Title of article :
Fabrication of Hollow poly acrylic acid Nano gels via Emulsion polymerization as a Model for loading of Drugs
Author/Authors :
Askarizadeh, E. Department of Applied Chemistry - Faculty of Pharmaceutical Chemistry - Tehran Medical Sciences - Islamic Azad University, Tehran, Iran
Pages :
7
From page :
233
To page :
239
Abstract :
Nanogels are nano-sized hydrogel networks formed by chemically or physically crosslinked polymer particles. Their colloidal stability affords them as good candidates for drug delivery systems. Like nanoparticles, nanogels are injectable and responsive to environmental factors, such pH, and temperature. This work presents a facile and large-scale fabrication of poly(acrylic acid) (PAA) hollow nanogels via in situ Pickering miniemulsion polymerization method. Cross-linked polyacrylonitrile (PAN) nanoparticles with hollow structure were prepared by using hydrophobic solvent as liquid core. The complete hydrolysis reaction process of PAN shell leads to the successful formation of hollow PAA nanogels. The properties of PAA nanogel were characterized by FT-IR, Scanning electron microscope and Dynamic light scattering. It is found that the nanogels have a hollow core-porous shell structure. Protein, bovine serum albumin (BSA) was used as model drugs to investigate their loading abilities as versatile drug-delivery vehicles. The nanogel exhibits high loading ability to protein. The maximum BSA loading capacity of PAA nanogel can reach at pH=5. This high loading capacity may be related to the hollow core-porous shell structure of PAA nanogels. Considering the high stability of the materials, simple and mild preparation procedure, high loading capacity, and ability to protect biological agents from denaturation, PAA nanogels should be promising drug-delivery carriers for drug-delivery systems.
Farsi abstract :
فاقد چكيده فارسي
Keywords :
BSA , Drug delivery , Nanogel , Pickeing miniemulsion
Journal title :
International Journal of Bio-Inorganic Hybrid Nanomaterials
Serial Year :
2020
Record number :
2630251
Link To Document :
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