Method for reducing biofilm formation

US10092308B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10092308-B2
Application numberUS-201514939552-A
CountryUS
Kind codeB2
Filing dateNov 12, 2015
Priority dateNov 12, 2014
Publication dateOct 9, 2018
Grant dateOct 9, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A two phase method for reducing the formation of biofilm includes an evacuation of ambient air from a region about the surgical or treatment site, to extract airborne or aerosolized bacteria ejected from the site by the treatment. The extracted bacteria are prevented from settling back onto the cleansed tissue surface, thus at least reducing colonial bacteriological growth and concomitantly exuded biofilm material. A second phase involves the attachment of one or more ultrasonic transducers to the patient over or near a surgical treatment site after the surgery is terminated. Each applied ultrasonic transducer is used to vibrate the patient's tissues at the treatment site to disrupt biofilm formation.

First claim

Opening claim text (preview).

What is claimed is: 1. An ultrasonic debridement instrument assembly comprising: a probe including a proximal body section, a smaller-diameter horn section, and a probe head, the horn section extending distally of said body section, said head being formed at a distal end of said horn section; and a rigid sheath shiftable relative to said probe for assuming a continuous range of longitudinal positions relative to the probe, said probe having a longitudinal channel for the delivery of liquid irrigant to an outlet in a distal end face of said probe head, said probe and said sheath defining a first space or channel and a second space or channel, said second space or channel being located proximally of said first space or channel and having a larger transverse cross-sectional area, in a plane orthogonal to an axis of said probe, than said first space or channel, said probe being provided at in a distal end portion with at least one aperture spaced from said outlet and communicating with said first space or channel, said sheath being configured to shift between a distal-most position wherein said probe head is covered and a proximal-most position wherein at least a portion of said probe head is exposed, said sheath being provided with an aspiration arm having an aspiration channel communicating with said first space or channel and said second space or channel. 2. The ultrasonic debridement instrument assembly defined in claim 1 wherein said rigid sheath includes a cylindrical rear section and a rectangularly prismatic forward section. 3. The ultrasonic debridement instrument assembly defined in claim 2 wherein said proximal body section is cylindrical and defines with said cylindrical rear section of said rigid sheath said second space or channel, said rectangularly prismatic forward section of said rigid sheath and said smaller-diameter horn section defining said first space or channel. 4. The ultrasonic debridement instrument assembly defined in claim 3 wherein said probe and said rigid sheath define an enlarged space or chamber between said first space or channel and said second space of channel. 5. The ultrasonic debridement instrument assembly defined in claim 4 wherein said aspiration channel of said aspiration arm communicates directly with said enlarged space or chamber. 6. The ultrasonic debridement instrument assembly defined in claim 4 wherein said aspiration channel of said aspiration arm is in direct communication with said first space or channel, distally of said enlarged space or chamber. 7. The ultrasonic debridement instrument assembly defined in claim 6 wherein said rigid sheath includes a rear sheath section inserted inside a handpiece casing, an O-ring seal being disposed between an outer surface of said rear sheath section and said handpiece casing. 8. The ultrasonic debridement instrument assembly defined in claim 7 wherein said probe head includes a plurality of teeth arranged in two mutually parallel rows along opposing edges or sides of a distal end face of said probe head. 9. The ultrasonic debridement instrument assembly defined in claim 1 wherein said probe and said rigid sheath define an enlarged space or chamber at a junction of said proximal body section and said smaller-diameter horn section, said aspiration channel communicating directly with or opening into said enlarged space or chamber. 10. The ultrasonic debridement instrument assembly defined in claim 1 wherein said aspiration channel of said aspiration arm is in direct communication with said first space or channel, distally of a junction between said proximal body section and said smaller-diameter horn section. 11. The ultrasonic debridement instrument assembly defined in claim 1 wherein said rigid sheath includes a rear sheath section inserted inside a handpiece casing, an O-ring seal being disposed between an outer surface of said rear sheath section and said handpiece casing. 12. The ultrasonic debridement instrument assembly defined in claim 1 wherein said probe head includes a plurality of teeth arranged in two mutually parallel rows along opposing edges or sides of a distal end face of said probe head.

Assignees

Inventors

Classifications

  • using mechanical vibrations, e.g. ultrasonic (A61B17/22012 takes precedence; dental tooth drilling devices operated by vibration A61C3/03; removing intra-ocular material using mechanical vibrations A61F9/00745) · CPC title

  • using mechanical vibrations, e.g. ultrasonic shock waves (A61B17/225 takes precedence) · CPC title

  • Effects, e.g. on tissue · CPC title

  • with suction drainage system · CPC title

  • Irrigation sleeves · CPC title

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Frequently asked questions

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What does patent US10092308B2 cover?
A two phase method for reducing the formation of biofilm includes an evacuation of ambient air from a region about the surgical or treatment site, to extract airborne or aerosolized bacteria ejected from the site by the treatment. The extracted bacteria are prevented from settling back onto the cleansed tissue surface, thus at least reducing colonial bacteriological growth and concomitantly exu…
Who is the assignee on this patent?
Misonix Inc, Misonix Inc
What technology area does this patent fall under?
Primary CPC classification A61B17/22004. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Oct 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).