کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
591924 | 1453887 | 2015 | 9 صفحه PDF | دانلود رایگان |

• Biocompatible dextran-covered nanoparticles are obtained by miniemulsion AGET-ATRP.
• Amphiphilic dextran derivatives and M810 are used as stabilizer and costabilizer.
• M810 prevents Ostwald ripening and contributes to ATRP catalyst solubilization.
• Control of polymerization and object size improve with M810 compared to hexadecane.
Aiming to prepare potentially biocompatible dextran-covered nanoparticles (NPs), the use of a pharmaceutically acceptable oil (Miglyol 810, M810—a medium chain saturated triglyceride) as co-stabilizer and of amphiphilic dextran derivatives (DexPτ) as stabilizers was investigated for Activator Generated by Electron Transfer Atom Transfer Radical Polymerization (AGET ATRP) of methyl methacrylate in miniemulsion. We showed that, as compared to several oils, M810 was the most suitable co-stabilizer. Indeed, it efficiently prevented diffusional degradation and contributed to solubilize ATRP catalytic systems in organic phase (methyl methacrylate + 5 vol% of co-stabilizer). Better control over polymerization and nano-objects size was achieved for polymerization with M810 compared to a standard co-stabilizer (hexadecane). Indeed, with the appropriate formulation conditions, NPs size was very similar to the one of initial emulsion nanodroplets and more than 85% of the initial DexPτ amount was adsorbed at NPs surface. A convenient procedure to eliminate copper from the finals NPs was also experienced.
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Journal: Colloids and Surfaces A: Physicochemical and Engineering Aspects - Volume 486, 5 December 2015, Pages 60–68