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R. N. Chena, H. O. Hob, C. Y. Yu and M. T. Sheub, “Development of Swelling/Floating Gastroretentive Drug Delivery System Based on a Combination of Hydroxyethyl Cellulose and Sodium Carboxymethyl Cellulose for Losartan and Its Clinical Relevance in Healthy Volunteers with CYP2C9 Polymorphism,” European Journal of Pharmaceutical Sciences, Vol. 39, No. 1, 2010, pp. 82-89. doi:10.1016/j.ejps.2009.10.015

has been cited by the following article:

• TITLE: Pharmacokinetics of Hydrochlorothiazide, Losartan and E3174 after Oral Doses of Losartan and Losartan/Hydrochlorothiazide in Healthy Chinese Male Volunteers

  AUTHORS: Sha Liu, Fan-Long Bu, Chun-Min Wei, Gui-Yan Yuan, Ben-Jie Wang, Rui-Chen Guo

  KEYWORDS: Losartan; E3174; hydrochlorothiazide; Pharmacokinetic; Phenotype; LC-MS

  JOURNAL NAME: Pharmacology & Pharmacy, Vol.3 No.1, January 12, 2012

  ABSTRACT: Aims: A simple and highly sensitive LC-MS method was used to determine the concentrations of losartan, its major active metabolite E3174 and hydrochlorothiazide in human plasma and pharmacokinetic characteristics and metabolism phenotype observation after administration of losartan tablets and losartan/hydrochlorothiazide combination tablets. Methods: An open, randomized cross-over single-dose study was designed in forty healthy male volunteers, A single-dose of 50 mg losartan tablets or 50 mg losartan/12.5 mg hydrochlorothiazide combination tablets was orally given and blood samples were collected at scheduled time. A LC-MS method was established and evaluated for determining the plasma concentrations of losartan, E3174 and hydrochlorothiazide. The pharmacokinetic parameters and characteristic of metabolism phenotypes were calculated and compared via this test. Results: The elimination rate of E3174 (t1/2) was significantly shorter (P 0–t was lower (P 1/2, AUC0–t and AUC0–inf of E3174.