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@ARTICLE{Rai:1028278,
author = {Rai, Ragini and Kumar, Deepak and Dhule, Anjali A. and
Rudani, Binny and Tiwari, Sanjay},
title = {{A}lkanols {R}egulate the {F}luidity of {P}hospholipid
{B}ilayer in {A}ccordance to {T}heir {C}oncentration and
{P}olarity},
journal = {Langmuir},
volume = {40},
number = {27},
issn = {0743-7463},
address = {Washington, DC},
publisher = {ACS Publ.},
reportid = {FZJ-2024-04459},
pages = {acs.langmuir.4c01499},
year = {2024},
abstract = {In spite of the widespread use of alkanols as penetration
enhancers, their effect on vesicular formulations remains
largely unexplored. These can affect the stability and
integrity of the phospholipid bilayers. In this study, we
have investigated the interaction of linear (ethanol,
butanol, hexanol, octanol) and branched alkanols (t-amylol
and t-butanol) with three phospholipids (soya lecithin, SL;
soy L-α-phosphatidylcholine, SPC; and
1,2-dipalmitoyl-sn-glycero-3-phosphocholine, DPPC).
Thermodynamic and structural aspects of these interactions
were studied as a function of the alkanol concentration and
chain length. Our interpretations are based on isothermal
titration calorimetry (ITC) and dynamic light scattering
(DLS) experiments. We observed one-site interactions wherein
hydroxyl and acyl groups interacted with the polar and
nonpolar regions of the phospholipid, respectively. The
stability and structural integrity of bilayers appeared to
be dependent upon (a) the hydrocarbon chain length and
concentration of alcohols, and (b) the degree of
unsaturation in the phospholipid molecule. We found that
these interactions triggered a reduction in the enthalpy
which was compensated by increased entropy, keeping free
energy negative. Drop in enthalpy indicates reversible
disordering of the bilayer which enables the diffusion of
alcohol without triggering destabilization. Ethanol engaged
predominantly with the interface, and it resulted in higher
enthalpic changes. Interactions became increasingly
unfavorable with longer alcohols – a cutoff point was
recorded with hexanol. The overall sequence of membrane
disordering capability was recorded as follows: ethanol <
butanol < octanol < hexanol. Octanol’s larger size
restricted its penetration in the bilayer, and hence it
caused less enthalpic changes relative to hexanol. This
could also be verified from the trends in the area ratio of
these vesicles obtained from the DLS data. Branched alkanols
displayed a lower binding affinity with the phospholipids
relative to their linear counterparts. These data are useful
while contemplating the inclusion of short-chain alcohols as
penetration enhancers in phospholipid vesicles.},
cin = {IBI-4},
ddc = {540},
cid = {I:(DE-Juel1)IBI-4-20200312},
pnm = {5241 - Molecular Information Processing in Cellular Systems
(POF4-524)},
pid = {G:(DE-HGF)POF4-5241},
typ = {PUB:(DE-HGF)16},
pubmed = {38935825},
UT = {WOS:001258205900001},
doi = {10.1021/acs.langmuir.4c01499},
url = {https://juser.fz-juelich.de/record/1028278},
}