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. 2012 Jan 17;4(1):71–92. doi: 10.3390/pharmaceutics4010071

Table 1.

Skin penetration enhancers studied (listed alphabetically according to chemical classes).

Chemical Log Koctanol/PBS or Log Koctanol/water Class References
Ethanol −0.30 a Alcohol Kim et al. [6]
1-Propanol 0.25 a Alcohol Kim et al. [6]
1-Butanol 0.84 a Alcohol Kim et al. [6], Chantasart and Li [36]
1-Pentanol 1.5 a Alcohol Kim et al. [6], Chantasart and Li [36]
1-Hexanol 2.1 b Alcohol Warner et al. [24], Ibrahim and Li [40,56]
1-Heptanol 2.5 b Alcohol Warner et al. [24], Chantasart et al. [27]
1-Octanol 3.1 b Alcohol Warner et al. [24], Ibrahim and Li [40,56]
1-Nonanol 3.5 b Alcohol Chantasart et al. [27]
1-Undecanol 4.2 c Alcohol Ibrahim and Li [40,56]
Oleyl alcohol 7.0 d Alcohol Ibrahim and Li [40,56]
2-Hexanol 1.83 b Alcohol Chantasart et al. [27]
3-Hexanol 1.81 b Alcohol Chantasart et al. [27]
2-Heptanol 2.43 b Alcohol Chantasart et al. [27]
3-Heptanol 2.42 b Alcohol Chantasart et al. [27]
4-Heptanol 2.32 b Alcohol Chantasart et al. [27]
2-Octanol 3.03 b Alcohol Chantasart et al. [27]
3-Octanol 2.94 b Alcohol Chantasart et al. [27]
4-Octanol 2.88 b Alcohol Chantasart et al. [27]
2-Nonanol 3.48 b Alcohol Chantasart et al. [27]
3-Nonanol 3.47 b Alcohol Chantasart et al. [27]
4-Nonanol 3.46 b Alcohol Chantasart et al. [27]
5-Nonanol 3.42 b Alcohol Chantasart et al. [27]
cis-3-Penten-1-ol 1.08 e Alcohol He et al. [26]
cis-3-Hexen-1-ol 1.63 e Alcohol He et al. [26]
cis-3-Octen-1-ol 2.71 e Alcohol He et al. [26]
cis-3-Nonen-1-ol 3.25 e Alcohol He et al. [26]
trans-3-Hexen-1-ol 1.76 e Alcohol He et al. [26]
trans-Hydroxyproline-N-decanamide-C-ethylamide 2.9 f Amide/Alcohol Warner et al. [24]
N,N-Dimethylhexanamide 1.4 g Amide Warner et al. [23]
N,N-Dimethylheptanamide 1.9 g Amide Warner et al. [23]
N,N-Dimethyloctanamide 2.6 g Amide Warner et al. [23]
N,N-Dimethylnonanamide 1.9 g Amide Warner et al. [23]
Benzyl alcohol 1.1 d Aromatic ring: alcohol Ibrahim and Li [40,56]
2-Phenoxyethanol 1.2 h Aromatic ring: alcohol Ibrahim and Li [40,56]
2-Phenylethanol 1.6 i Aromatic ring: alcohol Chantasart et al. [30]
Padimate O (PadO) 5.8 d Aromatic ring: aminobenzoate Ibrahim and Li [40,56]
Butylated hydroxyanisole 3.1 j Aromatic ring: hydroxyanisole Ibrahim and Li [40,56]
2-Ethylhexyl salicylate 6.0 d Aromatic ring: salicylate Ibrahim and Li [40,56]
Salicylaldehyde 2.0 d Aromatic ring: salicylate Ibrahim and Li [40,56]
1-Butyl-2-azacycloheptanones 1.8 f Azone He et al. [25]
1-Hexyl-2-azacycloheptanones 2.9 f Azone He et al. [25]
1-Octyl-2-azacycloheptanones 4.0 f Azone He et al. [25]
Laurocapram (Azone) 6.3 k Azone Ibrahim and Li [40,56]
1,2-Hexanediol 0.78 f Diol Warner et al. [23]
1,2-Octanediol 2.1 f Diol Warner et al. [23]
1-2-Decanediol 3.2 f Diol Warner et al. [23]
2-(1-Butyl)-2-methyl-1,3 dioxolane 2.1 f Dioxolane Warner et al. [24]
2-(1-Hexyl)-2-methyl-1,3 dioxolane 3.5 f Dioxolane Warner et al. [24]
Isopropyl myristate 7.3 d Ester Ibrahim and Li [40,56]
Decanoic acid 4.0 d Fatty acid Ibrahim and Li [41]
Undecanoic acid 4.5 d Fatty acid Ibrahim and Li [41]
Lauric acid 5.0 d Fatty acid Ibrahim and Li [41]
Tridecanoic acid 5.5 d Fatty acid Ibrahim and Li [41]
Myristic acid 6.0 d Fatty acid Ibrahim and Li [41]
Pentadecanoic acid 6.5 d Fatty acid Ibrahim and Li [41]
Palmitic acid 7.0 d Fatty acid Ibrahim and Li [41]
Stearic acid 7.9 d Fatty acid Ibrahim and Li [41]
Linoleic acid 7.5 d Fatty acid Ibrahim and Li [41]
Oleic acid 7.6 d Fatty acid Ibrahim and Li [40,41,56]
Ricinoleic acid 6.2 d Fatty acid Ibrahim and Li [41]
1-Octyl-β-D-glucopyranoside 1.9 f Glucoside Warner et al. [24]
1-Decyl-β-D-glucopyranoside 3.1 f Glucoside Warner et al. [24]
1,2-Dihydroxypropyl octanoate 2.4 f Monoglyceride Warner et al. [24]
1,2-Dihydroxypropyl decanoate 3.1 f Monoglyceride Warner et al. [24]
1-Butyl-2-piperidinone 1.4 f Piperidinone Warner et al. [24]
1-Hexyl-2-piperidinone 2.6 f Piperidinone Warner et al. [24]
1-Octyl-2-piperidinone 3.4 f Piperidinone Warner et al. [24]
1-Ethyl-2-pyrrolidone −0.04 d Pyrrolidone Yoneto et al. [22,45]
1-Butyl-2-pyrrolidones 1.02 f Pyrrolidone Yoneto et al. [22,45]
1-Hexyl-2-pyrrolidinone 2.1 f Pyrrolidone Yoneto et al. [22] He et al. [25], Ibrahim and Li [40]
1-Octyl-2-pyrrolidinone 3.0 f Pyrrolidone Yoneto et al. [22] He et al. [25], Ibrahim and Li [40,56]
1-Decyl-2-pyrrolidinone 4.1 l Pyrrolidone Warner et al. [39]
1-Dodecyl-2-pyrrolidinone 4.9 l Pyrrolidone Warner et al. [39]
Thymol 2.5 m Terpene Chantasart et al. [31]
Menthol 3.4 m Terpene Chantasart et al. [31]
Menthone 2.9 m Terpene Chantasart et al. [31] Ibrahim and Li [40]
Carvacrol 2.5 m Terpene Chantasart et al. [31]
Cineole 3.1 m Terpene Chantasart et al. [31]
1,2,3-Nonanetriol 1.6 f Triol Warner et al. [24]

a Values from the literature [57]; b Experimental values from the literature [27]; c Experimental values from the literature [58]; d Calculated values based on the chemical structure of the compound, obtained from EPI suite database; e Experimental values from the literature [26]; f Experimental values from the literature [24]; g Experimental values from the literature [23]; h Experimental values from the literature [59]; i Experimental values from the literature [30]; j Experimental values from the literature [60]; k Experimental values from the literature [61]; l Experimental values from the literature [39]; m Experimental values from the literature [31].