In vitro dissolution and in vivo gamma scintigraphic evaluation of press-coated salbutamol sulfate tablets

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Abstract

The aim of this study was to investigate the in vitro and in vivo performance of salbutamol sulfate press-coated tablets for delayed release. The in vitro release behavior of press-coated tablets with the outer layer of PEG 6000/ Eudragit S100 blends (2:1) in pH 1.2 (0.1 mol L-1 HCl) and then pH 6.8 buffer solution was examined. Morphological change of the press-coated tablet during in vitro release was recorded with a digital camera. Release of salbutamol sulfate from press-coated tablets was less than 5 % before 3 h and was completed after 8 h in pH 6.8 phosphate buffer solution. In vivo gamma scintigraphy study carried out on healthy men indicated that the designed system released the drug in lower parts of the GI tract after a lag time of 5 hours. The results showed the capability of the system of achieving delayed release of the drug in both in vitro and in vivo gamma scintigraphy studies.

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Li, W., Shi, C. H., Sheng, Y. L., Cui, P., Zhao, Y. Q., & Zhang, X. R. (2013). In vitro dissolution and in vivo gamma scintigraphic evaluation of press-coated salbutamol sulfate tablets. Acta Pharmaceutica, 63(4), 545–551. https://doi.org/10.2478/acph-2013-0035

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