Preparation and characterization of stereocomplex aggregates based on PLA–P188–PLA

RSC Advances ◽  
2016 ◽  
Vol 6 (56) ◽  
pp. 50543-50552 ◽  
Author(s):  
Weiwei Zhang ◽  
Delong Zhang ◽  
Xiaoshan Fan ◽  
Guangyue Bai ◽  
Yuqin Jiang ◽  
...  

Novel dumbbell-shaped amphiphilic copolymers based on P188 and PLA were synthesized by click chemistry and ring opening polymerization. The self-assembly behavior of the stereocomplexes and the DOX release profile from the aggregates were studied.

Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1357
Author(s):  
Michel Nguyen ◽  
Khalid Ferji ◽  
Sébastien Lecommandoux ◽  
Colin Bonduelle

Nucleobase-containing polymers are an emerging class of building blocks for the self-assembly of nanoobjects with promising applications in nanomedicine and biology. Here we present a macromolecular engineering approach to design nucleobase-containing polypeptide polymers incorporating thymine that further self-assemble in nanomaterials. Diblock and triblock copolypeptide polymers were prepared using sequential ring-opening polymerization of γ-Benzyl-l-glutamate N-carboxyanhydride (BLG-NCA) and γ-Propargyl-l-glutamate N-carboxyanhydride (PLG-NCA), followed by an efficient copper(I)-catalyzed azide alkyne cycloaddition (CuAAc) functionalization with thymidine monophosphate. Resulting amphiphilic copolymers were able to spontaneously form nanoobjects in aqueous solutions avoiding a pre-solubilization step with an organic solvent. Upon self-assembly, light scattering measurements and transmission electron microscopy (TEM) revealed the impact of the architecture (diblock versus triblock) on the morphology of the resulted nanoassemblies. Interestingly, the nucleobase-containing nanoobjects displayed free thymine units in the shell that were found available for further DNA-binding.


2014 ◽  
Vol 215 (12) ◽  
pp. 1218-1229 ◽  
Author(s):  
Pasquale Tirino ◽  
Claudia Conte ◽  
Monica Ordegno ◽  
Rosario Palumbo ◽  
Francesca Ungaro ◽  
...  

2014 ◽  
Vol 513-517 ◽  
pp. 86-90
Author(s):  
Feng Hong Li ◽  
Wen Jing Zhang ◽  
San Xi Li ◽  
Yan Ming Chen ◽  
Xin Rui Zhang

The amphiphilic chitosan oligosaccharides graft copolymer (PHCSO-g-PCL) was synthesized via ring-opening polymerization (ROP) of ε-caprolactone (ε-CL) through an amino group protection route using phthaloyl chitosan oligosaccharide (PHCSO) as intermediate. The graft reaction was carried out in Pyridine at 120 °C with a chitosan oligosaccharide (CSO) initiator and a tin 2-ethylhexanoate (Sn (Oct)2) catalyst. The amphiphilic PHCSO-g-PCL nanoparticles were prepared through the self-assembled in DMF organic solvents. PHCSO-PCL copolymer was characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The physicochemical properties of the hydrophobized PHCSO-g-PCL nanoparticles were investigated by using dynamic light scattering (DLS). The results of DLS showed that the hydrodynamic diameters and particle size distribution with various concentrations of PHCSO-g-PCL nanoparticles were from 69.82 nm to 195.9 nm with a narrow polydispersity factor of 0.212 to 0.172.


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