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  3. Vol. 21 No. 1 (2025): IJPS_Volume 21_Issue 1 (2025)
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Vol. 21 No. 1 (2025)

January 2025

Synthesis, Characterization, and Investigation of Performance of Fe-MOF and Fe-MOF/Fe3O4 in Adsorption and Release of Naproxen as a Non-steroid Anti-inflammatory Drug (NSAID) Synthesis, Characterization, and Investigation of Performance of Fe-MOF

  • Sayyde Shadi Hosseini
  • Seyed Ali Hosseini
  • Mahin Broukanlou

Iranian Journal of Pharmaceutical Sciences, Vol. 21 No. 1 (2025), 21 January 2025 , Page 134-144
https://doi.org/10.22037/ijps.v21i1.44760 Published: 2025-04-26

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Abstract

Developing materials with a high capacity for drug adsorption and slow-releasing properties is promising in drug delivery. Metal-organic frameworks (MOFs) are materials with high adsorption and desorption capacities. Therefore, they can be very effective in targeted drug therapy. In this study, two Fe-MIL101 samples with different synthesis times (24 and 48 hours) were synthesized by solvothermal method and used as a naproxen carrier for the first time. The samples were analyzed using BET, FT-IR, XRD, and FESEM structural analyses at the nanoscale. The pHpzc of the Fe-MIL101 (48h) and Fe-MIL101/Fe3O4 was determined to be 3.3 and 3.5, respectively. The adsorption of the Naproxen on Fe-MIL-101/Fe3O4 followed the Freundlich adsorption isotherm (R²=0.996), indicating the multilayer adsorption of Naproxen molecules on the carriers. The release of naproxen from carriers was investigated at a phosphate-buffered saline (PBS( with a pH of 7.4 (the pH of human blood). The variables of release time, carrier synthesis time, and pH of the environment were considered in this study. The most effective release was with Fe-MIL-101/Fe3O4 synthesized over 48 hours. This method followed the kinetic model of Korsmeyer-Peppas (R²= 0.9843) with a release exponent (n) of 0.63, meaning that the naproxen release from MOFs follows the non-Fickian mechanism. To develop a magnetic and slow-releasing carrier, Fe-MIL-101/Fe3O4 was synthesized. The studies showed that naproxen release from Fe-MIL-101/Fe3O4 is slow and takes a long time. The n in Korsmeyer-Peppas mole for naproxen release from Fe-MIL-101/Fe3O4 was 0.886, indicating a case II transport mechanism for naproxen release with a constant release rate. The findings highlight the significant potential of Fe-MIL-101/Fe3O4 for enhancing targeted drug delivery, underscoring its importance in improving therapeutic outcomes.

Keywords:
  • Drug Delivery
  • Metal-organic framework (MOF)
  • Fe-MIL-101/Fe3O4
  • Korsmeyer-Peppas
  • non-Fickian mechanism
  • Naproxen
  • IJPS_Volume21_Issue1_Pages134-144

How to Cite

Hosseini, S. S., Hosseini, S. A., & Broukanlou, M. (2025). Synthesis, Characterization, and Investigation of Performance of Fe-MOF and Fe-MOF/Fe3O4 in Adsorption and Release of Naproxen as a Non-steroid Anti-inflammatory Drug (NSAID): Synthesis, Characterization, and Investigation of Performance of Fe-MOF. Iranian Journal of Pharmaceutical Sciences, 21(1), 134–144. https://doi.org/10.22037/ijps.v21i1.44760
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