High airway-to-blood transport of an opioid tetrapeptide in the isolated rat lung after aerosol delivery

被引:19
作者
Tronde, A [1 ]
Krondahl, E
von Euler-Chelpin, H
Brunmark, P
Bengtsson, UH
Ekström, G
Lennernäs, H
机构
[1] AstraZeneca R&D Lund, Discovery DMPK, SE-22187 Lund, Sweden
[2] BMC, Dept Pharm, SE-75123 Uppsala, Sweden
[3] AstraZeneca R&D Sodertalje, DMPK, SE-15185 Sodertalje, Sweden
[4] AstraZeneca R&D Sodertalje, BAC, SE-15185 Sodertalje, Sweden
[5] AstraZeneca R&D Sodertalje, TA Pain Control, SE-15185 Sodertalje, Sweden
关键词
opioid peptide; peptide metabolism; first-pass metabolism; drug delivery; absorption; permeability; inhalation; pulmonary; lung; isolated perfused lung; rat; Caco-2;
D O I
10.1016/S0196-9781(01)00624-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The airway-to-blood absorption of the mu-selective opioid tetrapeptide agonist Tyr-D-Arg-Phe-Phe-NH2 (MW 631.) was investigated in the isolated, perfused, and ventilated rat lung model. The lung metabolism of the peptide was compared after airway and vascular delivery. The concentrations of the parent tetrapeptide and five of its metabolites in the perfusate and in bronchoalveolar lavage fluid were analyzed by LC-MS. The metabolism of the peptide was higher after delivery to the airways compared to vascular delivery. However, the tetrapeptide was highly transported from the air-to-blood side to an extent of 47.8 +/- 10.7% in 2 h. In conclusion, the results prompt investigations of the pulmonary route as a successful alternative to parenteral delivery for this tetrapeptide. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:469 / 478
页数:10
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