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Bio Barrier, Inc.

Clive C Solomons

Robin R Shlenker

Clayton S Smith

David J Lester

Jerry D Plunkett

Sebastian S Plamthottam

Single and multiple layer membranes such as gloves and condoms include one or more deactivating barrier layers and/or indicating layers to indicate to a user membrane breach or the presence of a harmful substance in blood or body fluids. A membrane may include one or more permeable or semipermeable layers to disperse contained substances such as lubricants, biocides, spermicides, or indicators outwardly, and may also include permeable or semipermeable layers to allow transmission of body fluids or other environmental fluids inwardly into contact with an indicating or treating substance. An intermediate layer of a multi-layer membrane may include a substance to wipe, cleanse, sterilize, or otherwise treat a piercing needle. A membrane may include a sealing or coating to entrap indicators or other agents such as biocides therein. A method of making membranes such as gloves results in a double glove having discrete inner or outer layers joined only in a cuff region. Admixing of gentian violet with latex prior to membrane formation provides biocidal properties, anti-aging effects prolonging shelf-life and tear resistance, and reduces allergic reactions in latex-allergic users.

Method of forming a membrane especially a latex or polymer membrane

Method of forming a membrane, especially a latex or polymer membrane,

Methods of forming a chemical barrier against the transmission of disease-causing microbes and other harmful agents through a membrane such as latex. In the principal method, a mold or former is coded with a coagulant, which is dried, and then the former is dipped into liquid latex, which is allowed to gel, and then the former is dipped into a solution containing the biocide, and then the former is dipped again into the liquid latex, after which the entire coating on the former is cured. Alternatively, the biocide may be sprayed or otherwise applied onto the gelled latex.

Method of forming a membrane, especially a latex membrane, having a

Various methods of forming a chemical barrier against the transmission of disease-causing microbes and other harmful agents through a membrane fashioned of latex or other material. In one method, the latex material is provided with microbe sterilization properties by deforming the latex material from a relaxed condition such that the pores therein are deformed, then washing the deformed latex material with a biocide, which is entrapped in the pores, and then relaxing the latex material. Alternatively, instead of washing the deformed latex material with the biocide, the biocide may be mixed directly with the liquid latex preferably along with a buffer agent and then the liquid latex can be cured. In yet another method, the latex material is treated with a silicone, protein or high molecular polyion to form a water resistant surface. A method of inhibiting the deterioration, extending the effective life, increasing the strength, and increasing the elasticity of the latex material is to mix an oxidation reducing agent that chelates iron and other heavy metals with the liquid latex and then to cure the latex. The latex materials produced by the foregoing methods are also disclosed.

Membranes fashioned from latex and other materials and methods of

Methods of forming a chemical barrier against the transmission of disease-causing microbes and other harmful agents through a membrane such as latex. In the principal method, a mold or former is coded with a coagulant, which is dried, and then the former is dipped into liquid latex, which is allowed to gel, and then the former is dipped into a solution containing the biocide, and then the former is dipped again into the liquid latex, after which the entire coating on the former is cured. Alternatively, the biocide may be sprayed otherwise applied onto the gelled latex.

A kit is provided for measuring chemical and physical stresses on the blood platelets of a human patient by measuring reduction in ATP (adenosine triphosphate) and ADP (adenosine diphosphate) concentrations while measuring increases in the ATP degradation products HYPX (hypoxanthine) and the AMP (adenosine monophosphate). The kit is useful for measuring a human patient's risk to internal stress such as reduction in the size of blood vessels, to response to various environmental changes as well as to a variety of treatments including drug treatment, risk of malignant hyperthermia in response to anesthetic administration or in response to vascular or organ transplant.

Kit for determining blood platelet stress

A process and kit are provided for measuring chemical and physical stresses on the blood platelets of a human patient by measuring reduction in ATP (adenosine triphosphate) and ADP (adenosine diphosphate) concentrations while measuring increases in the ATP degradation products HYPX (hypoxanthine) and AMP (adenosine monophosphate). The process is useful for measuring a human patient's risk to internal stress such as reduction in the size of blood vessels, to response to various environmental changes as well as to a variety of treatments including drug treatment, risk of malignant hyperthermia in response to anesthetic administration or in response to vascular or organ transplant.

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Denver, CO, United States of America

Clive C Solomons