Search results for "Copolymer"
showing 10 items of 1003 documents
Biodegradable tablets having a matrix of low molecular weight poly-L-lactic acid and poly-D,L-lactic acid.
1990
Biodegradable Homo- and Copolymers of lactic and glycolic acids have been used for manufacture of microparticles and matrix implants1,5). To ensure sufficient hydrolytic matrix stability lactic acids of high and medium degree of polymerization have been used. The manufacture of poly lactic acid tablets with an average molecular weight of 25000 and 6000 was reported recently, after finishing the following study2). Bioabbaubare Gerusttabletten aus niedermolekularer poly-L-Milchsaure und poly-D,L-Milchsaure
Development of polymer-based nanoparticles for Zileuton delivery to the lung : PMeOx and PMeOzi surface chemistry reduces interactions with mucins
2021
In this paper, two amphiphilic graft copolymers were synthesized by grafting polylactic acid (PLA) as hydrophobic chain and poly(2-methyl-2-oxazoline) (PMeOx) or poly(2-methyl-2-oxazine) (PMeOzi) as hydrophilic chain, respectively, to a backbone of α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA). These original graft copolymers were used to prepare nanoparticles delivering Zileuton in inhalation therapy. Among various tested methods, direct nanoprecipitation proved to be the best technique to prepare nanoparticles with the smallest dimensions, the narrowest dimensional distribution and a spherical shape. To overcome the size limitations for administration by inhalation, the nano-into-micr…
1991
L'etude viscosimetrique, potentiometrique et conductimetrique montre que le copolymere forme un complexe de stœchiometrie 2:1 avec le chlorure de palmityltrimethylammonium. Avec le laurylsuslfate de sodium, il y a d'abord formation d'un complexe de composition 2:1 puis par addition supplementaire du surfactant, formation d'un complexe 1:1
Cationic polyaspartamide-based nanocomplexes mediate siRNA entry and down-regulation of the pro-inflammatory mediator high mobility group box 1 in ai…
2015
Abstract High-mobility group box 1 (HMGB1) is a nonhistone protein secreted by airway epithelial cells in hyperinflammatory diseases such as asthma. In order to down-regulate HMGB1 expression in airway epithelial cells, siRNA directed against HMGB1 was delivered through nanocomplexes based on a cationic copolymer of poly(N-2-hydroxyethyl)- d,l -aspartamide (PHEA) by using H441 cells. Two copolymers were used in these experiments bearing respectively spermine side chains (PHEA-Spm) and both spermine and PEG2000 chains (PHEA-PEG-Spm). PHEA-Spm and PHEA-PEG-Spm derivatives complexed dsDNA oligonucleotides with a w/w ratio of 1 and higher as shown by a gel retardation assay. PHEA-Spm and PHEA-P…
Amphiphilic derivatives of a polyaspartamide: their aggregation and solubilization ability.Tensiometric and spectrophotometric studies
2006
The self-aggregation and solubilization capability of a series of amphiphilic copolymers obtained by derivatisation of polymeric chain of α,β-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) with polyethylene glycols (PEG, being different molecular weight 2000 or 5000 Da, PEG2000 and PEG5000, respectively) and/or hexadecylamine alkyl chain (C16), namely PHEA–PEG2000, PHEA–PEG5000, PHEA–C16, PHEA–PEG2000–C16 and PHEA–PEG5000–C16, have been evidenced by performing systematic tensiometric and spectrophotometric studies. All measurements have been performed at 25.0 °C over a wide copolymer concentration range. The tensiometric results have shown that, for all copolymers studied, the surface tension…
2019
Lamella-forming ABC triblock terpolymers are convenient building blocks for the synthesis of soft Janus nanoparticles (JNPs) by crosslinking the B domain that is “sandwiched” between A and C lamellae. Despite thorough synthetic variation of the B fraction to control the geometry of the sandwiched microphase, so far only Janus spheres, cylinders, and sheets have been obtained. In this combined theoretical and experimental work, we show that the blending of polybutadiene homopolymer (hPB) into lamella morphologies of polystyrene-block-polybutadiene-block-polymethylmethacrylate (SBM) triblock terpolymers allows the continuous tuning of the polybutadiene (PB) microphase. We systematically vary …
Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. I: Preliminary study in a batch mixer
2005
Abstract Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis-(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6,-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) at 25/75 w/w and 75/25 w/w composition. In order to perform a preliminary analysis on the behaviour of the blends, the materials were prepared in a batch mixer. The materials have been completely characterized from a rheological, morphological, mechanical point of view. The results indic…
Controlled Synthesis of Multi-Arm Star Polyether-Polycarbonate Polyols Based on Propylene Oxide and CO2
2013
Multi-arm star copolymers based on a hyperbranched poly(propylene oxide) polyether-polyol (hbPPO) as a core and poly(propylene carbonate) (PPC) arms are synthesized in two steps from propylene oxide (PO), a small amount of glycidol and CO2 . The PPC arms are prepared via carbon dioxide (CO2 )/PO copolymerization, using hbPPO as a multifunctional macroinitiator and the (R,R)-(salcy)CoOBzF5 catalyst. Star copolymers with 14 and 28 PPC arms, respectively, and controlled molecular weights in the range of 2700-8800 g mol(-1) are prepared (Mw /Mn = 1.23-1.61). Thermal analysis reveals lowered glass transition temperatures in the range of -8 to 10 °C for the PPC star polymers compared with linear …
Core–shell-type multiarm star polyethylenimine-block-poly(ɛ-caprolactone): Synthesis and guest encapsulation potential
2006
Novel multiarm star copolymers with poly(e-caprolactone) (PCL) as the arms and hyperbranched polyethylenimine (HPEI) as the core have been successfully prepared by the tin(II) 2-ethylhexanoate catalyzed ring-opening polymerization of e-caprolactone (CL) with HPEI used directly as a macroinitiator. Not only primary but also secondary amine groups of HPEI participate in initiating the ring-opening polymerization of CL with almost 100% initiation efficiency. The average degree of polymerization of the PCL arms can be controlled by the feed ratio of the monomers to the initiating sites. Because of the polarity difference of the PCL arms and HPEI core, the obtained multiarm star polymers display…