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Methods and systems for modifying bioactive agent use

  • US 9,282,927 B2
  • Filed: 08/22/2008
  • Issued: 03/15/2016
  • Est. Priority Date: 04/24/2008
  • Status: Active Grant
First Claim
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1. A combination treatment system comprising:

  • at least one in vivo type administration unit that includes at leastat least one housing;

    at least one reservoir within the at least one housing and that is operable to contain at least one antidepressant agent;

    at least one controllable valve or pump mechanism operable to transfer the at least one antidepressant agent from the at least one reservoir for delivery to at least one bodily site;

    at least one wireless receiver operable to receive one or more wirelessly transmitted instructions; and

    at least one controller communicably linked with the at least one wireless receiver and that at least one controllable valve or pump mechanism, which at least one controller is operable to control the at least one controllable valve or pump mechanism to deliver one or more dosages of the at least one antidepressant agent in accordance with one or more wirelessly transmitted instructions received by the at least one wireless receiver; and

    at least one smartphone device communicably linked with the at least one administration unit, the at least one smartphone device including at least;

    at least one sensor for monitoring visual appearance of an individual;

    at least one wireless transmitter operable to communicate wirelessly with the at least one administration unit;

    at least one display;

    one or more media including one or more executable instructions; and

    at least one processor operatively connected to the one or more media, wherein the at least one processor is configured to execute the one or more executable instructions to perform operations including at least;

    monitoring appearance of the individual using the at least one sensor;

    detecting at least one depression symptom of the individual based at least partly on monitored appearance of the individual which deviates from one or more specified levels of normalcy for the individual;

    transmitting one or more instructions wirelessly to the at least one administration unit that control the at least one controllable valve or pump mechanism to deliver one or more dosages of the at least one antidepressant agent to at least one bodily site at least partly in response to detection of the at least one depression symptom of the individual based at least partly on monitored appearance of the individual which deviates from one or more specified levels of normalcy for the individual; and

    implementing one or more modifications to at least one interpersonal interaction application at one or more staggered times relative to administration of the at least one antidepressant agent based at least partly on one or more pharmacokinetic profiles of the at least one antidepressant agent, the one or more staggered times corresponding to when the antidepressant agent is expected to be least effective.

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