Polyurea systems, processes for preparing the same and use thereof for postoperative adhesion barriers
Polyurea systems comprising: (a) an amino-functional aspartic ester of the general formula (I) wherein X represents an n-valent organic radical derived from a corresponding n-functional primary amine X(NH 2 ) n , R 1 and R 2 each independently represent an organic radical having no Zerevitinov active hydrogens and n represents an integer of at least 2; and (b) an isocyanate functional prepolymer having a residual monomer content of less than 1% by weight, the prepolymer prepared by reacting: (b1) an aliphatic isocyante; and (b2) a polyol component having a number average molecular weight of ≥400 g/mol and an average OH functionality of 2 to 6, wherein the polyol component comprises one or more constituents selected from the group consisting of polyester polyols, polyester-polyether polyols and mixtures thereof; processes for making the same; postoperative adhesions barriers prepared therewith and dispensing systems for such polyurea systems.
1. A polyurea system comprising:
(a) an amino-functional aspartic ester of the general formula (I)
wherein
X is an n-valent organic radical having 2 to 5 carbon atoms,
R 1 and R 2 each independently represent an organic radical having no Zerevitinov active hydrogens and n represents an integer of at least 2;
(b) an isocyanate functional prepolymer having a residual monomer content of less than 1% by weight, the prepolymer prepared by reacting:
(b1) an aliphatic isocyante; and
(b2) a polyol component comprising:
a polyether polyol which has a number-average molecular weight of 100 to 2,000 g/mol; and
a polyol component comprising one or more constituents selected from the group consisting of polyester polyols, polyester-polyether polyols and mixtures thereof having a number average molecular weight of ≥400 g/mol and an average OH functionality of 2 to 6;
wherein the ether groups are derived from, 60% to 90% of ethylene oxide units, based on the amounts of alkylene oxide units that are present in total,
(c) an organic filler comprising a hydroxy-functional polyether polyol compound having a DIN 53019 viscosity at 23° C. of 10 to 6000 mPas, and
wherein the ratio of free or blocked amino groups to free NCO groups is about 1:1.
2. The polyurea system according to claim 1 , further comprising: (d) a reaction product of an isocyanate functional prepolymer according to (b) and an amino-functional aspartic ester according to (a).
3. The polyurea system according to claim 1 , further comprising: (d) a reaction product of an isocyanate functional prepolymer according to (b); an amino-functional aspartic ester according to (a); and (c) an organic filler having a DIN 53019 viscosity at 23° C. of 10 to 6000 mPas.
4. The polyurea system according to claim 1 , wherein the polyol component has a hydroxyl number of 30 to 140 mg KOH/g, an acid number of 0.05 to 10 mg KOH/g and a DIN 53019 shear viscosity at 23° C. of 200 to 8000 mPas.
5. The polyurea system according to claim 1 , wherein the polyol component comprises ≤50% by weight of polyether polyols based on the polyol component.
6. The polyurea system according to claim 1 , wherein the polyol component has an ester group concentrations of 0.5 to 5.5 moles per kg.
7. The polyurea system according to claim 1 , further comprising: (d) a reaction product of an isocyanate functional prepolymer according to (b) and an amino-functional aspartic ester according to (a); wherein the polyol component has a hydroxyl number of 30 to 140 mg KOH/g, an acid number of 0.05 to 10 mg KOH/g and a DIN 53019 shear viscosity at 23° C. of 200 to 8000 mPas; wherein the polyol component comprises ≤50% by weight of polyether polyols based on the polyol component.
8. The polyurea system according to claim 1 , wherein the weight ratio of the organic filler (c) to the amino-functional aspartic ester component (a) is from 0:1 to 12:1.
9. A process for preparing a polyurea system, the process comprising:
(i) providing (a) an amino-functional aspartic ester of the general formula (I)
wherein
X is an n-valent organic radical having 2 to 5 carbon atoms,
R 1 and R 2 each independently represent an organic radical having no Zerevitinov active hydrogens and n represents an integer of at least 2;
(ii) providing (b) an isocyanate functional prepolymer having a residual monomer content of less than 1% by weight, the prepolymer prepared by reacting:
(b1) an aliphatic isocyante; and
(b2) a polyol component comprising:
a polyether polyol which has a number-average molecular weight of 100 to 2,000 g/mol; and
a polyol component comprising one or more constituents selected from the group consisting of polyester polyols, polyester-polyether polyols and mixtures thereof having a number average molecular weight of ≥400 g/mol and an average OH functionality of 2 to 6;
wherein the ether groups are derived from, 60% to 90% of ethylene oxide units, based on the amounts of alkylene oxide units that are present in total;
(iii) providing (c) an organic filler comprising a hydroxy-functional polyether polyol compound having a DIN 53019 viscosity at 23° C. of 10 to 6000 mPas; and wherein the (c) organic filler is mixed with the (a) amino-functional aspartic ester and the (b) isocyanate functional prepolymer at a weight ratio of organic filler to amino-functional aspartic ester of 0:1 to 20:1; and
(iv) mixing the (a) amino-functional aspartic ester and the (b) isocyanate functional prepolymer in a ratio of free or blocked amino groups to free NCO groups of 1:1.
10. A polyurea system prepared according to the process of claim 9 .
11. A method comprising:
(i) providing cell tissue to be treated;
(ii) providing a polyurea system according to claim 1 ; and
(iii) contacting the cell tissue to be treated with the polyurea system.
12. A post operative adhesion barrier comprising a polyurea system according to claim 1 .
13. A film comprising a polyurea system according to claim 1 .
14. A dispensing system comprising a first chamber and a second chamber; wherein the first chamber comprises (a) an amino-functional aspartic ester of the general formula (I)
wherein
X is an n-valent organic optionally branched or cyclic organic radical having 2 to 5 carbon atoms,
R 1 and R 2 each independently represent an organic radical having no Zerevitinov active hydrogens and n represents an integer of at least 2; and wherein the second chamber comprises (b) an isocyanate functional prepolymer having a residual monomer content of less than 1% by weight, the prepolymer prepared by reacting:
(b1) an aliphatic isocyante; and
(b2) a polyol component comprising:
a polyether polyol which has a number-average molecular weight of 100 to 2,000 g/mol; and
a polyol component comprising one or more constituents selected from the group consisting of polyester polyols, polyester-polyether polyols and mixtures thereof having a number average molecular weight of ≥400 g/mol and an average OH functionality of 2 to 6;
wherein the ether groups are derived from, 60% to 90% of ethylene oxide units, based on the amounts of alkylene oxide units that are present in total.