List of Articles Particle Size

• Open Access Article
  • Abstract Page
  • Full-Text
  
  1 - Investigating the Particle Size of Chitosan-Based Drug Carriers for the Release of 5-Fluorouracil Antitumor Drug
  Mohammad Hossein Karami Majid Abdouss Mandana Karami
  Chitosan has been widely used as a natural biopolymer. The modification of chitosan for various applications can be easily achieved due to the abundant active groups (NH2 and OH) in the main chain. Controlled drug release makes the drug release rate predictable and repe More

  Chitosan has been widely used as a natural biopolymer. The modification of chitosan for various applications can be easily achieved due to the abundant active groups (NH2 and OH) in the main chain. Controlled drug release makes the drug release rate predictable and repeatable for prolonged release drugs. Drug delivery systems prepared from nanoparticles show several advantages, including improved efficiency and reduced toxicity. Using drug delivery systems based on nanoparticles loaded with anti-cancer agents is an effective method for targeting cancer cells. These systems, with the ability to penetrate better inside the cells, combine the drug in a targeted way in the cells. Also, due to the enhanced permeability and retention (EPR), the possibility of better accumulation of drugs in the tumor site is provided. In most researches, the suitable particle size for the targeted release of drug nanocarriers has been reported to be less than 300 or 200 nm. This amount is suitable for the application of drug release for diffusion among tissues and causes the effect of increasing permeability. In this study, for the first time, it examines and analyzes the particle size and zeta potential (surface charge) of chitosan-based nanocarriers through dynamic light scattering and electron microscope tests in improving the release of the antitumor drug, 5-fluorouracil. Manuscript profile
• Open Access Article
  • Abstract Page
  • Full-Text
  
  2 - A review of polymer bonded explosive rheology
  Mahmoud Heydari
  Polymer-bonded explosives are widely used in defense and commercial industries. In this type of explosive, very high amounts of explosive crystals (about 90% by weight) are surrounded by a polymeric binder (about 10%), which leads to a decrease in sensitivity and a sign More

  Polymer-bonded explosives are widely used in defense and commercial industries. In this type of explosive, very high amounts of explosive crystals (about 90% by weight) are surrounded by a polymeric binder (about 10%), which leads to a decrease in sensitivity and a significant increase in safety during application and storage. These mixtures are molded in different ways, such as pressing, casting, extrusion, and injection. Studying the rheology of these mixtures with a high percentage of solid loading leads to finding the appropriate quality control method at different production stages. The first step was to review studies on alternatives to simulating explosive rheological behavior, such as dechlorane, calcium carbonate, sugar, etc. The general behavior of simulated mixtures, such as yield stress, shear rate dependence, time dependence, etc., is compared with original explosive. The results showed that despite the similarity in some rheological behaviors, it is impossible to predict and study all the rheological behaviors of polymer-bonded explosives using simulating materials. This paper discusses factors affecting the rheology of polymer-bonded explosives, such as particle size distribution, modification of explosive crystal surfaces, and plasticizer. A review of scientific sources showed that using a wide distribution of explosive crystal particles compared to a narrow distribution led to a significant reduction in viscosity and dependence on shear rate and time. The absence of strong interactions between crystal particles and polymer binder leads to no observation of quasi-solid behavior even in 85% by weight of explosive crystals such as octogen in hydroxyl-terminated polybutadiene Manuscript profile
• Open Access Article
  • Abstract Page
  • Full-Text
  
  3 - Investigating the Particle Size of Chitosan-Based Drug Carriers for the Release of 5-Fluorouracil Antitumor Drug
  Mohammad Hossein Karami Majid Abdouss Mandana Karami
  Chitosan has been widely used as a natural biopolymer. The modification of chitosan for various applications can be easily achieved due to the abundant active groups (NH2 and OH) in the main chain. Controlled drug release makes the drug release rate predictable and repe More

  Chitosan has been widely used as a natural biopolymer. The modification of chitosan for various applications can be easily achieved due to the abundant active groups (NH2 and OH) in the main chain. Controlled drug release makes the drug release rate predictable and repeatable for prolonged release drugs. Drug delivery systems prepared from nanoparticles show several advantages, including improved efficiency and reduced toxicity. Using drug delivery systems based on nanoparticles loaded with anti-cancer agents is an effective method for targeting cancer cells. These systems, with the ability to penetrate better inside the cells, combine the drug in a targeted way in the cells. Also, due to the enhanced permeability and retention (EPR), the possibility of better accumulation of drugs in the tumor site is provided. In most researches, the suitable particle size for the targeted release of drug nanocarriers has been reported to be less than 300 or 200 nm. This amount is suitable for the application of drug release for diffusion among tissues and causes the effect of increasing permeability. In this study, for the first time, it examines and analyzes the particle size and zeta potential (surface charge) of chitosan-based nanocarriers through dynamic light scattering and electron microscope tests in improving the release of the antitumor drug, 5-fluorouracil. Manuscript profile