Radiation synthesis and characterization of pH-Responsive sodium Alginate/Poly(acrylic acid) nanogel loaded with ferulic acid for anticancer drug delivery

被引:6
|
作者
El-Adl, Khaled [1 ,2 ]
Ghobashy, Mohamed M. [3 ]
Ismail, Amel F. M. [4 ]
El-morsy, Ahmed [5 ,6 ]
Shoman, Nabil A. [7 ]
机构
[1] Heliopolis Univ Sustainable Dev, Fac Pharm, Chem Dept, Cairo, Egypt
[2] Al Azhar Univ, Fac Pharm Boys, Pharmaceut Med Chem & Drug Design Dept, Nasr City 11884, Cairo, Egypt
[3] Egyptian Atom Energy Author EAEA, Natl Ctr Radiat Res & Technol NCRRT, Radiat Res Polymer Chem Dept, Cairo, Egypt
[4] Egyptian Atom Energy Author EAEA, Natl Ctr Radiat Res & Technol NCRRT, Drug Radiat Res Dept, Cairo, Egypt
[5] Al Azhar Univ, Fac Pharm Boys, Pharmaceut Organ Chem Dept, Nasr City 11884, Cairo, Egypt
[6] Islamic Univ, Coll Pharm, Pharmaceut Chem Dept, Najaf, Iraq
[7] Ahram Canadian Univ, Fac Pharm, Dept Pharmaceut & Pharmaceut Technol, Giza, Egypt
关键词
Anticancer agent; Molecular docking; Nanogel; Gamma radiation; Ferulic acid; DESIGN; EGFR; DERIVATIVES; INHIBITORS; DISCOVERY; GROWTH; RECEPTORS; SURVIVAL; ASSAY;
D O I
10.1016/j.matchemphys.2024.129564
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This study focuses on the synthesis and characterization of a pH-responsive nanogel system composed of sodium alginate (NaAlg) and poly(acrylic acid) loaded with ferulic acid. The mechanism of nanogel formation by gamma irradiation was elucidated, highlighting the role of polymer interactions and crosslinking agents. The pHdependent release of ferulic acid from the nanogel carrier was investigated, revealing a controlled release behavior in response to pH variations. The zeta potential values remained slightly negative across the pH range, indicating the presence of surface functional groups. Transmission electron microscopy confirmed the nanogel's formation and uniform particle size at pH 1. This nanogel was considered for controlled drug delivery applications, exhibiting high physical and chemical stability of ferulic acid. Our nanogel compound 5 decreased IC50 against HepG2, A549, MCF-7 and HCT-116 by 58.22 %, 78.35 %, 45.81 %, and 47.94 % respectively. Additionally, it decreased IC50 against VEGFR2 and EGFRT790 M by 41.94 %, and 70.59 % respectively.
引用
收藏
页数:13
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