1987 Fiscal Year Final Research Report Summary
New Mechod on Evaluating Fibrinolytic Activity using Calormitry
Project/Area Number |
60870079
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Research Category |
Grant-in-Aid for Developmental Scientific Research
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Allocation Type | Single-year Grants |
Research Field |
Physical pharmacy
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Research Institution | Toyama Medical & Pharmaceutical Univerisity |
Principal Investigator |
UENO Masaharu Department of Hospital Pharmacy, Toyama Medical & Pharmaceutical University, Associate Professor, 附属病院, 助教授 (40080197)
|
Co-Investigator(Kenkyū-buntansha) |
TAKAHASHI Kaoru Department of Central Clinical Laboratory, Toyama Medical & Pharmaceutical Unive, 附属病院, 助教授 (70135028)
ADACHI Isao Department of Hospital Pharmacy, Toyama Medical & Pharmaceutical University, Res, 附属病院, 助手 (30151070)
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Project Period (FY) |
1985 – 1987
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Keywords | Calorimetry / Fibrinolytic activity / Microcalorimeter / Flow-throgh-Cell / Urokinase / Fibrinogen / Plasminogen / プラスミン |
Research Abstract |
A novel method using calormetry on the evaluation of activity of fibrinolytic enzyme was developed. LKB microcaolrimeter equipped by flow-throug-cell was used. The protocol of the method was as follows: An enzyme and an excess amount of the substrate were mixed. The solution, in which the fibrinolytic reaction was in the steady state, was led to a thermodetector. The heat produced in unit time was measured. First, the reaction heat in two component system was measuted. Plasmin was used as a fibrinolytic enzyme. The reaction heat for fibrinogen, fibrin and casein as substrates of plasmin were measured. As fibrinogen showed the highest reaction heat, fibrinogen was adoptted as the substrate. Next, 3 component system i.e. urokinase, plasminogen and fibrinogen, was studied. Because of the practical 0 heat of the reaction from plasmininogen to plasmin, the heat observed in this system can be regraded as that of the reaction from fibrinogen to FDP by Plasmin. A linear relationship between UK concentration and observed heat was obtaind within the UK concentration of 0.5-20 unit/ml. Thus the method on evaluation of fibrinolitic activity using calorimetry was established. The methods using vescoelasticity and light transmittance were also studied.
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Research Products
(6 results)