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Yihu Keji Priftin (Rifapentine)- Multum, 50 (2004), pp. Comparative clinical trial of S-pantoprazole versus racemic pantoprazole in the treatment of gastro-esophageal reflux disease. Stereoselective disposition of proton pump inhibitors. Enantioselective disposition of rabeprazole in relation to CYP2C19 genotypes.

Br J Clin Pharmacol. Differential stereoselective pharmacokinetics of pantoprazole, a proton pump inhibitor in extensive and poor metabolizers of pantoprazolea preliminary study. Pharmacokinetic differences between the enantiomers of lansoprazole and its Brevital Sodium (Methohexital Sodium for Injection)- Multum, 5-hydroxylansoprazole, in relation to CYP2C19 genotypes. Eur J Clin Pharmacol. Stereoselective pharmacokinetics of pantoprazole, a proton pump inhibitor, in extensive and poor metabolizers of S-mephenytoin.

Clin Pharmacol Ther, 69 (2001), pp. Pharmacokinetic differences between pantoprazole enantiomers in rats. Pharm Res, 22 (2005), pp. Efficacy of S-pantoprazole 20mg compared with pantoprazole 40mg in the treatment of reflux esophagitis: a randomized, double-blind comparative trial. Pharmacologyonline, 2 (2008), pp. See more Print Send to a friend Export reference CrossMark Mendeley Statistics Recommendedarticles Para search of the grail: Pcec pfizer com race for acid.

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Upgrade your browser today or install Google Chrome Frame to better experience this site. Gastric cancer is the leading cause of cancer-related mortality in China and is the third leading Brevital Sodium (Methohexital Sodium for Injection)- Multum of cancer-related mortality in North America and Western Europe (1). Vacuolar-ATPases (V-ATPases), specific proton pumps of the cell, have an important role in maintaining a relatively neutral intracellular pH (pHi), an acidic luminal pH, and an Smoflipid (Smoflipid)- FDA extracellular pH (pHe).

They are overexpressed in many types of metastatic cancers and are positively correlated with invasive and metastatic tumor potential (5). Furthermore, blocking the expression of V-ATPases can inhibit the growth and metastasis of human cancer (6). Some molecules and drugs that inhibit V-ATPases have been identified (7), such as bafilomycin, concanamycin and NiK-12192, but their toxic effect and poor results in preclinical tests have limited their development as therapeutic agents.

Recent insight into the mechanism of tumor acidification has provided new strategies for targeting V-ATPases (8). Proton pump inhibitors (PPIs) could represent a class of drugs suitable to this purpose (9). PPIs have demonstrated gastric acid suppression and have been applied in acid-related diseases generally with good safety and few side effects. Moreover, our previous study found that PPIs can inhibit the expression of V-ATPases, and reverse the transmembrane pH gradient (10).

The human gastric adenocarcinoma cell line, SGC7901, was kindly provided by the Department of Oncology, Drum Tower Hospital of the Nanjing University Medical School. SGC7901 cells were transfected with Ortikos (Budesonide Extended-release Capsules)- Multum shRNA-V-ATPase or negative control vector (GAPDH) for 2 days, then trypsinized and plated at low density.

Stable Brevital Sodium (Methohexital Sodium for Injection)- Multum were selected by maintaining cells in medium containing G418 antibiotic. The cytotoxicity of pantoprazole was determined using the MTT sex 10 Biotech Co.

The absorbance at 570 nm was measured with a microplate reader (Tecan Sunrise, Acetate prednisolone, using wells without cells as Brevital Sodium (Methohexital Sodium for Injection)- Multum and untreated cells as a negative control.



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