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. 2022 Jul 29;14(8):1587. doi: 10.3390/pharmaceutics14081587

Table 1.

Descriptive characteristics of included laboratory Demodex studies (n = 8).

Study Setting Study Design Method/Assay Intervention Outcome Measure(s) Treatment Outcome(s) Quality Score
Bulut and Tanriverdi, 2021 [70], Turkey In vitro (n = 4.8 (mean) Demodex (no report on species type) randomly assigned to each group) In vitro killing assay: direct application of test solutions onto epilated eyelashes with mites placed on the glass slides and microscopic examination of their non-viability for 360 min n = mean number of 4.8 mites in each group
TTO (2 %, Osto®) solution (n = 5)
TTO (7.5 %, Blefaritto®) solution
Terpinen-4-ol (T4O, 0.5%, Blefastop plus®) wipe
Saline solution (Control)
Mite survival time (MST): from treatment to non-viability (absence of limb and body movement during an observation period of 1 min) MST (Mean ± SD): 95.9 ± 25.2 min for TTO (2%) vs. 67.1 ± 21.8 for TTO (7.5%) vs. 27.3 ± 6.0 for T4O (0.5%) vs. 323.5 ± 21.1 for Saline (p < 0.001)
MST (Mean ± SD): T4O (0.5%) vs. TTO (2%) vs. TTO (7.5%) (p < 0.001); TTO (7.5%) vs. TTO (2%) (p < 0.001)
17
(Reliable without restriction)
Yurekli and Botsali, 2021 [71], Turkey In vitro (n = 35 D. folliculorum randomly assigned to each group) In vitro killing assay: direct application of test solutions onto diagnostic Standardized Skin Surface Biopsy samples with mites placed on glass slides and microscopic examination of their non-viability for 240 min TTO (2.5%)
TTO (5%)
TTO (10%) (n = 5)
TTO (25%) (n = 5)
TTO (50%) (n = 11)
TTO (100%) (n = 21) solutions
Permethrin (5%) solution (positive control)
Immersion oil (negative control)
MST: from treatment to non-viability (absence of body and leg movements during an observation period of 1 min) MST (Mean ± SD): 54.0 ± 6.1 min for TTO (2.5%) vs. 39.0 ± 3.9 for TTO (5%) vs. 22.0 ± 2.5 for TTO (10%) vs. 13.0 ± 2.5 for TTO (25%) vs. 7.8 ± 0.6 for TTO (50%) vs. 3.3 ± 1.3 for TTO (100%) (p < 0.001) vs. 12.5 ± 1.9 for Permethrin 5% vs. 196.0 ± 23.6 for Immersion oil
MST (Mean ± SD): 13.0 ± 2.5 for TTO (25%) vs. 12.5 ± 1.9 for Permethrin 5% (p = 0.628) (no p-value is reported for TTO solutions vs. negative control)
17
(Reliable without restriction)
Cheung et al., 2018 [112], New Zealand In vitro (n = 93 Demodex (no report on species type) randomly assigned to each group) In vitro killing assay: direct application of test solutions onto epilated eyelashes with mites placed on the glass slides and microscopic examination of their non-viability for 300 min TTO (100%) solution (n = 10)
TTO (50%) solution (n = 10)
Terpinen-4-ol (T4O, 100%) solution (n = 11)
Linalool (100%) solution (n = 10)
T4O (Cliradex®, 4 mg/mL) towelette cleanser (n = 10)
T4O (Oust Demodex®, 0.29 mg/mL) cleanser (n = 11)
T4O (Blephadex, 0.03 mg/mL) eyelid foam (n = 10)
T4O (0.02 mg/mL) and linalool (76%) (TheraTears® SteriLid®) eyelid cleanser (n = 11)
No treatment (n = 10)
Mite survival time (MST): from treatment to non-viability (absence of limb and body movement over two consecutive observations periods) MST (Median [range]): 10 (7–24) mins for TTO (100%) vs. 28 (24–75) for TTO (50%) vs. 12 (5–18) for T4O (100%) vs. 7 (5–21) for Linalool vs. 37.5 (15–240) for Cliradex® vs. 90 (30–150) for Oust Demodex® vs. 60 (15–240) for Blephadex vs. 70 (30–145) for TheraTears® SteriLid® vs. ≥ 300 min for No treatment groups (p < 0.0001) 17
(Reliable without restriction)
Frame et al., 2018 [114], New Zealand In vitro (n = 52 Demodex (no report on species type) randomly assigned to each group) In vitro killing assay: direct application of TTO solutions onto epilated eyelashes with mites placed on glass slides or placing the mites onto slides smeared with the honey and microscopic examination of their non-viability for 240 min TTO (100%) solution (n = 10)
TTO (50%) solution (n = 12)
Cyclodextrin- complexed manuka honey MGO (CyCMH, n = 12)
Uncomplexed manuka honey MGO (UCMH, n = 10)
No treatment (n = 8)
MST: from treatment to non-viability (absence of limb and body movement) MST (Median (range)): 9 (6–10) mins for TTO (100%) vs. 121 (8–190) for TTO (50%) vs. 141 (34–185) for CyCMH vs. 190 (190–censored) for UCMH vs. ≥ 250 min for No treatment groups (p < 0.001) 17
(Reliable without restriction)
Gao et al., 2005 [97], USA In vitro (n = 116 D. folliculorum mites randomly assigned to each group) In vitro killing assay: direct application of test solutions onto epilated eyelashes with mites placed on glass slides and microscopic examination of their non-viability for 150 min TTO (100%) (n = 21); TTO (50%) (n = 11); TTO (25%) (n = 5) TTO (10%) (n = 5) solutions; Baby shampoo (50%) (BS, n = 9); Mineral oil (MO, n = 5); Povidone-iodine (10%) (PI, n = 4); Alcohol (100%) (Alc, n = 7); Alcohol (75%) (Alc, n = 8); Caraway oil (100%) (CWO, n = 16); Dill weed oil (100%) (DWO, n = 5); and Pilocarpine (Pilo, n = 3) MST: from treatment to non-viability (absence of limb and body movement) MST (Mean ± SD): 3.7 ± 0.8mins for TTO (100%) vs. 14.8 ± 9.5 for TTO (50%) vs. 34.7 ± 4.3 for TTO (25%) vs. 150 (no SD) for TTO (10%) vs. 150 (no SD) for BS vs. 150 (no SD) for MO vs. 150 (no SD) for PI vs. 39 ± 1.2 for 100% Alc vs. 150 (no SD) for 75% Alc vs. 4.4 ± 2.5 CWO vs. 14 ± 8.3 for DWO vs. 150 (no SD) for Pilo (no p-value is reported)
TTO: 3.7 ± 0.8mins for TTO (100%) vs. 14.8 ± 9.5 for TTO (50%) vs. 34.7 ± 4.3 for TTO (25%) vs. 150 (no SD) for TTO (10%) (p < 0.01)
16
(Reliable without restriction)
Kabat 2019 [100], USA In vitro (n = 35 D. folliculorum randomly assigned to each group) In vitro killing assay: immersion of epilated eyelashes with mites placed on glass slides with test solutions and microscopic examination of their non-viability for 90 min T4O (4%) solution (n = 12)
Hypochlorous acid (0.01%) solution (HOCl, n = 14)
Mineral oil (100%) (MO, n = 9)
MST or kill time: from treatment to non-viability (absence of limb and body movement) MST (Mean ± SD):
T4O: 40 ± 0.0 min for T4O vs. 87.9 ± 4.2 for HOCl (p = 0.0005)
HOCl: 87.9 ± 4.2mins for HOCl vs. 90 ± 0.0 for MO (p = 0.25)
18
(Reliable without restriction)
Oseka and Sedzikowska, 2014 [64], Poland In vitro (n = not reported, no report on species type) In vitro killing assay: immersion of mites in test solutions placed on glass slides and microscopic examination of their non-viability for about 6 days TTO (50%) solution
Sage oil (100%) solution
Peppermint oil (100%) solution
Aloe oil (100%) solution
Seabuckthorn oil (100%) solution
Physiological saline (control)
MST: from treatment to non-viability (absence of limb and body movement) MST (Mean): 7 min for TTO (50%) vs. 7 min for Sage oil vs. 11 min for Peppermint oil vs. 9 h for Aloe vs. 3 days for Seabuckthorn vs. 82 h for Control (no p-value is reported) 4 (Not assignable)
Tighe et al., 2013 [81], China In vitro (n = 292, no species type is reported) In vitro killing assay: immersion of epilated eyelashes with mites placed on glass slides with test solutions and microscopic examination of their non-viability for 150 min n = 6 for each group
T4O: 100%; 50% 25%, and 10% solutions
γ-Terpinene: 100%; 50% and 25%
α -Terpinene:100%; 50% 25%, and 10%
α-Terpineol: 100%; 50% 25%, and 10%
1,8-Cineole: 100%; 50% 25%, and 10%
Mineral oil (100%) control
(NB: only the top five major components are considered here)
MST: from treatment to non-viability (absence of movement of legs) MST (Mean ± SD):
T4O: 3.6 ± 1.1 min for 100% vs. 4.5 ± 1.0 for 50% vs. 8.3 ± 3.1 for 25% vs. 12.3 ± 8.8 for 10% T4O; γ-Terpinene: 8.3 ± 6.2 for 100% vs. 75.9 ± 29.8 for 50% vs. > 150 for 25%; α -Terpinene:13.6 ± 4.4 min for 100% vs. 21.0 ± 2.2 for 50% vs. 61.6 ± 11.6 for 25% vs. > 150 for 10%; α-Terpineol: 3.8 ± 0.8 for 100% vs. 12.5 ± 2.9 for 50% vs. 22.8 ± 3.9 for 25% vs. 43.4 ± 4.3 for 10%; 1,8-Cineole: 13.5 ± 2.0 for 100% vs. 18.8 ± 4.1 for 50% vs. 23.5 ± 3.9 for 25% vs. 44.4 ± 7.2 for 10% vs. no effect for MO (no p-value is reported for each comparison)
17
(Reliable without restriction)