Abstract

Three-dimensional porous architectures have gained popularity as advanced materials in emerging therapeutics, drug delivery systems and tissue regeneration. This is largely due to their porosity, inter-connectivity, and mechanical properties. However, current approaches to derive such three-dimensional structures are stochastic and therefore density uniformity varies, with innermost components exhibiting dense attributes. This also limits the encapsulation ability and quality of compounds. In this study, multifunctional structures comprising multi-layered particles are developed. Polycaprolactone (PCL)/ethyl cellulose (EC)/ganoderma lucidum polysaccharide (GLP) is the outer layer; silicone oil (SO) is the intermediate layer; PCL and magnetic Fe 3 O 4 nanoparticles (MNP) are the inner-most (core) component. Particles are initially formed using single step tri-needle co-axial electrostatic jetting, followed by sacrificial template removal to enable multifunctional porous structures. Using this approach, deployment of layered bodies enables the formation of homogeneous particles (150 µm) with tunable pore sizes of 100 s of nanometers to 350 s of microns. The process is versatile, and results indicate multi-scale pore size and hybrid pore connectivity are regulated through manipulation of the sacrificial agent. These structures are therefore promising for several multi-faceted healthcare applications e.g. targeted drug delivery, 3D cell culture , and real-time MRI imaging.