Vodouhê Constant, Le Guen Erell, Garza Juan Mendez, Francius Gregory, Déjugnat Christophe, Ogier Joëlle, Schaaf Pierre, Voegel Jean-Claude, Lavalle Philippe
INSERM Unité 595, 11 rue Humann, F-67085 Strasbourg Cedex, France.
Biomaterials. 2006 Aug;27(22):4149-56. doi: 10.1016/j.biomaterials.2006.03.024. Epub 2006 Apr 4.
A surface coating based on polylysine/hyaluronic acid multilayers was designed and acted as a reservoir for an antiproliferative agent, paclitaxel (Taxol). Absolutely no chemical modification of polyelectrolytes or of the drug was needed and the final architecture was obtained in an extremely simple way using the layer-by-layer method. The paclitaxel dose available for human colonic adenocarcinoma cells HT29 seeded on the films could be finely tuned. Moreover, the accessibility of the drugs was controlled by adding on the top of the drug reservoir a capping made of synthetic polyelectrolyte multilayers. This capping was also required to allow adhesion of HT29 cells. Paclitaxel activity was maintained after embedding in the polyelectrolyte multilayers and cellular viability could be reduced by about 80% 96 h after seeding. The strategy described in this paper could be valuable for various other drug/cell systems.
设计了一种基于聚赖氨酸/透明质酸多层膜的表面涂层,该涂层可作为抗增殖剂紫杉醇(泰素)的储存库。无需对聚电解质或药物进行任何化学修饰,并且使用逐层方法以极其简单的方式获得了最终结构。可精确调节接种在薄膜上的人结肠腺癌细胞HT29可用的紫杉醇剂量。此外,通过在药物储存库顶部添加由合成聚电解质多层膜制成的封盖来控制药物的可及性。该封盖对于使HT29细胞粘附也是必需的。紫杉醇包埋在聚电解质多层膜中后仍保持活性,接种96小时后细胞活力可降低约80%。本文所述策略对于各种其他药物/细胞系统可能具有重要价值。