METHOD AND SYSTEM TO DETECT MALFUNCTIONS IN AN IONTOPHORESIS DEVICE THAT DELIVERS ACTIVE AGENTS TO BIOLOGICAL INTERFACES
An active agent delivery device is operable to deliver an active agent such as a drug or therapeutic agent to a biological interface such as skin or mucous membrane. The device, such as an iontophoresis device, may include one or more human-perceptible indicators operable to provide an indication of a malfunction or other defective condition of the device. Detectors may be provided to detect a value of a characteristic or parameter associated with one or more components of the device, with the value being usable to determine whether a defective condition may exist.
1 . A method usable with an iontophoresis device that delivers an active agent to a biological interface, the method comprising:
detecting a value of a characteristic associated with at least one component of the iontophoresis device;
evaluating the detected value of the characteristic to determine whether the detected value is indicative of a possible defective condition of the iontophoresis device; and
if the evaluated value is determined to be indicative of the possible defective condition, generating at least one human-perceptible indication that is indicative of the possible defective condition of the iontophoresis device, including providing the human-perceptible indication in a manner that is perceivable from an exterior of the iontophoresis device.
2 . The method of claim 1 wherein detecting the value of the characteristic comprises detecting a value of one or combination of a current, voltage, power, impedance, capacitance, inductance, and impedance spectrum.
3 . The method of claim 1 wherein evaluating the detected value includes comparing the detected value with a stored value representing a threshold.
4 . The method of claim 1 wherein generating at least one-human perceptible indication includes generating a visual indication.
5 . The method of claim 1 wherein generating at least one-human perceptible indication includes generating an audible indication.
6 . The method of claim 1 wherein generating at least one-human perceptible indication includes generating a tactile indication.
7 . The method of claim 1 wherein the possible defective condition includes improper placement of the iontophoresis device on the biological interface.
8 . The method of claim 1 wherein the possible defective condition includes a damage or improper operation of at least one component of the iontophoresis device.
9 . An article of manufacture, comprising:
a machine-readable medium usable with an iontophoresis device and having instructions stored thereon that are executable by a processor to determine whether a possible defective condition of the iontophoresis device exists, by:
evaluating a detected value of a characteristic associated with operation of the iontophoresis device to determine whether the detected value is indicative of the possible defective condition; and
initiating generation of at least one human-perceptible indication that is indicative of the possible defective condition of the iontophoresis device, if the evaluated value is determined to be indicative of the possible defective condition.
10 . The article of manufacture of claim 9 wherein the instructions to initiate generation of at least one-human perceptible indication includes instructions to provide the human-perceptible indication in a manner that is perceivable from an exterior of the iontophoresis device.
11 . The article of manufacture of claim 9 wherein the machine-readable medium is located within a common housing material as the iontophoresis device.
12 . The article of manufacture of claim 9 wherein the machine-readable medium further includes instructions executable by the processor to determine whether the possible defective condition exists, by:
applying an impedance spectroscopy technique to at least one component of the iontophoresis device; and
obtaining the detected value of the characteristic, which is to be evaluated, from results from the applied impedance spectroscopy technique.
13 . The article of manufacture of claim 9 wherein the machine-readable medium further includes instructions executable by the processor to determine whether the possible defective condition exists, by:
controlling at least one detector to obtain the value of the characteristic.
14 . A system, comprising:
iontophoresis device means for delivering an active agent to a biological interface;
detector means for obtaining a value of a parameter associated with operation of at least one component of the iontophoresis device means;
evaluation means for evaluating the obtained value of the parameter to determine whether there may be a possible malfunction of the iontophoresis device means; and
indicator means for providing, based on the evaluated value of the parameter, a human-perceptible indication of whether the possible malfunction of the iontophoresis device means may exist.
15 . The system of claim 14 wherein the evaluation means includes circuit means for comparing the value of the parameter with a reference value.
16 . The system of claim 14 wherein the evaluation means includes processing means in cooperation with machine-readable instruction means for determining if the value of the parameter is indicative of the possible malfunction of the iontophoresis device means.
17 . The system of claim 14 wherein the evaluating means is externally and separately located from the iontophoresis device means.
18 . An iontophoresis device, comprising:
an active electrode assembly to deliver an active agent to a biological interface;
a power supply coupled to the active electrode assembly to apply a current to the active electrode assembly to induce delivery of the active agent to the biological interface;
a counter electrode assembly coupled to the power supply; and
a control unit coupled to the electrode assemblies and to the power supply, the control unit including:
at least one detector to detect a value of a characteristic associated with any one or combination of the electrode assemblies and the power supply;
an evaluation unit coupled to the detector to receive an input based on the detected value and to determine whether the input is indicative of a possible malfunction; and
an indicator coupled to the evaluation unit and responsive to the evaluation unit to provide a human-perceptible indication of the possible malfunction.
19 . The device of claim 18 wherein the evaluation unit comprises circuitry coupled to compare the input with at least one specified value.
20 . The device of claim 18 wherein the evaluation unit comprises a processor able to execute machine-readable instructions to determine whether the input is indicative of the possible malfunction.
21 . The device of claim 18 wherein the indicator provides a graphical display output.
22 . The device of claim 18 , further comprising an input unit coupled to the evaluation unit to receive information pertaining to evaluation of the input to the evaluation unit.
23 . The device of claim 18 wherein the indicator provides a visual indication that includes at least one or more of an optical indication, a mechanical indication, an electrochemical indication.
24 . The device of claim 18 wherein the indicator provides an audible indication.
25 . The device of claim 18 wherein the indicator provides an indication that can be sensed by user touching.
26 . The device of claim 18 wherein said at least one detector includes a voltage detector to detect a voltage across at least one layer of one of said electrode assemblies.
27 . The device of claim 18 wherein said at least one detector includes a current detector placed coupled between said electrode assemblies.
28 . The device of claim 18 wherein said at least one detector includes a detector coupled to said power supply.