Provided are devices and methods that combine material anisotropy with nonlinear structural design to produce structures that precisely and sequentially actuate in response to multiple stimuli, such as water or non-polar solvents. These devices and methods can include bistable anisotropic elements that convert to monostable element upon exposure to a particular stimulus, and anisotropic distortions can be harnessed to change the geometric properties of the element to cross phase boundaries and trigger shape changes at precise times. One can incorporate complex logic into these devices and methods.

Apparatus and methods for mixing and dispersing a dispersed phase in a medium comprise a rotating surface for receiving the medium and an atomizing apparatus positioned at the rotating surface for depositing aerosolized constituents of the dispersed phase into the medium. The medium is made receptive and the dispersed phase is aerosolized. Constituents of the aerosolized dispersed phase are deposited into the receptive medium to form a compound or composite. The medium may be deposited onto a rotating disk, and the dispersed phase may be sprayed onto the disk. A thin film can be generated on the disk to transfer, distribute, and disperse the dispersed phase. Liquid ligaments formed at the edge of the rotating disk further transfer, distribute, and disperse the dispersed phase into the medium. Ligaments may be broken into aerosols or deformed by attenuation/drawing to further promote transfer, distribution, and dispersion. A bulk composite/compound may be collected.

An isokinetic oscillation exercise device of an elongated flexible blade having a first and second end and a grip portion coupled to a middle portion of the elongated flexible blade. End caps coupled to said first and second ends adapted to storage. Further, a method is disclosed of manufacturing an isokinetic oscillation exercise device that provides a flexible elongated flexible blade, a grip portion injection molding, a pliable ring injection moldings, and end caps injection molding; slides the pliable rings on the elongated flexible blade separated by a length of the grip portion, overmolds a first-shot of the grip portion over the pliable rings, overmolds a second-shot of the grip portion to the first-shot of the grip portion to the elongated flexible blade, seals the first-shot to the second-shot of the grip portion against the pliable rings; and attaches the end caps to the elongated flexible blade.

Described are techniques for additive manufacturing of deformable objects. The techniques including a method comprising generating printing parameters for a deformable component. The method further comprises fabricating the deformable component by additive manufacturing, where a smart material is located at an articulation point of the deformable component, and where a base material is located at a static portion of the deformable component. The method further comprises supplying an environmental stimulus to the deformable component that causes the deformable component to transition from a first state to a second state.

A bedding product having a cooling layer and a method therefor. The bedding product has a gel layer having an outside surface, a bonding surface opposite the outside surface, and a perimeter. A memory foam layer surrounds the perimeter and is disposed on the bonding surface. A textile layer having a first rectangular portion and a second rectangular portion affixed on a perimeter thereof to the first rectangular portion retains the gel layer and memory foam layer therebetween. The textile layer has a cooling surface, an opposing surface opposite the cooling surface, and at least one vent disposed adjacent to an edge portion of the first or second rectangular portion. The gel layer contains a plurality of hexagonal prism-shaped peaks and valleys on the outside surface thereof, and the gel layer and memory foam layer have a plurality of air conduits for air flow communication with the vent.

Methods of tissue engineering, and more particularly methods and compositions for generating various vascularized 3D tissues, such as 3D vascularized embryoid bodies and organoids are described. Certain embodiments relate to a method of generating functional human tissue, the method comprising embedding an embryoid body or organoid in a tissue construct comprising a first vascular network and a second vascular network, each vascular network comprising one or more interconnected vascular channels; exposing the embryoid body or organoid to one or more biological agents, a biological agent gradient, a pressure, and/or an oxygen tension gradient, thereby inducing angiogenesis of capillary vessels to and/or from the embryoid body or organoid; and vascularizing the embryoid body or organoid, the capillary vessels connecting the first vascular network to the second vascular network, thereby creating a single vascular network and a perfusable tissue structure.

The present invention enables three-dimensional nanofabrication by isotropic shrinking of patterned hydrogels. A hydrogel is first expanded, the rate of expansion being controlled by the concentration of the crosslinker. The hydrogel is then infused with a reactive group and patterned in three dimensions using a photon beam through a limited-diffraction microscope. Functional particles or materials are then deposited on the pattern. The hydrogel is then shrunk and cleaved from the pattern.

There is provided a method of forming a 3-dimensional structure from a hydrogel, the process comprising the steps of: (a) placing a hydrogel polymerisation solution into a reaction vessel, and (b) allowing the hydrogel polymerisation solution to react without mixing for a period of time at ambient temperature, while introducing a polymerisation modulator to the reaction solution through a reaction solution/polymerisation modulator interface, wherein over the period of time, a modulation effect gradient is established in the reaction solution, where the modulation effect has a maximal value at the reaction solution/polymerisation modulator interface and a minimal value at a point furthest away from said interface. The said method additionally includes the use of physical constraint members such as wires and/or threads.

Microchannels in hydrogels play an essential role in enabling a smart contact lens. A wearable contact lens is disclosed herein that uses microchannels and connected chambers located in poly-2-hydroxyethyl methacrylate (poly(HEMA)) hydrogel that is used in a commercial contact lens with three-dimensional (3D) printed mold. The corresponding capillary flow behaviors in these microchannels were investigated. Different capillary flow regimes were observed in these microchannels, depending on the hydration level of the hydrogel material. In particular, it was found that a peristaltic pressure could reinstate flow in a dehydrated microchannel, indicating the motion of eye-blinking may help tear flow in a microchannel-containing contact lens. Colorimetric pH and electrochemical Na.sup.+ sensing capabilities were demonstrated in these microchannels. Micro-engineered contact lenses formed using poly(HEMA) hydrogel can be used for various biomedical applications such as eye-care and wearable biosensing.

A method for producing a 3D-printed tissue substitute is disclosed, utilizing a 3D printing device including a tank including a yield stress fluid in which the material is printed, the printing material delivered by the cartridge includes polyvinyl alcohol and gelatin, the method including a step following which, after printing the material in the yield stress fluid, a printed intermediate device is solidified in the yield stress fluid by lowering the temperature of the tank. The intermediate device is removed from the tank, rinsed and dried in order to obtain the tissue substitute.