The toxic side effects of chemotherapy have long limited its efficacy, prompting expensive and long-drawn efforts to develop more targeted cancer therapeutics. An alternative approach to mitigate off-target toxicity is to develop a device that can sequester chemotherapeutic agents from the veins that drain the target organ before they enter systemic circulation. This effectively localizes the chemotherapy to the target organ, minimizing any hazardous side effects. 3D printing is ideal for fabricating these devices, as the geometric control afforded allows us to precisely dictate its hemodynamic performance in vivo. However, the existing materials compatible with 3D printing do not have drug-binding capabilities. Here, we report the stable coating of genomic DNA on a 3D-printed structure for the capture of doxorubicin. Genomic DNA is an effective chemotherapeutic-agent capture material due to the intrinsic DNA-targeting mechanism of action of these drugs. Stable DNA coatings were achieved through a combination of electrostatic interactions and ultraviolet C (UVC, 254 nm) cross-linking. These UVC cross-linked DNA coatings were extremely stable-leaching on average 100 pg of genomic DNA per mm2 of 3D-printed structure over a period of 30 min. In vitro studies of these materials in phosphate buffered saline and human serum demonstrated that they were able to capture, on average, 72 and 60 ng of doxorubicin per mm2 of structure, respectively. The stability and efficacy of these genomic DNA-coated 3D-printed materials represent a significant step forward towards the translation of these devices to clinical applications for the potential improvement of chemotherapy treatment.

Designing mechanical metamaterials is overwhelming for most computational approaches because of the staggering number and complexity of flexible elements that constitute their architecture-particularly if these elements don't repeat in periodic patterns or collectively occupy irregular bulk shapes. We introduce an approach, inspired by the freedom and constraint topologies (FACT) methodology, that leverages simplified assumptions to enable the design of such materials with ~6 orders of magnitude greater computational efficiency than other approaches (e.g., topology optimization). Metamaterials designed using this approach are called directionally compliant metamaterials (DCMs) because they manifest prescribed compliant directions while possessing high stiffness in all other directions. Since their compliant directions are governed by both macroscale shape and microscale architecture, DCMs can be engineered with the necessary design freedom to facilitate arbitrary form and unprecedented anisotropy. Thus, DCMs show promise as irregularly shaped flexure bearings, compliant prosthetics, morphing structures, and soft robots.