Search Results (7)

Melanin-like polymers, particularly polydopamine, have gained significant attention as photothermal materials due to their broad light absorption (ultraviolet to near-infrared), high photothermal conversion efficiency, negligible fluorescence, good biocompatibility regarding unmodified melanin-like polymers, and universal adhesion. Upon light irradiation, these bioinspired polymers convert absorbed optical energy into heat through molecular vibration and electron–phonon coupling, making them ideal for diverse photothermal applications. This review comprehensively summarizes recent advances in using melanin-like polymers for photothermal purposes. In biomedical engineering, they serve as efficient agents for photothermal therapy and synergistic antibacterial treatment. In catalysis, their photothermal effect enhances pollutant degradation, hydrogen production, and chemical warfare agent detoxification. For water remediation, melanin-like polymers are fabricated into evaporators, membranes, and aerogels for solar-driven steam generation, desalination, and oil spill cleanup. They also enable sensitive photothermal sensing, near-infrared imaging, and laser desorption ionization mass spectrometry imaging. Furthermore, these materials are incorporated into soft actuators and self-healing elastomers for light-controlled shape memory, programmable folding, and remote manipulation. Finally, we discuss remaining challenges such as long-term stability, biocompatibility, scalability, and color limitations and provide future perspectives for advancing melanin-like photothermal materials toward practical applications. Full article

Droplet-based microfluidics has emerged as a powerful platform for precise fluid manipulation in biomedical, chemical, and material science applications. Among various geometries, T-junction microchannels are widely utilized for droplet generation and splitting due to their simplicity and reliability. This review provides a comprehensive overview of droplet splitting mechanisms in T-junction microfluidic systems, with particular emphasis on the role of actuation methods in enhancing control and functionality. We first discuss the fundamental physics governing droplet behavior, including the influence of capillary and viscous forces, flow regimes, and geometric parameters. Passive strategies based on flow rate tuning and channel design are outlined, followed by an in-depth examination of active actuation techniques: thermal, electrical, magnetic, acoustic, and pneumatic and their effects on droplet dynamics. In addition, the review highlights computational modeling approaches and experimental tools used to characterize and predict splitting behavior. Finally, we explore the current challenges and future directions in integrating multifunctional actuation systems for real-time, programmable droplet control in lab-on-a-chip platforms. This article serves as a foundational resource for researchers aiming to advance microfluidic droplet manipulation through actuator-enabled strategies. Full article

Natural rubber biosynthesis is catalyzed by a unilamella membrane-bound heterologous complex with multiple different subunits (rubber transferase, RTase). Two substrates and divalent metal cation activators are required, and their concentrations affect biosynthetic rate and polymer molecular weight. Rate, molecular weight, and complex stability are highly sensitive to Mg²⁺ and Mn²⁺ concentration, but studies are challenging because methods to control ion concentration may dislodge the elongating rubber polymers from the RTase complexes, halting synthesis and producing low-molecular-weight polymer. Here, programmable chemical actuators (PCAs) are used to electrochemically control rubber biosynthetic rate and subsequent molecular weight in enzymatically active rubber particles purified from Ficus elastica (Indian rubber tree). RTase activity was assayed using ³H-FPP (initiator) and ¹⁴C-IPP (monomer). Since only one FPP molecular is needed to initiate a new rubber polymer, the ratio of incorporated ³H-FPP to ¹⁴C-IPP was used to calculate the mean molecular weight of newly synthesized polymers. PCAs exchange ions in solution through REDOX reactions which we show control cation concentration without dislodging the elongating rubber polymers from the RTase. PCAs demonstrated highly tunable control over monomer incorporation and molecular weight in both Mg²⁺ and Mn²⁺ cations. REDOX cycling PCAs did not irreversibly inhibit the rubber transferase complex, and no indication of enzymatic damage was observed. Precise PCA control of RTase activity may pave the way for rubber eventually to be produced in bioreactors. Full article

Engineered living materials (ELMs) integrate living cells—such as bacteria, yeast, or mammalian cells—with synthetic matrices to create responsive, adaptive systems for sensing and actuation. Among ELMs, those endowed with sensing capabilities are gaining increasing attention for applications in environmental monitoring, biomedicine, and smart infrastructure. Central to these sensing functions are synthetic gene circuits, which enable cells to detect and respond to specific signals. This mini-review focuses on recent advances in sensing ELMs empowered by synthetic gene circuits. Here, we highlight how rationally designed genetic circuits enable living materials to sense and respond to diverse inputs—including environmental chemicals, light, heat, and mechanical loadings—via programmable signal transduction and tailored output behaviors. Input signals are classified by their source and physicochemical properties, including synthetic inducers, environmental chemicals, light, thermal, mechanical, and electrical signals. Particular emphasis is placed on the integration of genetically engineered microbial cells with hydrogels and other functional scaffolds to construct robust and tunable sensing platforms. Finally, we discuss the current challenges and future opportunities in this rapidly evolving field, providing insights to guide the rational design of next-generation sensing ELMs. Full article

Four-dimensional (4D) printing is an innovative additive manufacturing technology used to fabricate structures that can evolve over time when exposed to a predefined environmental stimulus. 4D printed objects are no longer static objects but programmable active structures that accomplish their functions thanks to a change over time in their physical/chemical properties that usually displays macroscopically as a shapeshifting in response to an external stimulus. 4D printing is characterized by several entangled features (e.g., involved material(s), structure geometry, and applied stimulus entities) that need to be carefully coupled to obtain a favorable fabrication and a functioning structure. Overall, the integration of micro-/nanofabrication methods of biomaterials with nanomaterials represents a promising approach for the development of advanced materials. The ability to construct complex and multifunctional triggerable structures capable of being activated allows for the control of biomedical device activity, reducing the need for invasive interventions. Such advancements provide new tools to biomedical engineers and clinicians to design dynamically actuated implantable devices. In this context, the aim of this review is to demonstrate the potential of 4D printing as an enabling manufacturing technology to code the environmentally triggered physical evolution of structures and devices of biomedical interest. Full article

DNA origami has garnered great attention due to its excellent programmability and precision. It offers a powerful means to create complex nanostructures which may not be possible by other methods. The macromolecular structures may be used as static templates for arranging proteins and other molecules. They are also capable of undergoing structural transformation in response to external signals, which may be exploited for sensing and actuation at the nanoscale. Such on-demand reconfigurations are executed mostly by DNA oligomers through base-pairing and/or strand displacement, demonstrating drastic shape changes between two different states, for example, open and close. Recent studies have developed new mechanisms to modulate the origami conformation in a controllable, progressive manner. Here we present several methods for conformational control of DNA origami nanostructures including chemical adducts and UV light as well as widely applied DNA oligomers. The detailed methods should be useful for beginners in the field of DNA nanotechnology. Full article

In order to fabricate a digital microfluidic (DMF) chip, which requires a patterned array of electrodes coated with a dielectric film, we explored two simple methods: Ballpoint pen printing to generate the electrodes, and wrapping of a dielectric plastic film to coat the electrodes. For precise and programmable printing of the patterned electrodes, we used a digital plotter with a ballpoint pen filled with a silver nanoparticle (AgNP) ink. Instead of using conventional material deposition methods, such as chemical vapor deposition, printing, and spin coating, for fabricating the thin dielectric layer, we used a simple method in which we prepared a thin dielectric layer using pre-made linear, low-density polyethylene (LLDPE) plastic (17-μm thick) by simple wrapping. We then sealed it tightly with thin silicone oil layers so that it could be used as a DMF chip. Such a treated dielectric layer showed good electrowetting performance for a sessile drop without contact angle hysteresis under an applied voltage of less than 170 V. By using this straightforward fabrication method, we quickly and affordably fabricated a paper-based DMF chip and demonstrated the digital electrofluidic actuation and manipulation of drops. Full article