scholarly journals Regional Differences in the Components of Luminal Water from Rat Gastrointestinal Tract and Comparison with Other Species.

2012 ◽  
Vol 15 (4) ◽  
pp. 510 ◽  
Author(s):  
Yusuke Tanaka ◽  
Toshihiro Hara ◽  
Ryoichi Waki ◽  
Shunji Nagata

Purpose. The bile acids, phospholipids, inorganic ions, and pH in luminal fluid are very important factors for the dissolution and oral absorption of solid drugs. In this study, we evaluated the regional differences in these factors in the rat GI tract. The solubility of griseofulvin, a poorly water-soluble drug, in the luminal fluid in each segment was also measured. In addition, the data from rats were compared with those from other species published previously to evaluate the species differences in the composition of luminal fluid. Methods. Rat abdomen was opened and residual water was sampled from each region of GI tract to measure the various components concentrations. Results. The total bile acid and phospholipid concentrations were much higher in the lower jejunum and upper jejunum, respectively, than in the other regions. The solubilities of griseofulvin in the lower jejunal fluid (153-260 g/mL) were about 1.5-2 times higher than those in the upper jejunal fluid (99-146 g/mL). The regional differences in inorganic ions and pH were also observed. As for species differences, the total bile acid and phospholipid concentration in rats GI tract were much higher than those of dogs and humans. Conclusion. These informations about the regional differences and species differences of the components in the GI fluid should be very useful to consider dissolution and oral absorption of solid drugs.

2019 ◽  
Vol 24 (8) ◽  
pp. 992-1001
Author(s):  
Yuri Ikeuchi-Takahashi ◽  
Yudai Shiokawa ◽  
Kazuki Sekita ◽  
Etsuo Yonemochi ◽  
Hiraku Onishi

Drug Delivery ◽  
2008 ◽  
Vol 15 (8) ◽  
pp. 503-514 ◽  
Author(s):  
Stéphanie Poullain-Termeau ◽  
Sylvie Crauste-Manciet ◽  
Denis Brossard ◽  
Saleh Muhamed ◽  
Georges Nicolaos ◽  
...  

2011 ◽  
Vol 140 ◽  
pp. 200-205
Author(s):  
Na Zhang ◽  
Na Zhang ◽  
Dan Dan She ◽  
Lian Dong Hu ◽  
Hong Fang Liu

The purpose of the current investigation was to improve the solubility of daidzein, a poorly water-soluble drug which exhibits low oral absorption bioavailability, in a self-micro-emulsifying drug delivery system that is suitable for oral administration. A carefully executed central composite design was applied to screen the optimal formulation of daidzein SMEDDS. The formulations were characterized by solubility of the drug in the vehicle, droplet size, and emulsification time. The optimal formulation consists of 20 % ethyl oleate, 64 % OP emulsifier, and 16 % polyethylene glycol 400. The droplet sizes of drug-free SMEDDS and drug-loaded SMEDDS were 66.4 nm and 77.9 nm respectively. Additionally, the dissolution rate of daidzein from SMEDDS was significantly enhanced in comparison to pure drug. The data suggested that the daidzein SMEDDS was prepared successfully.


2011 ◽  
Vol 8 (3) ◽  
pp. 807-813 ◽  
Author(s):  
Shaoling Zhang ◽  
Kohsaku Kawakami ◽  
Marina Yamamoto ◽  
Yoshie Masaoka ◽  
Makoto Kataoka ◽  
...  

2011 ◽  
Vol 59 (6) ◽  
pp. 686-691 ◽  
Author(s):  
Hiroshi Miura ◽  
Makoto Kanebako ◽  
Hiroyuki Shirai ◽  
Hiroshi Nakao ◽  
Toshio Inagi ◽  
...  

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