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. 2021 Dec 6;87(3):1791–1804. doi: 10.1021/acs.joc.1c02308

Table 3. Kinetic Parametersa,b Determined for Peroxidation of MeLin in DMPC/DMPG LUVs without Added Phenols or Inhibited by 1 μM PMHC or 5 μM DAc.

  no additive 1 μM PMHC
5 μM DA
model vox1a vinha effinhb vox2a effox2b vinha effinhb vox2a effox2b
micellesd 92.5 ± 7.3 4.6 ± 0.3 20.2 ± 0.9 57.2 ± 3.4 1.6 ± 0.1 no antioxidant activity
LUVse (XDMPG = 0.00) 16.8 ± 1.4 3.7 ± 0.4 4.3 ± 0.5 18.3 ± 2.5 0.9 ± 0.1 3.7 ± 0.2 4.7 ± 0.3 14.2 ± 0.9 1.2 ± 0.1
LUVse (XDMPG = 0.25) 14.1 ± 1.1 2.1 ± 0.2 6.6 ± 0.5 16.1 ± 0.9 0.9 ± 0.1 3.6 ± 0.5 4.0 ± 0.6 14.2 ± 1.3 1.0 ± 0.1
LUVse (XDMPG = 0.50) 13.6 ± 0.3 2.5 ± 0.3 6.7 ± 0.2 16.3 ± 0.5 0.9 ± 0.1 4.0 ± 0.3 3.6 ± 0.3 12.2 ± 1.0 1.2 ± 0.1
LUVse (XDMPG = 0.75) 13.0 ± 1.3 2.4 ± 0.4 5.5 ± 0.9 13.8 ± 1.6 1.0 ± 0.1 4.1 ± 0.4 3.3 ± 0.3 11.7 ± 1.3 1.2 ± 0.1
LUVse (XDMPG = 1.00) 10.1 ± 0.6 2.5 ± 0.5 4.3 ± 0.9 12.1 ± 1.1 0.8 ± 0.1 3.4 ± 0.2 3.4 ± 0.2 6.0 ± 0.5 1.9 ± 0.2
a

Kinetic chain lengths for uninhibited (vox1), inhibited (vinh), and postinhibited (vox2) peroxidation (i.e., vox1 = Rox1/Ri, vinh = Rinh/Ri, and vox2 = Rox2/Ri).

b

Efficiencies of suppressing peroxidation calculated for the induction period (effinh = Rox1/Rinh) and for the postinhibited process (effox2 = Rox1/Rox2).

c

Experiments were performed at 310 K and pH 7.0 with ABAP as an initiator. All numbers represent the average values obtained from a series of measurements with calculated standard deviations.

d

Kinetic parameters obtained for 2.74 mM MeLin peroxidation in Triton X-100 micelles were added for comparison.

e

LUVs consisted of DMPC and DMPG, with XDMPG being the molar fraction of DMPG in phospholipids, see footnote c in Table 2.