Simultaneous disease detection system method and devices

An apparatus comprising:

• a first conductive layer deposited and cured to couple to a substrate configured for a lysis function;
• wherein the substrate is configured to support deposited materials;
• a temperature controlling conductive layer deposited and cured to couple on top of a portion of the first conductive layer configured to create a heating element that serves as the lysis function;
• an insulating layer deposited and cured to couple on top of the temperature controlling conductive layer, and a portion of the first conductive layer, configured to insulate the temperature controlling conductive layer and a portion of the first conductive layer;
• a second conductive layer deposited and cured to couple on top of a portion of the first conductive layer configured to bind with at least one molecule;
• a conductive adhesive layer deposited on a portion of the first conductive layer and coupled to a memory device, coupled to the conductive adhesive layer, configured to adhere the memory device to the first conductive layer;
• wherein the memory device is coupled to the conductive adhesive, and then the conductive adhesive is cured;
• wherein the memory device is conductively coupled to the first conductive layer and configured to store analyte signatures;
• a temperature control device coupled to the bodily fluid test sample compartment and a temperature measurement device, configured to regulate the bodily fluid test sample at a uniform temperature;
• a meter coupled to an electrode graphene layer configured to measure the circuit electrical current passing through the electrode graphene layer, with and without the deposition of a prepared bodily fluid test sample to measure an electrical field and ionic strength of a bodily fluid test sample;
• wherein a meter reading with no bodily fluid test sample shows a base current to compare the meter reading of the current in the presence of the bodily fluid test sample to determine a concentration level of a functionalized analyte signature detection;
• and
• at least one molecule layer deposited and dried to couple on top of the second conductive layer, configured to promote hybridization of the atomic orbitals of the at least one molecule on the surface of the second conductive layer and the atomic orbitals of the at least one molecule in the test sample.

An apparatus comprising:

• a first conductive layer deposited and cured to couple to a substrate configured for a lysis function;
• wherein the substrate is configured to support deposited materials;
• a temperature controlling conductive layer deposited and cured to couple on top of a portion of the first conductive layer, configured to create a heating element that serves as the lysis function;
• an insulating layer deposited and cured to couple on top of the temperature controlling conductive layer, and a portion of the first conductive layer configured to insulate the temperature controlling conductive layer and a portion of the first conductive layer;
• a second conductive layer deposited and cured to couple on top of a portion of the first conductive layer configured to bind with at least one molecule;
• a conductive adhesive layer deposited on a portion of the first conductive layer and coupled to a memory device, coupled to the conductive adhesive layer, configured to adhere the memory device to the first conductive layer;
• wherein the memory device is conductively coupled to the first conductive layer and configured to store analyte signatures;
• a temperature control device coupled to the bodily fluid test sample compartment and a temperature measurement device, configured to regulate the bodily fluid test sample at a uniform temperature;
• a monitor/detector coupled to a monitor system configured to detect positive bodily fluid test samples based on molecule hybridization;
• a meter coupled to an electrode graphene layer configured to measure the circuit electrical current passing through the electrode graphene layer, with and without the deposition of a prepared bodily fluid test sample to measure an electrical field and ionic strength of a bodily fluid test sample;
• wherein a meter reading with no bodily fluid test sample shows a base current to compare the meter reading of the current in the presence of the bodily fluid test sample to determine the concentration level of a functionalized analyte signature detection;
• and
• at least one molecule layer deposited and dried to couple on top of the second conductive layer, configured to promote hybridization of the atomic orbitals of the at least one molecule on the surface of the second conductive layer and the atomic orbitals of the at least one molecule in the bodily fluid test sample.