The present invention relates generally to devices and methods for extracting and macerating tissue.
Bone grafts are often used to treat fractures, gaps in bones caused by trauma or infection, revision joint surgery, and oral/maxillofacial surgery. Bone grafts provide a framework into which the host bone can regenerate and heal. Once implanted, the bone cells weave into and through the porous microstructure of the bone graft to support the new tissue, blood cells and soft tissue as they grow to connect fractured bone segments.
The loss or failure of tissue is one of the most frequent and costly problems in human health care. In recent years, grafting has evolved from the initial autograft and allograft preparations to biosynthetic and tissue-engineered living replacements. Tissue engineering enables the growth of transplantable functional tissue replacements starting from samples of autologous cells of the patient. The cells are obtained by harvesting tissue from a patient using a biopsy and then cells are extracted from the tissue sample and cultured to the appropriate numbers in the laboratory. These living cells are then placed in a three-dimensional natural or synthetic scaffold or matrix, and are kept under tissue specific culture conditions to ensure differentiation and tissue maturation. If provided with the appropriate conditions and signals, the cells will secrete various matrix materials to create an actual living tissue that can be used as a replacement tissue to be implanted back into the defective site in the patient.
Current tissue engineering procedures involve a multi-step process. First, a biopsy is performed to remove a tissue sample from a patient's body. A variety of biopsy devices are well known in the art, including, for example, high-pressure fluid jets that are effective to cut and retrieve a tissue sample. Once the biopsy procedure is complete, the tissue sample is then sent to a laboratory, where the tissue is prepared for cell isolation. The isolated cells can then be placed into a three-dimensional scaffold for subsequent growth and eventually implantation back into the patient.
While current procedures have proven effective, they can be very time-consuming and costly. Accordingly, there exists a need for more efficient and effective methods and devices for obtaining and processing a tissue sample. There also remains a need for an improved biopsy device that maximizes cell viability.
The present invention provides a tissue extraction and maceration device that is designed to effectively remove a viable tissue sample, to control the volume of tissue removed, and to macerate the tissue sample into particles having a predetermined size. In general, the device includes an outer tube having a substantially open distal end that is adapted to be placed on and to form a seal with a tissue surface, and a shaft that is rotatably disposed within the outer tube and that is movable between a first, proximal position in which the shaft is fully disposed within the outer tube, and a second, distal position in which a portion of a distal end of the shaft extends through the opening in the distal end of the outer tube. In one embodiment, a biasing element can be provided for biasing the shaft to the proximal position, and a trigger mechanism can be connected to the shaft to, upon actuation, overcome the biasing force to move the shaft from the proximal position to the distal position.
The device also includes a tissue harvesting tip formed on the distal end of the shaft. The tissue harvesting tip is effective to excise a tissue sample. In one embodiment, the harvesting tip can be a cone-shaped member having a plurality of cutting teeth formed on an outer surface thereof. In another embodiment, the harvesting tip can be a substantially semi-cylindrical housing having a cutting surface formed around a periphery thereof. While the harvesting tip can have a variety of configurations, it is preferably adapted to penetrate tissue to remove a predetermined volume of tissue when the shaft is moved from the proximal position to the distal position.
The device can further include a cutting member coupled to the shaft at a position proximal to the tissue harvesting tip. The cutting member, which is preferably in the form of at least one blade member extending radially from the shaft, is effective to macerate a tissue sample excised by the tissue harvesting tip. Each blade member can have a shape such as, for example, a rectangular shape, a curved shaped, a triangular shape, a square shape, an irregular shape, and combinations thereof.
In another embodiment, the device includes a sizing screen disposed within the outer tube and positioned proximal to the harvesting tip and the cutting member of the shaft. The sizing screen can have several openings formed therein for allowing tissue of a predetermined size to pass therethrough. The openings can optionally be defined by a wall having an upstream edge that is effective to cut tissue having a size greater than the circumference of the openings.
The present invention also provides a method for harvesting a tissue sample using a tissue extraction and preparation device having an outer tube with an open distal end, and a shaft rotatably disposed within the outer tube and including a tissue harvesting tip formed on the distal end thereof and a cutting member coupled to the shaft at a position proximal to the tissue harvesting tip. The method includes the steps of coupling the proximal end of the shaft to a driver mechanism, and positioning the open distal end of the outer tube against a tissue surface at a desired tissue sample site. The driver mechanism is then actuated to effect rotation of the shaft within the outer tube, and the shaft is moved from a proximal position, wherein the harvesting tip of the shaft is disposed within the outer tube, to a distal position, wherein the harvesting tip extends distally from the outer tube, thereby causing the harvesting tip to obtain a tissue sample. The shaft is then returned to the proximal position wherein the tissue sample is macerated by the cutting member. In a further embodiment, the outer tube can be coupled to a tissue dispensing device that is effective to deposit the macerated tissue sample onto a tissue scaffold.
The invention will be more fully understood from the following detailed description taken in conjunction with the accompanying drawings, in which like reference numerals designate like parts throughout the various figures, and wherein:
The present invention provides devices and methods for extracting and macerating tissue, and optionally for depositing the tissue onto a tissue scaffold. As shown in
The device is particularly advantageous in that it provides a simple, all-in-one device that can be operated using one hand. The device is designed to effectively remove a viable tissue sample, to control the volume of tissue removed, and to macerate the tissue sample into particles having a predetermined size.
The outer tube 12 of the device 10, which is shown in more detail in
In another embodiment, the outer tube 12 can include a sidearm 20 for mating the device 10 to a tissue collection device, or for otherwise allowing the tissue sample to be collected. The sidearm 20 is preferably disposed adjacent to the proximal end 12a of the device 10, and it preferably extends in a direction substantially transverse to the longitudinal axis L of the tube 12. The sidearm 20 can optionally be coupled to the outer tube 12 by a second tube 21 that extends around a portion of the outer tube 12 and that is attached to the sidearm 20. The sidearm 20 includes an inner lumen 20c that is in communication with the inner lumen 12c of the tube 12, such that all material flowing into the distal end 12b of the tube 12 and through the inner lumen 12c of the tube 12 will enter into the inner lumen 20c in the sidearm 20, rather than exit through the proximal end 12a of the outer tube 12. The distal end 20b of the sidearm 20 can include a connector 22 formed thereon for mating with an entry port formed in a tissue collection device, which will be discussed in more detail with respect to
The device 10 can also optionally include an outer housing 26 that extends around a portion of the proximal end 12a of the outer tube 12, and the sidearm 20, to facilitate handling of the device 10. The outer housing 26 can have virtually any shape and size, but it is preferably adapted to fit within a user's hands. In an exemplary embodiment, the outer housing 26 can include a rotating member 26a formed on a distal portion thereof for allowing rotation of the outer tube 12. As shown, the rotating member 26a is rotatably coupled to the housing 26, and it is positioned around and attached to the outer tube 12. As a result, the rotating member 26a can be used to control the position of the distal end 12b of the outer tube 12, thereby facilitating the proper placement of the distal end 12b of the outer tube 12 on a tissue surface. The rotating member 26a is preferably rotatable in a controlled fashion, rather than freely rotatable, such that the position of the outer tube 12 can be maintained during use.
Referring back to
The proximal end 14a of the shaft 14 also includes a trigger mechanism 24 that is effective to move the shaft 14 between the proximal and distal positions. While the trigger mechanism 24 can have a variety of configurations,
In order to allow the shaft 14 to return to the proximal position after the trigger mechanism 24 is actuated, the device 10 can include a biasing element that is effective to bias the shaft 14 to the proximal position. The biasing element can have a variety of configurations, such as, for example, a spring 28, and it can be coupled to the trigger mechanism 24, the driver mechanism 22, and/or the shaft 14. As shown in
In use, the spring 28 is compressed between the driver mechanism 22 and the outer tube 12, thereby creating a biasing force that is effective to push the driver mechanism 22, as well as the inner shaft 14, back into the proximal position. The spring 28 is also effective to create a hard stop between the driver mechanism 22 and the outer tube 12, thereby limiting the distance that the inner shaft 14 can extend from the distal end 12b of the outer tube 12. In an exemplary embodiment, the shaft 14 moves a distance, between the proximal and distal positions, that is in the range of about 1 mm to 5 mm, and more preferably about 3 mm. A person skilled in the art will appreciate that a variety of other techniques can be used to move the shaft 14 between the proximal and distal positions.
The distal end of the inner shaft 14, which is adapted to extend from outer tube 12 when moved into the distal position, preferably includes a tissue harvesting tip 16 that is adapted to retrieve a tissue sample. The tissue harvesting tip 16 can have a variety of configurations, but it is preferably adapted to retrieve a viable tissue sample without tearing or otherwise causing damage to the tissue. More particularly, the tissue harvesting tip 16 should allow for the rapid removal of cleanly cut tissue, rather than crushed or torn tissue. By way of non-limiting example,
While the harvesting tip 16 used with the device 10 of the present invention can have a variety of configurations, shapes, and sizes, the harvesting tip 16 is preferably effective to retrieve a predetermined amount of tissue. In an exemplary embodiment, the predetermined volume of tissue, per tissue sample, retrieve by the harvesting tip 16 is in the range of about 0.5 cm3 to 1.5 cm3, and more preferably about 0.9 cm3. A person skilled in the art will appreciate that a variety of tissue harvesting tips can be used with the present invention, and that
The distal end 14b of the shaft 14 can also include a cutting member 18, which is preferably disposed around the shaft 14 at a positioned just proximal to the tissue harvesting tip 16. The cutting member 18 can have a variety of shapes and sizes, but it is preferably effective to macerate the tissue sample excised by the tissue harvesting tip 16. Similar to the tissue harvesting tip 16, the cutting member 18 should be effective to cut, rather than tear, the tissue to allow a viable tissue sample to be obtained. By way of non-limiting example,
The device 10 can also optionally include a sizing screen 32, as shown in
In use, the device 10 is connected to a vacuum source (preferably via the sidearm 20) that is effective to create a vacuum within the inner lumen 12c of the outer tube 12, and the distal end 12b of the outer tube is positioned against tissue surface 50, as shown in
As previously indicated, the tissue sample can be collected into a tissue collection device. While virtually any tissue collection device can be used,
The features and other details of the invention will now be more particularly described and pointed out in the claims. It will be understood that the particular embodiments of the invention are shown by way of illustration and not as limitations of the invention. Those skilled in the art will know, or be able to ascertain, using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. These and all other equivalents are intended to be encompassed by the following claims.
This application is a divisional of U.S. application Ser. No. 10/661,460 filed Sep. 11, 2003, and entitled “Tissue Extraction and Maceration Device,” which is hereby incorporated by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
1337998 | Church | Apr 1920 | A |
3604417 | Stolzenberg | Sep 1971 | A |
3698561 | Babson | Oct 1972 | A |
3810545 | Filz et al. | May 1974 | A |
3814079 | Le Roy, Sr. | Jun 1974 | A |
3937222 | Banko | Feb 1976 | A |
4366822 | Altshuler | Jan 1983 | A |
4438769 | Pratt et al. | Mar 1984 | A |
4469153 | Morrisette | Sep 1984 | A |
4553553 | Homann et al. | Nov 1985 | A |
4649919 | Thimsen et al. | Mar 1987 | A |
4690672 | Veltrup | Sep 1987 | A |
4842578 | Johnson et al. | Jun 1989 | A |
4844064 | Thimsen et al. | Jul 1989 | A |
4960130 | Guirguis | Oct 1990 | A |
5041138 | Vacanti et al. | Aug 1991 | A |
5077012 | Guirguis | Dec 1991 | A |
5108381 | Kolozsi | Apr 1992 | A |
5108422 | Green et al. | Apr 1992 | A |
5186714 | Boudreault et al. | Feb 1993 | A |
5195956 | Stockmeier et al. | Mar 1993 | A |
5197483 | Rogalsky et al. | Mar 1993 | A |
5206023 | Hunziker et al. | Apr 1993 | A |
5252301 | Nilson et al. | Oct 1993 | A |
5269785 | Bonutti | Dec 1993 | A |
5333627 | Mehringer et al. | Aug 1994 | A |
5338294 | Blake, III | Aug 1994 | A |
5370609 | Drasler et al. | Dec 1994 | A |
5387236 | Noishiki et al. | Feb 1995 | A |
5398690 | Batten et al. | Mar 1995 | A |
5403317 | Bonutti | Apr 1995 | A |
5489291 | Wiley | Feb 1996 | A |
5494044 | Sundberg | Feb 1996 | A |
5526822 | Burbank et al. | Jun 1996 | A |
5527330 | Tovey | Jun 1996 | A |
5551778 | Hauke et al. | Sep 1996 | A |
5575293 | Miller et al. | Nov 1996 | A |
5593423 | Person et al. | Jan 1997 | A |
5649547 | Ritchart | Jul 1997 | A |
5694951 | Bonutti | Dec 1997 | A |
5759190 | Vibe-Hansen et al. | Jun 1998 | A |
5788667 | Stoller | Aug 1998 | A |
5804366 | Hu et al. | Sep 1998 | A |
5827305 | Gordon | Oct 1998 | A |
5871454 | Majlessi | Feb 1999 | A |
5871462 | Yoder et al. | Feb 1999 | A |
5900361 | Klebe | May 1999 | A |
5913859 | Shapira | Jun 1999 | A |
5944686 | Patterson et al. | Aug 1999 | A |
5949044 | Walker et al. | Sep 1999 | A |
6010476 | Saadat | Jan 2000 | A |
6017348 | Hart et al. | Jan 2000 | A |
6022354 | Mercuri et al. | Feb 2000 | A |
6053923 | Veca et al. | Apr 2000 | A |
6066153 | Lev et al. | May 2000 | A |
6071284 | Fox | Jun 2000 | A |
6110176 | Shapira | Aug 2000 | A |
6120514 | Vibe-Hansen et al. | Sep 2000 | A |
6135977 | Drasler et al. | Oct 2000 | A |
6174313 | Bonutti | Jan 2001 | B1 |
6179840 | Bowman | Jan 2001 | B1 |
6214369 | Grande et al. | Apr 2001 | B1 |
6216573 | Moutafis et al. | Apr 2001 | B1 |
6218182 | Naughton et al. | Apr 2001 | B1 |
6242247 | Rieser et al. | Jun 2001 | B1 |
6280398 | Ritchart et al. | Aug 2001 | B1 |
6299763 | Ashman | Oct 2001 | B1 |
6325806 | Fox | Dec 2001 | B1 |
6352555 | Dzau et al. | Mar 2002 | B1 |
6358252 | Shapira | Mar 2002 | B1 |
6364884 | Bowman et al. | Apr 2002 | B1 |
6375635 | Moutafis et al. | Apr 2002 | B1 |
6378527 | Hungerford et al. | Apr 2002 | B1 |
6402766 | Bowman et al. | Jun 2002 | B2 |
6423073 | Bowman | Jul 2002 | B2 |
6436110 | Bowman et al. | Aug 2002 | B2 |
6447517 | Bowman | Sep 2002 | B1 |
6451017 | Moutafis et al. | Sep 2002 | B1 |
6485436 | Truckai et al. | Nov 2002 | B1 |
6497707 | Bowman et al. | Dec 2002 | B1 |
6511493 | Moutafis et al. | Jan 2003 | B1 |
6537567 | Niklason et al. | Mar 2003 | B1 |
6543455 | Bonutti | Apr 2003 | B2 |
6554852 | Oberlander | Apr 2003 | B1 |
6572578 | Blanchard | Jun 2003 | B1 |
6669710 | Moutafis et al. | Dec 2003 | B2 |
6736799 | Erbe et al. | May 2004 | B1 |
D491807 | Cauldwell et al. | Jun 2004 | S |
D494063 | Cauldwell et al. | Aug 2004 | S |
6783532 | Steiner et al. | Aug 2004 | B2 |
6846314 | Shapira | Jan 2005 | B2 |
6852330 | Bowman et al. | Feb 2005 | B2 |
6875442 | Holy et al. | Apr 2005 | B2 |
6878338 | Taylor et al. | Apr 2005 | B2 |
6884428 | Binette et al. | Apr 2005 | B2 |
6921380 | Epstein et al. | Jul 2005 | B1 |
7115100 | McRury et al. | Oct 2006 | B2 |
7270284 | Liao et al. | Sep 2007 | B2 |
7611473 | Boock et al. | Nov 2009 | B2 |
7794408 | Binette et al. | Sep 2010 | B2 |
20010043918 | Masini et al. | Nov 2001 | A1 |
20020007190 | Wulfman et al. | Jan 2002 | A1 |
20020029055 | Bonutti | Mar 2002 | A1 |
20020045903 | Bonutti | Apr 2002 | A1 |
20020052628 | Bowman | May 2002 | A1 |
20020055755 | Bonutti | May 2002 | A1 |
20020082631 | Bonutti | Jun 2002 | A1 |
20020091401 | Hellenkamp | Jul 2002 | A1 |
20020091403 | Bonutti | Jul 2002 | A1 |
20020091406 | Bonutti | Jul 2002 | A1 |
20020095157 | Bowman | Jul 2002 | A1 |
20020099401 | Bonutti | Jul 2002 | A1 |
20020099403 | Yoo | Jul 2002 | A1 |
20020106625 | Hung et al. | Aug 2002 | A1 |
20020119177 | Bowman et al. | Aug 2002 | A1 |
20020127265 | Bowman et al. | Sep 2002 | A1 |
20020161449 | Muschler | Oct 2002 | A1 |
20020169465 | Bowman et al. | Nov 2002 | A1 |
20020177802 | Moutafis et al. | Nov 2002 | A1 |
20030009237 | Bonutti | Jan 2003 | A1 |
20030012805 | Chen et al. | Jan 2003 | A1 |
20030032961 | Pelo et al. | Feb 2003 | A1 |
20030036801 | Schwartz et al. | Feb 2003 | A1 |
20030044444 | Malaviya et al. | Mar 2003 | A1 |
20030049299 | Malaviya et al. | Mar 2003 | A1 |
20030114875 | Sjostrom | Jun 2003 | A1 |
20030114936 | Sherwood et al. | Jun 2003 | A1 |
20030147935 | Binette et al. | Aug 2003 | A1 |
20030176881 | Barlev | Sep 2003 | A1 |
20030212456 | Lipchitz et al. | Nov 2003 | A1 |
20030225344 | Miller | Dec 2003 | A1 |
20040010320 | Huckle et al. | Jan 2004 | A1 |
20040078090 | Binette et al. | Apr 2004 | A1 |
20040092992 | Adams et al. | May 2004 | A1 |
20040097829 | McRury et al. | May 2004 | A1 |
20040121459 | Liao et al. | Jun 2004 | A1 |
20040126405 | Sahatjian et al. | Jul 2004 | A1 |
20040134502 | Mizuno et al. | Jul 2004 | A1 |
20040138664 | Bowman | Jul 2004 | A1 |
20040142861 | Mansbridge | Jul 2004 | A1 |
20040146546 | Gravett et al. | Jul 2004 | A1 |
20040169311 | Bonutti | Sep 2004 | A1 |
20040175408 | Chun et al. | Sep 2004 | A1 |
20040193071 | Binette et al. | Sep 2004 | A1 |
20040219182 | Gomes et al. | Nov 2004 | A1 |
20040243157 | Connor et al. | Dec 2004 | A1 |
20040267362 | Hwang et al. | Dec 2004 | A1 |
20050014252 | Chu et al. | Jan 2005 | A1 |
20050021035 | Groiso | Jan 2005 | A1 |
20050038520 | Binette et al. | Feb 2005 | A1 |
20050048644 | Hedrick et al. | Mar 2005 | A1 |
20050059905 | Boock et al. | Mar 2005 | A1 |
20050059986 | Bowman | Mar 2005 | A1 |
20050107814 | Johnston et al. | May 2005 | A1 |
20050113736 | Orr et al. | May 2005 | A1 |
20050113937 | Binette et al. | May 2005 | A1 |
20050113938 | Jamiolkowski et al. | May 2005 | A1 |
20050125077 | Harmon et al. | Jun 2005 | A1 |
20050177249 | Kladakis et al. | Aug 2005 | A1 |
20050203527 | Carrison et al. | Sep 2005 | A1 |
20050222687 | Vunjak-Novakovic et al. | Oct 2005 | A1 |
20050232967 | Kladakis et al. | Oct 2005 | A1 |
20050234549 | Kladakis et al. | Oct 2005 | A1 |
20060100569 | McRury et al. | May 2006 | A1 |
20060129086 | McRury et al. | Jun 2006 | A1 |
20070032740 | Quick et al. | Feb 2007 | A1 |
20070239067 | Hibner | Oct 2007 | A1 |
20080071192 | Hynes | Mar 2008 | A1 |
20080114389 | Johnston et al. | May 2008 | A1 |
20080234715 | Pesce et al. | Sep 2008 | A1 |
20100022915 | Boock et al. | Jan 2010 | A1 |
20100280406 | Binette et al. | Nov 2010 | A1 |
Number | Date | Country |
---|---|---|
0527312 | Feb 1993 | EP |
1389548 | Feb 2004 | EP |
1433423 | Jun 2004 | EP |
1514521 | Mar 2008 | EP |
3136640 | Jun 1991 | JP |
2001505460 | Apr 2001 | JP |
2001524844 | Dec 2001 | JP |
2003320013 | Nov 2003 | JP |
2004121167 | Apr 2004 | JP |
WO-9601135 | Jan 1996 | WO |
WO-9824372 | Jun 1998 | WO |
WO-9824373 | Jun 1998 | WO |
WO-9958066 | Nov 1999 | WO |
WO-9959500 | Nov 1999 | WO |
WO-0041648 | Jul 2000 | WO |
WO 2002015950 | Feb 2002 | WO |
WO-02089722 | Nov 2002 | WO |
WO-03045259 | Jun 2003 | WO |
2005086874 | Sep 2005 | WO |
WO-2007112751 | Oct 2007 | WO |
Number | Date | Country | |
---|---|---|---|
20100022915 A1 | Jan 2010 | US |
Number | Date | Country | |
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Parent | 10661460 | Sep 2003 | US |
Child | 12569165 | US |