Assessment of treated wastewater produced from Al-Lajoun collection tanks of the wastewater treatment plant in Karak province was carried out in term of physical properties, its major ionic composition, heavy metals and general organic content, for both wastewater influent and effluent. Sampling was done in two periods during (2005-2006) summer season and during winter season to detect the impact of climate on treated wastewater quality. Soil samples were collected from Al-Lajoun valley where the treated wastewater drained, to determine the heavy metal and total organic carbon concentrations at same time. The study showed that the treated wastewater was low in its heavy metals contents during both winter and summer seasons, which was attributed to high pH value enhancing their precipitations. Some of the major ions such as Cl-, Na+, HCO33-, Mg2+in addition to biological oxygen demand and chemical oxygen demand were higher than the recommended Jordanian guidelines for drained water in valleys. The treated wastewater contained some organic compounds of toxic type such as polycyclic aromatic hydrocarbons. Results showed that the soil was low in its heavy metal contents and total organic carbon with distance from the discharging pond, which attributed to the adsorption of heavy metals, total organic carbon and sedimentation of suspended particulates. From this study it was concluded that the treated wastewater must be used in situ for production of animal fodder and prohibit its contact with the surface and groundwater resources of the area specially Al-Mujeb dam where it is collected.

Sixty-five sediment samples and 25 water samples were collected from Al-Mujib reservoir, central Jordan, in order to investigate the heavy metal and ionic contamination assessment. Therefore, to achieve this aim, water and sediment samples were collected during winter and summer seasons (2007) from Al-Mujib reservoir and the areas surrounding it. The study shows that there are elevated levels of SO 4 2-, Cl -and Na ? in reservoir water, which might originate from anthropogenic activities in the reservoir catchment area. In addition, the reservoir water has higher total hardness (TH) values together with high Ca and Mg contents. This might be attributed to pH of reservoir water and the nature of the rocks exposed in the catchment area. The average levels of heavy metals in reservoir sediments are Fe = 14,888.1, Cu = 17.8, Zn = 88.6, Ni = 38.7, Cd = 4.4, Mn = 337.9 and Pb = 6.1 mg/kg, which are lower than that observed in Wadi Al-Arab reservoir, northern Jordan. The values of enrichment factor are Cd = 35.5, Ni = 3.02, Zn = 2.54, Cu = 1.26, Mn = 1.2 and Pb = 0.57; these values indicate that heavy metals in sediments of Al-Mujeb reservoir have a different anthropogenic incrimination inputs. The study showed that the sediments are polluted with Cd, relatively contaminated with Ni and Zn and uncontaminated with respect to Mn, Pb and Cu.

Objective: A simple, Rapid, and sensitive HPLC method utilizing UV detection was developed and validated for the simultaneous estimation of Fluticasone propionate (FP) and Salmeterol xinafoate (SX) in solutions and in vitro human plasma. Methods: Chromatographic analysis was done on SUPELCO® RP-C18 column (150 x 4.6 mm, 5 μm particle size) with an isocratic mobile phase composed of methanol, acetonitrile, and water (50:20:30, v/v) mixture while flow rate was set to 1 ml/min. Detection with UV at maximum absorbance wavelength (ʎmax) values of 236 and 252 for FP and SX, respectively. Spiked plasma samples were liquid-liquid extracted by diethyl ether and reconstituted using methanol. Results: Method was accurate and precise over a linear (R2>0.995) range of (0.067-100 µg/ml) and (0.0333-50 µg/ml) for FP and SX, respectively. LOD/lOQ values were 0.13/0.6 and 0.06/0.3 µg/ml for FP and SX, respectively. The developed method was successfully applied for the analysis of FP and SX in spiked human plasma samples. The method is considered to be accurate and precise over a linear (R2>0.9969) range of (6.67-66.67 µg/ml) and (3.33-33.3 µg/ml) for FP and SX, respectively. Extraction efficiency was approved by recovery values of (94.98–102.46 %) and (96.54–102.62 %) for FP and SX, respectively. Conclusion: This validated method revealed simple and cheap extraction procedures and detectors, non-buffered mobile phase, and short retention times with excellent resolution.