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methoxyPEG

Methoxy polyethylene glycol, commonly abbreviated mPEG, is a monomethyl ether derivative of poly(ethylene glycol). In mPEG, one end of the polymer chain is capped with a methoxy group, while the opposite end is available for further functionalization. Depending on the derivative, the free end may be a hydroxyl group or carry a reactive moiety such as an NHS carbonate, maleimide, aldehyde, or other functional group used for conjugation to biomolecules or surfaces.

mPEG is highly water-soluble and chemically inert under many biological conditions, factors that contribute to its

Applications of mPEG include PEGylation of therapeutic proteins and peptides to extend circulatory half-life, reduce immunogenicity,

Safety and regulatory considerations generally reflect PEG’s long-standing use and favorable biocompatibility, though rare anti-PEG antibodies

widespread
use
in
biotechnology
and
pharmaceuticals.
Typical
mPEG
reagents
span
a
broad
range
of
molecular
weights,
from
roughly
500
Da
to
tens
of
kilodaltons,
and
many
derivatives
are
available
with
predefined
end
groups
to
suit
specific
conjugation
strategies.
The
polymer’s
hydrophilic
corona
can
improve
solubility,
stabilize
proteins,
and
reduce
nonspecific
interactions.
and
improve
pharmacokinetic
profiles.
It
is
also
used
to
functionalize
nanoparticles,
liposomes,
and
biosensors,
as
well
as
to
modify
surfaces
and
create
stealth
coatings.
Common
conjugation
chemistries
involve
amine
groups
on
proteins
(via
NHS
esters
or
carbonates)
or
thiols
(via
maleimide
or
related
partners),
enabling
selective,
mild
coupling
under
aqueous
conditions.
have
been
reported
in
some
contexts.
Overall,
mPEG
remains
a
versatile
tool
for
improving
solubility,
stability,
and
biocompatibility
in
a
wide
range
of
bioconjugate
applications.