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Preparation and characterization of a novel magnetized nanosphere as a carrier system for drug delivery using Plantago ovata Forssk. hydrogel combined with mefenamic acid as the drug model
Institution:1. Department of Chemistry, Faculty of Science, Hakim Sabzevari University, 96179-76487 Sabzevar, Iran;2. Department of Chemistry, College of Basic Science, Shahrood Branch, Islamic Azad University, Shahrood, Iran;3. Department of Chemistry, Sabzevar Branch, Islamic Azad University, Sabzevar, Iran
Abstract:The aim of the present study was to magnetize Plantago ovata Forssk. hydrogel and produce a nanosphere system to carrier mefenamic acid as the drug model. For this propose, P. ovata seeds hydrogel (POSH) was extracted and magnetized by Fe3O4 being functionalized using tetraethyl orthosilicate and trimethoxyvinysilane. Thereafter, mefenamic acid (MFA) was loaded on the carrier system. The final product, as the magnetic drug loaded nanosphere (Fe/POSH/MFA), was fully characterized through different techniques involving X-ray diffraction (XRD), scanning electron microscopy (SEM), vibrating-sample magnetometer (VSM), thermal gravimetric analysis (TGA), dynamic light scattering (DLS), and FT-IR spectroscopy. The results confirmed the successful production of the drug loaded nanosphere system with particles magnetization of 25 emu/g over a range size of 40–50 nm. However, the size distribution less than 100 nm was measured through DLS analysis. The hydrogel showed a pH sensitivity swelling behavior representing the best efficacy at pH 7.4. The efficiency of the drug encapsulation was found to be 64.35%. The drug releasing was studied using a dialysis bag at pH = 7.4. The highest in vitro drug releasing was found to be 57.3 ± 0.6% after 72 h, as well. The findings of the current report account for the potential use of P. ovata hydrogel as an effective delivery system for encapsulation of water insoluble basic drugs, e.g., MFA in a magnetized carrier system.
Keywords:Drug delivery  magnetized hydrogel  Mefenamic acid  AIBN"}  {"#name":"keyword"  "$":{"id":"k0025"}  "$$":[{"#name":"text"  "_":"A  A'-Azoisobutyronitrile  CTAB"}  {"#name":"keyword"  "$":{"id":"k0035"}  "$$":[{"#name":"text"  "_":"Cetyl trimethylammonium bromide  DEE"}  {"#name":"keyword"  "$":{"id":"k0045"}  "$$":[{"#name":"text"  "_":"Drug encapsulation efficiency  DLS"}  {"#name":"keyword"  "$":{"id":"k0055"}  "$$":[{"#name":"text"  "_":"Dynamic light scattering  DRE"}  {"#name":"keyword"  "$":{"id":"k0065"}  "$$":[{"#name":"text"  "_":"Drug releasing evaluation  EGDMA"}  {"#name":"keyword"  "$":{"id":"k0075"}  "$$":[{"#name":"text"  "_":"Ethylene glycol dimethacrylate  FE-SEM"}  {"#name":"keyword"  "$":{"id":"k0085"}  "$$":[{"#name":"text"  "_":"Field emission scanning electron microscope  FT-IR"}  {"#name":"keyword"  "$":{"id":"k0095"}  "$$":[{"#name":"text"  "_":"Fourier-transform infrared spectroscopy  MAA"}  {"#name":"keyword"  "$":{"id":"k0105"}  "$$":[{"#name":"text"  "_":"Methacrylic acid  MFA"}  {"#name":"keyword"  "$":{"id":"k0115"}  "$$":[{"#name":"text"  "_":"Mefenamic acid  NPs"}  {"#name":"keyword"  "$":{"id":"k0125"}  "$$":[{"#name":"text"  "_":"Nanoparticles  POSH"}  {"#name":"keyword"  "$":{"id":"k0135"}  "$$":[{"#name":"text"  "$$":[{"#name":"italic"  "_":"P  ovata"}  {"#name":"__text__"  "_":" seeds hydrogel  SEM"}  {"#name":"keyword"  "$":{"id":"k0145"}  "$$":[{"#name":"text"  "_":"Scanning electron microscopy  TEOS"}  {"#name":"keyword"  "$":{"id":"k0155"}  "$$":[{"#name":"text"  "_":"Tetraethyl orthosilicate  TGA"}  {"#name":"keyword"  "$":{"id":"k0165"}  "$$":[{"#name":"text"  "_":"Thermal gravimetric analysis  TMVS"}  {"#name":"keyword"  "$":{"id":"k0175"}  "$$":[{"#name":"text"  "_":"Trimethoxyvinysilane  VSM"}  {"#name":"keyword"  "$":{"id":"k0185"}  "$$":[{"#name":"text"  "_":"Vibrating-sample magnetometer  XRD"}  {"#name":"keyword"  "$":{"id":"k0195"}  "$$":[{"#name":"text"  "_":"X-Ray diffraction
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