Patent Grant
9022975
The present disclosure relates to flexible drip tip assemblies for use with devices that mix and apply two or more biologic components. More particularly, the present disclosure relates to a drip tip assembly for use with a biologic drip device, wherein the drip tip is capable of self-clearing as a result of a flexible outlet design.
Drip devices for dispensing two or more biocomponents are known. In the medical device field, such devices are typically used for applying bioadhesives, polymers and other synthetic material used in wound closure. Because of the reactant nature of the biocomponents used to form the bioadhesive, mixing of the components does not occur until the solution is ready to be applied. Mixing of the components too soon before application may result in premature hardening of the mixture, thereby making application of the solution impossible. Thus, in known drip devices, the two or more components are maintained separately until just prior to application. The drip devices include one or more mixing means for mixing the two or more solutions prior to application. The mixing means may be passive, i.e., spiral configuration in the tubing, or instead may be active, i.e., mixing blade or impeller. Once mixed, the solution may be applied through a needle-like output or may instead be ejected through a spray assembly. Thorough mixing of the two or more components prior to application is important to ensure that the solution will perform as intended.
An exemplary device is taught in U.S. Pat. No. 5,116,315, entitled “Biological Syringe System”, which discloses a system for delivery two fluids in a mixed composition, comprising a manifold and a discharge assembly. The discharge assembly mixes fluids in a mixing space and then atomizes the mixed fluids in a spray delivered from the assembly. Similarly, the device shown in U.S. Pat. No. 5,605,255, entitled, “Apparatus for Spraying a mixture of Two Components’, is an apparatus for spraying a liquid mixture having two syringes, a connecting piece, a premixing chamber, and a reduced volume section downstream from premixing chamber, and an exit aperture for spraying the mixture. The reduced volume section terminates in a homogenization region. U.S. Pat. No. 6,063,055, entitled “Turbulence Mixing Head for a Tissue Sealant Applicator and Spray Head for Same”, illustrates a device in which the mixing is performed in a mixing head.
Intermittent use of a biologics spray device, as may be required during a procedure, tends to clog the outlet of the applicator tip. As a result, most applicator assemblies are provided with a number of replacement tips for when clogging of the tip occurs. Replacing clogged applicator tips interrupts the flow of a procedure, is time consuming and is an added expense. The device in published U.S. Patent Application 2010/0096481, “Self-Cleaning Spray Tip”, is described as having the distal end of drip cap assembly with an outlet that changes its configuration—at rest and at a second condition (e.g. during expression). The distal end is described as comprised of a material that permits flexion and expansion. The first and second reactive components are introduced into swirl chambers before mixing and are atomized as ejected through the outlet in a cone-shaped spray
The invention described herein is a device for dripping a tissue sealant and/or adhesive that comprises a) first and second barrels or syringes that contain first and second biocomponents that are disposed between proximal and distal ends; b) a plunger in each barrel and c) a drip tip comprising i) a support having distal and proximal ends and at least two fluid passageways from the distal to the proximal end that are in fluid communication with one of the barrels of the dispensing device on the proximal end; and ii) an endcap that fits over the support having at least two flexible hinges, each hinge having a portion of their interior surface resting on a top surface of the distal end of the dual lumen support and distal outlets for the fluid passageways, wherein a mix chamber and an outlet are formed by expansion only when the first and second biocomponents are under sufficient dispensing pressure.
The present invention is in one embodiment directed to a device for mixing and drip dispensing two reactive biologic components as tissue sealant and/or hemostatic agent with a syringe support having holding elements for at least two syringes and an associated handle; at least a pair of syringes each having an outlet and containing a reactive biologic component; a first piston and second piston within the first and second syringes, respectively; a support having two separate fluid channels in communication with the syringe outlets for the first and second syringes; and an endcap that is positioned at the outlet of the support having an open proximal end and a closed distal end with a flexible diaphragm. The flexible diaphragm in combination with the distal face of the dual lumen support define a first volume and a second volume and a dispensing passageway, wherein said first volume is substantially zero and said second volume is sufficient to allow the two reactive biologic components to mix just prior to and/or during dispensing. Further, the dispensing passageway is closed when the first volume is substantially zero. The first volume of the flexible diaphragm transitions to said second volume in response to a dispensing pressure from the reactive biologic components flowing through the two fluid channels and transitions back to said first volume in response to a reduction of pressure acting on the biologic components within the fluid channels. The distal end of the endcap can be substantially circular, while the flexible diaphragm can be at least two flexible flaps that are circumferentially affixed to the endcap. Preferably, at least a portion of an interior-facing edge from each flexible flap is not affixed to the circumference of the endcap. The dispensing passageway through the endcap is preferably a linear gap as the flexible diaphragm expands distally in response to pressure from the lumens to dispense the components from the mixing volume.
In one embodiment, a polymeric layer or silicone oil is applied over at least one surface of the flexible diaphragm. The polymeric layer can contain a poly-para-xylylene material and/or derivatives thereof.
In another embodiment, the first syringe contains thrombin and the second syringe contains fibrinogen. Hence, the present invention is also directed to a method for delivering biologic components to achieve hemostasis and/or tissue sealant by drip dispensing from the device described above. The biologic components are preferably delivered in a surgical setting.
In another embodiment, the present invention is directed to an assembly for mixing and drip dispensing two reactive biologic components as tissue sealant and/or hemostatic agent having an endcap having a proximal end and distal end, wherein the proximal end is open and the distal end has a flexible diaphragm covering outlet of fluid passages, said flexible diaphragm in combination with the distal face of fluid passage outlets, defining a first volume and a second volume and a dispensing passageway, wherein said first volume is substantially zero and said second volume is sufficient to allow the two reactive biologic components to mix just prior to and/or during dispensing; and a support having at least two fluid passages that is positioned in the distal end of the endcap. Further, the dispensing passageway is closed when the first volume is substantially zero, and said first volume transitions to said second volume in response to a dispensing pressure from the reactive biologic components flowing through the fluid passages and transitions back to said first volume in response to a reduction of pressure acting on the biologic components within the fluid passages. The distal end of the endcap can be substantially circular while the flexible diaphragm can be at least two flexible flaps that are circumferentially affixed to the endcap. Preferably, at least a portion of an interior-facing edge from each flexible flap is not affixed to the circumference of the endcap. In one embodiment, a polymeric layer or silicone oil is applied over at least one surface of the flexible diaphragm. The polymeric layer is preferably poly-para-xylylene polymeric material and/or derivatives thereof.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the disclosure and, together with a general description of the disclosure given above, and the detailed description of the embodiment(s) given below, serve to explain the principles of the disclosure, wherein:
Referring initially to
The syringe bodies 14 are supported for sliding displacement on the holding element 38, because the resilient elastic holding clamps 40 extend by more than 180° and preferably by up to 200° around the syringe bodies 14 and thus enclose the syringe bodies 14 with a clamping force allowing for a relative displacement. The holding element 38 is arranged to bear on laterally protruding flanges 46 on the rear ends 22 of the syringe bodies 14, thus providing for a mutual abutment of holding element 38 and syringe body 14.
As evident from
With reference now to
Referring back to
With reference now to
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Mixing volume 88 is created as a result of pressure from the incoming biologic components flowing through first and second lumens 73, 75 that flexes and expands flaps 83, 85, while it holds the remainder of drip cap assembly 80 stays in place. Mixing volume 88 will exist for so long as sufficient pressure is applied against drip cap assembly 80. In the absence of sufficient pressure from the liquid components, drip cap assembly returns to the first operational state in which there is no liquid component mixing in mixing volume 88.
Mixing volume 88, when present, defines a substantially curved conical volume having a flat proximal surface formed by the outlets from first and second lumens 73, 75. The shape and volume mixing volume 88 must be sufficient to allow mixing of the two liquid components. Additionally, in order to ensure drip cap assembly 80 and flaps 83, 85 retain sufficient flexibility and functionality, it has been found that a coating of Parylene, silicone oil or similar materials should be applied. Parylene is the generic name for members of a specific polymer series. The basic members of the series, called Parylene N, is poly-para-xylylene, a completely linear, highly crystalline material. Parylene C is produced from the same monomer modified only by the substitution of a chlorine atom for one of the aromatic hydrogens. Parylene D is produced from the same monomer modified by the substitution of the chlorine atom for two of the aromatic hydrogens. Parylene coatings are applied by vacuum deposition. The Parylene series of polymers are known in the art and commercially available. Additionally, it has been found desirable to ensure complete curing of the flexible diaphragm prior to placement of the slit so that subsequent sterilization activities do not induce further curing or crosslinking reactions that can cause the slit to reseal.
The operation of spray device 10 will now be described as relates to the figures. Prior to use, drip cap assembly 80 is affixed to the distal end of elongated shaft 68. First and second holders (23, 24) with vessels 42 for sources of first and second component are next connected to first and second fluid control devices 48 and drawn into syringes 12. Once secured to manifold 60, first and second components may be activated by depression of syringe plungers (not shown), to initiate the flow of first and second components within first and second component channels 63, 65, respectively. The first and second components flow through first and second component channels 62, 64, through first and second component lumen 73, 75, respectively, and into drip cap assembly 80. The first and second components flowing from first and second component lumens 73, 75 enter mixing volume 88 where they are mix and are directed out through flaps 83, 85 and outlet 89.
During operation of drip cap assembly 80, momentary stoppages in the application of pressure for a period of time could result in the formation of a clog or obstruction that may obstruct outlet 89. However, as pressure is released, drip cap assembly 80 returns to its first operational state in which flaps 83, 83 rest directly against the outlets for first and second lumens 73, 75 to eliminate any clog or obstruction.
Although the illustrative embodiments of the present disclosure have been described herein with reference to the accompanying drawings, it is to be understood that the disclosure is not limited to those precise embodiments, and that various other changes and modifications may be effected therein by one skilled in the art without departing from the scope or spirit of the disclosure.
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| Number | Date | Country |
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| Number | Date | Country | |
|---|---|---|---|
| 20140074154 A1 | Mar 2014 | US |
