Transdermal Micro-Patch

• US 20100292632A1
• Filed: 02/13/2009
• Published: 11/18/2010
• Est. Priority Date: 02/15/2008
• Status: Abandoned Application

• Current Assignee: Piezo Resonance Innovations, Inc.
• Original Assignee: Piezo Resonance Innovations, Inc.
• Inventors: Knowles, Gareth, Mulvihill, Maureen L., Park, Brian M.
• Application Number:
  US12/812,799
• Publication Number:
  US 20100292632A1
• Time in Patent Office: Days
• US Class Current: 604/22
• CPC Class Codes: A61K 9/703 characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
• CPC Class Codes: A61M 37/0092 using ultrasonic, sonic or infrasonic vibrations, e.g. phonophoresis
• CPC Class Codes: A61N 7/00 Ultrasound therapy lithotripsy A61B17/22, A61B17/225; massage using supersonic vibration A61H23/00 ; using ultrasound for introducing media into the body A61M37/0092

Abstract

A transdermal micro-patch for use with living tissue is provided. The micro-patch includes a first membrane, a reservoir, a micro-pump, flextensional transducers, a microelectronics circuit, and an optional sensor. The first membrane is permeable to allow the passage of fluid in either a unidirectional or bidirectional fashion. The reservoir is a container-like element capable of storing a fluid removed from or communicated into the tissue. The micro-pump facilitates transport of the fluid between the reservoir and first membrane. The flextensional transducers generate ultrasonic waves which are separately communicated into the tissue to transport fluid between the first membrane and tissue. Ultrasonic waves could interact to enhance the performance of the micro-patch. The microelectronics circuit controls both flextensional transducers and the micro-pump. The sensor could be embedded within the micro-patch to monitor temperature, pressure, or flow rate so as to avoid damage or irritation to the tissue.

Claims

1. A transdermal micro-patch for use on a living tissue comprising:

(a) a first membrane being permeable so as to allow passage of a fluid;

(b) a reservoir which stores said fluid;

(c) a micro-pump which communicates said fluid between said reservoir and said first membrane;

(d) at least one flextensional transducer which independently generate ultrasonic waves that are separately communicated into said living tissue and increase the permeability of said living tissue so as to facilitate transport of said fluid between said living tissue and said first membrane; and

(e) a microelectronics circuit which controls functionality of said at least one flextensional transducer and said micro-pump, said reservoir, said micro-pump, said at least one flextensional transducer, and said microelectronics disposed along one side of said first membrane.

2. The transdermal micro-patch of claim 1, further comprising:

(f) an adhesive dispose along said first membrane opposite of said at least one flextensional transducer.

3. The transdermal micro-patch of claim 1, further comprising:

(f) a second membrane with said micro-pump, said reservoir, said at least one flextensional transducer, and said microelectronics circuit disposed between said first membrane and said second membrane.

4. The transdermal micro-patch of claim 1, further comprising:

(f) a matrix disposed about said at least one flextensional transducer.

5. The transdermal micro-patch of claim 1, wherein said transdermal micro-patch delivers said fluid into said living tissue and/or removes said fluid from said living tissue.

6. The transdermal micro-patch of claim 1, wherein at least two of said flextensional transducers communicate separate waves into said living tissue which interact along at least one interaction zone.

7. The transdermal micro-patch of claim 1, further comprising:

(f) a sensor which monitors at least one condition within said transdermal micro-patch or said living tissue so as to facilitate adjustments to the performance of said at least one flextensional transducer and/or said micro-pump when said at least one condition is indicative of damage or irritation to said living tissue.

8. A method of delivering or extracting a fluid between a tissue and a transdermal micro-patch including a reservoir, a micro-pump, at least one flextensional transducer, a membrane, and a microelectronics circuit comprising the steps of:

(a) actuating said micro-pump to communicate said fluid between said reservoir and said membrane;

(b) actuating said at least one flextensional transducer to separately generate ultrasonic waves within said wound area, said ultrasonic waves increase the permeability within said tissue; and

(c) transporting said fluid between said membrane and said tissue, said actuating steps controlled by said microelectronics circuit.

9. The method of claim 8, wherein a large quantity of said fluid is extracted or delivered uninterrupted.

10. The method of claim 8, wherein said micro-pump has a removable cartridge that facilitates continuous transdermal fluidic delivery or extraction without adjustment, removal, or reconfiguration of said reservoir, said micro-pump, said at least one flextensional transducer, said membrane, and/or said microelectronics circuit, said transdermal micro-patch attached to said tissue so that said membrane acts as a barrier until the transdermal fluidic transfer is safe to continue.

11. The method of claim 8, wherein said actuating step is performed at a frequency in the range of 10 to 100 kHz.

12. The method of claim 8, wherein said transporting step moves said fluid from said tissue to said transdermal micro-patch and/or from said transdermal micro-patch to said tissue.

13. The method of claim 8, wherein said actuating step communicates at least two separate waves into said tissue which interact to enhance the performance of said transdermal micro-patch.

14. The method of claim 8, further comprising the steps of:

(d) sensing a condition within said transdermal micro-patch and/or said tissue; and

(e) adjusting the performance of said at least one flextensional transducer and/or said micro-pump when said condition is indicative of damage or irritation to said tissue.

15. The method of claim 14, wherein said condition is flow rate, pressure, temperature, voltage, current, frequency, or amplitude.

16. The method of claim 8, wherein a digital controlled piezo-transformer and a piezoelectric pump mechanism are electrically interconnected in a feedback arrangement so as to enable the highly efficient transfer of said fluid between said tissue and said membrane and between said membrane and said reservoir in a manner that is highly compact and lightweight.