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@ARTICLE{PuigRigall:890359,
author = {Puig-Rigall, Joan and Blanco-Prieto, María J. and Aydillo,
Carlos and Radulescu, Aurel and Molero-Vilchez, Dolores and
Dreiss, Cécile A. and González-Gaitano, Gustavo},
title = {{P}oloxamine/{D}-α-{T}ocopheryl polyethylene glycol
succinate ({TPGS}) mixed micelles and gels: {M}orphology,
loading capacity and skin drug permeability},
journal = {Journal of molecular liquids},
volume = {324},
issn = {0167-7322},
address = {New York, NY [u.a.]},
publisher = {Elsevier},
reportid = {FZJ-2021-00904},
pages = {114930},
year = {2021},
abstract = {The combination of polymeric surfactants with different
features into mixed micelles give access to properties that
may be superior to the single-component micelles. In this
work, we investigated synergistic effects in mixtures of
D-α-Tocopheryl polyethylene glycol succinate (TPGS) with
poloxamines (also known as Tetronic), pH-responsive and
thermogelling polyethylene oxide (PEO)-polypropylene oxide
(PPO) 4-arm block copolymers. We examined the morphology of
the self-assembled micelles of TPGS with Tetronic 1107
(T1107) and 908 (T908) in the presence of naproxen (NA),
used as a model drug, and assessed the capacity of the
single and mixed micelles to trap the guest, using a
combination of small-angle neutron scattering (SANS) and NMR
spectroscopy (1D, 2D-NOESY and diffusion NMR), over a range
of compositions and temperatures, in the dilute regime and
gel state. NA did not interact with T1107 or T908 in their
unimer form, but it was incorporated into the hydrophobic
core of the micelles above the critical micellar temperature
(CMT). In contrast, TPGS dissolved NA at any temperature,
mainly in the tocopherol core, with some partitioning in the
PEG-shell. The micellar structure was not altered by the
presence of NA, except for an expansion of the core size, a
result of the preferential accumulation of NA in that
compartment. The solubility of the drug in single component
micelles increased markedly with temperature, while mixed
micelles produced an intermediate enhancement of the
solubility between that of TPGS and the poloxamines, which
increased at higher TPGS/poloxamine ratios. Micellar
hydrogels formed by the packing of the polymeric mixed
micelles in a BCC macrolattice, whose structure was not
altered by the presence of the drug (at least at 0.2
$wt\%).$ The applicability of the drug-loaded gels for
topical formulations was explored by transdermal diffusion
testing using a synthetic model of skin, showing that the
diffusion of NA across the membrane was enhanced by
incorporating small amounts of TPGS to the hydrogel,
especially with the more hydrophilic T908.},
cin = {JCNS-FRM-II / MLZ},
ddc = {540},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 / I:(DE-588b)4597118-3},
pnm = {6G4 - Jülich Centre for Neutron Research (JCNS) (FZJ)
(POF4-6G4)},
pid = {G:(DE-HGF)POF4-6G4},
experiment = {EXP:(DE-MLZ)KWS2-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000632343700086},
doi = {10.1016/j.molliq.2020.114930},
url = {https://juser.fz-juelich.de/record/890359},
}