Channeled by 213 nm The apparent permeability Tskoeffizient was prepared using the equation. in Section 2.5. 2.3. Initial screening of drug candidates in Calu-3 cell line model 2.3.1. Effect of concentration on the permeability tons of drug candidates by Calu 3 cell line model, each of the four drugs were dissolved in HBSS st, so prepare three levels of assessment: for rizatriptan, 5 × 104, 1103 and 5 × × 103 M were for meloxicam and lornoxicam, 5 prepared × 105, 1104 and 2 × × 104 M were used for nebivolol, a × 105, 2105 and 5 produced × × 105 M in HBSS were prepared 1% DMSO. The permeation studies were carried out in the same manner as the Durchl Described permeability of marker compounds. The concentrations of the drugs tested were determined by HPLC. The recovery and apparent permeability Tskoeffizienten of the tested compounds were cozy the equations. and in each case. 2.3.2. Effect of pH on the permeability T of drug candidates by Calu 3 cell line Rifapentine 61379-65-5 models rizatriptan, meloxicam and lornoxicam in HBSS, and concentrations of 5104 resolved St were became a × × 104 and 1104 m respectively defined. The pH value of L Shop solutions of drugs were adjusted to 6, 7, 8 and 9 with phosphorus Acid or sodium hydroxide prior to loading on heart tee apical Calu 3 monolayers. The permeation studies, the analysis of samples and calculations were as described above. 2.4. In studies in vivo absorption of meloxicam in the rat model 2.4.1. Animal M Nnliche Sprague Dawley rats weighing 220 240 g were provided by the Center for Animal Laboratory Services at the Chinese University of Hong Kong are available.
The rats were kept in a conditioned room under a 12/12 h light / dark cycle. The experiment was conducted after approval by the Animal Ethics Committee of the Chinese University of Hong Kong. Based on in vitro results for meloxicam in vivo study weight Was selected. Three groups of Diosmetin rats were assigned to different modes of administration of meloxicam with 7 8 rats in each group received. For oral and intravenous S administration was performed minor surgery, the rats on the day before the experiment. The rat was at Sthesiert by intraperitoneal injection of a mixture containing 60 mg / kg ketamine and 6 mg / kg xylazine. For oral administration, the right jugular vein of rats and was cannulated with a poly-. For the intravenous S administration, was the right jugular vein of rats and introduced with two polyethylene tubes for drug administration and blood sampling a cannula, respectively. The polyethylene-R Hrchen Were put out is then injected subcutaneously into the back of the rat. After surgery, the rat was to recover overnight fasting conditions with free access to water. For nasal administration, the rats were the first to Sthesiert by intraperitoneal injection of a mixture containing 60 mg / kg ketamine and 6 mg / kg xylazine on the day of the experiment. The rats were then placed in the supine position and the K Body temperature was passed through a W Rmelampe held. The Luftr Hre rats was through an incision in the neck pierced with a polyethylene tube inserted to assist breathing. In addition, a polyethylene-R hre Sealingly in the feeder HRE in the rear part of the Nasenh cave introduced to the flow of Arzneimittell Solution is to prevent.
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