Thromb Haemost 1995; 73(03): 488-494
DOI: 10.1055/s-0038-1653802
Original Articles
Fibrinolysis
Schattauer GmbH Stuttgart

Thrombolytic Treatment with Tissue-type Plasminogen Activator (t-PA) Containing Liposomes in Rabbits: a Comparison with Free t-PA

J L M Heeremans
The Dept. of Pharmaceutics, Utrecht Inst, for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands
,
R Prevost
The Dept. of Pharmaceutics, Utrecht Inst, for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands
,
M E A Bekkers
*   Gaubius Laboratory, TNO-PG, Leiden, The Netherlands
,
P Los
*   Gaubius Laboratory, TNO-PG, Leiden, The Netherlands
,
J J Emeis
*   Gaubius Laboratory, TNO-PG, Leiden, The Netherlands
,
C Kluft
*   Gaubius Laboratory, TNO-PG, Leiden, The Netherlands
,
D J A Crommelin
The Dept. of Pharmaceutics, Utrecht Inst, for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received 25. August 1994

Accepted after resubmission 29. November 1994

Publikationsdatum:
26. Juli 2018 (online)

Summary

In this study, we aimed at improving the therapeutic index of tissue- type Plasminogen Activator (t-PA) as thrombolytic agent in the treatment of myocardial infarction. Liposome-encapsulated t-PA was tested in a rabbit jugular vein thrombosis model: administration of free t-PA (t-PA) as a bolus injection in the ear vein was compared to a similar administration of liposomal t-PA (t-PA-lip), liposomal t-PA in plasminogen-coated liposomes (Plg-t-PA-lip), a mixture of free t-PA and empty liposomes (t-PA+empty lip) and a saline-blank (blank) in terms of thrombolytic activity and side effects.

Liposomal t-PA (t-PA-lip/Plg-t-PA-lip) showed a significantly better thrombolysis efficiency than equimolar doses of free t-PA (t-PA/ t-PA+ empty lip): about 0.24 mg/kg of liposomal t-PA practically equalled the lysis-activity of a dose of free t-PA of 1.0 mg/kg (t-PAlmg/kg). On the other hand, liposome encapsulation did not affect the systemic activation of alpha2-antiplasmin and plasminogen by t-PA.

We conclude that for this model an improvement in thrombolytic efficacy of t-PA is achieved by liposome encapsulation of t-PA. As t-PA-lip and Plg-t-PA-lip -treatment induced similar results, targeting of liposomal t-PA by coupled glu-Plg remains a topic to be optimized in future studies.

 
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