Abstract: A method for providing portable biological testing capabilities free from biological contamination from an environment outside the device is provided. The method includes providing components configured to be assembled together to seal a volume against passage of biological materials between the volume and an environment outside the volume. The method further includes sterilizing the components and providing a sterilized culture medium. The method further includes assembling the components together with the sterilized culture medium within the volume. The method further includes sterilizing the assembled components by elevating the temperature. The method further includes flowing gas from within the volume to the environment while at an elevated temperature.

Abstract: A method for providing portable biological testing capabilities free from biological contamination from an environment outside the device is provided. The method includes providing components configured to be assembled together to seal a volume against passage of biological materials between the volume and an environment outside the volume. The method further includes sterilizing the components and providing a sterilized culture medium. The method further includes assembling the components together with the sterilized culture medium within the volume. The method further includes sterilizing the assembled components by elevating the temperature. The method further includes flowing gas from within the volume to the environment while at an elevated temperature.

Abstract: A device and method for providing portable biological testing capabilities free from biological contamination from an environment outside the device are provided. The device includes a portable housing. The device further includes a volume surrounded by the housing and sealed against passage of biological materials between the volume and the environment outside the device. The device further includes a culture medium within the volume. The device further includes one or more ports configured to provide access to the volume while avoiding biological contamination of the volume. The device further includes a valve in fluidic communication with the volume and the environment. The valve has an open state in which the valve allows gas to flow from within the volume to the environment outside the device and a closed state in which the valve inhibits gas from flowing between the volume and the environment.

Abstract: A device and method for providing portable biological testing capabilities free from biological contamination from an environment outside the device are provided. The device includes a portable housing. The device further includes a volume surrounded by the housing and sealed against passage of biological materials between the volume and the environment outside the device. The device further includes a culture medium within the volume. The device further includes one or more ports configured to provide access to the volume while avoiding biological contamination of the volume. The device further includes a valve in fluidic communication with the volume and the environment. The valve has an open state in which the valve allows gas to flow from within the volume to the environment outside the device and a closed state in which the valve inhibits gas from flowing between the volume and the environment.

Abstract: A patient replica is created from layered culture medium where solid culture medium is formed so that a discontinuity exists, for example, between layers of culture medium or between culture medium and the container holding the medium. An injection port is provided in registration with the discontinuity so that a sample of patient blood can be infused into the discontinuity to form a thin layer of blood in contact with a surface of culture medium. The thin layer of blood obviates the requirement for any anticoagulant allowing blood-borne pathogens to be readily cultured without using broth. Further antibiotics or other drug samples may be placed on an exposed surface of the culture medium above the blood layer so that the antibiotic can diffuse through the culture medium and reveal the sensitivities of the cultured pathogens.

Abstract: A patient replica is created from a layered culture medium where solid culture medium is formed so that a discontinuity exists between the layers. An infusion port is provided in registration with the discontinuity so that a fresh unadulterated sample of patient blood can be infused into the discontinuity to form a thin layer of blood between the layers of culture medium. The thin layer obviates the requirement for any anticoagulant allowing blood-borne pathogens to be readily cultured without using broth. Further antibiotics or other drug samples may be placed on the surface of the culture medium above the blood layer so that the antibiotic can diffuse through the culture medium and reveal the sensitivities of the cultured pathogens. Other samples of pathogens or tissues can be placed on the surface of the culture medium so that effects of drugs or growth factors present in the patient blood can be observed thereby allowing the entrapped blood layer to act as a biological replica of the patient.