MC for Gastroretentive Drug Delivery

Recently, bacterial nanocellulose (BNC), a biological material produced by non-pathogenic bacteria that possesses excellent material properties for various medical applications, has received increased interest as a carrier system for drug delivery. However, the vast majority of existing studies on drug release from BNC are feasibility studies with modeling and design aspects remaining largely unexplored. To narrow this research gap, this paper proposes a novel model for the drug release from BNC. Specifically, the drug delivery system considered in this paper consists of a BNC fleece coated with a polymer. The polymer coating is used as an additional diffusion barrier, enabling the controlled release of an active pharmaceutical ingredient. The proposed physics-based model reflects the geometry of the BNC and incorporates the impact of the polymer coating on the drug release. Hence, it can be useful for designing BNC-based drug delivery systems in the future. The accuracy of the model is validated with experimental data obtained in wet lab experiments.

Microparticle-based Controlled Drug Delivery Systems: From Experiments to Statistical Analysis and Design

Controlled drug delivery (CDD), the controlled release and delivery of therapeutic drugs inside the human body, is a promising approach to increase the efficacy of drug administration and reduce harmful side effects to the body. CDD has been a major research focus in the field of molecular communications (MC) with the goal to aid the design and optimization of CDD systems with communication theoretical analysis. However, the existing studies of CDD under the MC framework are purely theoretical, and the potential of MC for the development of practical CDD applications remains yet to be shown. This paper presents a step towards filling this research gap. Specifically, we present a novel MC-based model for a specific CDD system in which drugs are embedded into microparticles and released gradually towards the target site. It is demonstrated that the proposed model is able to faithfully reproduce experimental data. Furthermore, statistical analysis is conducted to explore the impact of the microparticle size on the drug release. The presented results reveal the sensitivity of the drug release to changes in the microparticle size. In this way, the proposed model can be used for the design of future microparticle-based CDD systems.