Age-related Percutaneous Penetration Part 1: Skin Factors
Sailesh Konda, MD1; Susan R. Meier-Davis, DVM, PhD2; Brenda Cayme, RN2; Jutaro Shudo, PhD2; Howard I. Maibach, MD3
1Department of Dermatology, Howard University College of Medicine, Washington, DC, USA
2Teikoku Pharma USA, Inc., San Jose, CA, USA
3Department of Dermatology, University of California, San Francisco, CA, USA
Changes in the skin that occur in the elderly may put them at increased risk for altered percutaneous penetration from pharmacotherapy along with potential adverse effects. Skin factors that may have a role in age-related percutaneous penetration include blood flow, pH, skin thickness, hair and pore density, and the content and structure of proteins, glycosaminoglycans (GAGs), water, and lipids. Each factor is examined as a function of increasing age along with its potential impact on percutaneous penetration. Additionally, topical drugs that successfully overcome the barrier function of the skin can still fall victim to cutaneous metabolism, thereby producing metabolites that may have increased or decreased activity. This overview discusses the current data and highlights the importance of further studies to evaluate the impact of skin factors in age-related percutaneous penetration.
transdermal, elderly, dermatopharmacokinetics, percutaneous penetration, cutaneous metabolism
Human skin changes with increasing age due to both intrinsic and extrinsic factors. Intrinsic skin aging is primarily determined by genetics and extrinsic aging (photoaging) is primarily caused by environmental exposure to ultraviolet light. In sun-exposed skin, these two processes of aging are superimposed. Age-related skin changes may affect the percutaneous penetration of drugs and ultimately their systemic absorption. Numerous physiological and biochemical changes within the skin have been identified, but it is not clear how these factors have a role, if any, in the degree of percutaneous penetration.1
Changes that occur in aged skin include increased stratum corneum dryness,2,3 reduction in sebaceous gland activity resulting in a decrease in skin surface lipids,4 flattening of the dermal-epidermal junction,1,5 and atrophy of the skin capillary network resulting in a gradual attenuation of blood supply to the viable epidermis.6 This overview provides a basis for understanding the effect of skin aging on percutaneous penetration and discusses the individual skin factors and inherent cutaneous metabolism that may be contributing factors. While this is a relatively new and continually evolving area of investigation, we hope that the data consolidated here will serve as a stepping ground for future studies.
Skin Factors Affecting Age-related Percutaneous Penetration
Humans are exposed to drugs by the oral, pulmonary, or percutaneous routes through intentional or accidental means. The route of exposure as well as other factors can have an impact on the absorption of a drug and its resulting effects either locally or systemically. Percutaneous penetration of a drug occurs with its concentration on the skin's surface as the main driving force for a series of partitioning and passive diffusion steps through the stratum corneum, underlying viable epidermis, dermis, and then finally into the circulatory of lymphatic system. Percutaneous penetration may occur through the intercellular, transcellular, and appendegeal routes. The intercellular route is thought to have a major role in drug penetration, which involves partitioning of the drug into the lipid laden extracellular regions of the stratum corneum. Lipophilic drugs diffuse through the lamellar acyl chains of the lipid, while hydrophilic drugs diffuse through the polar head groups of the lipid. The transcellular route involves the drug going through the corneocytes of the stratum corneum and the appendegeal route involves the drug entering the shunts of hair follicles and sebaceous and sweat glands, effectively bypassing the stratum corneum.
Percutaneous absorption of drugs can be affected by drug, exposure, and skin related factors. Drug-related factors include molecular weight, lipid solubility, water solubility, vehicle, irritancy, and other drugs that may serve as enhancers. Exposurerelated factors include drug concentration, duration, use of protective equipment, climate (temperature and humidity), and the matrix (e.g., soil). Skin-related factors include blood flow, pH, skin thickness, hair and pore density, and the content and structure of proteins, glycosaminoglycans (GAGs), water, and lipids (Table 1).7,8 Cutaneous metabolism also has a role and will be covered in a separate section. The following sections serve as an overview for how some of these skin-related factors change as a function of increasing age. There is limited data available on how these age-related changes may directly or indirectly affect the percutaneous penetration of drugs.
As we review skin-related factors, keep in mind that percutaneous penetration varies depending on the regional site of the body.9 There is also considerable variability within a given site as well as within and between individuals, which can result in confounding factors.
||Implication for Percutaneous Penetration
|Cutaneous blood perfusion
- Studies are conflicting; overall trends indicate that blood flow may decrease
|Enhanced local delivery and diminished systemic delivery
- Studies are conflicting, some report an increased pH
|Fluctuation in amount of unionized (lipophilic) drug available for percutaneous penetration
- Stratum corneum maintains thickness; epidermal, dermal, and whole thickness changes are controversial
|Not always an inverse relationship with the degree of percutaneous penetration
|Hair and pore density
- Reduction in hair follicles
- Sebaceous glands increase in size but produce less sebum
- Decreased sweat glands
|Decreased percutaneous penetration through the shunt route
- Intrinsic: collagen is sparser and less soluble, elastin degrades slower and accumulates damage
- Extrinsic: collagen is thickened and more soluble, increased synthesis of abnormal elastin
- Increased folding and decreased interaction of proteins with water
|Increased xerosis, leading to decreased percutaneous penetration
- Increased GAGs but abnormally deposited on elastoic material; cannot interact properly with water
|Improper deposition may decrease percutaneous penetration
- More water is found in the tetrahedron form, instead of bound to proteins
|Increased xerosis, leading to decreased percutaneous penetration
- Studies are conflicting; lipid content appears to decrease
|Enhanced percutaneous penetration
Table 1. Skin factors affecting age-related percutaneous penetration
Cutaneous Blood Perfusion
Cutaneous blood perfusion has been quantitatively studied in vitro using histologic sections stained for alkaline phosphatase or the CD31 antigen. The former is inversely correlated with the degree of blood perfusion and the latter is a marker for endothelial cells.10,11 In vivo methods allow for three-dimensional visualization of cutaneous blood flow and include intravital capillaroscopy (native microscopy and fluorescein angiography), laser Doppler flowmetry (LDF), laser Doppler velocimetry, and photoplethysmography. Intravital capillaroscopy measurements of 26 subjects found a decrease in dermal papillary loops and little change in horizontal vessels with increasing age.10 Kelly and colleagues used LDF and found little difference in blood flow between young (18-26 years) and elderly (65-88 years) subjects; however, there were only 10 subjects in each group.10 Another LDF study of 201 people (10-89 years) revealed that areas with high blood flow, such as the lip, cushion of the third finger, nasal tip, and forehead, decreased with age while areas with initially low blood flow, such as the trunk, had no clear variation with age.12 A photoplethysmographic study including 69 individuals (3-99 years) revealed significantly decreased capillary circulation in forehead skin with advancing age.13 Despite the many tools and techniques available, age studies are often conflicting in the area of blood flow. Overall trends indicate that blood flow may decrease with age, especially in photo-exposed areas. With topically applied drugs, a reduction in blood flow may enhance local delivery, but diminish systemic delivery.
pH contributes to defense against microbiological or drug insults and plays a role in skin barrier homeostasis and stratum corneum desquamation.14 Instruments using a glass planar electrode are primarily used for pH measurement and they function based on a potential difference in H+ concentration between the skin surface and the solution (HgCl + KCl) contained in a reference electrode. Fluhr and colleagues measured 44 adults (21-44 years) and 44 of the adults' children (1-6 years) and found no significant difference in pH between the two groups.15 However, another study involving 11 anatomic locations in 14 adults (26.7 ± 2.8 years) and 15 aged adults (70.5 ± 13.8 years) found pH was significantly higher in the aged group on the ankle and the forehead. Mean pH varied from 4.8 (ankle) to 5.5 (thigh) in the young group and from 5.0 (forehead) to 5.5 (abdomen) in aged individuals.16
Most drugs are weak organic acids or bases and exist in unionized and ionized forms in an aqueous environment. The unionized form is usually lipophilic and the ionized form is hydrophilic. The portion of the unionized form present is determined by the pH and the drug's pKa (acid dissociation constant). When the pH is lower than the pKa, the unionized form of a weak acid predominates, but the ionized form of a weak base predominates. Thus, the skin's pH can affect the amount of unionized drug available for percutaneous penetration. At present, it is unclear to what degree the skin's pH changes with advancing age and more studies are needed in this area.
While the stratum corneum is generally accepted to maintain its thickness during aging,17 epidermal, dermal, and whole skin thickness changes are controversial. In vitro analyses of images taken from light, scanning electron, and transmission electron microscopies have been used to determine the thickness of various skin layers. Recently, confocal laser scanning microscopy (CSLM) has allowed for direct measurement of stratum corneum and epidermal thickness and is considered to be the "gold standard." A CSLM study of 34 subjects (18-69 years) found that the epidermis on the arm thinned with increasing age.18 However, a study of 71 people (20-68 years) involved punch biopsies from the dorsal forearm, buttock, and shoulder found no significant difference in epidermal thickness associated with increasing age.19 Hull and colleagues used scanning electron microscopy to reveal that the corrugated papillary interface between the dermis and epidermis is visible up through the sixth decade and flattens thereafter.20 Flattening may be associated with decreased proliferative potential and could affect percutaneous penetration.
Pulsed ultrasound has also been used for the determination of whole skin thickness. An ultrasound (B-mode) study of 40 subjects (25-90 years) found an increase in facial skin thickness with age.21 However, another ultrasound study showed thinning of forehead skin with age.22 Comparing skin layer thickness is challenging because of significant variation in measurements between individuals and between sites within each individual. The skin thickness of the eyelid is approximately 0.05 cm and that of the palm and sole is about 0.4 cm.23 Note that percutaneous penetration is not exclusively a function of skin thickness. The skin on the sole or palm has a higher rate of diffusion than the skin of the forearm or abdomen, even though it is much thicker. Furthermore, hormonal differences (e.g., estrogen) during the aging process may confound studies of skin thickness.
Hair and Pore Density
Hair follicles and sebaceous and sweat glands represent an important shunt route into the skin for topical drugs. In vitro studies have demonstrated the importance of these skin appendages for percutaneous penetration by hydrophilic drugs.24 The hair follicle infundibulum also has a large storage reservoir capacity, about 10 times more than the stratum corneum.25 There may be a reduction in the amount of hair follicles with age, not only in the scalp, but also throughout the body. The mechanism for this hair follicle dropout is unclear, though it may be similar to the programmed hair follicle organ deletion that can occur in mice with age.26 Sebaceous glands continually secrete sebum, which prevents the loss of water from the skin. In the elderly, sebaceous glands increase in size, but produce less sebum, which may contribute to xerosis. The number of sweat glands also decreases with age, but also shows variation between individuals after adjustment for age and sex.27 All of these appendegeal changes may contribute to decreased percutaneous penetration in aged skin.
Collagen comprises 70-80% of the dry weight of the dermis and is primarily responsible for the skin's tensile strength. The rate of collagen synthesis, activity of post-translational enzymes, collagen solubility, thickness of collagen fiber bundles, and density of the collagen network all decrease in intrinsically aged skin.28-30 However, extrinsically aged skin is characterized by collagen fibers that are fragmented, thickened, and more soluble.28 The elastic fiber network occupies 2-4% of dermal volume and provides resilience and suppleness. Elastin is degraded slowly and accumulates damage with intrinsic aging; also, increased synthesis of abnormally structured elastin occurs in extrinsically aged skin.31 This leads to age-related accumulation of aberrant elastoic material, clumped in the papillary dermis. Age also leads to increased folding and decreased interaction of proteins with water, which may contribute to increased xerosis, and thus, decreased percutaneous penetration.32
Most GAGs are present in human skin as hyaluronic acid and the proteoglycan family of chondroitin sulfates, including dermatan sulfate. Skin hydration is closely linked to the content and distribution of dermal GAGs, which can bind up to 1000 times their volume in water. Despite increased GAGs in extrinsically aged skin, these are abnormally deposited on elastoic material and cannot interact properly with water.33 Brown and colleagues found that topical hyaluronic acid significantly enhanced the partitioning of both diclofenac and ibuprofen into human skin when compared to an aqueous control, pectin, and carboxymethylcellulose.34 This suggests that GAGs, when allowed to interact with water, can enhance the percutaneous penetration of some drugs. The details of their interaction remain to be elucidated.
In young skin, water is usually bound to proteins and is known as bound water, which is important for the structure and mechanical properties of proteins and their interactions. Water molecules not bound to proteins bind to each other and are found in a tetrahedron form. In aged skin, significantly more water is found in the tetrahedron form, which may result in delayed percutaneous penetration, especially for hydrophilic drugs.35 Diridollou and colleagues utilized an active capacitance imaging system to investigate the hydration of dorsal and ventral forearm sites and, as expected, found skin dryness to increase with age.36 Interestingly, they found ethnicity to be a significant factor with elderly African American and Caucasian women (>51 years) having increased skin dryness when compared to their Chinese or Mexican counterparts.
Lipids form multilamellar sheets among the intercellular spaces of the stratum corneum and are critical to the stratum corneum's mechanical and cohesive properties, allowing it to function as an effective water barrier. Lipid content appears to decrease with age, although the proportion of different lipid classes seems to remain fairly constant.37,38 A study of 28 subjects (21-50 years) utilized high performance thin layer chromatography to separate lipid extracts from stratum corneum tape strippings and found a 30% decrease in the face, hands, and legs in older subjects.39 However, Cua and colleagues studied 11 sites on 29 subjects and noted little relation between skin surface lipid content and age, except on the ankle, where the elderly demonstrated decreased lipid content.40 These conflicting results may be due to significant regional variation within individuals they studied. It is generally accepted that percutaneous penetration is increased as the percentage of lipid weight in the stratum corneum is decreased. Both in vitro and in vivo studies have demonstrated enhanced percutaneous penetration following delipidization with polar and nontoxic solvents.41
The impact of cutaneous metabolism and how it changes as a function of increasing age is an area of growing interest on percutaneous drug delivery. Skin contains the major enzymes found in other tissues of the body. These enzymes have the ability to metabolize both endogenous drugs (e.g., hormones, steroids, and inflammatory mediators) and topically applied exogenous compounds (e.g., drugs, pesticides, and industrial and environmental agents). This cutaneous metabolism may result in activation of inert compounds to toxicologically active species, detoxification of toxicologically active drugs to inactive metabolites, conversion of active drugs to active metabolites, and activation of prodrugs. If transport through the epidermis is the rate limiting step and the metabolite is less hydrophobic than the parent compound, then percutaneous absorption of the metabolized compound could be faster than the parent compound, resulting in enhanced local and/or systemic toxicity. Examples of some drugs and compounds that undergo cutaneous metabolism are betamethasone 17-valerate, propranolol, nitroglycerin, theophylline, polycyclic aromatic hydrocarbons, butachlor, and atrazine.42
The skin contains enzymes that undergo Phase 1 (e.g., oxidation, reduction, and hydrolysis) and Phase 2 (e.g., conjugation) reactions. Although the extent of cutaneous metabolism is modest when compared to hepatic metabolism (0.1-28% of the activities in the liver for Phase 1; 0.6-50% for Phase 2), it is important to consider the effect of cutaneous metabolism on percutaneous drug delivery.43,44
Sotaniemi and colleagues measured cytochrome P-450 content in liver biopsy samples from 226 subjects and levels were found to be increased during the fourth decade, declined after 40 years to a level that remained unaltered up to 69 years, then declined further after 70 years.45 Extrapolating this to the skin, one would expect cutaneous metabolism to follow a similar pattern with increasing age. While a study found a 15-25% decrease in the activity of most cutaneous enzymes,46 other studies have reported no significant differences in relation to age.47 Yamasawa and colleagues obtained skin biopsies from the abdomen of 63 subjects (1 month to 90 years) and enzyme activity was assayed using fluorometric methods. Fourteen enzymes, representative of the glycolytic pathway, tricarboxylic acid cycle, the transamination linkages between amino acid and carbohydrate metabolism, the pentose phosphate pathway, and fatty acid metabolism were studied. No significant differences in enzyme activity were observed in relation to age.48
The effect of cutaneous metabolism on the biological response to topically applied drugs is only beginning to be investigated. Work has been directed towards the use of topical prodrugs and the design of molecules better able to transport across the stratum corneum and then undergo local enzymatic activation. This task is complicated since skin metabolism is difficult to measure in vivo without interference from systemic enzymes. In addition, certain cutaneous metabolic systems, such as cytochrome P-450, have relatively low activity when compared with the liver. Further research in this area requires a more specific quantitative understanding of the metabolic capabilities of human skin in vivo.
We are currently facing a dramatic demographic shift as the average age of the population steadily increases secondary to the baby boomer generation and advances in medicine allow for longer life expectancy. Consequently, it is crucial that we gain a better understanding of how age-related changes in the skin affect percutaneous drug penetration. Presently, studies focusing on dermatopharmacokinetics as a function of increasing age have conflicting results. If there is in fact a difference in percutaneous penetration between the young and the elderly, potential skin factors that may have a direct or indirect role have been outlined. Furthermore, cutaneous metabolism may provide an additional variable even if a drug is able to successfully navigate the barrier function of the skin. The crux of these evaluations is the assumption that individuals have similar pharmacodynamics, which may not be the case. In the future, metabolic phenotyping may be able to overcome inter-individual variation.
- Gilchrest BA. Skin and aging processes. Boca Raton, FL: CRC Press; 1984.
- Potts RO, Buras EM, Jr., Chrisman DA, Jr. Changes with age in the moisture content of human skin. J Invest Dermatol. 1984 Jan;82(1):97-100.
- Potts RO, Buras EM. In vivo changes in the dynamic viscosity of human stratum corneum as a function of age and ambient moisture. J Soc Cosmet Chem. 1985;36:169-76.
- Pochi PE, Strauss JS, Downing DT. Age-related changes in sebaceous gland activity. J Invest Dermatol. 1979 Jul;73(1):108-11.
- Lavker RM, Zheng PS, Dong G. Morphology of aged skin. Dermatol Clin. 1986 Jul;4(3):379-89.
- Ryan TJ. Cutaneous circulation. In Goldsmith LA, ed. Biochemistry and physiology of the skin. Vol II. New York/Oxford: Oxford University Press; 1983:817-77.
- Waller JM, Maibach HI. Age and skin structure and function, a quantitative approach (I): blood flow, pH, thickness, and ultrasound echogenicity. Skin Res Technol. 2005 Nov;11(4):221-35.
- Waller JM, Maibach HI. Age and skin structure and function, a quantitative approach (II): protein, glycosaminoglycan, water, and lipid content and structure. Skin Res Technol. 2006 Aug;12(3):145-54.
- Feldmann RJ, Maibach HI. Regional variation in percutaneous penetration of 14C cortisol in man. J Invest Dermatol. 1967 Feb;48(2):181-3.
- Kelly RI, Pearse R, Bull RH, et al. The effects of aging on the cutaneous microvasculature. J Am Acad Dermatol. 1995 Nov;33(5 Pt 1):749-56.
- Chung JH, Yano K, Lee MK, et al. Differential effects of photoaging vs intrinsic aging on the vascularization of human skin. Arch Dermatol. 2002 Nov;138(11):1437-42.
- Ishihara M, Itoh M, Ohsawa K, et al. Blood flow. In: Kligman AM, Takase Y, eds. Cutaneous aging. Tokyo: University of Tokyo Press; 1988:167-81.
- Leveque JL, Corcuff P, de Rigal J, et al. In vivo studies of the evolution of physical properties of the human skin with age. Int J Dermatol. 1984 Jun;23(5):322-9.
- Rippke F, Schreiner V, Doering T, et al. Stratum corneum pH in atopic dermatitis: impact on skin barrier function and colonization with Staphylococcus aureus. Am J Clin Dermatol. 2004;5(4):217-23.
- Fluhr JW, Pfisterer S, Gloor M. Direct comparison of skin physiology in children and adults with bioengineering methods. Pediatr Dermatol. 2000 Nov-Dec;17(6):436-9.
- Wilhelm KP, Cua AB, Maibach HI. Skin aging. Effect on transepidermal water loss, stratum corneum hydration, skin surface pH, and casual sebum content. Arch Dermatol. 1991 Dec;127(12):1806-9.
- Batisse D, Bazin R, Baldeweck T, et al. Influence of age on the wrinkling capacities of skin. Skin Res Technol. 2002 Aug;8(3):148-54.
- Sandby-Moller J, Poulsen T, Wulf HC. Epidermal thickness at different body sites: relationship to age, gender, pigmentation, blood content, skin type and smoking habits. Acta Derm Venereol. 2003;83(6):410-3.
- Branchet MC, Boisnic S, Frances C, et al. Skin thickness changes in normal aging skin. Gerontology. 1990;36(1):28-35.
- Hull MT, Warfel KA. Age-related changes in the cutaneous basal lamina: scanning electron microscopic study. J Invest Dermatol. 1983 Oct;81(4):378- 80.
- Pellacani G, Seidenari S. Variations in facial skin thickness and echogenicity with site and age. Acta Derm Venereol. 1999 Sep;79(5):366-9.
- Gniadecka M, Jemec GB. Quantitative evaluation of chronological ageing and photoageing in vivo: studies on skin echogenicity and thickness. Br J Dermatol. 1998 Nov;139(5):815-21.
- Maibach HI, Patrick E. Dermatotoxicology. In: Hayes WA, ed. Principles and methods of toxicology. 4th ed. Philadelphia, PA: Taylor and Francis; 2001:1039- 1046.
- Essa EA, Bonner MC, Barry BW. Human skin sandwich for assessing shunt route penetration during passive and iontophoretic drug and liposome delivery. J Pharm Pharmacol. 2002 Nov;54(11):1481-90.
- Lademann J, Richter H, Schaefer UF, et al. Hair follicles - a long-term reservoir for drug delivery. Skin Pharmacol Physiol. 2006;19(4):232-6.
- Eichmuller S, van der Veen C, Moll I, et al. Clusters of perifollicular macrophages in normal murine skin: physiological degeneration of selected hair follicles by programmed organ deletion. J Histochem Cytochem. 1998 Mar;46(3):361-70.
- Scobbie RB, Sofaer JA. Sweat pore count, hair density and tooth size: heritability and genetic correlation. Hum Hered. 1987;37(6):349-53.
- Gniadecka M, Gniadecki R, Serup J, et al. Ultrasound structure and digital image analysis of the subepidermal low echogenic band in aged human skin: diurnal changes and interindividual variability. J Invest Dermatol. 1994 Mar;102(3):362-5.
- Uitto J. Connective tissue biochemistry of the aging dermis. Age-associated alterations in collagen and elastin. Clin Geriatr Med. 1989 Feb;5(1):127-47.
- Lavker RM, Zheng PS, Dong G. Aged skin: a study by light, transmission electron, and scanning electron microscopy. J Invest Dermatol. 1987 Mar;88(3 Suppl):44s-51s.
- Bernstein EF, Chen YQ, Tamai K, et al. Enhanced elastin and fibrillin gene expression in chronically photodamaged skin. J Invest Dermatol. 1994 Aug;103(2):182-6.
- Gniadecka M, Nielsen OF, Wessel S, et al. Water and protein structure in photoaged and chronically aged skin. J Invest Dermatol. 1998 Dec;111(6): 1129-33.
- Bernstein EF, Underhill CB, Hahn PJ, et al. Chronic sun exposure alters both the content and distribution of dermal glycosaminoglycans. Br J Dermatol. 1996 Aug;135(2):255-62.
- Brown MB, Hanpanitcharoen M, Martin GP. An in vitro investigation into the effect of glycosaminoglycans on the skin partitioning and deposition of NSAIDs. Int J Pharm. 2001 Aug 28;225(1-2):113-21.
- Gniadecka M, Faurskov Nielsen O, Christensen DH, et al. Structure of water, proteins, and lipids in intact human skin, hair, and nail. J Invest Dermatol. 1998 Apr;110(4):393-8.
- Diridollou S, de Rigal J, Querleux B, et al. Comparative study of the hydration of the stratum corneum between four ethnic groups: influence of age. Int J Dermatol. 2007 Oct;46 Suppl 1:11-4.
- Roskos KV. The effect of skin aging on the percutaneous penetration of chemicals through human skin. Dissertation, University of California, San Francisco, CA, 1989.
- Saint Leger D, Francois AM, Leveque JL, et al. Age-associated changes in stratum corneum lipids and their relation to dryness. Dermatologica. 1988;177(3):159-64.
- Rogers J, Harding C, Mayo A, et al. Stratum corneum lipids: the effect of ageing and the seasons. Arch Dermatol Res. 1996 Nov;288(12):765-70.
- Cua AB, Wilhelm KP, Maibach HI. Skin surface lipid and skin friction: relation to age, sex and anatomical region. Skin Pharmacol. 1995;8(5):246-51.
- Menczel EM. Delipidization of the cutaneous permeability barrier and percutaneous penetration. In: Smith EW, Maibach HI, eds. Percutaneous penetration enhancers. 1st ed. Boca Raton, FL: CRC Press; 1995:383-92.
- Bashir S, Maibach HI. Cutaneous metabolism of xenobiotics. In: Bronaugh RL, Maibach HI, eds. Percutaneous absorption: drugs-cosmetics-mechanismmethodology. 3rd ed. New York, NY: Marcel Dekker; 1999:65-80.
- Kao J, Carver MP. Cutaneous metabolism of xenobiotics. Drug Metab Rev. 1990;22(4):363-410.
- Hotchkiss SAM. Dermal metabolism. In: Roberts MS, Walter KA, eds. Dermal absorption and toxicity assessment. Vol 91. New York, NY: Marcel Dekker; 1998:43-101.
- Sotaniemi EA, Arranto AJ, Pelkonen O, et al. Age and cytochrome P450- linked drug metabolism in humans: an analysis of 226 subjects with equal histopathologic conditions. Clin Pharmacol Ther. 1997 Mar;61(3):331-9.
- Salfeld K. [On the problem of energy producing metabolism and amino acid metabolism in the aging skin. II. Enzymatic activity in the epidermis of adults of advanced age depending on the localization]. Arch Klin Exp Dermatol. 1966 May 27;225(1):93-100.
- Ribuffo A. Metabolismo glicidico cutaneo nell'invecchiamento. In: Dinamico dell'invecchiamento della pelle. Italy: Minerva Medica; 1967:74-104.
- Yamasawa S, Cerimele D, Serri F. The activity of metabolic enzymes of human epidermis in relation to age. Br J Dermatol. 1972 Feb;86(2):134-40.
In this issue:
- Age-related Percutaneous Penetration Part 1: Skin Factors
- Excimer Laser Therapy for Hairline Psoriasis: A Useful Addition to the Scalp Psoriasis Treatment Algorithm
- Update on Drugs and Drug News - May 2012
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