Biomolecule drying process for long-term storage
The present invention relates to a method for producing a storable dry composition of biomolecule. First a composition is dispensed on a surface. The composition comprises at least a biomolecule, at least a liquid volatile component, at least a polysaccharide being designed for forming together with the at least a biomolecule and a part of the at least a liquid volatile component a matrix displaying a glass transition temperature Tg. Secondly, at least a part of the liquid volatile component is evaporated by adjusting the temperature of said composition to allow the formation of the matrix. Said evaporation step is initiated at an initial temperature T 1 , and finished up at a final temperature T 2 , said final temperature T 2 being above said initial temperature T 1.
1. A method for producing a storable dry composition of biomolecule, comprising:
(a) Dispensing at least a composition on a surface, the composition comprising:
(i) at least a biomolecule,
(ii) at least a liquid volatile component,
(iii) at least a polysaccharide being designed for forming together with the at least a biomolecule and a part of the at least a liquid volatile component a matrix displaying a glass transition temperature Tg,
(b) Evaporating at least a part of the at least a liquid volatile component by adjusting a temperature of said composition to allow formation of the matrix,
wherein step (b) is initiated at an initial temperature T 1 , and finished up at a final temperature T 2 , said final temperature T 2 being above said initial temperature T 1 .
2. A method according to claim 1 , wherein the initial temperature T 1 and final temperature T 2 are above the glass transition temperature Tg.
3. A method according to claim 1 , wherein a difference between the initial temperature T 1 and the glass transition temperature Tg and a difference between the final temperature T 2 and the glass transition temperature Tg remain constant and positive.
4. A method according to claim 1 , wherein the initial temperature T 1 is maintained between about 30° C. and about 50° C. during 30 minutes, and the final temperature T 2 is maintained between about 60° C. and about 90° C. during 30 minutes.
5. A method according to claim 1 , wherein step (b) is performed until a fraction of liquid volatile component of the composition reaches about 3%.
6. A method according to claim 1 , wherein step (b) is performed at initial temperature T 1 until a fraction of liquid volatile component of the composition reaches about 10%.
7. A method according to claim 1 , wherein the initial temperature T 1 is below 40° C.
8. A method according to claim 1 , wherein the final temperature T 2 is above 80° C.
9. A method according to claim 1 , wherein step (b) further makes use of a gas flow.
10. A method according to claim 1 , wherein the liquid volatile component is selected from a group comprising: water, alcohol, or a mixture thereof.
11. A method according to claim 1 , wherein the biomolecule is an enzyme for amplification reaction of nucleic acid.
12. A method according to claim 1 , wherein the composition comprises at least 0.1 M to 0.6 M of trehalose.
13. A method according to claim 1 , wherein the composition comprises at least 4.0 ug/uL to 8.0 ug/ul of Bovine Serum Albumin.
14. A method according to claim 1 , wherein the composition comprises at least 1.0% to 30.0% of glycerol.
15. A method according to claim 1 , wherein step (b) is performed until a fraction of liquid volatile component of the composition reaches about 2%.
16. A method according to claim 1 , wherein the composition comprises at least 0.15 M to 0.3 M of trehalose.
17. A method according to claim 1 , wherein the composition comprises at least 5.5 ug/uL to 6.5 ug/ul of Bovine Serum Albumin.
18. A method according to claim 1 , wherein the composition comprises at least 5.0% to 15.0% of glycerol.