• Yun-Seok Rhee, Seok Park, Tae-Won Lee, Chun-Woong Park, Tae-Young Nam, Tack-Oon Oh, Ji-Woong Jeon, Sang Beom Han, Dong-Soo Lee, and Eun-Seok Park.
• College of Pharmacy, Sungkyunkwan University, Suwon, Korea.
• Arch Pharm Res. 2008 Jul 1;31(7):911-7.

AbstractThe aim of this study was to examine the in vitro/in vivo relationship of the drug release behavior of a sustained-release formulation of gabapentin. The immediate-release formulation was used as the reference formulation. The dissolution test was employed using pH 1.2, 4.0, or 6.8 buffer solution, or water, to determine the in vitro release behaviors of gabapentin tablets. Gabapentin was released completely within 1 h from the immediate-release tablet and released for 12 h from the sustained-release tablet. A single dose (600 mg) of each formulation was orally administered to four beagle dogs under fasted conditions, and the pharmacokinetic parameters were calculated. Although the sustained-release tablet did not disintegrate and had slow drug release characteristics, it showed similar pharmacokinetic parameters to the immediate-release tablet, which rapidly disintegrated and showed fast drug release. Thus, the in vivo release of gabapentin did not correlate with in vitro release of drug.

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