نتایج جستجو برای: oral drug administrations

تعداد نتایج: 813791  

2014
F. Shi H. Tang W. Xie A. Anees Z. Yang X. Zhang

The pharmacokinetic behavior of enrofloxacin (EF) was investigated in geese after oral (p.o.) and intravenous (i.v.) administrations of a single dose of 20 mg/kg body weight. Plasma concentrations of EF and its active metabolite, ciprofloxacin, were determined by high performance liquid chromatography fluorescence method. Plasma concentrations versus time were analyzed by non-compartmental meth...

Esmaeil Tamadonfard, Firooz Hamzeh goshchi Nasrin Hamzeh gooshchi

In the present study, the effects of the acute and chronic oral administrations (po) of curcumin in the absence and presence of morphine and naloxone was investigated on the sensation of acute corneal pain in rats. Acute corneal pain was induced by the local application of hypertonic saline (5 M NaCl) on the corneal surface, and the number of eye wipes was then counted for 30 s. Subcutaneous (s...

Journal: :Anticancer research 2009
Jean-Pierre Delord Christian Puozzo Florence Lefresne Roland Bugat

BACKGROUND Vinorelbine (VRL)-cisplatin (CDDP) is an active doublet for advanced non-small cell lung cancer. CDDP has a narrow therapeutic index and may produce a cumulative nephrotoxicity over the treatment period. This study was to assess the risks of drug-drug interaction (DDI) over 3 consecutive cycles of VRL-CDDP combined treatments. PATIENTS AND METHODS An open-label, nonrandomised, phas...

Journal: :Antimicrobial agents and chemotherapy 2009
Min Zhu Sanjeev Kaul Partha Nandy Dennis M Grasela Marc Pfister

Characterization of the time course and magnitude of enzyme induction due to multiple inducers is important for interpretation of clinical data from drug-drug interaction studies. A population interaction model was developed to quantify efavirenz autoinduction and further induction with concurrent carbamazepine coadministration. Efavirenz concentration data in the absence and presence of carbam...

2011
Shuyu Xie Luyan Zhu Zhao Dong Yan Wang Xiaofang Wang WenZhong Zhou

The purpose of this study was to use solid lipid nanoparticles (SLN) to improve the pharmacological activity of ofloxacin. Ofloxacin-loaded SLN were prepared using palmitic acid as lipid matrix and poly vinyl alcohol (PVA) as emulsifier by a hot homogenization and ultrasonication method. The physicochemical characteristics of SLN were investigated by optical microscope, scanning electron micros...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2018
Naohiro Narita Akio Morohashi Kimio Tohyama Toshiyuki Takeuchi Yoshihiko Tagawa Takahiro Kondo Satoru Asahi

N-{4-Chloro-2-[(1-oxidopyridin-4-yl)carbonyl]phenyl}-4-(propan-2-yloxy)benzenesulfonamide (MLN3126) is an orally available chemokine C-C motif receptor 9 selective antagonist. In nonclinical pharmacokinetic studies of MLN3126, nonextractable radioactivity was observed in plasma after oral administration of 14C-labeled MLN3126 ([14C]MLN3126) to Sprague-Dawley (SD) rats. In this study, the nonext...

Journal: :Physiology & behavior 1976
R E Davis M Mitchell L Dolson

DAVIS, R. E., M. MITCHELL AND L. DOLSON. The effects of methallibure on conspeeific visual reinfbrcement, social display .frequency, and spawning in the Paradise Fish, Macropodus opercularis, {L.J Belontiidae. PHYSIOL. BEHAV. 17(1 ) 47 52, 1976 . Pretrial intramuscular administration of the antigonadotropin, methallibure suppressed operant responding for conspecific visual stimulation. Four adm...

2015
Megan J. Shram Bernard Silverman Elliot Ehrich Edward M. Sellers Ryan Turncliff

A novel clinical study design was used to evaluate the blockade of a selective short-acting μ-opioid agonist (remifentanil) in 24 opioid-experienced subjects. Samidorphan (3-carboxamido-4-hydroxynaltrexone) is a novel opioid modulator with μ-antagonist properties. Objective (pupil diameter) and subjective (visual analog scale) responses to repeated remifentanil and saline infusion challenges we...

2017
Bilin Liu Dan He Jianyong Wu Quan Sun Mi Zhang Qunyou Tan Yao Li Jingqing Zhang

To date there has not been any report on catan-ionic hybrid lipidic nano-carriers, let alone a report on applying them to deliver insoluble anti-tumor drugs. Catan-ionic hybrid lipidic nano-carriers containing curcumin (CUR-C-HLN) inherit the merits of catan-ionic systems, hybrid lipidic systems and nano-structured carriers (the second-generation substitute of solid lipidic nano-systems). Catan...

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