Abstract: Embodiments of a pharmaceutical formulation comprising an enteric material are disclosed. The embodiments release at least a portion of an active ingredient upon contacting gastric fluid. The remaining portion of the formulation releases active ingredient upon contacting intestinal fluid. Certain embodiments of the pharmaceutical composition comprise at least one active ingredient in a core and a leaky enteric coating, such as an enteric coating comprising a gastric fluid channeling agent. Other embodiments of the pharmaceutical composition comprise at least one active ingredient substantially homogeneously admixed with at least one enteric material, such as an enteric material comprising a gastric fluid channeling agent. Disclosed embodiments of the pharmaceutical composition may comprise a single active ingredient, or may comprise plural active ingredients. Generally, but not necessarily, the active ingredient has a window of absorption.

Abstract: A plunger switch comprises a switch body housing a first contact element, a second contact element and an elongate plunger. The first contact element is partially housed in the switch body and extends out for operative communication with a circuit. The second contact element is movable along a longitudinal axis of the switch body and is aligned to contact the first contact element through movement. The elongate plunger is movable along the longitudinal axis of the switch body, and is able to be completely recessed in the switch body. Movement of the plunger in a first direction facilitates contact between the first and second contact elements. The contact elements contact at contact portions. At least a pair of the contact portions may have ridged surfaces that are oriented so as to have intersecting points at contact and configured to perform oxidation cleanup. At least a pair of the contact portions may include silver nitride.

Abstract: A method of coating a pharmaceutical substrate which is not a hot-melt coating by fluid bed method comprises applying a molten coating material to the pharmaceutical substrate wherein the substrate is coated with the coating material; optionally applying to the coated substrate the same or different molten coating material, and optionally repeating the second applying step; wherein the coated substrate contains an antigen or a pharmaceutical agent or drug; and wherein the molten coating contains less than 10% solvent. Coated substrates include those made by this process.

Abstract: An expandable crate, such as an expandable animal crate, is disclosed that optionally is expandable and collapsible in multi-dimensions, most preferably in three dimensions, and has a usable interior space in the collapsed or expanded or in-between states. That is, the crate may be expanded or collapsed in one dimension, or two dimensions, or three dimensions, or even more than three dimensions. The size of the crate is adjustable by expansion or collapsing to provide a variety of sizes for use.

Abstract: A cooking device for cooking an item where the device includes an input for a source of cooking energy; a cooking element for applying the cooking energy to the item; a cooking control for controlling the application of the cooking energy to the item; a lockout selectable for preventing application of the cooking energy to the cooking element, the lockout being non-selectable when the cooking control is activated; and a user interface, the interface providing an indication of selection of the lockout in response to a user attempt to activate the cooking control when the lockout is selected.

Abstract: A method of making microcapsules including activating a fluid ejector at a frequency greater than 10 kilohertz where each activation of the fluid ejector generates essentially a drop, and the fluid ejector is fluidically coupled to a first fluid including a core component. The method further includes ejecting the drop of the first fluid into a second fluid, the drop having a volume. In addition, the method includes generating a microcapsule, that includes the core component, in the second fluid for each drop of the first fluid ejected.

Abstract: A method of dispensing a medicament. A treatment plan having at least two rates of action for a medicament may be provided. A droplet characteristic corresponding to each rate of action may be selected. Medicament droplets having each droplet characteristic may be ejected into a mucosal tract according to the treatment plan, thereby allowing the medicament to act at two or more rates.

Abstract: Sheets of base substrate (e.g., transparency film, glass, or other suitable growth material) are coated with an array of spots of the same or different growth media and/or nutrients. Coating may be accomplished using an ink-jet printer, which deposits droplets of a growth medium and/or one or more nutrients on the substrate.