TY - JOUR
T1 - Effect of lipophilization on the distribution and reactivity of ingredients in emulsions
AU - Leong, Wai Fun
AU - Berton-Carabin, C.C.
AU - Elias, Ryan J.
AU - Lecomte, Jérôme
AU - Villeneuve, Pierre
AU - Zhao, Yu
AU - Coupland, John N.
PY - 2015
Y1 - 2015
N2 - Hypothesis: The reactivity of small molecules in emulsions is believed to depend on their partitioning between phases, yet this is hard to verify experimentally in situ. In the present work, we use electron paramagnetic resonance (EPR) spectroscopy to simultaneously measure the distribution and reactivity of a homologous series of lipophilized spin probes in an emulsion. Experiments: 4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL) was derivatized with saturated fatty acids to create a series of spin probes with increasing lipophilicity (C4-, C8-, C12-, and C16-TEMPO). The probes were added to a 10wt.% tetradecane-in water emulsions (d32~190nm) stabilized with sodium caseinate (1wt.% in the aqueous phase, pH 7). The distribution of the probes between phases was measured by electron paramagnetic resonance (EPR) spectroscopy. Findings: TEMPOL partitioned into the aqueous phase, C4-TEMPO distributed between the lipid and aqueous phases (69% and 31% respectively) while the more lipophilic probes dissolved exclusively within the lipid droplets. Interestingly, the more lipophilic probes initially precipitated upon their addition to the emulsion, and only slowly redistributed to the droplets over hours or days, the rate of which was dependent on their carbon chain length. The reactivity of the probes with aqueous an aqueous phase reductant (ascorbate) generally depended on the proportion in the aqueous phase (i.e., TEMPOL. >C4-TEMPO. >C8-TEMPO~C12-TEMPO~C16-TEMPO).
AB - Hypothesis: The reactivity of small molecules in emulsions is believed to depend on their partitioning between phases, yet this is hard to verify experimentally in situ. In the present work, we use electron paramagnetic resonance (EPR) spectroscopy to simultaneously measure the distribution and reactivity of a homologous series of lipophilized spin probes in an emulsion. Experiments: 4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL) was derivatized with saturated fatty acids to create a series of spin probes with increasing lipophilicity (C4-, C8-, C12-, and C16-TEMPO). The probes were added to a 10wt.% tetradecane-in water emulsions (d32~190nm) stabilized with sodium caseinate (1wt.% in the aqueous phase, pH 7). The distribution of the probes between phases was measured by electron paramagnetic resonance (EPR) spectroscopy. Findings: TEMPOL partitioned into the aqueous phase, C4-TEMPO distributed between the lipid and aqueous phases (69% and 31% respectively) while the more lipophilic probes dissolved exclusively within the lipid droplets. Interestingly, the more lipophilic probes initially precipitated upon their addition to the emulsion, and only slowly redistributed to the droplets over hours or days, the rate of which was dependent on their carbon chain length. The reactivity of the probes with aqueous an aqueous phase reductant (ascorbate) generally depended on the proportion in the aqueous phase (i.e., TEMPOL. >C4-TEMPO. >C8-TEMPO~C12-TEMPO~C16-TEMPO).
KW - Electron paramagnetic resonance (EPR)
KW - Emulsion
KW - Small molecule partitioning
KW - Spin probe
KW - TEMPOL
U2 - 10.1016/j.jcis.2015.07.070
DO - 10.1016/j.jcis.2015.07.070
M3 - Article
AN - SCOPUS:84938784133
SN - 0021-9797
VL - 459
SP - 36
EP - 43
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -