Biomedical Engineering Reference
In-Depth Information
Crosslinked
poly(hydroxypropyl
L-glutamine) hydrogel
microspheres
Synthesized by treating the hydrophobic synthetic
polyamino acid poly(benzyl L-glutamate)
microspheres with aminopropyl alcohol
containing 5% (w/v) hexanediamine as a
crosslinker
As more phenyl groups were substituted by
hydroxypropyl groups, the microspheres
became increasingly hydrophilic, thereby
resulting in a substantial reduction in
liver uptake
[323]
Polyester-based bioerodible
hydrogel
Has been made as dried microspheres that can be
resuspended in water
Microspheres able to pass through a 22G
hypodermic needle and exhibited a
reasonably linear release of albumin by
matrix erosion
[324]
Bioerodible noncrosslinked
poly(methyl methacrylate-
co -methacrylic acid) beads
To achieve synchronization of swelling and
dissolution fronts of the spherical bead
Release of a GH-releasing peptide
[325]
Polyorganophosphazene
with amino omega
methylpolyethylene
glycol; polyepsilon
caprolactone- co -lactide-
polyethylene glycol; N -
isopropylacrylamide
Temperature sensitive hydrogels
Various proteins and peptides are
incorporated, like hGHs
[326,327]
Polyactive microspheres—
amphiphilic multiblock
copolymers
Hydrophilic poly(ethylene glycol)-terephthalate
(PEGT) segments have been coupled to more
hydrophobic poly(butylene terephthalate) (PBT)
segments. Variation in content and MWt of PEG
allows fine-tuning of release kinetics of proteins
Lysozyme used as model protein
[328]
Dextran methacrylate; dextran-
hydroxyethyl methacrylate;
dextran-hydroxyethyl
methacrylate-lactate
Release kinetics depends upon initial water
content, crosslink density, and the type of
polymeric precursor
Model drugs used for dextran hydrogel
were IgG, IL-2, hGH
[328,329]
Dextran hydrogel by PLA
stereocomplexing
D- and L-lactic acid oligomers can be grafted to
dextran. Release kinetics depend on the degree of
substitution, oligomer chain length, and MWt of
the protein
Model drugs used for dextran hydrogel:
IgG, IL-2, hGH
[330]
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