Pharmacokinetic investigation of a 14C-labelled β3/α tetrapeptide in rats

Hansjörg Wiegand, Bernard Wirz, Alain Schweitzer, Gerhard Gross, Maria I. Rodriguez Perez, Hendrik Andres, Thierry Kimmerlin, Magnus Rueping, Dieter Seebach

Research output: Contribution to journalArticlepeer-review

35 Scopus citations


The solid-phase synthesis and an ADME investigation with albino and pigmented male rats of the doubly 14C-labelled β/α-tetrapeptide derivative Ac-β3hTyr-(D)Trp-β3hLys-β3hThr-lactone (3; Fig. 3) are described. After intravenous (i.v.) and peroral (p.o.) administration of the peptide, its concentration in blood and plasma, its tissue distribution, and the metabolism and the excretion of the peptide were analyzed over a period of up to 7 days post dose. The tetrapeptide in its ring opened form, 5, has a bioavailability of ca. 25%; radioactivity is distributed in the animals in an organ-specific way, and the compound appears to pass the blood-brain barrier to a very small extent, if at all (Tables 1 - 3 and Figs. 2 - 6). Excretion (37% renal, 44% fecal, including biliary) of the tetrapeptide 4 days after i.v. administration is almost complete, with only 4.3% remaining in the carcass; 4 days after p.o. administration 97% of the dose has been excreted in the feces. Radiochromatograms taken of plasma (0.5 and 24 h after i.v. dosing) and of urine and feces extracts (0 - 48 h collected) reveal the presence of lactone 3 and/or the corresponding hydroxy acid 5 with essentially no or very minor other peaks, respectively, representing possible metabolites (Tables 4 - 6, and Fig. 7 and 8). A comparison with a previous ADME investigation of a β-nonapeptide show that - except for the lack of metabolism - all aspects of exposure, distribution, and elimination are different (structure-specific properties). The investigated tetrapeptide 3 is a potent and highly specific agonist of the somatostatin receptor hsst4 , rendering the results described herein promising for diagnostic and therapeutic applications of β-peptides.

Original languageEnglish (US)
Pages (from-to)1812-1828
Number of pages17
JournalChemistry and Biodiversity
Issue number11
StatePublished - Nov 2004
Externally publishedYes

ASJC Scopus subject areas

  • Bioengineering
  • Biochemistry
  • General Chemistry
  • Molecular Medicine
  • Molecular Biology


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