scholarly journals Mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) as multivalent lectin-binding nanomaterials

2019 ◽  
Vol 10 ◽  
pp. 2192-2206 ◽  
Author(s):  
Stefania Ordanini ◽  
Wanda Celentano ◽  
Anna Bernardi ◽  
Francesco Cellesi
Keyword(s):  
Molecular Weight ◽  
Ethylene Glycol ◽  
Ring Opening ◽  
Binding Assay ◽  
Lectin Binding ◽  
Aqueous Media ◽  
Poly Ethylene Glycol ◽  
High Control ◽  
Poly Ethylene ◽  
Macromolecular Architecture

A class of linear and four-arm mannosylated brush copolymers based on poly(ethylene glycol) and poly(ε-caprolactone) is presented here. The synthesis through ring-opening and atom transfer radical polymerizations provided high control over molecular weight and functionality. A post-polymerization azide–alkyne cycloaddition allowed for the formation of glycopolymers with different mannose valencies (1, 2, 4, and 8). In aqueous media, these macromolecules formed nanoparticles that were able to bind lectins, as investigated by concanavalin A binding assay. The results indicate that carbohydrate–lectin interactions can be tuned by the macromolecular architecture and functionality, hence the importance of these macromolecular properties in the design of targeted anti-pathogenic nanomaterials.

Synthesis and Properties of Biodegradable ABA Triblock Copolymers of Polylactide (A) and Polyethylene Glycol (B)

2006 ◽  
Vol 11-12 ◽  
pp. 469-472 ◽  
Author(s):  
Shu Xian Shi ◽  
Yu Zheng Xia ◽  
Xiao Yan Ma ◽  
Shu Ke Jiao ◽  
Xiao Yu Li
Keyword(s):  
Molecular Weight ◽  
Ethylene Glycol ◽  
Ring Opening ◽  
Average Molecular Weight ◽  
Analytical Techniques ◽  
Normal Pressure ◽  
Molar Ratio ◽  
Poly Ethylene Glycol ◽  
Molar Ratios ◽  
Poly Ethylene

The triblock ABA copolymers of poly (D,L-lactide)-b-poly (ethylene glycol)-b-poly (D,L-lactide) (PDLLA-PEG-PDLLA) were synthesized by bulk ring-opening polymerization in the presence of N2 under normal pressure, using the D,L-lactide (DLLA) as monomer, hydroxyl endgroups of poly(ethylene glycol) (PEG) as initiator and the stannous octoate as the catalyst. The resulting copolymers were characterized by various analytical techniques. Effects of molar ratios of lactide to PEG and the chain length of PEG on the viscosity-average molecular weight of the copolymers, the biodegradation behaviors and hydrophilicity of the copolymers were investigated in detail. The results showed that the viscosity-average molecular weight and the contact angle of the copolymers increased with the molar ratio of lactide to PEG, but water uptake and degradability decreased.

scholarly journals Poly(ethylene glycol)-b-poly(1,3-trimethylene carbonate) Amphiphilic Copolymers for Long-Acting Injectables: Synthesis, Non-Acylating Performance and In Vivo Degradation

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1438
Author(s):  
Silvio Curia ◽  
Feifei Ng ◽  
Marie-Emérentienne Cagnon ◽  
Victor Nicoulin ◽  
Adolfo Lopez-Noriega
Keyword(s):  
Ethylene Glycol ◽  
Ring Opening ◽  
Gel Chromatography ◽  
Amphiphilic Copolymers ◽  
Trimethylene Carbonate ◽  
Poly Ethylene Glycol ◽  
Poly Ethylene ◽  
Long Acting ◽  
In Vivo Degradation

This article presents the evaluation of diblock and triblock poly(ethylene glycol)-b-poly(1,3-trimethylene carbonate) amphiphilic copolymers (PEG-PTMCs) as excipients for the formulation of long-acting injectables (LAIs). Copolymers were successfully synthesised through bulk ring-opening polymerisation. The concomitant formation of PTMC homopolymer could not be avoided irrespective of the catalyst amount, but the by-product could easily be removed by gel chromatography. Pure PEG-PTMCs undergo faster erosion in vivo than their corresponding homopolymer. Furthermore, these copolymers show outstanding stability compared to their polyester analogues when formulated with amine-containing reactive drugs, which makes them particularly suitable as LAIs for the sustained release of drugs susceptible to acylation.

Hydrolytically and Reductively Degradable High-Molecular-Weight Poly(ethylene glycol)s

2007 ◽  
Vol 208 (24) ◽  
pp. 2642-2653 ◽  
Author(s):  
Alena Braunová ◽  
Michal Pechar ◽  
Richard Laga ◽  
Karel Ulbrich
Keyword(s):  
Molecular Weight ◽  
Ethylene Glycol ◽  
High Molecular Weight ◽  
Poly Ethylene Glycol ◽  
Poly Ethylene ◽  
High Molecular Weight Poly

Microporous Bio-Membrane Materials Based on High Molecular Weight Polylactide and Low Molecular Weight Poly(ethylene glycol)

2012 ◽  
Vol 567 ◽  
pp. 123-126
Author(s):  
Teng Fei Shen ◽  
Man Geng Lu ◽  
Li Yan Liang
Keyword(s):  
Molecular Weight ◽  
Ethylene Glycol ◽  
High Weight ◽  
Low Molecular Weight ◽  
Poly Ethylene Glycol ◽  
Degradation Rates ◽  
Degradation Behaviors ◽  
The Mean ◽  
Poly Ethylene ◽  
Lower Glass Transition Temperature

In this work, microporous membrane biomaterials based on high weight molecular polylactide (PLA) and low molecular weight poly(ethylene glycol) (PEG) using rapid solvent evaporation method were prepared and investigated. The effect of PEG segments added on the thermal and degradation behaviors was studied. According to the results, produced PLA/PEG biomaterial has lower glass transition temperature (Tg)in comparison with neat PLA. It was also found that the degradation rates of the PLA/PEG biomaterials were significantly increased with adding of PEG, which explained by increasing hydrophilic groups. For better porous fixation, CL-blocked polyisocyanate (CL-bp), which was synthesized from reaction of isophorone diisocyanate (IPDI) with dimethylol propionic acid (DMPA) and Trimethylolpropane (TMP) followed by addition of caprolactam (CL), were introduced. The microporous forms were observed by the scanning electron microscope (SEM), which showed the mean diameters of prepared PLA/PEG microporous were around 10μm.

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