Bari Elia, Scocozza Franca, Perteghella Sara, Sorlini Marzio, Auricchio Ferdinando, Torre Maria Luisa, Conti Michele
Department of Drug Sciences, University of Pavia, 27100 Pavia, Italy.
Department of Civil Engineering and Architecture, University of Pavia, 27100 Pavia, Italy.
Pharmaceutics. 2021 Apr 8;13(4):515. doi: 10.3390/pharmaceutics13040515.
Three-dimensional printing of poly(ε-caprolactone) (PCL) is a consolidated scaffold manufacturing technique for bone regenerative medicine. Simultaneously, the mesenchymal stem/stromal cell (MSC) secretome is osteoinductive, promoting scaffold colonization by cells, proliferation, and differentiation. The present paper combines 3D-printed PCL scaffolds with lyosecretome, a freeze-dried formulation of MSC secretome, containing proteins and extracellular vesicles (EVs). We designed a lyosecretome 3D-printed scaffold by two loading strategies: (i) MSC secretome adsorption on 3D-printed scaffold and (ii) coprinting of PCL with an alginate-based hydrogel containing MSC secretome (at two alginate concentrations, i.e., 6% or 10% /). A fast release of proteins and EVs (a burst of 75% after 30 min) was observed from scaffolds obtained by absorption loading, while coprinting of PCL and hydrogel, encapsulating lyosecretome, allowed a homogeneous loading of protein and EVs and a controlled slow release. For both loading modes, protein and EV release was governed by diffusion as revealed by the kinetic release study. The secretome's diffusion is influenced by alginate, its concentration, or its cross-linking modes with protamine due to the higher steric hindrance of the polymer chains. Moreover, it is possible to further slow down protein and EV release by changing the scaffold shape from parallelepiped to cylindrical. In conclusion, it is possible to control the release kinetics of proteins and EVs by changing the composition of the alginate hydrogel, the scaffold's shape, and hydrogel cross-linking. Such scaffold prototypes for bone regenerative medicine are now available for further testing of safety and efficacy.
聚(ε-己内酯)(PCL)的三维打印是一种用于骨再生医学的成熟支架制造技术。同时,间充质干/基质细胞(MSC)分泌组具有骨诱导性,可促进细胞在支架上的定植、增殖和分化。本文将3D打印的PCL支架与冻干的MSC分泌组(lyosecretome)相结合,后者包含蛋白质和细胞外囊泡(EVs)。我们通过两种加载策略设计了一种lyosecretome 3D打印支架:(i)将MSC分泌组吸附在3D打印支架上;(ii)将PCL与含有MSC分泌组的藻酸盐基水凝胶共打印(藻酸盐浓度为6%或10%)。通过吸附加载获得的支架观察到蛋白质和EVs的快速释放(30分钟后突发释放75%),而PCL与包裹lyosecretome的水凝胶共打印则允许蛋白质和EVs均匀加载并实现可控的缓慢释放。动力学释放研究表明,对于两种加载模式,蛋白质和EVs的释放均受扩散控制。由于聚合物链的空间位阻较大,分泌组的扩散受藻酸盐、其浓度或其与鱼精蛋白的交联模式影响。此外,通过将支架形状从平行六面体改为圆柱体,可以进一步减缓蛋白质和EVs的释放。总之,可以通过改变藻酸盐水凝胶的组成、支架形状和水凝胶交联来控制蛋白质和EVs的释放动力学。这种用于骨再生医学的支架原型现在可用于进一步的安全性和有效性测试。