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In recent decades, there has been a growing awareness in our society of the impor-
tance of medicines that are personalized to the needs of patients. This dissertation
contributes to the research on personalized dosage forms with controlled drug release.
The basis of our investigations is the simulation of the expected diffusion properties
of these personalized dosage forms using computer-aided statistical methods and the
subsequent adaptation of suitable models to experimentally obtained data. This
novel approach makes it possible to verify the parameters determined from exper-
imental data, such as the diffusion coefficient. A key finding is that, for instance,
the homogeneity of the sample, the precision of the measurement data collection
and the consideration of the measurement environment have a greater influence on
the validity of the diffusion coefficient than the choice of the diffusion model. The
experimental part of this thesis comprises the development and characterization of
drug-loaded polymer resins, the implant fabrication, and the pharmaceutical and
physical investigation of the polymer-drug implants. The formulation of polymer
resins and their suitability for 3D printing (3DP), as well as their use in pharmaceu-
tical applications, are extensively addressed. The release properties and, in partic-
ular, the polymer network’s mesh size influence on the active ingredient’s diffusion
rate in aqueous solution are studied. In addition, the production of polymer sam-
ples by means of UV photopolymerization in a molding process developed for this
purpose, as well as by using stereolithographic 3DP, are examined comparatively.
The polymerization process and the polymer properties resulting from the different
production methods are presented. The major findings from these studies include
the successful development of a polymer resin formulation whose release and swelling
properties are comprehensively demonstrated using a model drug. Furthermore, the
optimization of this resin for the use of the active pharmaceutical ingredient (API)
testosterone was achieved. A comparison of the two developed resin formulations
clearly shows the limitations and the possibilities of transferability of both systems.
In addition, the results concerning the release of API from the polymer, as well as
the diffusion of the solvent into the polymer and the resulting increase in the volume,
provide insight into the changed interfacial diffusion resistance in 3D printed poly-
mers compared to molded polymers. This work thus contributes to the development
of personalized drug forms and paves the way for the production of release-controlled
polymer resin implants for future follow-up work.