کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
600475 | 1454303 | 2013 | 9 صفحه PDF | دانلود رایگان |

This work focused on the design of new pH-responsive nanoparticles for controlled delivery of anticancer drug doxorubicin (Dox). Nanoparticles of poly(methacrylic acid)-polysorbate 80-grafted starch (PMAA-PS 80-g-St) were synthesized by using a one-pot method that enabled simultaneous grafting of PMAA and PS 80 onto starch and nanoparticle formation in an aqueous medium. The particles were characterized by FTIR, 1H NMR, TEM, DLS, and potentiometric titration. Dox loading and in vitro release from the nanoparticles were investigated. The FTIR and 1H NMR confirmed the chemical composition of the graft terpolymer. The nanoparticles were relatively spherical with narrow size distribution and porous morphology. They exhibited pH-dependent swelling in a physiological pH range. The particle size and magnitude of phase transition were dependent on polymer composition and formulation parameters such as concentrations of surfactant and cross-linking agent and total monomer concentration. The nanoparticles with optimized compositions showed high loading capacity for Dox and sustained Dox release. The results suggest that the new pH-responsive terpolymer nanoparticles are useful in controlled drug delivery.
Figure optionsDownload as PowerPoint slideHighlights
► pH-responsive nanoparticles of starch, methacrylic acid and polysorbate 80 terpolymer.
► Developed a method for simultaneous grafting and nanoparticle formation in one pot.
► Identified reaction parameters for tunable particle size and pH sensitivity.
► Identified properties of starch based nanoparticles useful for drug delivery.
Journal: Colloids and Surfaces B: Biointerfaces - Volume 101, 1 January 2013, Pages 405–413