Thromb Haemost 1985; 53(03): 415-418
DOI: 10.1055/s-0038-1661327
Original Article
Schattauer GmbH Stuttgart

Aspirin Kinetics and Inhibition of Platelet Thromboxane Generation-Relevance for a Solution of the “Aspirin Dilemma”

Chiara Cerletti
The Istituto di Ricerche Farmacologiche “Mario Negri”, Milano, Italy
,
Roberto Latini
The Istituto di Ricerche Farmacologiche “Mario Negri”, Milano, Italy
,
Aldo Del Maschio
The Istituto di Ricerche Farmacologiche “Mario Negri”, Milano, Italy
,
Ferruccio Galletti
The Istituto di Ricerche Farmacologiche “Mario Negri”, Milano, Italy
,
Elisabetta Dejana
The Istituto di Ricerche Farmacologiche “Mario Negri”, Milano, Italy
,
Giovanni de Gaetano
The Istituto di Ricerche Farmacologiche “Mario Negri”, Milano, Italy
› Institutsangaben
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Publikationsverlauf

Received 15. November 1984

Accepted 27. März 1985

Publikationsdatum:
18. Juli 2018 (online)

Summary

Six healthy male volunteers received aspirin (ASA) in a compressed (320 mg) and an enteric-coated (800 mg) formulation as single oral doses ten days apart. Ten plasma samples were obtained from each volunteer between 5 and 120 min after compressed ASA, and seven between 10 and 240 min after enteric-coated ASA.

ASA was undetectable (less than 100 ng/ml) in plasma from three subjects receiving compressed ASA and two receiving the enteric-coated preparation. Plasma levels and kinetic parameters of salicylate were the same in subjects with undetectable and detectable ASA plasma levels.

More than 98% inhibition of pre-drug serum TXB2 was noted in all samples collected one and four hours after either ASA preparation. TXB2 generation recovered on average by 3.5% at 24 hr with both preparations.

Thus inhibition of platelet TXB2 generation occurred independently of the amount of ASA reaching the peripheral circulation.

If this is due to inhibition of platelet function in the enterohepatic circulation followed by extensive first-pass deacetylation of ASA, vascular PGI2 synthesis could be spared.

A better knowledge of the kinetic parameters of ASA for each of the formulations used in thrombosis prevention trials might help in solving the “aspirin dilemma”.

 
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