Improving the Oral Bioavailability of Albendazole in Rabbits by the Solid Dispersion Technique

Author:

Kohri Naonori1,Yamayoshi Yasuko2,Xin He2,Iseki Ken2,Sato Naoki3,Todo Satoru3,Miyazaki Katsumi2

Affiliation:

1. Department of Pharmacy, Hokkaido College of Pharmacy, Hokkaido University, Kita-14-jo, Nishi-5-chome, Kita-ku, Sapporo 060-8648, Japan

2. Department of Pharmacy, School of Medicine, Hokkaido University, Kita-14-jo, Nishi-5-chome, Kita-ku, Sapporo 060-8648, Japan

3. First Department of Surgery, Hokkaido University Hospital, School of Medicine, Hokkaido University, Kita-14-jo, Nishi-5-chome, Kita-ku, Sapporo 060-8648, Japan

Abstract

Abstract We have investigated the oral bioavailability of granules of albendazole, a drug used for treating echinococcosis in man, prepared by the solid dispersion technique. Rapid dissolution and supersaturation were observed when hydroxypropylmethylcellulose and hydroxypropylmethylcellulose phthalate were used as carriers in the solid dispersion. They inhibited the crystallization of albendazole from the supersaturated solution and maintained an amorphous state for 8h. Gastric acidity-controlled rabbits were used to evaluate the variation in absorption after oral administration of the albendazole solid dispersion. For rabbits with low gastric acidity the bioavailability of orally administered albendazole in the granular form prepared by solid dispersion was more than three times that of albendazole in physical mixtures. These results suggest that the bioavailability of albendazole in solid dispersions might be high even if there is a great variation in the gastric pH of patients.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference18 articles.

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