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14C-NaVP and 14C-PEV Repeated Dose Study in Rat. Pharmacokinetic Study in Rats After Repeated Oral Administrations of 14C-valproic Acid Sodium Salt and 14C-valproic Acid Pivaloyl Oxymethyl Ester

14C-NaVP and 14C-PEV Repeated Dose Study in Rat. Pharmacokinetic Study in Rats After Repeated Oral Administrations of 14C-valproic Acid Sodium Salt and 14C-valproic Acid Pivaloyl Oxymethyl Ester

M Bertolino, D Acerbi, S Canali, C Giachetti, G Poli, P Ventura, G Zanolo

Eur J Drug Metab Pharmacokinet. Apr-Jun 1998;23(2):223-9.

PMID: 9725486

Abstract:

The absorption, excretion and tissue distribution of radioactivity after repeated oral equimolar doses of 14C-valproic acid sodium salt (NaVP) or 14C-valproic acid pivaloyl oxymethyl ester (PEV) was investigated in male rats treated once a day for 14 consecutive days. The 14th day plasma time-course of radioactivity after PEV administrations was characterised by a slow absorption rate with a delayed peak (tmax 2 h, Cmax 7.52 +/- 1.35 microg eq./ml), followed by a plateau lasting up to 8 h. After NaVP treatment, the main peak of radioactivity was observed 0.5 h after administration (Cmax 8.30 +/- 1.26 microg eq./ml) followed by a secondary peak due to biliary enterohepatic recycling. Starting from 4 h onwards, radioactivity levels after PEV treatment were higher than those after NaVP (AUCtau = 113.3 h.microg eq./ml after PEV vs 71.9 h.microg eq./ml after NaVP), but concentrations declined with similar terminal half-lives (52.8 h for PEV and 49.7 h for NaVP). Radioactivity recovered (0-432 h interval) in urine accounted for 79.3% (PEV) and 56.1% (NaVP) while, in faeces accounted for 9.1% (PEV) and 26.1% (NaVP) of total administered dose (14 days). The difference is attributable to a higher excretion of radioactivity in the bile for NaVP. The missing fraction in the total radioactivity balance is probably excreted in expired air, as observed in single dose studies. Radioactivity excreted in bile (0-8 h interval of the last 14th day) accounted for 5.1% (NaVP) and 0.23% (PEV) of the total administered dose (14 days). A possible explanation of this difference may be a different metabolism pattern for the two compounds. The negligible biliary excretion observed after PEV administration is probably due to an inhibition of the glucuronation of valproic acid (or other metabolites) caused by the pivalic acid. Due to the presence of the enterohepatic recycle, the radioactivity levels in intestine, 0.5 and 2 h after administration, were higher after NaVP administration. According to higher plasma levels, the radioactivity concentrations in liver, kidneys and some fat tissues were found to be slightly higher after PEV administration. At 120 h after the last treatment of both compounds, relevant tissue concentrations were observed in mesenteric lymphnodes, perirenal and brown fat. The tissue-plasma radio activity ratio appeared quite similar for the two compounds.

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Catalog Number	Product Name	Structure	CAS Number	Price
AP127062220	Biotinamidohexanoic acid 3-sulfo-N-hydroxysuccinimide ester sodium salt		127062-22-0	Price

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