Background: The study's objective was to estimate the effects of radiation on testosterone-related hormones and blood components in prostate cancer patients. N Materials and Method: This study aims to investigate the effects of radiation on 20 male prostate cancer patients at the Middle Euphrates Oncology Centre. Blood samples were collected before and after radiation treatment, with a total dose of 60- 70 Gy, The blood parameters were analyzed. The hospital laboratory conducted the blood analysis using an analyzer (Diagon D-cell5D) to test blood components before and after radiation. Hormonal examinations included testosterone levels, using the VIDASR 30 for Multiparametric immunoassay system Results: The study assessed the socio-demography of prostate cancer male patients, revealing that the majority were aged 69.55 t 10.76 years, with a weight of 75.3 t 10.84 Kg and height of 170.50 t 8.70 cm. The stage of cancer was assessed, with 25% of patients being IV and IIV, followed by II, IB, and V. Only one patient was at stage III. The Gleason Score (GS) was used to classify patients, with 40% being given a score of 7, followed by 6, 8, and 9 equally (20%). Total Prostate-specific Antigen (PSA) had a mean value of 12.87 t 2.78. Hematological analysis showed a significant decrease in random blood sugar levels, white blood cells, lymphocytes platelets, and hemoglobin levels after radiotherapy. Testosterone levels also declined after radiotherapy fractions. However, kidney functions like urea and creatinine levels increased after pelvic irradiation Conclusion: The study found that radiation treatment for prostate cancer significantly impacted blood components and hormones associated with testosterone. It led to reduced levels of random blood sugar, white blood cells, lymphocytes, platelets, haemoglobin, and testosterone. Additionally, high-energy therapeutic x-rays increased_ levels of urea and creatinine, indicating the need for strict monitoring and management of adverse effects.
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Siderophores are low molecular weight organic compounds produced by microorganisms growing under low iron concentration.In this study we describe the detection, production and extraction of siderophores secreted by Acinetobacter baumannii (Multiple-drug resistant ) pathogens. One hundered twenty Gram –negative non lactose fermenter bacilli isolates have been collected from three hospitals at Baghdad city over three months. Primary identification of these isolates is performed by standard diagnostic methods (biochemical tests and API 20 NE); 19 clinical isolates of A. baumannii are cultured on CHROMagar (highly selective medium for detection of MDR Acinetobacter) as well as diagnoses is documented by using Vitek 2 system. Isolates are exa
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Nanosponges (NS) of etodolac(ETO) was prepared using the emulsion solvent diffusion method ; the effects of drug: polymer ratio, the effect of level concentration of internal phase and stirring time and other variables that effect on the physical characteristics of NS were investigated and characterized, The selected formula was lyophilized then incorporated into hydrogel ; which also evaluated .The results show that the formulation that contain Drug: PVA:EC in ratio 1:3:2 is the best with smallest particle size 40.2±0.098 with polydispersibility0.005 and in vitro release 97.6±0.11%, , ETO NS Carbopol hydrogel produced a significant(p<0.05) improvement of the in vitro release than pure ETO hydrogel.
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The antibacterial activity of some extracts of A. eupatoria (aqueous and ethanolic) against some pathogenic bacteria (Staphylococcus aureus, Pseudomonas aeruginosa and Escherichia coli ) and their activity on wound healing in rats , also the presence of some active compounds in both extracts were detected . The results showed that the ethanolic extract was more effective on inhibiting tested bacteria than the aqueous extract . P.aeruginosa was the most resistant bacteria, while highest inhibition zone appeared on E.coli (20 mm) .There was a moderate activity against S.aureus with inhibition zone 15 mm. by using ethanolic extract (10 mg/ml) . The phytochemical analysis for detection of active compounds revealed the presence of Carbohydrate
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