Abstract: The use of protected active ingredients, preferably methionine, protected against degradation in the rumen as a hepatoprotective agent is disclosed.

Abstract: A wound dressing is provided which comprises a blend of silicone fluid and fumed silica having the consistency of a stiff cream prepared in the presence of a volatile diluent that reduces the consistency of the silicon fluid-fumed silica blend to that of a spreadable cream or grease which can applied to a wound without producing further injury or undue discomfort. After the blend is in place on the wound, evaporation of the volatile diluent restores the consistency of the silicone fluid silica blend to its undiluted state, thereby allowing the advantages of increased wound adhesion and "smear proofing" to be achieved without producing further damage to the wound or undue pain and discomfort during application. The consistency of any particular blend of silicone fluid and fumed silica may be adjusted by varying the quantity of volatile diluent, thereby allowing the physician to vary the thickness of the film to help control the loss of water from the protected area.

Abstract: A drug delivery system useful in treating individuals having maladies requiring topical, subcutaneous and intra-lesional administration of one or more drugs for a prolonged period of time. A method for treating individuals with noduloulcerative carcinomas using the present invention drug delivery system and intra-lesional administration of interferon to the individual in a controlled, sustained release manner such that long-term therapeutic levels of interferon are provided to the individual. A method of treating an individual having certain skin infections using the present invention drug delivery system including topical and/or subcutaneous administration of one or more drugs to the individual in a controlled, sustained release manner such that long-term therapeutic levels of the drug(s) are provided to the individual.

Abstract: A transdermal patch useful for evaluating the therapeutic effectiveness of a transdermally delivered medicinal agent is disclosed. The patch includes a substantially impermeable backing layer, a delivery layer containing a medicament and a substantially impermeable blocking layer. The delivery layer is arranged between the backing and blocking layers to prevent the release of the medicament contents from the delivery layer when the transdermal patch is affixed to the skin of a mammal. In alternative embodiments, non-transdermal placebo systems such as oral dosage forms which are coated with substantially impermeable layers to create virtually identical placebos of active oral delivery systems such as tablets, capsules and osmotic tablets are disclosed. Methods of comparing the therapeutic effectiveness of active dosage forms, i.e. transdermal units containing a medicament to placebo or to comparable active agents in either similar or different delivery systems are also disclosed.

Abstract: A transdermal drug delivery device has a drug containing element containing a drug which is preferably charged and first and second electrodes for conducting a current flow through the drug containing element. The current flow causes the drug to be released from the drug containing element and to permeate through the skin of a user to which the device has been fixed. A power source is connected to the first and second electrodes for providing the energy necessary to generate the current flow. The power source comprises a thermocouple or thermopile having two different poles which are connected to the first and/or second electrodes, whereby a self-contained drug delivery device is formed which provides the energy necessary for generating the current flow by means of a difference in temperature of the skin of the user and the ambient air (environment), thus providing a device free of batteries, accumulators or other external energy sources.

Abstract: A delivery system for providing antiparasitic agents to animals is provided and a method of treating parasitic infections in animals using such delivery systems is described. The delivery system is particularly useful for treatment with avermectins and milbemycins in lactide/glycolide polymeric matrices.

Abstract: A delivery system is disclosed for delivering a fluid-sensitive active agent such as a somatotropin, or an analogue or derivative thereof, to an animal such as a bovine. The delivery system comprises a first wall section, a second wall section and a locking coupling therebetween. The coupled wall sections define a compartment, enclosing an active agent and an expandable driving member. Various embodiments of the locking coupling are disclosed.

Abstract: The invention is directed to a device for delivering an active agent formulation for a predetermined administration period. An impermeable reservoir is divided into a water-swellable agent chamber and an active agent formulation chamber. Fluid from the environment is imbibed through a semipermeable plug into the water-swellable agent chamber and the active agent formulation is released through a back-diffusion regulating outlet. Delivery periods of up to 2 years are achieved.

Abstract: The present invention provides a transdermal absorption preparation whereby a drug, which takes effect with a small amount, and is liable to be decomposed, solid at ordinary temperatures, water-soluble and less absorbable into the skin, can be stored stably for a long period of time and, can be transdermally administered at a high releasing ratio and yet releasing slowly, when applied to the skin. The constitution of the present invention is as follows: a transdermal absorption preparation which comprises a drug-storing layer containing a drug and having a drug-releasing face coated with a drug-releasing controlling membrane, wherein said drug-storing layer comprises as a base a heat-sensitive segmented polyurethane represented by the general formula:R--A--(U)--F--(U)--B--R'wherein A and B each represents a polymer of ethylene oxide, propylene oxide, tetramethylene oxide or 1,2-butylene oxide, or a random or block copolymer thereof, R and R' each represents a terminal H, CH.sub.3, C.sub.2 H.sub.5, C.sub.3 H.

Abstract: A method for supplementing the amino acid levels in ruminants is provided where rumen-protected amino acids, particularly lysine and/or methionine, are used to supplement ruminant feed.

Abstract: The invention described is a bolus for the controlled release of a beneficial agent in the rumen of a ruminant animal. The bolus consists in a core containing a binder, solubilising agent, the beneficial agent to be released and, when required, a densifier. The core is coated with a wax coating, preferably with an opening exposing a small part of the core to rumen juices. The core is gradually dissolved releasing the beneficial agent. As the core dissolves the wax coating erodes until the bolus disappears completely.

Abstract: The reservoir loaded with a divided material which can be impregnated with the solution of active principle, comprises a) a support sheet (1) made of a cavitied material which is permeable to the solution and capable of contributing to the mechanical strength of the reservoir b) a layer (3) of particles of the impregnatable material and c) a substrative layer (2) interposed between one face of the support sheet (1) and the layer of particles (3) in order to hold the latter on the support sheet (1), this substrative layer (2) consisting of a substance which is miscible with the solution of active principle.

Abstract: A transdermal patch containing an extract of the herb Plantago major is presented. Use of the transdermal patch, of the present invention, produces a diminished desire for tobacco (i.e., nicotine) without the use of nicotine itself.

Abstract: Transdermal therapeutic system comprising the active substance acetylsalicylic acid, having a layered structure consisting of a backing layer which is substantially impermeable to active substances and moisture and one or several active substance-containing matrix layers, which is characterized in that at least one of said matrix layers comprises acetylsalicylic acid in mainly crystalline form.

Abstract: A scopolamine-containing transdermal therapeutic system in the form of a patch is described whose active substance-containing layers comprise as base polymer copolymers of acrylic acid or methacrylic acid derivatives and scopolamine base in a concentration corresponding to 50-100% of the saturation solubility, preferably 60-100% of the saturation solubility, in the total vehicle formulation.

Abstract: Disclosed is a novel transdermal delivery system for dehydroepiandrosterone (DHEA). Using phospholipids as vehicles, DHEA can be administered into and through the skin when topically applied. Numerous advantages apply to this modality of therapy.

Abstract: The present invention relates to a transdermal delivery device for estradiol where the metabolic degradation of estradiol to estrone during permeation is inhibited by another substance in the transdermal delivery device. The transdermal device also includes a compound for enhancing the rate of estradiol permeation. The transdermal delivery device containing the inhibitor and enhancer can also be used to simultaneously deliver both estradiol and a progestin at therapeutic rates.

Abstract: The present invention is a method for releasing an active agent into a use nvironment, by disposing this active agent within the lumen of a population of tubules, and disposing the tubules into a use environment, either directly or in some matrix such as a paint in contact with the use environment. The tubules have a preselected release profile to provide a preselected release rate curve. The preselected release profile may be achieved by controlling the length or length distribution of the tubules, or by placing degradable endcaps over some or all of the tubules in the population, or by combinations of these methods. The invention is also a population of tubules having a preselected release profile to provide a preselected release rate curve.

Abstract: A pharmaceutical composition for systemic transdermal administration containing morphine-6-glucuronide or a pharmaceutically acceptable acid addition salt thereof as the active agent.

Abstract: Absorbent products, especially catamenial tampons, for absorbing body fluids, such as menstrual fluid, blood and wound exudates, comprise an amount of a compound effective to inhibit the production of toxic shock syndrome toxin-1 by Staphylococcus aureus bacteria when the products are brought into contact with the bacteria. The compound is selected from the group consisting of monoesters of a polyhydric aliphatic alcohol and a C.sub.8 -C.sub.18 fatty acid; diesters of a polyhydric aliphatic alcohol and a C.sub.8 -C.sub.18 fatty acid; and mixtures thereof. The monoesters and diesters have at least one hydroxyl group associated with their aliphatic alcohol residue.