In Vitro Percutaneous Absorption of Thiamine Disulfide through Rat Skin from a Mixtrure of Propylene Glycol and Fatty Acid or Its Analog

抄録

Percutaneous absorption of thiamine disulfide, (TDS), a lipophilic derivative of thiamine, from a mixture of propylene glycol (PG) and fatty acid (FA) or its analog through rat skin was tested in vitro. Lauric acid (12 : 0) enhanced the absorption depending on its concentation in PG and showed a maximal enhancement at 10% w/v. At 10% w/v, lauryl alcohol also enhanced the absorption, but less than 12 : 0, while lauric acid methyl ester suppressed the absorption. The flux of TDS did not depend on the solubility of TDS in the vehicle, but on the permeability coefficient. From these rsults, it is suggested that FA increases the permeability coefficient not only because FA increases TDS diffusion by disrupting lipid packing in the stratum corneum but also, FA increases TDS partition to lipid plase by interacting with TDS.