Methods and compositions for use in perfusion applications
Methods and compositions for use in perfusion applications are provided. In the subject methods, a subject or derivative thereof, e.g. isolated organ or tissue, is infused, perfused and/or transfused with at least two fluid compositions. The first fluid composition is a non-naturally occurring biological buffer free plasma-like solution and the second fluid composition is a fluid blood composition. In a preferred embodiment, an additional volume of the first solution, or a derivative thereof, is administered to the patient following introduction of the fluid blood composition. Also provided are kits and systems for performing the subject methods. The subject methods and compositions find use in variety of perfusion applications, including the treatment of hypothermic surgical applications, cryogenic procedures, and the like.
1. A method of treating a subject for hypovolemia, said method comprising:
sequentially introducing to said subject at least one quantity of first, second and third types of fluid compositions, wherein:
(a) said first fluid composition is a conventional biological buffer free non-naturally occurring plasma-like solution comprising:
(i) electrolytes;
(ii) an oncotic agent;
(iii) and a dynamic buffering system;
(b) said second fluid composition is a fluid blood composition; and
(c) said third fluid composition is the same as said first fluid composition or is a derivative thereof;
to treat said subject for hypovolemia.
2. The method according to claim 1 , wherein said electrolytes include; Na + , Mg 2+ , Ca 2+ , and Cl—.
3. The method according to claim 2 , wherein said non-naturally occurring plasma-like solution further includes K + .
4. The method according to claim 1 , wherein said oncotic agent is a polymer.
5. The method according to claim 1 , wherein said dynamic buffering system comprises an organic carboxylic acid, salt or ester thereof.
6. The method according to claim 1 , wherein said non-naturally occurring plasma-like solution further includes a sugar selected from the group consisting of monosaccharides and disaccharides.
7. The method according to claim 1 , wherein said fluid blood composition is whole blood or a derivative thereof.
8. The method according to claim 7 , wherein said fluid blood composition is not terminally sterilizable.
9. The method according to claim 1 , wherein said method further comprises the introduction of at least one additional fluid composition.
10. The method according to claim 1 , wherein said method further comprises reducing the temperature of said subject.
11. The method according to claim 1 , wherein said method further comprises placing said subject into a hyperbaric environment.