PubMed · 16102388
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
Uri Zilberman. 2005. Formaldehyde from POM brackets.. https://doi.org/10.1016/j.ajodo.2005.06.008
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
Chitosan is functionalized with poly(ethylene glycol) methyl ether (mPEG) at the amino and hydroxyl groups via a single step reaction in a homogeneous aqueous system. A chitosan aqueous solution obtained from the mixture of chitosan and hydroxybenzotriazole (HOBt) in water is a key factor in providing mild conditions to conjugate mPEG by using a carbodiimide conjugating agent. The reaction at ambient temperature for 24 h gives chitosan-g-mPEG with water solubility with mPEG content as high as 42%. This work demonstrates that a water-soluble chitosan-HOBt complex is an effective system for the preparation of chitosan derivatives via the aqueous system without the use of acids or organic solvents.
Poly(propylene carbonate)/starch (PPC/starch) composites with different starch contents were prepared by melt compounding. The biodegradability of the composites was studied by soil burial for a period of 6 months. FTIR study, thermal analysis and morphology observation indicated clearly the changes of the buried specimens. The weight loss curves and the molecular weight changes of the specimens revealed a three-stage biodegradation, corresponding to the propagation of microorganisms, the degradation of starch and the degradation of PPC. The experimental results showed that the addition of starch accelerated the degradation of PPC. Specimens with higher starch content exhibited greater weight loss in the second stage and smaller weight loss in the third stage.
Delivery of genetic substance to target cells remains an obstacle for efficient utilization of gene therapy approaches. In this study, we describe a formulation of methacrylate acid copolymer carrier of DNA, in which the release rate of the gene can be controlled by pH. Plasmid release was coupled with the polymer's dissolution, which was accelerated in alkali conditions. The released plasmid was intact and bioactive, although alteration from closed circular supercoil to relaxed conformation was observed. Confocal laser scanning microscopy detected the plasmid DNA along the central layers of the polymeric film. Gene delivery systems controlled by the dissolution of the polymeric films offer flexibility in quantity and size of the incorporated DNA, and therefore could have a potential for in vivo use.