Nano‐ and micromotors are fascinating objects that can navigate in complex fluidic environments. Their active motion can be triggered by external power sources or they can exhibit self‐propulsion using fuel extracted from their surroundings. The research field is rapidly evolving and has produced nano/micromotors of different geometrical designs, exploiting a variety of mechanisms of locomotion, being capable of achieving remarkable speeds in diverse environments ranging from simple aqueous solutions to complex media including cell cultures or animal tissue. This review aims to provide an overview of the recent developments with focus on predominantly experimental demonstrations of the various motor designs developed in the past 24 months. First, externally driven motors are discussed followed by considering fuel‐driven approaches. Finally, a short future perspective is provided.

Micro-and nanoswimmers are a fast emerging concept that changes how colloidal and biological systems interact. They can support drug delivery vehicles, assist in crossing biological barriers, or improve diagnostics. We report microswimmers that employ collagen, a major extracellular matrix (ECM) constituent, as fuel and that have the ability to deliver heat via incorporated magnetic nanoparticles when exposed to an alternating magnetic field (AMF). Their assembly and heating properties are outlined followed by the assessment of their calcium-triggered mobility in aqueous solution and collagen gels. It is illustrated that the swimmers in collagen gel in the presence of a steep calcium gradient exhibit fast and directed mobility. The experimental data are supported with theoretical considerations. Finally, the successful penetration of the swimmers into 3D cell spheroids is shown, and upon exposure to an AMF, the cell viability is impaired due to the locally delivered heat. This report illustrates an opportunity to employ swimmers to enhance tissue penetration for cargo delivery via controlled interaction with the ECM.

Colloidal systems with autonomous mobility are attractive alternatives to static particles for diverse applications.

Implantable devices equipped with coatings which have the ability to carry and deliver active compounds are of great interest. We report the assembly of liposome-containing poly(dopamine) films, and their interaction with adhering cells. The liposome composition is varied by adding lipophilic dopamine-conjugates and charged lipids. The cell mean fluorescence (CMF) of adhering cells due to the internalization of fluorescent cargo is found to be similar for coatings with the lipophilic-dopamine conjugates, while the charge affects the amount and location of the internalized cargo. The uptake mechanism for cargo by myoblasts using chemical inhibitors is found to be dependent on the used type of liposome. The CMF is significantly reduced for endothelial cells adhering to coatings with applied shear stress.