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Development of Timolol Maleate-Loaded Poloxamer-co-Poly (acrylic acid) based hydrogel for controlled drug delivery
R. Mansoor, K. Barkat, I. Anjum, M. Aamir, SF. Badshah, R. Ullah, Z. Iqbal, MA. Raza
Language English Country United States
Document type Journal Article
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- MeSH
- Acrylic Resins * chemistry MeSH
- Calorimetry, Differential Scanning MeSH
- X-Ray Diffraction MeSH
- Hydrogels * chemistry MeSH
- Hydrogen-Ion Concentration MeSH
- Rabbits MeSH
- Drug Delivery Systems MeSH
- Delayed-Action Preparations chemistry pharmacokinetics MeSH
- Microscopy, Electron, Scanning MeSH
- Drug Carriers chemistry MeSH
- Poloxamer * chemistry MeSH
- Spectroscopy, Fourier Transform Infrared MeSH
- Thermogravimetry MeSH
- Timolol * administration & dosage pharmacokinetics chemistry MeSH
- Drug Liberation MeSH
- Animals MeSH
- Check Tag
- Rabbits MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Free radical polymerization technique was used to formulate Poloxamer-188 based hydrogels for controlled delivery. A total of seven formulations were formulated with varying concentrations of polymer, monomer ad cross linker. In order to assess the structural properties of the formulated hydrogels, Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric analysis (TGA), Differential Scanning Calorimetry (DSC), Scanning electron microscopy (SEM), and X-ray diffraction (XRD) were carried out. To assess the effect of pH on the release of the drug from the polymeric system, drug release studies were carried in pH 1.2 and 7.4 and it was found that release of the drug was significant in pH 7.4 as compared to that of pH 1.2 which confirmed the pH responsiveness of the system. Different kinetic models were also applied to the drug release to evaluate the mechanism of the drug release from the system. To determine the safety and biocompatibility of the system, toxicity study was also carried out for which healthy rabbits were selected and formulated hydrogels were orally administered to the rabbits. The results obtained suggested that the formulated poloxamer-188 hydrogels are biocompatible with biological system and have the potential to serve as controlled drug delivery vehicles.
Department of Pharmacognosy College of Pharmacy King Saud University Riyadh Saudi Arabia
Department of Surgery College of Medicine King Saud University Riyadh Kingdom of Saudi Arabia
Faculty of Health Sciences Equator University of Science and Technology Masaka Uganda
Faculty of Pharmacy The University of Lahore Lahore Pakistan
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