Development of [NH3] Ammonia target for Cyclone-30 at KFSH&RC

Introduction Nitrogen [13N] NH3 is a liquid radioisotope, produced by medical cyclotrons for nuclear medicine application and widely applied for evaluation of myocardial perfusion in clinical assessments [1,2]. Owing to its short half-life (10 minutes), the unloading procedure of the radio-active solution of [13N]NH3 from the target is crucial in saving the activity produced for patient. Therefore, an efficient technique in un-loading the radioactive solution from the target body was developed using COMSOL Multiphysics. The new design of the target with improved unloading technique resulted in 30% increase of the available 13N activity. In our experiments, 13N was produced by the 16O(p,α)13N reaction. The energy of proton beam was 16.5 MeV. Material and Methods A 2D model was developed using COMSOL Multiphysics to simulate the inner geometry of [13N] Ammonia target. In the 2D model, water and aluminum were used as materials for the inner body and outer boundary (walls), respectively. The physical equations used to solve the problem of allocating proper place for the loading/unloading opening is turbulent, k-ε Module being extracted from fluid flow module. FIGURE 1 shows the result of simulating water flow on the target water channels. The entrance of the pushing solution (for unloading) was designed to create a turbulent flow inside the target body and, hence, to collect most of the activity inside the target. FIGURE 2 shows the setup for 13N production. A peristaltic pump is used to push the solution after irradiation to the hotcell at 6 ml/min flowrate. The distance from the target to the hotcell is approximately 30 meters. Results and Conclusion FIGURE 3 presents activity produced in milicurie (mCi) for several patient runs. The activity obtained in some experiments reached up to 330 mCi when we irradiated the target with 25 μA for 15 min. This was satisfactory for delivery to the patient at the nuclear medicine department. Moreover, purity of [13N] purity was above 95 % what meets the standard regulation for administration to a patient

A COMPARATIVE STUDY BETWEEN SIMULATED AND MEASURED BEAM'S QUALITY OF 30 MeV CYCLOTRON AT KFSHRC

Abstract At King Faisal Specialist Hospital and Research Centre (KFSHRC), the C-30 Cyclotron (manufactured by IBA) is used to produce radioisotopes for medical purposes. Working with very expensive machine dedicated for patients needs full attention and understanding of how beam can be controlled safely inside beam transport system. Moreover, knowledge of influence of magnetic lenses on charged particles is desired. Therefore, using off-line source such as PC-based beam simulator allows an operator to immediately see the effect of various magnetic lenses attached to the beam line. Initially, the magnetic field of quadruples and steering magnet was recorded using Hall probe Teslameter. The magnetic field values then uploaded into the Beam simulator in which beam quality was recorded and analysed

Dietary Patterns of Females with Cholecystolithiasis: A Comprehensive Study from Central Region of Saudi Arabia

BACKGROUND: Cholecystolithiasis is a worldwide gastrointestinal disorder and dietary pattern is one of the major risk factors involved in formation of cholelithiasis. AIM: This study was undertaken to determine the dietary patterns of female patients with cholecystolithiasis in the central region of Saudi Arabia. METHODS: A total of 332 females respondents were included, among them 157 were cholecystolithiasis cases, whereas 175 were healthy female subjects. All respondents were from central region of Saudi Arabia. Data were collected from a self-administered questionnaire and dietary patterns of studied population samples were compared by Chi-square test using SPSS software. RESULTS: The data showed that the consumption of meat from beef, lamb or goat, butter, ghee, pizza, cereals, legumes, coffee, tea, kabsa rice, tomatoes, and eggs was found to be positively associated with the risk of cholelithiasis. Interestingly, the data also demonstrated that consumption of cakes, chocolates, cookies, ice cream, doughnuts, chicken, fish or other sea foods, French fries, and hot dogs showed no relation with the risk of cholelithiasis. CONCLUSIONS: This study provides a comprehensive description of the dietary patterns of females from central region of Saudi Arabia and their association with the risk of onset of cholelithiasis. Specifically, the majority of non-vegetarian food stuffs showed positive association with the risk of development of cholelithiasis. These findings strongly recommended that the Health Ministry of Saudi Arabia should initiate the specific intervention public health programs on the dietary pattern in relation with the risk of cholelithiasis

Development of [NH3] Ammonia target for Cyclone-30 at KFSH&RC

Introduction Nitrogen [13N] NH3 is a liquid radioisotope, produced by medical cyclotrons for nuclear medicine application and widely applied for evaluation of myocardial perfusion in clinical assessments [1,2]. Owing to its short half-life (10 minutes), the unloading procedure of the radio-active solution of [13N]NH3 from the target is crucial in saving the activity produced for patient. Therefore, an efficient technique in un-loading the radioactive solution from the target body was developed using COMSOL Multiphysics. The new design of the target with improved unloading technique resulted in 30% increase of the available 13N activity. In our experiments, 13N was produced by the 16O(p,α)13N reaction. The energy of proton beam was 16.5 MeV. Material and Methods A 2D model was developed using COMSOL Multiphysics to simulate the inner geometry of [13N] Ammonia target. In the 2D model, water and aluminum were used as materials for the inner body and outer boundary (walls), respectively. The physical equations used to solve the problem of allocating proper place for the loading/unloading opening is turbulent, k-ε Module being extracted from fluid flow module. FIGURE 1 shows the result of simulating water flow on the target water channels. The entrance of the pushing solution (for unloading) was designed to create a turbulent flow inside the target body and, hence, to collect most of the activity inside the target. FIGURE 2 shows the setup for 13N production. A peristaltic pump is used to push the solution after irradiation to the hotcell at 6 ml/min flowrate. The distance from the target to the hotcell is approximately 30 meters. Results and Conclusion FIGURE 3 presents activity produced in milicurie (mCi) for several patient runs. The activity obtained in some experiments reached up to 330 mCi when we irradiated the target with 25 μA for 15 min. This was satisfactory for delivery to the patient at the nuclear medicine department. Moreover, purity of [13N] purity was above 95 % what meets the standard regulation for administration to a patient

Development of [NH3] Ammonia target for Cyclone-30 at KFSH&RC

Introduction Nitrogen [13N] NH3 is a liquid radioisotope, produced by medical cyclotrons for nuclear medicine application and widely applied for evaluation of myocardial perfusion in clinical assessments [1,2]. Owing to its short half-life (10 minutes), the unloading procedure of the radio-active solution of [13N]NH3 from the target is crucial in saving the activity produced for patient. Therefore, an efficient technique in un-loading the radioactive solution from the target body was developed using COMSOL Multiphysics. The new design of the target with improved unloading technique resulted in 30% increase of the available 13N activity. In our experiments, 13N was produced by the 16O(p,α)13N reaction. The energy of proton beam was 16.5 MeV. Material and Methods A 2D model was developed using COMSOL Multiphysics to simulate the inner geometry of [13N] Ammonia target. In the 2D model, water and aluminum were used as materials for the inner body and outer boundary (walls), respectively. The physical equations used to solve the problem of allocating proper place for the loading/unloading opening is turbulent, k-ε Module being extracted from fluid flow module. FIGURE 1 shows the result of simulating water flow on the target water channels. The entrance of the pushing solution (for unloading) was designed to create a turbulent flow inside the target body and, hence, to collect most of the activity inside the target. FIGURE 2 shows the setup for 13N production. A peristaltic pump is used to push the solution after irradiation to the hotcell at 6 ml/min flowrate. The distance from the target to the hotcell is approximately 30 meters. Results and Conclusion FIGURE 3 presents activity produced in milicurie (mCi) for several patient runs. The activity obtained in some experiments reached up to 330 mCi when we irradiated the target with 25 μA for 15 min. This was satisfactory for delivery to the patient at the nuclear medicine department. Moreover, purity of [13N] purity was above 95 % what meets the standard regulation for administration to a patient

Solubility and Thermodynamic Properties of Febuxostat in Various (PEG 400 + Water) Mixtures

The solubility of the poorly soluble medicine febuxostat (FXT) (3) in various {polyethylene glycol 400 (PEG 400) (1) + water (H2O) (2)} mixtures has been examined at 298.2–318.2 K and 101.1 kPa. FXT solubility was measured using an isothermal method and correlated with “van’t Hoff, Apelblat, Buchowski–Ksiazczak λh, Yalkowsky–Roseman, Jouyban–Acree, and Jouyban–Acree-van’t Hoff models”. FXT mole fraction solubility was enhanced via an increase in temperature and PEG 400 mass fraction in {(PEG 400 (1) + H2O (2)} mixtures. Neat PEG 400 showed the highest mole fraction solubility of FXT (3.11 × 10–2 at 318.2 K), while neat H2O had the lowest (1.91 × 10–7 at 298.2 K). The overall error value was less than 6.0% for each computational model, indicating good correlations. Based on the positive values of apparent standard enthalpies (46.72–70.30 kJ mol−1) and apparent standard entropies (106.4–118.5 J mol−1 K−1), the dissolution of FXT was “endothermic and entropy-driven” in all {PEG 400 (1) + H2O (2)} mixtures examined. The main mechanism for FXT solvation in {PEG 400 (1) + H2O (2)} mixtures was discovered to be an enthalpy-driven process. In comparison to FXT-H2O, FXT-PEG 400 showed the strongest molecular interactions. In conclusion, these results suggested that PEG 400 has considerable potential for solubilizing a poorly soluble FXT in H2O

Cellulosic biomass biocomposites with polyaniline, polypyrrole and sodium alginate: Insecticide adsorption-desorption, equilibrium and kinetics studies

This work was designed to synthesize and characterize biocomposites for the adsorptive elimination of insecticide (nitenpyram). Different biocomposites were synthesized of polyaniline (PAN-PH), polypyrrole (PPY-PH) and sodium alginate (Na-Al-PH) with cellulosic biomass of peanut husk (PH), which was characterized fourier-transform infrared spectroscopy (FTIR), pHpzc and scanning electron microscope (SEM). In batch mode, different variables, i.e., contact time, pH, temperature, NP (nitenpyram) concentration and adsorbent dose effects were investigated. The adsorption capacities of PH, PAN-PH, PPY-PH and Na-Al-PH were recorded to be 13.0, 14.43, 13.61 and 11.91 (mg/g), respectively at 30 °C, 60 min contact time, 0.05 g and 2.0 pH. Pseudo second order kinetic and Freundlich isotherm models best explained the NP adsorption data. An exothermic adsorption nature of NP adsorption was observed on to PH, PAN-PH, PPY-PH and Na-Al-PH. The NP desorption was efficient with NaOH and biocomposites are competent for the adsorptive removal of NP, which can utilized for NP remediation in effluents

The Optimization and Evaluation of Flibanserin Fast-Dissolving Oral Films

Flibanserin (FLB) is a drug used for female hypotensive sexual desire disorder approved by the FDA in August 2015. FLB exhibits extensive hepatic first-pass metabolism and low aqueous solubility, hence poor oral bioavailability. In this study, beta hydroxypropyl cyclodextrin-FLB inclusion complexes were incorporated into orally fast dissolving films. This dosage form was expected to improve FLB aqueous solubility, which would give fast onset of action and decrease presystemic metabolism, hence improving oral bioavailability. The inclusion complex at a ratio of 1:1 was prepared by the kneading method. Differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), and powder X-ray diffractometry (XRD) were used to confirm complex formation. The Box–Behnken design (15 different formulae of FLB fast-dissolving oral films (FLBFDOFs) were utilized for the optimization of the prepared films. The Expert Design 11 program was utilized to examine the effects of three selected factors, polymer concentration (X1), plasticizer concentration (X2), and disintegrant concentration (X3) on four responses: disintegration time (DT), initial dissolution rate (IDR), dissolution efficiency (DE), and film quality (QF). Numerical optimization was performed by minimizing disintegration time (Y1), while maximizing the initial drug dissolution rate (Y2), dissolution efficiency (Y3), and the quality factor (Y4). The statistical analysis showed that X1 has a significant positive effect on the disintegration time and a significant negative effect on IDR. While X2 and X3 produced a nonsignificant negative effect on IDR. Dissolution efficiency was maximized at the middle concentration of both X2 and X3. The best film quality was observed at the middle concentration of both X1 and X2. In addition, increasing X3 leads to an improvement in film quality. The optimized film cast from an aqueous solution contains hydroxypropyl cellulose (2%) as a hydrophilic film-forming agent and propylene glycol (0.8%) as a plasticizer and cross povidone (0.2%) as a disintegrant. The prepared film released 98% of FLB after 10 min and showed good physical and mechanical properties. The optimized formula showed a disintegration time of 30 s, IDR of 16.6% per minute, DE15 of 77.7%, and QF of 90%. This dosage form is expected to partially avoid the pre-systemic metabolism with a fast onset of action, hence improving its bioavailability that favors an advantage over conventional dosage forms

Amitriptyline-Based Biodegradable PEG-PLGA Self-Assembled Nanoparticles Accelerate Cutaneous Wound Healing in Diabetic Rats

The aim of this work was to study the healing activity of amitriptyline (Amitrip) in rat diabetic wounds. A nanoformula of the drug was prepared as Amitrip-based biodegradable PEG-PLGA self-assembled nanoparticles (Amitrip-NPs) with a mean particle size of 67.4 nm. An in vivo investigation was conducted to evaluate the wound-healing process of Amitrip-NPs in streptozotocin-induced diabetic rats. Wound contraction was accelerated in rats treated with Amitrip-NPs. Histological examinations confirmed these findings, with expedited remodeling and collagen deposition in the NPs-treated animals. The formula showed anti-inflammatory activities as demonstrated by inhibition of interleukin-6 (IL-6) expression and tumor necrosis factor-α (TNF-α) expression, as well as enhanced expression of interleukin-10 (IL-10). In addition, Amitrip-NPs protected against malondialdehyde (MDA) buildup and superoxide dismutase (SOD) and glutathione peroxidase (GPx) enzymatic exhaustion. The pro-collagen activity of Amitrip-NPs was confirmed by the observed enhancement of hydroxyproline wounded skin content, upregulation of Col 1A1 mRNA expression and immune expression of collagen type IV expression. Further, Amitrip-NPs significantly increased expression transforming growth factor-β1 (TGF-β1), vascular endothelial growth factor-A (VEGF-A), platelet-derived growth factor-B (PDGF-B) and cluster of differentiation 31 (CD31). In conclusion, the developed Amitrip-NPs expedited wound healing in diabetic rats. This involves anti-inflammatory, antioxidant, pro-collagen and angiogenic activities of the prepared NPs. This opens the gate for evaluating the usefulness of other structurally related tricyclic antidepressants in diabetic wounds

Effectiveness of using e-government platform "Absher" as a tool for noncommunicable diseases survey in Saudi Arabia 2019-2020: A cross-sectional study

Background: E-government platforms provide an opportunity to use a novel data source for population health surveillance (also known as e-health). Absher is a Saudi e-government platform with 23 million authenticated users, including residents and citizens in Saudi Arabia. All Absher users were invited to participate in a web-based survey to estimate the prevalence of noncommunicable diseases and their risk factors in Saudi Arabia. Objective: To assess the potential of using an e-government platform (Absher) to administer web-based health surveys. Methods: A cross-sectional, web-based health survey was administered to Absher users between April 2019 and March 2020. The survey instrument included eight items and too