Physikalisches Institut and Center für Soft Nanoscience, Westfälische Wilhelms-Universität Münster, Busso-Peus Straße 10, D-48149 Münster, Germany.
J Mater Chem B. 2019 Apr 14;7(14):2362-2371. doi: 10.1039/c8tb02507j. Epub 2019 Mar 8.
We present the preparation of self-assembled monolayers (SAMs) of pH responsive chiral periodic mesoporous organosilicas (PMOs) as model implants with drug delivery ability. SAMs of pH responsive PMOs were prepared by layer-by-layer coating of PMOs with polyelectrolytes (e.g. the enantiomers of a polycation biopolymer), for delivering organic molecules and anticancer drug molecules locally in a controlled manner to the adhered cells. We demonstrate that the amount of primary fibroblast, immortal NIH 3T3, and malignant Colo 818 cells adhered to the SAM of the d-enantiomer of polycation-functionalized PMOs was higher in comparison to that of the l-enantiomer of the polycation-functionalized PMO monolayer. In addition, we observe that the 3T3 and Colo cells internalized more of the organic and anticancer drug molecules (released from pH responsive PMOs) than the primary cells did due to the local acidic environment of them. Therefore, as the chirality of the PMOs influenced the amount of cells that adhered, the released molecules interacted with different amounts of cells which allowed us to tune the extent of local drug delivery.
我们制备了具有药物输送能力的 pH 响应手性介孔有机硅(PMO)自组装单层(SAM)作为模型植入物。通过 PMO 与聚电解质(例如聚阳离子生物聚合物的对映异构体)的层层涂覆,制备了 pH 响应 PMO 的 SAM,以将有机分子和抗癌药物分子以受控的方式局部递送到附着的细胞中。我们证明,与聚阳离子功能化 PMO 的 l-对映体单层相比,附着在 d-对映体聚阳离子功能化 PMO SAM 上的原代成纤维细胞、永生化 NIH 3T3 和恶性 Colo 818 细胞的数量更高。此外,我们观察到由于这些细胞的局部酸性环境,3T3 和 Colo 细胞内化了更多的有机和抗癌药物分子(从 pH 响应 PMO 中释放),而原代细胞则没有。因此,由于 PMO 的手性影响了附着的细胞数量,释放的分子与不同数量的细胞相互作用,这使我们能够调节局部药物输送的程度。