pH responsive character of the HPMCP-based capsule was evidenced in the release profiles of FD4 in a sequence of release media, i.e. simulated gastric fluid pH 1.2, simulated intestinal fluid pH 6.8 and phosphate buffer saline pH 7.4. The results supported the combinatorial formulation approach as a promising system for the efficient oral delivery of biomacromolecules.
时至今日,将生物大分子经口递送给仍具有重大的发展意义。本研究采用了一种组合方法,以开发一种有效的载体来递送模型生物大分子,即异硫氰酸荧光素标记的 4kDa 葡聚糖(FD4)。在将模型生物大分子递送到自组装肽水凝胶(ac-(RADA)-CONH)中之前,将其先包裹在羟丙基甲基纤维素邻苯二甲酸酯(HPMCP)的 3D 打印胶囊中。FD4 的载药量考察了对肽载体结构(AFM)和胶凝性能的潜在影响。通过 TGA、DSC 和显微镜研究评估了 3D 打印胶囊的热分析和形态学特性。对于肽水凝胶,在 pH1.2 的模拟胃液和 pH7.4 的磷酸盐缓冲液中记录到 FD4 的相似释放曲线,表明需要一个结构屏障来保护肽载体免受胃的酸性环境的影响。在一系列释放介质中,即 pH1.2 的模拟胃液、pH6.8 的模拟肠液和 pH7.4 的磷酸盐缓冲液中,HPMCP 基胶囊的 pH 响应特性在 FD4 的释放曲线中得到了证明。研究结果支持了组合配方方法作为高效经口递送生物大分子的有前途的系统。