US2019143000A1PendingUtilityA1

Methods of transplanting chondrocytes

Assignee: SCRIPPS HEALTHPriority: Oct 29, 2012Filed: Dec 7, 2018Published: May 16, 2019
Est. expiryOct 29, 2032(~6.3 yrs left)· nominal 20-yr term from priority
A61L 27/26A61L 27/54A61L 2430/06A61P 19/02A61L 27/3821A61L 27/44A61L 2430/02A61L 2300/64A61L 27/3817A61L 2300/412
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Claims

Abstract

Provided are tri-component matrices having collagen, hyaluronan, and chondroitin sulfate. Also provided are processes for producing a tri-component matrix. Additionally, provided are processes for providing cells capable of producing cartilage to a bone or cartilage defects.

Claims

exact text as granted — not AI-modified
1 .- 15 . (canceled) 
     
     
         16 . A process for producing a transplantation composition for cartilage engineering comprising:
 a) dissolving 0.5 mg to 5 mg of type II collagen per milliliter of a solution comprising an acid;   b) neutralizing the acid;   c) adding 0.25 mg to 3 mg of hyaluronan per milliliter of the solution; and   d) adding 0.25 mg to 3 mg of chondroitin sulfate per milliliter of the solution,   thereby producing a transplantation composition comprising a tri component matrix.   
     
     
         17 . The process of  claim 16 , wherein the acid is acetic acid. 
     
     
         18 . The process of  claim 16 , wherein the acetic acid is at a concentration of 0.01 M. 
     
     
         19 . The process of  claim 16 , wherein the acetic acid is neutralized with NaHCO 3  and HEPES. 
     
     
         20 . The process of  claim 16 , further comprising adding Medium 199 to the tri-component matrix. 
     
     
         21 . The process of  claim 16 , wherein step (c) comprises adding 1 mg/ml 1 mg of hyaluronan per milliliter of the solution. 
     
     
         22 . The process of  claim 16 , wherein step (d) comprises adding 1 mg/ml 1 mg of chondroitin sulfate per milliliter of the solution. 
     
     
         23 . The process of  claim 16 , wherein step (a) comprises dissolving 3 mg/ml 3 mg of type II collagen per milliliter of the solution. 
     
     
         24 . The process of  claim 16 , further comprising adding a plurality of cells comprising chondrocytes, chondroprogenitor cells, mesenchymal stem cells, iPS cells, iPS cells derived from chondrocytes, H9-derived chondroprogenitor cells, Sox-9 transduced chondrocytes, or any combinations thereof, to the tri-component matrix. 
     
     
         25 . The process of  claim 24 , wherein adding the plurality of cells comprises adding chondrocytes to the tri-component matrix. 
     
     
         26 . The process of  claim 24 , wherein adding the plurality of cells comprises adding chondroprogenitor cells to the tri-component matrix. 
     
     
         27 . The process of  claim 24 , wherein adding the plurality of cells comprises adding iPS cells to the tri-component matrix. 
     
     
         28 - 49 . (canceled) 
     
     
         50 . The process of  claim 16 , further comprising adding a fibrin adhesive to the tri-component matrix. 
     
     
         51 . The process of  claim 16  wherein the type II collagen is isolated type II collagen. 
     
     
         52 . The process of  claim 16  wherein the type II collagen is purified type II collagen. 
     
     
         53 . The process of  claim 16  wherein the type II collagen is non-denatured type II collagen. 
     
     
         54 . The process of  claim 53  wherein the non-denatured type II collagen is purified non-denatured type II collagen.

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