Medical product comprising a bioactive molecule immobilized to nanofibrillar cellulose, and a method for preparing thereof
The present application provides a method for preparing a medical product for covering tissue, the method comprising providing nanofibrillar cellulose, providing a bioactive molecule, and covalently bonding the bioactive molecule to the nanofibrillar cellulose. The present application also provides a medical product for covering tissue comprising a bioactive molecule covalently bound to nanofibrillar cellulose.
1. A method for preparing a medical product for covering tissue, such as skin, the method comprising
providing nanofibrillar cellulose having an average diameter of 200 nm or less,
providing a gauze,
providing a bioactive molecule,
incorporating the nanofibrillar cellulose to the gauze, and
covalently bonding the bioactive molecule to the nanofibrillar cellulose,
wherein the nanofibrillar cellulose is provided at a moisture content of, or adjusted to, 0-20% (w/w).
2. The method of claim 1 , comprising preparing at least one layer comprising the nanofibrillar cellulose.
3. The method of claim 1 , comprising carrying out the covalent bonding through primary amines or through sulfhydryl groups.
4. The method of claim 1 , comprising carrying out the covalent bonding in an aqueous medium.
5. The method of claim 1 , wherein the bioactive molecule is selected from proteins, peptides, nucleic acids, hormones, cytokines, photosensitizing molecules, and anti-cancer drugs.
6. The method of claim 1 , wherein the bioactive molecule is a quorum quenching protein.
7. The method of claim 1 , comprising providing the nanofibrillar cellulose at a moisture content of, or adjusting the moisture content of the nanofibrillar cellulose to the range of 1-10% (w/w).
8. The method of claim 1 , wherein the nanofibrillar cellulose, when dispersed in water, provides a Brookfield viscosity of at least 2000 mPa·s, measured at a temperature of 20° C.±1° C., a consistency of 0.8% (w/w) and at 10 rpm.
9. The method of claim 1 , wherein the nanofibrillar cellulose has an average diameter of a fibril in the range of 1-200 nm.
10. The method of claim 1 , wherein the nanofibrillar cellulose is selected from anionically modified nanofibrillar cellulose, cationically modified nanofibrillar cellulose, unmodified nanofibrillar cellulose, and oxidized nanofibrillar cellulose.
11. The method of claim 1 , comprising forming the medical product into a membrane, a patch, a plaster, a bandage, a dressing or a filter, or into a part of a plaster, a patch or a dressing.
12. A medical product for covering tissue comprising nanofibrillar cellulose having an average diameter of 200 nm or less, and a gauze, and
a bioactive molecule covalently bound to the nanofibrillar cellulose,
wherein the medical product has a moisture content in the range of 0-20% (w/w).
13. The medical product of claim 12 , wherein the nanofibrillar cellulose is present as a layer.
14. The medical product of claim 13 having a moisture content in the range of 1-10% (w/w).
15. The medical product of claim 12 , wherein the bioactive molecule is selected from proteins, peptides, nucleic acids, hormones, cytokines, photosensitizing molecules, and anti-cancer drugs.
16. The medical product of claim 12 , wherein the bioactive molecule is a quorum quenching protein.
17. The medical product of claim 12 , wherein the nanofibrillar cellulose, when dispersed in water, provides a Brookfield viscosity of at least 2000 mPa·s, measured at a temperature of 20° C.±1° C., a consistency of 0.8% (w/w) and at 10 rpm.
18. The medical product of claim 12 , wherein the nanofibrillar cellulose has an average diameter of a fibril in the range of 1-200 nm.
19. The medical product of claim 12 , wherein the gauze is a nonwoven gauze.
20. The medical product of claim 12 obtained with the method of claim 1 .
21. The medical product of claim 12 in a form of a membrane, a patch, a plaster, a bandage, a dressing or a filter, or as a part of a plaster, a patch or a dressing.
22. A method for treating a subject, such as a human subject, the method comprising
providing the medical product of claim 12 , and
applying the medical product onto a tissue of the subject.
23. The method of claim 22 , wherein the bioactive molecule is a quorum quenching protein and the treatment is to suppress or prevent bacterial biofilm formation.
24. The method of claim 22 wherein the treatment is treatment of skin wounds or other skin damages or injuries and the method comprises applying the medical product onto the skin wound, damage, or injury.
25. The medical product of claim 12 , wherein the nanofibrillar cellulose is selected from anionically modified nanofibrillar cellulose, cationically modified nanofibrillar cellulose, unmodified nanofibrillar cellulose, and oxidized nanofibrillar cellulose.
26. The medical product of claim 12 , wherein the nanofibrillar cellulose is TEMPO oxidized nanofibrillar cellulose.