Sign in

Shea Butter Extract for Bioactive Skin Care

Contact Author Ann-Charlotte Andersson and Jari Alander, AAK Sweden AB, Karlshamn, Sweden
Fill out my online form.

The shea tree, also known as Butyrospermum parkii or Vitellaria paradoxa, is primarily found in the semi-arid savannah belt, extending across sub-Saharan Africa and ranging from Mali to Sudan and Uganda.1 The shea tree is most valued for its “butter” extracted from the fruit kernels, which commonly is used as a skin care emollient, but also as a replacement or addition to cocoa butter in the food industry.

Shea butter, also known as Karité butter, is highly appreciated in the cosmetics industry for its sensory and skin care properties. Its high unsaponifiable lipid content makes it a valuable source of bioactive triterpene esters, offering a naturally derived and functional ingredient for cosmetic formulations. The present article profiles this ingredient and reviews research in the literature on its various benefits. Further, it describes studies conducted to assess the effects of shea butter triterpene esters on several skin properties.

Shea Butter Composition

Much like other vegetable oils and fats, the main constituents of shea butter are triglycerides—esters of glycerol and fatty acids, showing an approximately equal mix of solid and liquid triglyceride fractions based on oleic and stearic acids.2, 3 Shea butter also contains especially high levels of non-glyceride components summarized by the collective term unsaponifiables or unsaponifiable matter. A typical vegetable oil contains less than 1% of unsaponifiables, mainly phytosterols and tocopherols, whereas shea butter can contain as much as 7% to 10% of unsaponifiables comprising triterpene esters as well as highly unsaturated isoprenoidal hydrocarbons.3, 4

Excerpt Only This is a shortened version or summary of the article you requested. To view the complete article, please log in or create an account. Registration is Free!

The tocopherol content in shea butter vs. vegetable oil is comparatively low; often ~100 ppm, corresponding to a low level of sensitive polyunsaturated fatty acids in the butter. On the other hand, the main shea butter fatty acids, oleic and stearic, are sufficiently stable against oxidation. Thus, if carefully purified and correctly handled, shea butter and its extracts show superior oxidative stability and do not require additional antioxidants.

Triterpenes originate from squalene, and the biosynthesis of these pentacyclic hydrocarbon structures consisting of six isoprene units is considered one of the most complex reactions occurring in nature. Even though triterpenes are among the most common plant secondary metabolites, their function in plants is not yet fully understood. They usually are concentrated as alcohols in the plant’s outermost layers such as the cuticle, fruit peel and bark. They also are found at lower concentrations in plant oils.

The dominating triterpenes in shea butter are lupeol, α- and β-amyrin and butyrospermol, which belong to the lupane, oleanane and ursane triterpene families, respectively (see Figure 1). These triterpenes occur as acetyl and cinnamoyl esters and are of interest as active ingredients in cosmetic formulations.

Lupeol Effects and Mechanisms

Triterpenes with varying structures are found widely in edible fruits and vegetables, including Butyrospermum parkii. These naturally occurring alcohols and their derivatives are reported to exhibit anti-inflammatory and anti-tumor activity.5-8 Extensive research over the last three decades has revealed several important pharmacological activities of lupeol.9 Besides its anti-inflammatory7, 10 action, in vitro and preclinical animal studies suggest lupeol could act as an:

  • antimicrobial11
  • antiprotozoal12, 13
  • antiproliferative11
  • anti-invasive agent9
  • anti-angiogenic active14, 15 and
  • cholesterol-lowering agent.16, 17

Various in vitro and in vivo models also have tested lupeol for its therapeutic effectiveness for:

  • wounds18
  • diabetes19
  • cardiovascular disease20
  • kidney disease21 and
  • arthritis.22

Lupeol also was found effective for treating various diseases in animal models under preclinical settings irrespective of varying routes of administration; i.e., topical, oral, intra-peritoneal and intravenous. Further, it was reported to selectively target diseased and unhealthy human cells while sparing normal and healthy cells.9

Additional studies provide evidence of lupeol modulating the expression or activity of several molecules such as cytokines IL-2, IL-4, IL-5 and IL-1β; proteases; α-glucosidase; cFLIP; Bcl-2; and NF-kB.23 Observations of lupeol from shea butter in particular show it significantly reduces the levels of LPS-induced nitric oxide, Tumour Necrosis Factor-α (TNF-α), and interleukins-1β (IL-1β) and -12 (IL-12). The expression of pro-inflammatory enzymes, inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) also were inhibited.

These anti-inflammatory effects were due to an inhibitory action of lupeol on lipopolysaccharide (LPS)-induced iNOS, COX-2, TNF-α, IL-1β and IL-12 mRNA expressions. Moreover, lupeol suppressed IκB phosphorylation and NF-κB nuclear translocation induced by LPS. These findings explain the molecular basis of shea butter’s bioactivity against various inflammatory conditions.

Another study showed the triterpenes lupeol, lupeol-3-palmitate and lupeol-3-linoleate reduced joint destruction in adjuvant arthritis.22 Here, the triterpenes were tested on the release of both collagenase by bone tumor cells and five lipoxygenase inflammatory products by human neutrophils. The effectiveness of the triterpenes in these models on inflammatory and arthritic processes correspond with their relative anti-arthritic effectiveness in adjuvant arthritis.

The activity of lupeol could be explained by the inhibition of protein kinase C (PKC) with the potential reduced formation of intracellular reactive oxygen species (ROS) and early inhibition of the inflammatory cascade—the anti-inflammatory activity of triterpenoids depending on the inhibition of protein kinase C without any involvement of neurogenic inflammatory mechanisms.5, 24

Human Skin, Stress and Triterpenes

Human skin, being the body’s outermost shield against various environmental conditions, responds to a number of stress conditions by a series of inflammatory reactions that aim to repair tissue and regain homeostasis.

Inflammation can be induced by injurious agents, chemical irritants, toxins, pathogens, burns, UV exposure and so forth. This condition often is caused by the formation of ROS, followed by the biosynthesis of inflammatory mediators such as the leukotrienes and prostaglandins.25 UV-induced ROS are shown to prematurely influence aging processes; one study by Surowiak et al.26 illustrates a higher expression of cyclooxygenase 2 (COX-2) in skin samples affected by photoaging.

Consequently, protection against premature aging, as well as treatment for sensitive and aged skin is a high priority for personal care product development. In relation, natural triterpenes are well-researched for their bioactivity and show potential not only within the pharmaceutical industry, as previously described, but also as potential new and valuable skin care ingredients.

For example, the anti-inflammatory activity of shea butter triterpenes was recently investigated by Akihisa et al.,7 who showed lupeol cinnamate to have the highest activity against 12-O-tetradecanoylphorbol-13-acetate (TPA), a protein kinase C activator, and carrageenan-induced inflammation in vivo; the anti-inflammatory activity of shea butter triterpenes also was more effective than the reference compound indomethacin.

Lupeol esters such as acetates, palmitates and linoleates also were demonstrated to have potent protease-inhibiting activity.27-29 Moreover, esters of lupeol and other triterpenes have shown potential for reducing arthritic joint destruction in rheumatoid arthritis via direct pharmacological action.23, 27 A selective inhibiting activity of both metallo- and serineproteases by lupeol esters also has been described by Hodges et al.27

The anti-inflammatory and protease-inhibiting activity of triterpene esters reported by several research teams indicate potential for reducing skin stress induced by environmental factors.29 Such effects suggest the use of triterpene esters in skin care formulations, to protect against stress-related effects. In consideration, the studies described here assessed the various effects of shea butter triterpene esters on skin inflammation, barrier thickness and collagen production.

Materials and Methods

To study the effects of triterpene esters on skin properties, the authors tested highly concentrated shea butter triterpene ester ingredients. The content of bioactive triterpene esters in shea butter varies between 2% to 10% depending on the origin and the quality of the shea kernels. However, this content can be increased by processes such as solvent fractionation or molecular distillation.30 In fact, the processing and characterization of shea butter fractions with ~24% triterpenesa and a further concentrated fraction with 60-65% triterpenesb have been achieved.31, 32 These concentrated triterpene ester ingredients were used for the described tests.

Anti-inflammatory activity: The 100-500 ppm triterpene ester shea butter ingredienta was tested at concentrations of 0.5-2.5 mg/mL by applying it to normal human epidermal keratinocytes maintained in complete growth medium. Effects on the pro-inflammatory mediator IL-1α cytokine in keratinocytes were evaluated after exposure to croton oil as a chemical irritant.31

Barrier thickness: To assess barrier-strengthening properties, a simple polymer-stabilized test cream containing 5% caprylic/capric triglycerides and the 3,000-ppm shea butter triterpene ester ingredientb (0.5%), and a placebo cream were applied for five days to living human skin explants obtained from the abdominoplasty of a 45-year-old woman. Barrier thickness was evaluated on day six by general morphology, after staining with Masson’s trichrome and using a microscopec at 25× magnification.

Collagen activity: The effects of shea butter triterpene esters on collagen in the papillary dermis was investigated in a similar manner, applying the same test and placebo creams to explants grown under normal growth conditions. Collagen content also was evaluated microscopicallyd at 20× magnification, after collagen staining with Picro Sirius according to SOP H-164.

Matrix metalloproteinases (MMPs): The deactivation of MMPs is required for collagen production, thus a gene expression analysis (RT-qPCR method) was initiated. MMP-3 is known to be up-regulated in aged skin after UV-exposure and is responsible for the breakdown of the skin collagen type III.

The effects of the shea butter triterpene ester ingredientb on MMPs were therefore evaluated at 0.05% and 0.1% in normal human epidermal keratinocytes (NHEK), grown in Keratinocyte-SFM Culture Medium. This medium was replaced by assay medium containing the test compound or calcium chloride at 1.5 mM, as a reference. The NHEKs were incubated for 24 hr before analysis.

Ex vivo: Living human skin explants, obtained from the mammary plasty from a 61-year-old woman, were kept in survival for eight days. The explants were exposed to the same placebo cream and test creams described previously; the latter containing 0.5% shea butter triterpene ester ingredientb. The explants were exposed twice to collagenase (50 U/ mL) and the resulting network of collagen was observed microscopicallyd at 20× and quantified by image analysise.


Anti-inflammatory activity: As shown in Figure 2, a significant 25% reduction in the release of the intracellular pro-inflammatory mediator IL-1α cytokine was observed, in comparison with control cells. This suggested an anti-inflammatory effect of shea butter triterpenes, even at a low 100-500 ppm concentration.

Barrier thickness: After six days, under normal ex vivo growth conditions, a thick, moderately laminated stratum corneum with an epidermal thickness presenting seven to eight cellular layers was observed for the active-treated explants. The explants also demonstrated a well-maintained epidermal morphology, with a clear relief of dermal-epidermal junction.

An 84% increase in epidermal thickness for treated explants, over the untreated control, and 26% increase over the placebo was observed (data not shown).33 These results indicate shea butter triterpenes may well contribute to skin barrier strength and protection.

Collagen activity: A significant 6% increase of surface percentage occupied by collagen in the papillary dermis of living human skin explants was observed after six days of treatment with the formulation including 0.5% shea butter triterpenes, as depicted in Figure 3.32, 34 In contrast, no significant increase was observed with the placebo. These results indicate the triterpenes hold collagen-enhancing and regenerating properties.

MMPs: Shea butter triterpene-treated keratinocytes demonstrated a significant (>50%) reduction in MMP-3 expression versus the control at triterpene concentrations as low as 300 ppm and >60% reduction with triterpenes at 600 ppm, as shown in Figure 4. Such gene expression analysis indicates a moderate inhibition effect of the shea butter triterpenes; in order to further elucidate mechanisms and inhibiting activities, further investigations are required.

Ex vivo: The ex vivo study of shea butter triterpene-treated keratinocytes confirmed collagen-protecting activity after exposure to collagenase. The treated explants demonstrated a significant 91% reduction in collagenase activity over the control and versus 21% by the placebo (data not shown).

Overall, the presented data supports the collagen-protecting activity of shea butter triterpenes. Additional studies could indicate a collagen-stimulating effect as well, which has been reported for triterpenes such as madecassoside and asiaticoside, the main active constituents of Centella asiatica.5, 35-37 In addition, shea butter and C. asiatica are known in traditional medicine for wound-healing properties, which could indicate activity on protein synthesis.29, 38

Discussion and Conclusions

The protease-inhibiting, collagen-enhancing and anti-inflammatory activities of shea butter triterpenes shown here, in vitro and ex vivo, correlate well with published studies on the activities of similar triterpene and triterpene esters. These findings further highlight the enriched shea extract as a potential bioactive lipid complex for protecting the skin against environmental stress conditions and treating aged skin.

The trend today, especially in cosmetics, is for natural and sustainably derived bioactive compounds that serve as lead compounds for skin benefits. Shea butter is a natural choice for formulations aimed at reducing the premature breakdown of skin and supporting the tissue matrix.


Acknowledgements: AAK would like to thank Theresa Callaghan, Ph.D., of Callaghan Consulting International, for fruitful discussions and the preparation of this manuscript.


  1. S Maranz et al, Nutritional values and indigenous preferences for Shea fruit (Vitalleria paradoxa Gaertn. F.) in African agroforestry parklands, Econ Bot 58 588-600 (2004)
  2. KE Peers, The non-glyceride saponifiables of Shea butter, J Sci Food Agric 28 1000-1009 (1977)
  3. T Akihisa et al, Triacylglycerol and triterpene ester composition of shea nuts from seven African countries, J Oleo Sci 60(8) 385-391 (2011)
  4. T Itoh, T Uetsuki, T Tamura and T Matsumoto, Characterization of triterpene alcohols of seed oils from some species of Theaceae, Phytolaccaceae and Sapotaceae, Lipids 15(6) 407-411 (1980)
  5. A Huguet et al, Effect of triterpenoids on the inflammation induced by protein kinase C activators, neuronally acting irritants and other agents, Eur J Pharmacol 410(1) 69-81 (2000)
  6. D Lucetti et al, Anti-inflammatory effects and possible mechanism of action of lupeol acetate isolated from Himatanthus drasticus (Mart.) Plumel, J Inflamm 7 60 (2010)
  7. T Akihisa et al, Anti-inflammatory and chemopreventative effects of triterpene cinnamates and acetates from shea fat, J Oleo Sci 59(6) 273-280 (2010)
  8. J Alex et al, Anticancer and anti-inflammatory activity of chemically modified lupeol derivatives, Ind J Pharmacol 40(suppl 2) S57-S59 (075) (2008)
  9. MBC Gallo et al, Biological activities of lupeol, Intl J Biomed and Pharma Sci 46–66 (Oct 2009)
  10. MA Fernández et al, New insights into the mechanism of action of the anti-inflammatory triterpene lupeol, J Pharm Pharmacol 53 1533-1539 (2001b)
  11. BKM Ahamed et al, Isolation of bactericidal constituents from the steam bark extract of Grewia tiliaefolia Vahl, Res J Medicinal Plant 1 72-82 (2007)
  12. J Fotie et al, Lupeol long-chain fatty acid esters with antimalarial activity from Holarrhena floribunda, J Nat Products 69 62-67 (2006)
  13. HL Ziegler et al, Loading of erythrocyte membrane with pentacyclic triterpenes inhibits Plasmodium falciparum invasion, Planta Medica 72, 640-642 (2006)
  14. YJ You et al, Antiangiogenic activity of lupeol from Bombax ceiba, Phytotherapy Res 17 341-344 (2003)
  15. S Käßmeyer et al, New insights in vascular development: Vasculogenesis and endothelial progenitor cells, Anat Hist Embryol 38 1-11 (2009)
  16. KP Reddy et al, Synthesis of novel triterpenoid (lupeol) derivatives and their in vivo antihyperglycemic and antidyslipidemic activity, Bioorganic Med Chem Lett 19 4463-4466 (2009)
  17. V Sudhahar et al, Remedial effect of lupeol and its ester derivative on hypercholesterolemia-induced oxidative and inflammatory stresses, Nutrition Research 27 778-787 (2007a)
  18. JB Nikiéma et al, Effects of anti-inflammatory triterpenes isolated from Leptadenia hastata latex on keratinocyte proliferation, Phytotherapy Res 15 31-134 (2001)
  19. OB Flekhter et al, The synthesis and hepatoprotective activity of esters of the lupine group triterpenoids, Russ J Bioorg Chem 26 192-200 (2000)
  20. R Saleem et al, Hypotensive activity and toxicology of constituents from Bombax ceiba stem bark, Biol Pharm Bull 26 41-46 (2003)
  21. M Malini M et al, Protective effect of triterpenes on calcium oxalate crystal-induced peroxidative changes in experimental urolithiasis, Pharmacol Res 41 413-418 (2000)
  22. G Kweifio-Okai et al, Antiarthritic mechanisms of lupeol triterpenes, Drug Dev Res 36 20–24 (1995)
  23. N Verma et al, Anti-inflammatory effects of shea butter through inhibition of iNOS, COX-2 and cytokines via the Nf-κB pathway in LPS-activated J774 macrophage cells, J Compl Integr Med 12 9 (2012)
  24. M Saleem et al, Lupeol, a fruit and vegetable based triterpene, induces apoptotic death of human pancreatic adenocarcinoma cells via inhibition of Ras signaling pathway, Carcinogenesis 26(11) 1956-64 (2005)
  25. Y Bellik et al, Molecular mechanism underlying anti-inflammatory and anti-allergic activities of phytochemicals: An update, Molecules 18 322-353 (2013)
  26. P Surowiak et al, Increase in cyclooxygenase-2 (COX-2) expression in keratinocytes and dermal fibroblasts in photoaged skin, J Cos Derm 13 195-201 (2014)
  27. L Hodges et al, Antiprotease effect of anti-inflammatory lupeol esters, Mol Cell Biochem 252(1-2) 97-101 (2003)
  28. Y Zhang et al, Triterpenoid resinous metabolites from the genus Boswellia: Pharmacological activities and potential species-identifying properties, Chem Cent J 7 1533 (2013)
  29. HR Siddique and M Saleem, Beneficial health effects of lupeol triterpene: A review of preclinical studies, Life Sci 88(7-8) 285-93 (2011)
  30. WO 99/63031, Fractionation process, J Alander, A-C Andersson, H Malmros and J Nilsson (1999)
  31. J Alander, Composition and bioactive properties of unsaponifiables from shea butter (Butyrospermum parkii), poster presentation, IFSCC Congress, Osaka (2006)
  32. J Alander and AC Andersson, Bioactive shea butter concentrate for skin care, poster presentation, IFSCC Conference, Rio de Janeiro (2013)
  33. AC Andersson and J Alander, Lipex shea butters—Emollients with high functionality, poster presentation, APGI Skin and Formulation 4th Symposium, Lyon (2012)
  34. AC Andersson, Protection against stress by natural triterpene esters, Personal Care (6)77-79 (Jun 2011)
  35. D Paolino et al, Improved in vitro and in vivo collagen biosynthesis by asiaticoside-loaded ultradeformable vesicles, J Control Release 162(1) 143-51 (2012)
  36. J Lee et al, Asiaticoside induces human collagen I synthesis through TGF-β receptor I kinase (TβRI kinase)-independent Smad signalling, Planta Med 72(4) 324-8 (2006)
  37. B Tang et al, Asiaticoside suppresses collagen expression and TGF-β/Smad signaling through inducing Smad7 and inhibiting TGF-βRI and TGF-βRII in keloid fibroblasts, Arch Dermatol Res 303(8) 563-72 (2011)
  38. W Bylka et al, Centella asiatica in dermatology: An overview, Phytother Res 28(8) 1117-24 (2014)

Related Content



Figure 1. Main triterpene structures found in shea butter

Figure 1. Main triterpene structures found in shea butter

The dominating triterpenes in shea butter are lupeol, α- and β-amyrin and butyrospermol, which belong to the lupane, oleanane and ursane triterpene families, respectively.

Figure 2. Anti-inflammatory properties

Figure 2. Anti-inflammatory properties

In vitro evaluation of cytokine release shows a significant reduction of IL-1α release after treatment with shea butter triterpene esters.

Figure 3. Collagen-enhancing activity

Figure 3. Collagen-enhancing activity

Ex vivo evaluation shows a significant increase of dermal collagen after six days of treatment with formulation including shea butter triterpene esters.

Figure 4. Collagen-protecting properties

Figure 4. Collagen-protecting properties

Shea butter triterpene esters down-regulate the expression of MMP-3 gene in human cultured keratinocyte.

Footnotes [Andersson 130(6)]

a Lipex Shea-U (INCI: Butyrospermum Parkii (Shea) Butter) and
b Lipex Shea Tris (LST) (INCI: Butyrospermum Parkii (Shea) Butter Extract), AAK Sweden AB

c Orthoplan microscope and
d DMLB microscope, Leica Microsystems

e DP 72 camera and Cell software, Olympus

Next image >