Acta Pharm. 63 (2013) 545-551

 

full paper

Short communication

 

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

WEI LI, CAI-HONG SHI, YI-LING SHENG, PING CUI, YU-QING ZHAO and XIANG-RONG ZHANG

zhangxr@vip.sina.com

1 Shenyang Pharmaceutical University, Shenyang 110016, Liaoning Province, China

2 The First Hospital of China Medical University, Shenyang 110001, Liaoning Province, China

Accepted July 3, 2013

 

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 L1 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.

 

Keywords: salbutamol sulfate, press-coated tablet, PEG 6000-Eudragit S100 blends, dissolution, gamma scintigraphy