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Pharmacokinetics studies of novel soybean iosflavone sulfonate in rats with HPLC

Zeyuan Deng

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Abstract

prodrug decision for novel soybean isoflavone sulfonate(DB) and study oral bioavailability of parent drug daidzein(DZ) in the prodrug were studied with HPLC.In the drug metabolism experiments,DZ were obviously detected in rat plasma after oral administration of DB.The results showed that the pharma cokinetic process of DZ was two compartment model after rats were ig given DB 50 mg/kg.The t1/2(h) was 7.86±3.60.The relative oral bioavailability of DZ in DB is only 26.8%.Although the relative oral bioavailability of parent drug DZ in prodrug did not achieve the desired improvement,the results show that DB is prodrug of DZ.

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What this paper is about

prodrug decision for novel soybean isoflavone sulfonate(DB) and study oral bioavailability of parent drug daidzein(DZ) in the prodrug were studied with HPLC.In the drug metabolism experiments,DZ were obviously detected in rat plasma after oral administration of DB.The results showed that the pharma cokinetic process of DZ was two compartment model after rats were ig given DB 50 mg/kg.The t1/2(h) was 7.86±3.60.The relative oral bioavailability of DZ in DB is only 26.8%.Although the relative oral bioavailability of parent drug DZ in prodrug did not achieve the desired improvement,the results show that DB is prodrug of DZ.

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Available abstract

prodrug decision for novel soybean isoflavone sulfonate(DB) and study oral bioavailability of parent drug daidzein(DZ) in the prodrug were studied with HPLC.In the drug metabolism experiments,DZ were obviously detected in rat plasma after oral administration of DB.The results showed that the pharma cokinetic process of DZ was two compartment model after rats were ig given DB 50 mg/kg.The t1/2(h) was 7.86±3.60.The relative oral bioavailability of DZ in DB is only 26.8%.Although the relative oral bioavailability of parent drug DZ in prodrug did not achieve the desired improvement,the results show that DB is prodrug of DZ.

Key concepts: Prodrug, Bioavailability, Pharmacokinetics, Chemistry, Oral administration, Pharmacology, High-performance liquid chromatography, Drug

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