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Therapeutic Methods and Therapies TCIM
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1.
Comput Methods Programs Biomed ; 172: 11-24, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30902122

ABSTRACT

BACKGROUND: Magnetic drug targeting improves effectiveness of medicine application and reduces its side effects. In this method, drugs with magnetic core are released in the lung and they are steered towards the tumor by applying an external magnetic field. A number of researchers utilized numerical methods to study particle deposition in the lung, but magnetic drug delivery to the tumors in the human lung has not been addressed yet. METHOD: In the present study, Weibel model is used for human airway geometry from generation G0-G3. Moreover, a tumor is considered in the lung, which is located in G2. Particles are made of iron oxide magnetic cores and poly lactic coglycolic acid shells. Fluid flow is assumed laminar and particles are coupled with the fluid by one-way method. The magnetic field is produced by a coil with law current intensities instead of a wire with high current intensities. Influences of various parameters such as particle diameter, magnetic source position, current intensity, and inlet mass flow rate and tumor size on the deposition efficiency on the tumor surface are reported. RESULTS: Results show that magnetic drug targeting enhances deposition efficiency on the tumor surface Furthermore, when the current intensity rises from 10 (A) to 20 (A), tumor enlarging, and increasing particle diameter, lead to deposition efficiency enhancement, but efficiency decreases by increasing mass flow rate. However, when current intensity is 20 (A), deposition efficiency decreases in two situations. The first situation is when mass flow rate is 7 (L/min) and particle diameter is 9 (µm), and the second one is in 10 (L/min) mass flow rate and 9 (µm) diameter. CONCLUSION: The results demonstrated that magnetic drug targeting is applicable and suitable for all tumors specially for small tumors (r/R = 0.5 in this case) that efficiency increase from 0% in the absence of magnetic field to more than 2% in the presence of magnetic field.


Subject(s)
Computer Simulation , Drug Delivery Systems , Lung Neoplasms/drug therapy , Magnetic Field Therapy , Neoplasms/drug therapy , Algorithms , Drug Delivery Systems/methods , Humans , Imaging, Three-Dimensional , Models, Biological
2.
Pak J Biol Sci ; 12(12): 924-8, 2009 Jun 15.
Article in English | MEDLINE | ID: mdl-19777787

ABSTRACT

An experiment was conducted by eight lactating Holstein cows with an average milk production of 32.75 kg day(-1) and body weight of 643.6 kg to evaluate the effects of propylene glycol (PG) on productive performance, blood metabolites and nutrients digestibilities. In this experiment a balanced change-over design with four treatments and four periods with 21 days were employed. Treatments included: (1) Control (without PG), (2) 250 g PG/cow/day, (3) 500 g PG/cow/day and (4) 750 g PG/cow/day. Daily milk yield recorded and milk samples were taken during seven and two last days of each period. The results show that dry matter intake, milk yield, fat corrected milk yield, milk compositions were not affected (p > 0.05) by different levels of PG. Supplementing diets with 500 and 750 g PG/cow/day, significantly increased plasma glucose (p < 0.05) but other blood metabolites such as blood urea nitrogen, triglyceride and cholesterol were not affected (p > 0.05) by PG. Apparent digestibility of dry matter and organic matte was not affected (p > 0.05) by PG administration. In conclusion, plasma glucose was increased by using 500 and 750 g PG/cow/day (as powder) in the first and mid lactation stage, but the levels of 250 g PG/cow/day did not have any significant effect on dry matter intake, milk yield, milk compositions and other blood metabolites.


Subject(s)
Cattle/physiology , Lactation/drug effects , Propylene Glycol/administration & dosage , Animal Feed/analysis , Animals , Blood Glucose/metabolism , Cattle/blood , Eating/drug effects , Female , Lactation/blood , Lactation/physiology , Milk/chemistry , Milk/metabolism , Powders
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