کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
601122 879931 2011 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis and characterization of novel amphiphilic copolymer stearic acid-coupled F127 nanoparticles for nano-technology based drug delivery system
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
پیش نمایش صفحه اول مقاله
Synthesis and characterization of novel amphiphilic copolymer stearic acid-coupled F127 nanoparticles for nano-technology based drug delivery system
چکیده انگلیسی

Pluronic, F127, amphiphilic block copolymers, are used for several applications, including drug delivery systems. The critical micelle concentration (CMC) of F127 is about 0.26–0.8 wt% so that the utility of F127 in nano-technology based drug delivery system is limited since the nano-sized micelles could dissociate upon dilution. Herein, stearic acid (SA) was simply coupled to F127 between the carboxyl group of SA and the hydroxyl group of F127, which formed a novel copolymer named as SA-coupled F127, with significantly lower CMC. Above the CMC 6.9 × 10−5 wt%, SA-coupled F127 self-assembled stable nanoparticles with Zeta potential −36 mV. Doxorubicin (DOX)-loaded nanoparticles were made, with drug loading (DL) 5.7 wt% and Zeta potential −36 to −39 mV, and the nanoparticles exhibited distinct shape with the size distribution from 20 to 50 nm. DOX-loaded nanoparticles were relatively stable and exhibited DOX dependant cytotoxicity toward MCF-7 cells in vitro. These results suggest that SA-coupled F127 potentially could be applied as a nano-technology based drug delivery method.

Figure optionsDownload as PowerPoint slideHighlights
► A novel amphiphilic copolymer stearic acid-coupled F127 was synthesized.
► The CMC for SA-coupled F127 was 6.9 × 10−5 wt%, lower about 2 × 103-fold than 0.388 wt% of F127.
► The Zeta potential of nanoparticles formed by SA-coupled F127 was around −36 mV.
► DOX loaded nanoparticles showed potential applications in drug delivery system.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Colloids and Surfaces B: Biointerfaces - Volume 88, Issue 2, 1 December 2011, Pages 741–748
نویسندگان
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