Department of Chemistry, Aarhus University, Aarhus, Denmark.
Nanoscale. 2013 Aug 7;5(15):6758-66. doi: 10.1039/c3nr01662e.
Drug-eluting engineered surface coatings are of paramount importance for many biomedical applications from implantable devices to tissue engineering. Herein, we present the assembly of lipogels, composite physical hydrogels assembled from poly(vinyl alcohol) and liposomes using thiol-disulfide exchange between end group modified PVA and thiocholesterol containing liposomes, and the response of adhering cells to these coatings. We demonstrate the controlled loading of liposomes into the polymer matrix and the preserved mechanical properties of the lipogels. Furthermore, the lipogels are successfully rendered cell adhesive by incorporation of poly(l-lysine) into the PVA polymer matrix or by poly(dopamine) coating of the lipogels. The successful lipid uptake from the lipogels by macrophages, hepatocytes, and myoblasts was monitored by flow cytometry. Finally, the delivery of active cargo, paclitaxel, to adherent myoblasts is shown, thus illustrating the potential of the lipogels as a drug eluting interface for biomedical applications.
载药工程表面涂层对于许多生物医学应用至关重要,从可植入设备到组织工程。在此,我们介绍了脂凝胶的组装,这是一种由聚(乙醇酸)和脂质体组成的复合物理水凝胶,通过端基修饰的 PVA 和含有硫胆固醇的脂质体之间的硫醇-二硫交换进行组装,以及黏附细胞对这些涂层的反应。我们证明了脂质体可以在聚合物基质中进行控制负载,并且脂凝胶的机械性能得到了保留。此外,通过将聚(L-赖氨酸)掺入 PVA 聚合物基质中或通过聚多巴胺对脂凝胶进行涂层,可以使脂凝胶成功地具有黏附性。通过流式细胞术监测了巨噬细胞、肝细胞和成肌细胞从脂凝胶中摄取脂质的情况。最后,展示了活性药物紫杉醇向黏附的成肌细胞的递送,从而说明了脂凝胶作为生物医学应用中药物洗脱界面的潜力。