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Novel Polymeric Nanomaterial Based on Poly(Hydroxyethyl Methacrylate-Methacryloylamidophenylalanine) for Hypertension Treatment: Properties and Drug Release Characteristics.
Bardakci, Fevzi; Kusat, Kevser; Adnan, Mohd; Badraoui, Riadh; Alam, Mohammad Jahoor; Alreshidi, Mousa M; Siddiqui, Arif Jamal; Sachidanandan, Manojkumar; Akgöl, Sinan.
  • Bardakci F; Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
  • Kusat K; Molecular Diagnostics and Personalized Therapeutics Unit, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
  • Adnan M; Department of Chemistry, Faculty of Science, Dokuz Eylül University, Izmir 35390, Turkey.
  • Badraoui R; Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
  • Alam MJ; Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
  • Alreshidi MM; Section of Histology-Cytology, Medicine Faculty of Tunis, University of Tunis El Manar, Tunis 1007, Tunisia.
  • Siddiqui AJ; Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
  • Sachidanandan M; Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
  • Akgöl S; Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
Polymers (Basel) ; 14(22)2022 Nov 21.
Article en En | MEDLINE | ID: mdl-36433166
ABSTRACT
In this study, a novel polymeric nanomaterial was synthesized and characterized, and it its potential usability in hypertension treatment was demonstrated. For these purposes, a poly(hydroxyethyl methacrylate-methacryloylamidophenylalanine)-based polymeric nanomaterial (p(HEMPA)) was synthesized using a mini-emulsion polymerization technique. The nanomaterials were characterized using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and zeta size analysis. The synthesized p(HEMPA) nanomaterial had a diameter of about 113 nm. Amlodipine-binding studies were optimized by changing the reaction conditions. Under optimum conditions, amlodipine's maximum adsorption value (Qmax) of the p(HEMPA) nanopolymer was found to be 145.8 mg/g. In vitro controlled drug release rates of amlodipine, bound to the nanopolymer at the optimum conditions, were studied with the dialysis method in a simulated gastrointestinal system with pH values of 1.2, 6.8 and 7.4. It was found that 99.5% of amlodipine loaded on the nanomaterial was released at pH 7.4 and 72 h. Even after 72 h, no difference was observed in the release of AML. It can be said that the synthesized nanomaterial is suitable for oral amlodipine release. In conclusion, the synthesized nanomaterial was studied for the first time in the literature as a drug delivery system for use in the treatment of hypertension. In addition, AML-p(HEMPA) nanomaterials may enable less frequent drug uptake, have higher bioavailability, and allow for prolonged release with minimal side effects.
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