2007, Number 1
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Bioquimia 2007; 32 (1)
Influence of vehicles on vanillin (4-hydroxy-3-metoxybenzaldehyde) pharmacokinetic, a single dose
Trapero-Quintana YM, Gonzáles-Delgado CA, Olivera-Ruano L, Correa A
Language: Spanish
References: 12
Page: 5-9
PDF size: 60.05 Kb.
ABSTRACT
The 4-hydroxy-3-metoxybenzaldehyde (vanillin) candidate agent for Sickle Cell Disease, a disease for which effective treatment doesn’t exist. It is necessary to develop preclinical studies of this made up with a formulation that guarantees its bioavailability. The references of the toxicological studies of 4-hydroxy-3-metoxybenzaldehyde only report its administration like component of the animal diet, reason why it is not safe to calculate the really absorbed quantity and the one wasted. It should be carried out a preformulation study looking for the vehicle that favors a better absorption and that you can use in the preclinical studies, through the oral administration for gastric intubation. We were studied three formulations (0.5% carboxymethylcelulose, 2% carboxymethylcelulose and 15% hydroalcoholic solution as reference) in Wistar rats. The purpose was to looking for the most appropriate for the toxicological studies of vanillin. We determined some pharmacokinetics parameters (ABCtotal, Cmax, tmax, t½, MRT, Tlag, Frel) of the three formulations. The 0.5% carboxymethylcelulose was selected because it offered the plasmatic levels that guarantee an appropriate exhibition level, determined using an analytic method for high performance liquid chromatography (HPLC), validated in the National Center of Toxicology.
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