The introduction of biodegradable implant materials as well as minimally invasive surgical procedures in medicine has substantially improved health care within the past few decades. This report describes a group of degradable thermoplastic polymers that are able to change their shape after an increase in temperature. Their shape-memory capability enables bulky implants to be placed in the body through small incisions or to perform complex mechanical deformations automatically. A smart degradable suture was created to illustrate the potential of these shape-memory thermoplastics in biomedical applications.

Shape-memory polymers are an emerging class of active polymers that have dual-shape capability. They can change their shape in a predefined way from shape A to shape B when exposed to an appropriate stimulus. While shape B is given by the initial processing step, shape A is determined by applying a process called programming. We review fundamental aspects of the molecular design of suitable polymer architectures, tailored programming and recovery processes, and the quantification of the shape-memory effect. Shape-memory research was initially founded on the thermally induced dual-shape effect. This concept has been extended to other stimuli by either indirect thermal actuation or direct actuation by addressing stimuli-sensitive groups on the molecular level. Finally, polymers are introduced that can be multifunctional. Besides their dual-shape capability, these active materials are biofunctional or biodegradable. Potential applications for such materials as active medical devices are highlighted.

In shape-memory polymers, changes in shape are mostly induced by heating, and exceeding a specific switching temperature,T_switch. If polymers cannot be warmed up by heat transfer using a hot liquid or gaseous medium, noncontact triggering will be required. In this article, the magnetically induced shape-memory effect of composites from magnetic nanoparticles and thermoplastic shape-memory polymers is introduced. A polyetherurethane (TFX) and a biodegradable multiblock copolymer (PDC) with poly(p-dioxanone) as hard segment and poly(ε-caprolactone) as soft segment were investigated as matrix component. Nanoparticles consisting of an iron(III)oxide core in a silica matrix could be processed into both polymers. A homogeneous particle distribution in TFX could be shown. Compounds have suitable elastic and thermal properties for the shape-memory functionalization. Temporary shapes of TFX compounds were obtained by elongating at increased temperature and subsequent cooling under constant stress. Cold-drawing of PDC compounds at 25°C resulted in temporary fixation of the mechanical deformation by 50–60%. The shape-memory effect of both composite systems could be induced by inductive heating in an alternating magnetic field (f= 258 kHz;H= 30 kA·m⁻¹). The maximum temperatures achievable by inductive heating in a specific magnetic field depend on sample geometry and nanoparticle content. Shape recovery rates of composites resulting from magnetic triggering are comparable to those obtained by increasing the environmental temperature.