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ELP nanoparticles have been produced to encapsulate and release bone morphogenetic proteins (BMP) for potential protein and drug delivery applications.
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These complexes were produced by encapsulating curcumin phytosomes in chitosan microspheres using ionotropic gelation.
An avian Metapneumovirus (aMPV) fusion (F) protein-encoding plasmid vaccine and the corresponding recombinant protein vaccine were produced and bound to or encapsulated by PLGA-MP, respectively.
Different formulations were produced according to an experimental mixture simplex-lattice design, where the independent variables were the concentrations of each encapsulating agent.
These were encapsulated in an alginate-polylysine matrix and biologically active endostatin (ie that retained its ability to inhibit angiogenesis) was produced for up to 4 weeks.
Nanoparticles were produced by double emulsion-solvent evaporation method to encapsulate bovine serum albumin into the PLGA matrix material.
Furthermore, a range of drug encapsulates NPs were produced and showed a sustained release of the encapsulated drug.
Between 12 and 22 encapsulated eggs are produced at a time, which the female attaches to the bottom.
The carbon encapsulated silicon composite is produced by a two-step thermal reduction of commercial wheat flour.
Herein, ultralong peapod-like nanowires (NWs) composed of short vanadium sesquioxide nanorods (V2O3 NRs) encapsulated with carbon are produced as high-performance anode materials.
In order to evaluate the ability of dextran nanoparticle to attenuate the acidic microenvironment, the dextran nanoparticle was encapsulated into PLGA microspheres in which acidic microenvironment can be produced via biodegradation of PLGA.
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