Agostini Elisa, Winter Gerhard, Engert Julia
Ludwig-Maximilians-University, Department of Pharmacy, Pharmaceutical Technology & Biopharmaceutics, Butenandtstr. 5, D-81377 Munich, Germany.
Ludwig-Maximilians-University, Department of Pharmacy, Pharmaceutical Technology & Biopharmaceutics, Butenandtstr. 5, D-81377 Munich, Germany.
J Control Release. 2015 Sep 10;213:134-141. doi: 10.1016/j.jconrel.2015.06.025. Epub 2015 Jun 20.
The main focus of this work was to obtain a drug delivery matrix characterized by biocompatibility, water insolubility and good mechanical properties. Moreover the preparation process has to be compatible with protein encapsulation and the obtained matrix should be able to sustain release a model protein. Spider silk proteins represent exceptional natural polymers due to their mechanical properties in combination with biocompatibility. As both hydrophobic and slowly biodegrading biopolymers, recombinant spider silk proteins fulfill the required properties for a drug delivery system. In this work, we present the preparation of eADF4(C16) films as drug delivery matrices without the use of any organic solvent. Water-based spider silk films were characterized in terms of protein secondary structure, thermal stability, zeta-potential, solubility, mechanical properties, and water absorption and desorption. Additionally, this study includes an evaluation of their application as a drug delivery system for both small molecular weight drugs and high molecular weight molecules such as proteins. Our investigation focused on possible improvements in the film's mechanical properties including plasticizers in the film matrix. Furthermore, different film designs were prepared, such as: monolayer, coated monolayer, multilayer (sandwich), and coated multilayer. The release of the model protein BSA from these new systems was studied. Results indicated that spider silk films are a promising protein drug delivery matrix, capable of releasing the model protein over 90 days with a release profile close to zero order kinetic. Such films could be used for several pharmaceutical and medical purposes, especially when mechanical strength of a drug eluting matrix is of high importance.
这项工作的主要重点是获得一种具有生物相容性、水不溶性和良好机械性能的药物递送基质。此外,制备过程必须与蛋白质包封兼容,并且所获得的基质应能够持续释放一种模型蛋白质。蜘蛛丝蛋白由于其机械性能与生物相容性相结合,是一类特殊的天然聚合物。作为疏水性且生物降解缓慢的生物聚合物,重组蜘蛛丝蛋白满足药物递送系统所需的特性。在这项工作中,我们展示了在不使用任何有机溶剂的情况下制备作为药物递送基质的eADF4(C16)薄膜。对水基蜘蛛丝薄膜进行了蛋白质二级结构、热稳定性、ζ电位、溶解度、机械性能以及吸水和解吸等方面的表征。此外,本研究还评估了它们作为小分子药物和蛋白质等高分子量分子的药物递送系统的应用。我们的研究重点是薄膜机械性能的可能改进,包括薄膜基质中的增塑剂。此外,还制备了不同的薄膜设计,如:单层、涂层单层、多层(三明治)和涂层多层。研究了这些新系统中模型蛋白牛血清白蛋白(BSA)的释放情况。结果表明,蜘蛛丝薄膜是一种很有前景的蛋白质药物递送基质,能够在90天内释放模型蛋白,释放曲线接近零级动力学。这种薄膜可用于多种制药和医疗目的,特别是当药物洗脱基质的机械强度至关重要时。