Skin Pigmentation Types, Causes and Treatment—A Review
Open accessAbstract
Human skin pigmentation and melanin synthesis are incredibly variable, and are impacted by genetics, UV exposure, and some drugs. Patients' physical appearance, psychological health, and social functioning are all impacted by a sizable number of skin conditions that cause pigmentary abnormalities. Hyperpigmentation, where pigment appears to overflow, and hypopigmentation, where pigment is reduced, are the two major classifications of skin pigmentation. Albinism, melasma, vitiligo, Addison's disease, and post-inflammatory hyperpigmentation, which can be brought on by eczema, acne vulgaris, and drug interactions, are the most common skin pigmentation disorders in clinical practice. Anti-inflammatory medications, antioxidants, and medications that inhibit tyrosinase, which prevents the production of melanin, are all possible treatments for pigmentation problems. Skin pigmentation can be treated orally and topically with medications, herbal remedies, and cosmetic products, but a doctor should always be consulted before beginning any new medicine or treatment plan. This review article explores the numerous types of pigmentation problems, their causes, and treatments, as well as the 25 plants, 4 marine species, and 17 topical and oral medications now on the market that have been clinically tested to treat skin diseases.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Light skin is deficient in the adequate pigmentation necessary to neutralize the destructive effects of UV radiation, contrasting with darker skin which is aided by the antioxidant properties of melanin.
“Contrasting with darker skin, which is aided by the antioxidant properties of melanin, light skin is deficient in the adequate pigmentation necessary to neutralize the destructive effects of UV radiation [57].”
From A Comprehensive Review of the Role of UV Radiation in Photoaging Processes Between Different Types of Skin (2025) · cites this paper as [57]
The Introduction (page not provided) says darker skin has more eumelanin, which absorbs UV rays and protects against sunburn, while lighter skin has less eumelanin and is more prone to sun damage. It does not attribute that protection to melanin’s antioxidant properties; the mechanism it describes is UV absorption. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 225 · Cited by 233
Research works printed but not linked: 203
- [1]Del Bino S. Duval C. Bernerd F. Clinical and biological characterization of skin pigmentation diversity and its consequences on UV impact Int. J. Mol. Sci. 2018 19 2668 10.3390/ijms19092668 30205563 PMC6163216 · DOI · Paper page
- [3]Nasti T.H. Timares L. MC 1R, Eumelanin and Pheomelanin: Their role in determining the susceptibility to skin cancer Photochem. Photobiol. 2015 91 188 200 10.1111/php.12335 25155575 PMC4299862 · DOI · Paper page
- [4]Solano F. Photoprotection and skin pigmentation: Melanin-related molecules and some other new agents obtained from natural sources Molecules 2020 25 1537 10.3390/molecules25071537 32230973 PMC7180973 · DOI
- [5]Polidori C. Jorge A. Ornosa C. Eumelanin and pheomelanin are predominant pigments in bumblebee (Apidae: Bombus) pubescence PeerJ 2017 5 e3300 e3321 10.7717/peerj.3300 28560094 PMC5445944 · DOI
- [6]Hu S. Zhai P. Chen Y. Zhao B. Yang N. Wang M. Xiao Y. Bao G. Wu X. Morphological characterization and gene expression patterns for melanin pigmentation in Rex rabbit Biochem. Genet. 2019 57 734 744 10.1007/s10528-019-09929-x 31302800 · DOI
- [7]Baek S.H. Lee S.H. Sesamol decreases melanin biosynthesis in melanocyte cells and zebrafish: Possible involvement of MITF via the intracellular cAMP and p38/JNK signalling pathways Exp. Dermatol. 2015 24 761 766 10.1111/exd.12765 26010596 PMC4744993 · DOI
- [8]Madelaine R. Ngo K.J. Skariah G. Mourrain P. Genetic deciphering of the antagonistic activities of the melanin-concentrating hormone and melanocortin pathways in skin pigmentation PLoS Genet. 2020 16 e1009244-65 10.1371/journal.pgen.1009244 33301440 PMC7755275 · DOI
- [9]Ozdeslik R.N. Olinski L.E. Trieu M.M. Oprian D.D. Oancea E. Human nonvisual opsin 3 regulates pigmentation of epidermal melanocytes through functional interaction with melanocortin 1 receptor Proc. Natl. Acad. Sci. USA 2019 116 11508 11517 10.1073/pnas.1902825116 31097585 PMC6561246 · DOI
- [10]Wolf Horrell E.M. Boulanger M.C. D’Orazio J.A. Melanocortin 1 receptor: Structure, function, and regulation Front. Genet. 2016 7 95 111 10.3389/fgene.2016.00095 27303435 PMC4885833 · DOI
- [12]Jablonski N.G. The evolution of human skin pigmentation involved the interactions of genetic, environmental, and cultural variables Pigment Cell Melanoma Res. 2021 34 707 729 10.1111/pcmr.12976 33825328 PMC8359960 · DOI
- [13]Ainger S.A. Jagirdar K. Lee K.J. Soyer H.P. Sturm R.A. Skin pigmentation genetics for the clinic Dermatology 2017 233 1 15 10.1159/000468538 28463841 · DOI
- [14]Feng Y. McQuillan M.A. Tishkoff S.A. Evolutionary genetics of skin pigmentation in African populations Human Mol. Genet. 2021 30 88 97 10.1093/hmg/ddab007 PMC8117430 33438000 · DOI
- [15]Kita R. Fraser H.B. Local adaptation of sun-exposure-dependent gene expression regulation in human skin PLoS Genet. 2016 12 e1006382 10.1371/journal.pgen.1006382 27760139 PMC5070784 · DOI
- [16]Armenta A.M. Henkel E.D. Ahmed A.M. Pigmentation disorders in the elderly Drugs Aging 2019 36 235 245 10.1007/s40266-018-00633-w 30637685 · DOI
- [17]Adigun C.G. Adverse drug reactions of the lower extremities Clin. Podiatr. Med. Surg. 2016 33 397 408 10.1016/j.cpm.2016.02.007 27215159 · DOI
- [18]Nicolaidou E. Katsambas A.D. Pigmentation disorders: Hyperpigmentation and hypopigmentation Clin. Dermatol. 2014 32 66 72 10.1016/j.clindermatol.2013.05.026 24314378 · DOI
- [19]Böhm M. Disorders of Melanin Pigmentation Braun-Falco’s Dermatology Springer Berlin/Heidelberg, Germany 2021 1 35
- [20]Ma E.Z. Zhou A.E. Hoegler K.M. Khachemoune A. Oculocutaneous albinism: Epidemiology, genetics, skin manifestation, and psychosocial issues Arch. Dermatol. Res. 2023 315 107 116 10.1007/s00403-022-02335-1 35217926 · DOI
- [22]Lee D.Y. Kim C.R. Lee J.H. Trichrome vitiligo in segmental type Photodermatol. Photoimmunol. Photomed. 2011 27 111 112 10.1111/j.1600-0781.2011.00572.x 21392115 · DOI
- [23]Hill J.P. Batchelor J.M. An approach to hypopigmentation BMJ 2017 356 356 362 10.1136/bmj.i6534 28082370 · DOI
- [24]Silpa-Archa N. Kohli I. Chaowattanapanit S. Lim H.W. Hamzavi I. Postinflammatory hyperpigmentation: A comprehensive overview: Epidemiology, pathogenesis, clinical presentation, and noninvasive assessment technique J. Am. Acad. Dermatol. 2017 77 591 605 10.1016/j.jaad.2017.01.035 28917451 · DOI
- [25]Kallini J.R. Riaz F. Khachemoune A. Tinea versicolor in dark-skinned individuals Int. J. Dermatol. 2014 53 137 141 10.1111/ijd.12345 24320140 · DOI
- [26]Miazek N. Michalek I. Pawlowska-Kisiel M. Olszewska M. Rudnicka L. Pityriasis Alba—Common Disease, Enigmatic Entity: Up-to-Date Review of the Literature Pediatr. Dermatol. 2015 32 786 791 10.1111/pde.12683 26477326 · DOI
- [27]Jing J. Man X.Y. Vitiligo-like depigmentation in a patient treated with PD-1 antibody BMJ 2021 374 n1982 10.1136/bmj.n1982 · DOI
- [28]McMichael L. Skin camouflage BMJ 2012 344 d7921 10.1136/bmj.d7921 22223831 · DOI
- [29]Sheth P.B. Shah H.A. Dave J.N. Periorbital hyperpigmentation: A study of its prevalence, common causative factors and its association with personal habits and other disorders Indian J. Dermatol. 2014 59 151 157 10.4103/0019-5154.127675 24700933 PMC3969674 · DOI
- [30]Choi W. Yin L. Smuda C. Batzer J. Hearing V.J. Kolbe L. Molecular and histological characterization of age spots Exp. Dermatol. 2017 26 242 248 10.1111/exd.13203 27621222 PMC5342934 · DOI
- [31]Baxter L.L. Pavan W.J. The etiology and molecular genetics of human pigmentation disorders Wiley Interdiscip. Rev. Dev. Biol. 2013 2 379 392 10.1002/wdev.72 23799582 PMC3694277 · DOI
- [32]Yadalla H.K.K. Aradhya S. Post acne hyperpigmentation: A brief review Our Dermatol. Online 2011 2 230 231
- [33]Plensdorf S. Livieratos M. Dada N. Pigmentation disorders: Diagnosis and management Am. Fam. Physician 2017 96 797 804 29431372
- [34]Woolery-Lloyd H. Kammer J.N. Treatment of Hyperpigmentation Seminars in Cutaneous Medicine and Surgery WB Saunders Philadelphia, PA, USA 2011 Volume 30 171 175 21925372
- [35]Bala H.R. Lee S. Wong C. Pandya A.G. Rodrigues M. Oral tranexamic acid for the treatment of melasma: A review Dermatol. Surg. 2018 44 814 825 10.1097/DSS.0000000000001518 29677015 · DOI
- [37]Kaur A. Bhalla M. Sarkar R. Tranexamic acid in melasma: A review Pigment Int. 2020 7 12 25
- [38]Maeda K. Mechanism of Action of Topical Tranexamic Acid in the Treatment of Melasma and Sun-Induced Skin Hyperpigmentation Cosmetics 2022 9 108 10.3390/cosmetics9050108 · DOI
- [39]McKesey J. Tovar-Garza A. Pandya A.G. Melasma treatment: An evidence-based review Am. J. Clin. Dermatol. 2020 21 173 225 10.1007/s40257-019-00488-w 31802394 · DOI
- [40]Grimes P.E. Ijaz S. Nashawati R. Kwak D. New oral and topical approaches for the treatment of melasma Int. J. Women’s Dermatol. 2019 5 30 36 10.1016/j.ijwd.2018.09.004 30809577 PMC6374710 · DOI
- [41]Artzi O. Horovitz T. Bar-Ilan E. Shehadeh W. Koren A. Zusmanovitch L. Mehrabi J. Salameh F. Nelkenbaum G.I. Zur E. The pathogenesis of melasma and implications for treatment J. Cosmet. Dermatol. 2021 20 3432 3445 10.1111/jocd.14382 34411403 · DOI
- [42]Taraz M. Niknam S. Ehsani A.H. Tranexamic acid in treatment of melasma: A comprehensive review of clinical studies Dermatol. Ther. 2017 30 e12465 10.1111/dth.12465 28133910 · DOI
- [43]Tse T.W. Hui E. Tranexamic acid: An important adjuvant in the treatment of melasma J. Cosmet. Dermatol. 2013 12 57 66 10.1111/jocd.12026 23438143 · DOI
- [44]Sharma R. Mahajan V.K. Mehta K.S. Chauhan P.S. Rawat R. Shiny T.N. Therapeutic efficacy and safety of oral tranexamic acid and that of tranexamic acid local infiltration with microinjections in patients with melasma: A comparative study Clin. Exp. Dermatol. 2017 42 728 734 10.1111/ced.13164 28649780 · DOI
- [45]Kim S.J. Park J.Y. Shibata T. Fujiwara R. Kang H.Y. Efficacy and possible mechanisms of topical tranexamic acid in melasma Clin. Exp. Dermatol. 2016 41 480 485 10.1111/ced.12835 27135282 · DOI
- [46]Sofen B. Prado G. Emer J. Melasma and post inflammatory hyperpigmentation: Management update and expert opinion Skin. Ther. Lett. 2016 21 1 7 27224897
- [48]Mysore V. Mahadevappa O.H. Barua S. Majid I. Viswanath V. Bhat R.M. Talwar S. Thurakkal S. Aurangabadkar S.J. Chatterjee M. Standard guidelines of care: Performing procedures in patients on or recently administered with isotretinoin J. Cutan. Aesthetic Surg. 2017 10 186 194 10.4103/JCAS.JCAS_110_17 29491653 PMC5820835 · DOI
- [49]Bagatin E. Costa C.S. The use of isotretinoin for acne–an update on optimal dosing, surveillance, and adverse effects Expert Rev. Clin. Pharmacol. 2020 13 885 897 10.1080/17512433.2020.1796637 32744074 · DOI
- [50]Fallah H. Rademaker M. Isotretinoin in the management of acne vulgaris: Practical prescribing Int. J. Dermatol. 2021 60 451 460 10.1111/ijd.15089 32860434 · DOI
- [52]Spring L.K. Krakowski A.C. Alam M. Bhatia A. Brauer J. Cohen J. Rosso J.Q. Diaz L. Dover J. Eichenfield L.F. Isotretinoin and timing of procedural interventions: A systematic review with consensus recommendations JAMA Dermatol. 2017 153 802 809 10.1001/jamadermatol.2017.2077 28658462 · DOI · Paper page
- [53]Chu S. Michelle L. Ekelem C. Sung C.T. Rojek N. Mesinkovska N.A. Oral isotretinoin for the treatment of dermatologic conditions other than acne: A systematic review and discussion of future directions Arch. Dermatol. Res. 2021 313 391 430 10.1007/s00403-020-02152-4 33151346 · DOI
- [54]Shao X. Chen Y. Zhang L. Zhang Y. Ariyawati A. Chen T. Chen J. Liu L. Pu Y. Li Y. Effect of 30% supramolecular salicylic acid peel on skin microbiota and inflammation in patients with moderate-to-severe acne vulgaris Dermatol. Ther. 2023 13 155 168 10.1007/s13555-022-00844-5 36350527 PMC9823178 · DOI
- [55]Dréno B. Araviiskaia E. Kerob D. Andriessen A. Anfilova M. Arenbergerova M. Barrios L.O. Mokos Z.B. Haedersdal M. Hofmann M.A. Nonprescription acne vulgaris treatments: Their role in our treatment armamentarium—An international panel discussion J. Cosmet. Dermatol. 2020 19 2201 2211 10.1111/jocd.13497 32426933 PMC7496538 · DOI
- [56]Rachmin I. Ostrowski S.M. Weng Q.Y. Fisher D.E. Topical treatment strategies to manipulate human skin pigmentation Adv. Drug Deliv. Rev. 2020 153 65 71 10.1016/j.addr.2020.02.002 32092380 PMC7442613 · DOI
- [58]Yasir M. Goyal A. Sonthalia S. Corticosteroid adverse effects StatPearls StatPearls Publishing Treasure Island, FL, USA 2022 30285357
- [59]Yélamos O. Alejo B. Ertekin SSVilla-Crespo L. Zamora-Barquero S. Martinez N. Domínguez M. Iglesias P. Herrero A. Malvehy J. Puig S. Non-invasive clinical and microscopic evaluation of the response to treatment with clobetasol cream vs. calcipotriol/betamethasone dipropionate foam in mild to moderate plaque psoriasis: An investigator-initiated, phase IV, unicentric, open, randomized clinical trial J. Eur. Acad. Dermatol. Venereol. 2021 35 143 149 32365242 PMC7818495
- [60]Cho J.H. Bhutani S. Kim C.H. Irwin M.R. Anti-inflammatory effects of melatonin: A systematic review and meta-analysis of clinical trials Brain Behav. Immun. 2021 93 245 253 10.1016/j.bbi.2021.01.034 33581247 PMC7979486 · DOI
- [61]Karekar S.R. Marathe P.A. Nagarajan V.B. Khopkar U.S. Chikhalkar S.B. Desai P.K. Dongre M.S. Use of topical steroids in dermatology: A questionnaire based study Indian Dermatol. Online J. 2020 11 725 730 33235837 PMC7678551
- [62]Chadderdon C. Gaston R.G. Loeffler B.J. Lewis D. Betamethasone Versus Ketorolac Injection for the Treatment of De Quervain’s Tenosynovitis: A Double-Blind Randomized Clinical Trial: Level 1 Evidence J. Hand Surg. 2017 42 S45 S46 10.1016/j.jhsa.2017.06.086 · DOI
- [63]Patel H.K. Barot B.S. Parejiya P.B. Shelat P.K. Shukla A. Topical delivery of clobetasol propionate loaded microemulsion based gel for effective treatment of vitiligo: Ex vivo permeation and skin irritation studies Colloids Surf. B Biointerfaces 2013 102 86 94 10.1016/j.colsurfb.2012.08.011 23000677 · DOI
- [64]Khaitan B.K. Sindhuja T. Autoimmunity in vitiligo: Therapeutic implications and opportunities Autoimmun. Rev. 2022 21 102932 10.1016/j.autrev.2021.102932 34506987 · DOI
- [65]Eleftheriadou V. Atkar R. Batchelor J. McDonald B. Novakovic L. Patel J.V. Ravenscroft J. Rush E. Shah D. Shah R. British Association of Dermatologists’ Clinical Standards Unit. British Association of Dermatologists guidelines for the management of people with vitiligo 2021 Br. J. Dermatol. 2022 186 18 29 10.1111/bjd.20596 34160061 · DOI · Paper page
- [66]Habet K.A. Kolli S.S. Pona A. Feldman S.R. A review of topical corticosteroid sprays for the treatment of inflammatory dermatoses Dermatol. Online J. 2019 25 3 12 10.5070/D3258045123 31553858 · DOI
- [67]Gajinov Z. Corticosteroid topical therapy range: Fluocinolone-acetonide gel Galen. Med. J. 2022 1 17 22 10.5937/Galmed2202017G · DOI
- [68]Medici S. Peana M. Nurchi V.M. Zoroddu M.A. Medical uses of silver: History, myths, and scientific evidence J. Med. Chem. 2019 62 5923 5943 10.1021/acs.jmedchem.8b01439 30735392 · DOI
- [69]Bandyopadhyay D. Topical antibacterials in dermatology Indian J. Dermatol. 2021 66 117 125 10.4103/ijd.IJD_99_18 34188265 PMC8208253 · DOI
- [70]Adhya A. Bain J. Ray O. Hazra A. Adhikari S. Dutta G. Ray S. Majumdar B.K. Healing of burn wounds by topical treatment: A randomized controlled comparison between silver sulfadiazine and nano-crystalline silver J. Basic Clin. Pharm. 2014 6 29 34 10.4103/0976-0105.145776 25538469 PMC4268627 · DOI
- [71]Nethi S.K. Das S. Patra C.R. Mukherjee S. Recent advances in inorganic nanomaterials for wound-healing applications Biomater. Sci. 2019 7 2652 2674 10.1039/C9BM00423H 31094374 · DOI
- [72]Srivastava S. Patil A. Prakash C. Kumari H. Comparison of intralesional triamcinolone acetonide, 5-fluorouracil, and their combination in treatment of keloids World J. Plast. Surg. 2018 7 212 219 10.1089/wound.2017.0741 30083505 PMC6066718 · DOI
- [73]Khan H.A. Sahibzada M.N. Paracha M.M. Comparison of the efficacy of intralesional bleomycin versus intralesional triamcinolone acetonide in the treatment of keloids Dermatol. Ther. 2019 32 e13036-40 10.1111/dth.13036 31361934 · DOI
- [74]Raman P. Pitty R. Krithika C.L. Anand S.N. Subramani G.P. Topical curcumin and triamcinolone acetonide in recurrent minor aphthous ulcers: A pilot trial J. Contemp. Dent. Pract. 2020 21 884 890 33568610
- [75]Kwiatkowska D. Wicka M. Bulska E. Kaliszewski P. Investigation of the Excretion of Triamcinolone Acetonide and Its Metabolite Separations 2023 10 164 10.3390/separations10030164 · DOI
- [76]Mangion S.E. Mackenzie L. Roberts M.S. Holmes A.M. Seborrheic dermatitis: Topical therapeutics and formulation design Eur. J. Pharm. Biopharm. 2023 185 148 164 10.1016/j.ejpb.2023.01.023 36842718 · DOI
- [77]Pinto L.M. Chiricozzi A. Calabrese L. Mannino M. Peris K. Novel Therapeutic Strategies in the Topical Treatment of Atopic Dermatitis Pharmaceutics 2022 14 2767 10.3390/pharmaceutics14122767 36559261 PMC9788207 · DOI
- [78]Sandhu S. Klein B.A. Al-Hadlaq M. Chirravur P. Bajonaid A. Xu Y. Intini R. Hussein M. Vacharotayangul P. Sroussi H. Oral lichen planus: Comparative efficacy and treatment costs—A systematic review BMC Oral Health 2022 22 161 10.1186/s12903-022-02168-4 35524296 PMC9074269 · DOI
- [79]Pakravan F. Ghalayani P. Emami H. Isfahani M.N. Noorshargh P. A novel formulation for radiotherapy-induced oral mucositis: Triamcinolone acetonide mucoadhesive film J. Res. Med. Sci. Off. J. Isfahan Univ. Med. Sci. 2019 24 63 PMC6669991 31523249
- [80]Mangold A.R. Pittelkow M.R. Lichen planus Clin. Basic Immunodermatology 2017 551 576 10.1007/978-3-319-29785-9_31 · DOI
- [81]Ahmad Nasrollahi S. Sabet Nematzadeh M. Samadi A. Ayatollahi A. Yadangi S. Abels C. Firooz A. Evaluation of the safety and efficacy of a triple combination cream (hydroquinone, tretinoin, and fluocinolone) for treatment of melasma in Middle Eastern skin Clin. Cosmet. Investig. Dermatol. 2019 12 437 444 10.2147/CCID.S202285 PMC6580938 31354327 · DOI
- [82]Dreher F. Draelos Z.D. Gold M.H. Goldman M.P. Fabi S.G. Puissegur Lupo M.L. Efficacy of hydroquinone-free skin-lightening cream for photoaging J. Cosmet. Dermatol. 2013 12 12 17 10.1111/jocd.12025 23438137 · DOI
- [83]Banihashemi M. Zabolinejad N. Jaafari M.R. Salehi M. Jabari A. Comparison of therapeutic effects of liposomal tranexamic acid and conventional hydroquinone on melasma J. Cosmet. Dermatol. 2015 14 174 177 10.1111/jocd.12152 26177992 · DOI
- [84]Pradhan M. Singh D. Murthy S.N. Singh M.R. Design, characterization and skin permeating potential of Fluocinolone acetonide loaded nanostructured lipid carriers for topical treatment of psoriasis Steroids 2015 101 56 63 10.1016/j.steroids.2015.05.012 26049018 · DOI
- [85]Treesirichod A. Chaithirayanon S. Chaikul T. Chansakulporn S. The randomized trials of 10% urea cream and 0.025% tretinoin cream in the treatment of acanthosis nigricans J. Dermatol. Treat. 2021 32 837 842 10.1080/09546634.2019.1708855 31868565 · DOI
- [86]Bagatin E. Gonçalves H.D.S. Sato M. Almeida L.M.C. Miot H.A. Comparable efficacy of adapalene 0.3% gel and tretinoin 0.05% cream as treatment for cutaneous photoaging Eur. J. Dermatol. 2018 28 343 350 10.1684/ejd.2018.3320 30105991 · DOI
- [87]Nautiyal A. Wairkar S. Management of hyperpigmentation: Current treatments and emerging therapies Pigment Cell Melanoma Res. 2021 34 1000 1014 10.1111/pcmr.12986 33998768 · DOI
- [88]Ferraris C. Rimicci C. Garelli S. Ugazio E. Battaglia L. Nanosystems in cosmetic products: A brief overview of functional, market, regulatory and safety concerns Pharmaceutics 2021 13 1408 10.3390/pharmaceutics13091408 34575484 PMC8470546 · DOI
- [89]Usatine R. Tinitigan M. Diagnosis and treatment of lichen planus Am. Fam. Physician 2011 84 53 60 21766756
- [91]Doucette K. Forster S. Marcus A. Study to Assess Visual Elimination of a Novel Otic Gel (Florfenicol, Terbinafine, Betamethasone Acetate) in Comparison to an Otic Solution (Florfenicol, Terbinafine, Mometasone Furoate) and an Otic Suspension (Gentamicin Sulfate, Clotrimazole, Mometasone Furoate Monohydrate) in Dogs Immediately after Application to the Ear Canal BSAVA Congress Proceedings 2018 BSAVA Library Gloucester, UK 2018 489
- [92]Grammatikova N.É. Comparative study of the antimicrobial activity of combined topical medicinal formulations of betamethasone, gentamicin, and clotrimazole in vitro Pharm. Chem. J. 2020 53 971 975 10.1007/s11094-020-02107-z · DOI
- [93]Cole L.K. Rajala-Schultz P.J. Lorch G. Conductive hearing loss in four dogs associated with the use of ointment-based otic medications Vet. Dermatol. 2018 29 341-e120 10.1111/vde.12542 29664150 · DOI
- [95]Harris J.E. Rashighi M. Nguyen N. Jabbari A. Ulerio G. Clynes R. Christiano A.M. Mackay-Wiggan J. Rapid skin repigmentation on oral ruxolitinib in a patient with coexistent vitiligo and alopecia areata (AA) J. Am. Acad. Dermatol. 2016 74 370 371 10.1016/j.jaad.2015.09.073 26685721 PMC4718770 · DOI
- [96]Rosmarin D. Pandya A.G. Lebwohl M. Grimes P. Hamzavi I. Gottlieb A.B. Butler K. Kuo F. Sun K. Ji T. Ruxolitinib cream for treatment of vitiligo: A randomised, controlled, phase 2 trial Lancet 2020 396 110 120 10.1016/S0140-6736(20)30609-7 32653055 · DOI
- [97]Rothstein B. Joshipura D. Saraiya A. Abdat R. Ashkar H. Turkowski Y. Vaneeta Sheth V. Huang V. Chung S. Kachuk C. Treatment of vitiligo with the topical Janus kinase inhibitor ruxolitinib J. Am. Acad. Dermatol. 2017 76 1054 1060 10.1016/j.jaad.2017.02.049 28390737 · DOI
- [98]Sheikh A. Rafique W. Owais R. Malik F. Ali E. FDA approves Ruxolitinib (Opzelura) for Vitiligo Therapy: A breakthrough in the field of dermatology Ann. Med. Surg. 2022 81 104499 104506 10.1016/j.amsu.2022.104499 PMC9486756 36147080 · DOI
- [99]Shreberk-Hassidim R. Ramot Y. Zlotogorski A. Janus kinase inhibitors in dermatology: A systematic review J. Am. Acad. Dermatol. 2017 76 745 753 10.1016/j.jaad.2016.12.004 28169015 · DOI
- [100]Chapman S. Kwa M. Gold L.S. Lim H.W. Janus kinase inhibitors in dermatology: Part I. A comprehensive review J. Am. Acad. Dermatol. 2022 86 406 413 10.1016/j.jaad.2021.07.002 34246698 · DOI
- [101]Rosmarin D. Passeron T. Pandya A.G. Grimes P. Harris J.E. Desai S.R. Lebwohl M. Mulard M. Seneschal J. Wolkerstorfer A. Two phase 3, randomized, controlled trials of ruxolitinib cream for vitiligo N. Engl. J. Med. 2022 387 1445 1455 10.1056/NEJMoa2118828 36260792 · DOI
- [102]Seneschal J. Wolkerstorfer A. Desai S.R. Grimes P. Ezzedine K. Kornacki D. Butler K. Kuo F.I. Sun K. Grimes P. Efficacy and safety of ruxolitinib cream for the treatment of vitiligo by patient demographics and baseline clinical characteristics: Week 52 pooled subgroup analysis from two randomized phase 3 studies Br. J. Dermatol. 2023 188 (Suppl. S1) ljac106-006 10.1093/bjd/ljac106.006 · DOI
- [104]Arif T. Salicylic acid as a peeling agent: A comprehensive review Clin. Cosmet. Investig. Dermatol. 2015 8 455 461 10.2147/CCID.S84765 26347269 PMC4554394 · DOI
- [105]Liu J. Jiang R. Zhou J. Xu X. Sun Z. Li J. Chen X. Li Z. Yan X. Zhao D. Salicylic acid in ginseng root alleviates skin hyperpigmentation disorders by inhibiting melanogenesis and melanosome transport Eur. J. Pharmacol. 2021 910 174458 10.1016/j.ejphar.2021.174458 34480884 · DOI
- [106]Karnes J.B. Usatine R.P. Management of external genital warts Am. Fam. Physician 2014 90 312 318 25251091
- [107]Lu J. Cong T. Wen X. Li X. Du D. He G. Jiang X. Salicylic acid treats acne vulgaris by suppressing AMPK/SREBP 1 pathway in sebocytes Exp. Dermatol. 2019 28 786 794 10.1111/exd.13934 30972839 · DOI
- [108]Yeoh S.C. Goh C.F. Topical delivery of salicylates Drug Deliv. Transl. Res. 2021 12 981 1001 10.1007/s13346-021-00988-5 33907986 · DOI
- [109]Ogbechie-Godec O.A. Elbuluk N. Melasma: An up-to-date comprehensive review Dermatol. Ther. 2017 7 305 318 10.1007/s13555-017-0194-1 28726212 PMC5574745 · DOI
- [111]Al-Niaimi F. Chiang N.Y.Z. Topical vitamin C and the skin: Mechanisms of action and clinical applications J. Clin. Aesthetic Dermatol. 2017 10 14 17 PMC5605218 29104718
- [112]Ravetti S. Clemente C. Brignone S. Hergert L. Allemandi D. Palma S. Ascorbic acid in skin health Cosmetics 2019 6 58 10.3390/cosmetics6040058 · DOI
- [113]Goik U. Goik T. Załęska I. The properties and application of argan oil in cosmetology Eur. J. Lipid Sci. Technol. 2019 121 1800313 1800342 10.1002/ejlt.201800313 · DOI
- [114]Phong C. Lee V. Yale K. Sung C. Mesinkovska N. Coconut, Castor, and Argan Oil for Hair in Skin of Color Patients: A Systematic Review J. Drugs Dermatol. JDD 2022 21 751 757 35816075
- [115]Charrouf Z. Guillaume D. The argan oil project: Going from utopia to reality in 20 years OCL 2018 25 D209 D214 10.1051/ocl/2018006 · DOI
- [116]Kanlayavattanakul M. Lourith N. Plants and natural products for the treatment of skin hyperpigmentation–A review Planta Med. 2018 84 988 1006 10.1055/a-0583-0410 29506294 · DOI
- [117]Hollinger J.C. Angra K. Halder R.M. Are natural ingredients effective in the management of hyperpigmentation? A systematic review J. Clin. Aesthetic Dermatol. 2018 11 28 37 PMC5843359 29552273
- [119]Grimes P. Bhawan J. Howell M. Desai S. Coryell E. Einziger M. Simpson A. Yaroshinsky A. McCraw T. Histopathological Changes Induced by Malassezin: A Novel Natural Microbiome Indole for Treatment of Facial Hyperpigmentation J. Drugs Dermatol. JDD 2022 21 141 145 10.36849/JDD.6596 35133118 · DOI
- [120]Karadas F. Erdoğan S. Kor D. Oto G. Uluman M. The effects of different types of antioxidants (Se, vitamin E and carotenoids) in broiler diets on the growth performance, skin pigmentation and liver and plasma antioxidant concentrations Braz. J. Poult. Sci. 2016 18 101 116 10.1590/18069061-2015-0155 · DOI
- [121]Lucock M.D. The evolution of human skin pigmentation: A changing medley of vitamins, genetic variability, and UV radiation during human expansion Am. J. Biol. Anthropol. 2023 180 252 271 10.1002/ajpa.24564 36790744 PMC10083917 · DOI
- [122]Rembe J.D. Fromm-Dornieden C. Stuermer E.K. Effects of vitamin B complex and vitamin C on human skin cells: Is the perceived effect measurable? Adv. Skin Wound Care 2018 31 225 233 10.1097/01.ASW.0000531351.85866.d9 29672394 · DOI
- [123]Farzanfar S. Kouzekonan G.S. Mirjani R. Shekarchi B. Vitamin B12-loaded polycaprolacton/gelatin nanofibrous scaffold as potential wound care material Biomed. Eng. Lett. 2020 10 547 554 10.1007/s13534-020-00165-6 33194247 PMC7655877 · DOI
- [124]Vivcharenko V. Wojcik M. Przekora A. Cellular response to vitamin C-enriched chitosan/agarose film with potential application as artificial skin substitute for chronic wound treatment Cells 2020 9 1185 10.3390/cells9051185 32397594 PMC7290375 · DOI
- [125]Barrios-Garay K. Toledano-Serrabona J. Gay-Escoda C. Sánchez-Garcés M.Á. Clinical effect of vitamin C supplementation on bone healing: A systematic review Med. Oral Patol. Oral Y Cirugía Bucal 2022 27 e205 e215 10.4317/medoral.24944 35368012 PMC9054165 · DOI
- [126]Ahn K.Y. Song H.J. Kim D.C. Effect of alpha-tocopheryl acetate, retinyl palmitate, and phytantriol on hair protection J. Appl. Biol. Chem. 2022 65 307 312 10.3839/jabc.2022.039 · DOI
- [128]Putranti A.R. Primaharinastiti R. Hendradi E. Effectivity and physicochemical stability of nanostructured lipid carrier coenzyme Q10 in different ratio of lipid cetyl palmitate and alpha tocopheryl acetate as carrier Asian J. Pharm. Clin. Res. 2017 10 146 152 10.22159/ajpcr.2017.v10i2.14835 · DOI
- [129]Panichakul T. Rodboon T. Suwannalert P. Tripetch C. Rungruang R. Boohuad N. Youdee P. Additive effect of a combination of Artocarpus lakoocha and Glycyrrhiza glabra extracts on tyrosinase inhibition in melanoma B16 cells Pharmaceuticals 2020 13 310 10.3390/ph13100310 33066628 PMC7602378 · DOI
- [130]Gupta A.K. Pathak U. Medhi M. Mastinu A. Sikarwar M.S. Mishra P. Botanical, chemical and pharmacological properties of artocarpus lakoocha (monkey fruit): A review Agric. Rev. 2020 41 305 316 10.18805/ag.R-1989 · DOI
- [131]Ullah S. Shoaib R. Khan S. Masood A. Phytochemicals; Targeted-Based Therapeutic Approaches for Pigmentation Disorders Open Access Indones. J. Med. Rev. 2023 3 368 381 10.37275/oaijmr.v3i2.287 · DOI
- [132]Vaughn A.R. Clark A.K. Sivamani R.K. Shi V.Y. Natural oils for skin-barrier repair: Ancient compounds now backed by modern science Am. J. Clin. Dermatol. 2018 19 103 117 10.1007/s40257-017-0301-1 28707186 · DOI
- [133]Sarkic A. Stappen I. Essential oils and their single compounds in cosmetics—A critical review Cosmetics 2018 5 11 10.3390/cosmetics5010011 · DOI
- [134]Ali S.A. Galgut J.M. Choudhary R.K. On the novel action of melanolysis by a leaf extract of Aloe vera and its active ingredient aloin, potent skin depigmenting agents Planta Med. 2012 78 767 771 10.1055/s-0031-1298406 22495441 · DOI
- [135]Gad H.A. Roberts A. Hamzi S.H. Gad H.A. Touiss I. Altyar A.E. Kensara A.O. Ashour M.L. Jojoba Oil: An updated comprehensive review on chemistry, pharmaceutical uses, and toxicity Polymers 2021 13 1711 10.3390/polym13111711 34073772 PMC8197201 · DOI
- [136]Matsumoto Y. Ma S. Tominaga T. Yokoyama K. Kitatani K. Horikawa K. Suzuki K. Acute effects of transdermal administration of jojoba oil on lipid metabolism in mice Medicina 2019 55 594 10.3390/medicina55090594 31540183 PMC6780807 · DOI
- [137]Blaak J. Staib P. An updated review on efficacy and benefits of sweet almond, evening primrose and jojoba oils in skin care applications Int. J. Cosmet. Sci. 2022 44 1 9 10.1111/ics.12758 34957578 · DOI
- [138]Sturtevant D. Lu S. Zhou Z.W. Shen Y. Wang S. Song J.M. Zhong J. Burks D.J. Yang Z.Q. Yang Q.Y. The genome of jojoba (Simmondsia chinensis): A taxonomically isolated species that directs wax ester accumulation in its seeds Sci. Adv. 2020 6 e3240 e3253 10.1126/sciadv.aay3240 PMC7065883 32195345 · DOI
- [139]Nasr M. Abdel-Hamid S. Moftah N.H. Fadel M. Alyoussef A.A. Jojoba oil soft colloidal nanocarrier of a synthetic retinoid: Preparation, characterization and clinical efficacy in psoriatic patients Curr. Drug Deliv. 2017 14 426 432 10.2174/1567201813666160513132321 27174314 · DOI · Paper page
- [140]Sánchez M. Avhad M.R. Marchetti J.M. Martínez M. Aracil J. Jojoba oil: A state of the art review and future prospects Energy Convers. Manag. 2016 129 293 304 10.1016/j.enconman.2016.10.038 · DOI
- [142]Leite C.D.S. Bonafé G.A. Carvalho Santos J. Martinez C.A.R. Ortega M.M. Ribeiro M.L. The anti-inflammatory properties of licorice (Glycyrrhiza glabra)-derived compounds in intestinal disorders Int. J. Mol. Sci. 2022 23 4121 10.3390/ijms23084121 35456938 PMC9025446 · DOI
- [143]Kwon Y.J. Son D.H. Chung T.H. Lee Y.J. A review of the pharmacological efficacy and safety of licorice root from corroborative clinical trial findings J. Med. Food 2020 23 12 20 10.1089/jmf.2019.4459 31874059 · DOI
- [145]Kimyon R.S. Liou Y.L. Schlarbaum J.P. Warshaw E.M. Allergic contact dermatitis to licorice root extract Dermatitis® 2019 30 227 228 10.1097/DER.0000000000000475 31045935 · DOI
- [146]Spencer J.M. Accioly J. Kitchen N. Double Blind, Placebo Controlled Evaluation of a Novel Skin Lightening Agent J. Drugs Dermatol. JDD 2018 17 113 115 29320596
- [147]Dhariwala M.Y. Ravikumar P. An overview of herbal alternatives in androgenetic alopecia J. Cosmet. Dermatol. 2019 18 966 975 10.1111/jocd.12930 30980598 · DOI
- [148]Boscariol R. Junior J.M.O. Baldo D.A. Balcão V.M. Vila M.M. Transdermal permeation of curcumin promoted by choline geranate ionic liquid: Potential for the treatment of skin diseases Saudi Pharm. J. 2022 30 382 397 10.1016/j.jsps.2022.01.023 35527836 PMC9068761 · DOI
- [149]Vo T.S. Vo T.T.B.C. Vo T.T.T.N. Lai T.N.H. Turmeric (Curcuma longa L.): Chemical components and their effective clinical applications J. Turk. Chem. Soc. Sect. A Chem. 2021 8 883 898 10.18596/jotcsa.913136 · DOI
- [150]Firmansyah D. Sumiwi S.A. Saptarini N.M. Levita J. Curcuma longa extract inhibits the activity of mushroom tyrosinase and the growth of murine skin cancer B16F10 cells J. Herbmed Pharmacol. 2023 12 153 158 10.34172/jhp.2023.15 · DOI
- [151]Farooqui R.K. Kaurav M. Kumar M. Sudheesh M.S. Pandey R.S. Permeation enhancer nanovesicles mediated topical delivery of curcumin for the treatment of hyperpigmentation J. Liposome Res. 2022 32 332 339 10.1080/08982104.2021.2024567 35099353 · DOI
- [152]Akter J. Islam M.Z. Hossain M.A. Takara K. Anti-tyrosinase properties of different species of turmeric and isolation of active compounds from Curcuma amada Med. Chem. Res. 2021 30 1669 1676 10.1007/s00044-021-02764-z · DOI
- [153]Rodríguez-Cid L. Qian W. Iribarra-Araya J. Etcheverry-Berríos Á. Martínez-Olmos E. Choquesillo-Lazarte D. Sañudo E.C. Roubeau O. Periago A.M.L. González-Camp A. Broadening the scope of high structural dimensionality nanomaterials using pyridine-based curcuminoids Dalton Trans. 2021 50 7056 7064 10.1039/D1DT00708D 33949538 PMC8145613 · DOI
- [154]Colantonio S. Rivers J.K. Botanicals with dermatologic properties derived from first nations healing: Part 2—Plants and algae J. Cutan. Med. Surg. 2017 21 299 307 10.1177/1203475416683390 28300437 · DOI
- [155]Vaughn A.R. Clark A.K. Notay M. Sivamani R.K. Randomized controlled pilot study of dietary supplementation with turmeric or herbal combination tablets on skin barrier function in healthy subjects J. Med. Food 2018 21 1260 1265 10.1089/jmf.2018.0015 30457892 · DOI
- [156]Kallis P.J. Price A. Dosal J.R. Nichols A.J. Keri J. A Biologically Based Approach to Acne and Rosacea J. Drugs Dermatol. JDD 2018 17 611 617 29879248
- [157]Song X.C. Canellas E. Wrona M. Becerril R. Nerin C. Comparison of two antioxidant packaging based on rosemary oleoresin and green tea extract coated on polyethylene terephthalate for extending the shelf life of minced pork meat Food Packag. Shelf Life 2020 26 100588 100597 10.1016/j.fpsl.2020.100588 · DOI
- [158]Bagheri R. Rashidlamir A. Ashtary-Larky D. Wong A. Alipour M. Motevalli M.S. Chebbi A. Laher I. Zouhal H. Does green tea extract enhance the anti-inflammatory effects of exercise on fat loss? Br. J. Clin. Pharmacol. 2020 86 753 762 10.1111/bcp.14176 31747468 PMC7098875 · DOI
- [159]Gaweł-Bęben K. Kukula-Koch W. Hoian U. Czop M. Strzępek-Gomółka M. Antosiewicz B. Characterization of Cistus× incanus L. and Cistus ladanifer L. extracts as potential multifunctional antioxidant ingredients for skin protecting cosmetics Antioxidants 2020 9 202 10.3390/antiox9030202 32121584 PMC7139296 · DOI
- [160]Tang G. Xu Y. Zhang C. Wang N. Li H. Feng Y. Green tea and epigallocatechin gallate (EGCG) for the management of nonalcoholic fatty liver diseases (NAFLD): Insights into the role of oxidative stress and antioxidant mechanism Antioxidants 2021 10 1076 10.3390/antiox10071076 34356308 PMC8301033 · DOI
- [161]Hodges J.K. Sasaki G.Y. Bruno R.S. Anti-inflammatory activities of green tea catechins along the gut–liver axis in nonalcoholic fatty liver disease: Lessons learned from preclinical and human studies J. Nutr. Biochem. 2020 85 108478 108524 10.1016/j.jnutbio.2020.108478 32801031 · DOI
- [162]Chaikul P. Sripisut T. Chanpirom S. Ditthawutthikul N. Anti-skin aging activities of green tea (Camelliasinensis (L) Kuntze) in B16F10 melanoma cells and human skin fibroblasts Eur. J. Integr. Med. 2020 40 101212 101240 10.1016/j.eujim.2020.101212 · DOI
- [163]Bhattacharya S. Sherje A.P. Development of resveratrol and green tea sunscreen formulation for combined photoprotective and antioxidant properties J. Drug Deliv. Sci. Technol. 2020 60 102000 102023 10.1016/j.jddst.2020.102000 · DOI · Paper page
- [164]Winkelman W.J. Aromatherapy, botanicals, and essential oils in acne Clin. Dermatol. 2018 36 299 305 10.1016/j.clindermatol.2018.03.004 29908571 · DOI
- [166]Phasha V. Senabe J. Ndzotoyi P. Okole B. Fouche G. Chuturgoon A. Review on the use of kojic acid—A skin-lightening ingredient Cosmetics 2022 9 64 10.3390/cosmetics9030064 · DOI
- [167]Saeedi M. Eslamifar M. Khezri K. Kojic acid applications in cosmetic and pharmaceutical preparations Biomed. Pharmacother. 2019 110 582 593 10.1016/j.biopha.2018.12.006 30537675 · DOI
- [168]Khezri K. Saeedi M. Morteza-Semnani K. Akbari J. Hedayatizadeh-Omran A. A promising and effective platform for delivering hydrophilic depigmenting agents in the treatment of cutaneous hyperpigmentation: Kojic acid nanostructured lipid carrier Artif. Cells Nanomed. Biotechnol. 2021 49 38 47 10.1080/21691401.2020.1865993 33438443 · DOI
- [169]Khan A. Park T.J. Ikram M. Ahmad S. Ahmad R. Jo M.G. Kim M.O. Antioxidative and Anti-inflammatory Effects of Kojic Acid in Aβ-Induced Mouse Model of Alzheimer’s Disease Mol. Neurobiol. 2021 58 5127 5140 10.1007/s12035-021-02460-4 34255249 · DOI
- [170]Zilles J.C. Dos Santos F.L. Kulkamp-Guerreiro I.C. Contri R.V. Biological activities and safety data of kojic acid and its derivatives: A review Exp. Dermatol. 2022 31 1500 1521 10.1111/exd.14662 35960194 · DOI
- [171]Bakhouche I. Aliat T. Boubellouta T. Gali L. Şen A. Bellik Y. Phenolic contents and in vitro antioxidant, anti-tyrosinase, and anti-inflammatory effects of leaves and roots extracts of the halophyte Limonium delicatulum S. Afr. J. Bot. 2021 139 42 49 10.1016/j.sajb.2021.01.030 · DOI
- [172]Li T.X. Liang J.X. Liu L.L. Shi F.C. Jia X.W. Li M.H. Xu C.P. Novel kojic acid derivatives with anti-inflammatory effects from Aspergillus versicolor Fitoterapia 2021 154 105027 105033 10.1016/j.fitote.2021.105027 34492330 · DOI
- [173]Gust P.J. Luke J.D. Kojic acid J. Dermatol. Nurses’ Assoc. 2016 8 338 340 10.1097/JDN.0000000000000247 · DOI
- [174]Searle T. Al-Niaimi F. Ali F.R. The top 10 cosmeceuticals for facial hyperpigmentation Dermatol. Ther. 2020 33 e14095 e14139 10.1111/dth.14095 32720446 · DOI
- [175]Ohno Y. Kondo S. Tajima K. Shibata T. Itoh T. Effect of phlorotannins isolated from Eisenia bicyclis on melanogenesis in mouse B16 melanoma cells Nat. Prod. Commun. 2021 16 1934578X211019264 10.1177/1934578X211019264 · DOI
- [176]Phang S.J. Teh H.X. Looi M.L. Arumugam B. Fauzi M.B. Kuppusamy U.R. Phlorotannins from brown algae: A review on their antioxidant mechanisms and applications in oxidative stress-mediated diseases J. Appl. Phycol. 2023 35 867 892 10.1007/s10811-023-02913-4 · DOI
- [177]Jesumani V. Du H. Aslam M. Pei P. Huang N. Potential use of seaweed bioactive compounds in skincare—A review Mar. Drugs 2019 17 688 10.3390/md17120688 31817709 PMC6950024 · DOI
- [178]Zhao W. Yang A. Wang J. Huang D. Deng Y. Zhang X. Qu Q. Ma W. Xiong R. Zhu M. Potential application of natural bioactive compounds as skin-whitening agents: A review J. Cosmet. Dermatol. 2022 21 6669 6687 10.1111/jocd.15437 36204978 · DOI
- [179]Kim K.N. Yang H.M. Kang S.M. Ahn G. Roh S.W. Lee W. Kim D.K. Jeon Y.J. Whitening effect of octaphlorethol A isolated from Ishige foliacea in an in vivo zebrafish model J. Microbiol. Biotechnol. 2015 25 448 451 10.4014/jmb.1409.09033 25341462 · DOI
- [180]Lee S.H. Kang N. Kim E.A. Heo S.J. Moon S.H. Jeon B.T. Jeon Y.J. Antidiabetogenic and antioxidative effects of octaphlorethol a isolated from the brown algae Ishige foliacea in streptozotocin-induced diabetic mice Food Sci. Biotechnol. 2014 23 1261 1266 10.1007/s10068-014-0173-6 · DOI
- [181]Thawabteh A.M. Swaileh Z. Ammar M. Jaghama W. Yousef M. Karaman R. Bufo S.A. Scrano L. Antifungal and Antibacterial Activities of Isolated Marine Compounds Toxins 2023 15 93 10.3390/toxins15020093 36828408 PMC9966175 · DOI
- [182]Shanura Fernando I.P. Asanka Sanjeewa K.K. Samarakoon K.W. Kim H.S. Gunasekara U.K.D.S.S. Park Y.J. Abeytunga D.T.U. Lee W.W. Jeon Y.J. The potential of fucoidans from Chnoospora minima and Sargassum polycystum in cosmetics: Antioxidant, anti-inflammatory, skin-whitening, and antiwrinkle activities J. Appl. Phycol. 2018 30 3223 3232 10.1007/s10811-018-1415-4 · DOI
- [183]Kok J.M.L. Jee J.M. Chew L.Y. Wong C.L. The potential of the brown seaweed Sargassum polycystum against acne vulgaris J. Appl. Phycol. 2016 28 3127 3133 10.1007/s10811-016-0825-4 · DOI
- [184]Lourenço-Lopes C. Fraga-Corral M. Soria-Lopez A. Nuñes-Estevez B. Barral-Martinez M. Silva A. Li N. Liu C. Gandara J.S. Prieto M.A. Fucoxanthin’s optimization from Undaria pinnatifida using conventional heat extraction, bioactivity assays and in silico studies Antioxidants 2022 11 1296 10.3390/antiox11071296 35883788 PMC9311727 · DOI
- [185]Park E.J. Choi J.I. Melanogenesis inhibitory effect of low molecular weight fucoidan from Undaria pinnatifida J. Appl. Phycol. 2017 29 2213 2217 10.1007/s10811-016-1048-4 · DOI
- [186]Lee S.H. Kang S.M. Ko S.C. Lee D.H. Jeon Y.J. Octaphlorethol A, a novel phenolic compound isolated from a brown alga, Ishige foliacea, increases glucose transporter 4-mediated glucose uptake in skeletal muscle cells Biochem. Biophys. Res. Commun. 2012 420 576 581 10.1016/j.bbrc.2012.03.036 22445752 · DOI
- [187]Lajis A.F.B. Ariff A.B. Discovery of new depigmenting compounds and their efficacy to treat hyperpigmentation: Evidence from in vitro study J. Cosmet. Dermatol. 2019 18 703 727 10.1111/jocd.12900 30866156 · DOI
- [188]Haggag Y.A. Abd Elrahman A.A. Ulber R. Zayed A. Fucoidan in pharmaceutical formulations: A comprehensive review for smart drug delivery systems Mar. Drugs 2023 21 112 10.3390/md21020112 36827153 PMC9965894 · DOI · Paper page
- [189]Guan B. Chen K. Tong Z. Chen L. Chen Q. Su J. Advances in fucoxanthin research for the prevention and treatment of inflammation-related diseases Nutrients 2022 14 4768 10.3390/nu14224768 36432455 PMC9694790 · DOI
- [190]Natsume C. Aoki N. Aoyama T. Senda K. Matsui M. Ikegami A. Tanaka K. Azuma Y.T. Fujita T. Fucoxanthin ameliorates atopic dermatitis symptoms by regulating keratinocytes and regulatory innate lymphoid cells Int. J. Mol. Sci. 2020 21 2180 10.3390/ijms21062180 32235696 PMC7139773 · DOI
- [191]Garcia-Jimenez A. Teruel-Puche J.A. Berna J. Rodriguez-Lopez J.N. Tudela J. Garcia-Ruiz P.A. Garcia-Canovas F. Characterization of the action of tyrosinase on resorcinols Bioorg. Med. Chem. 2016 24 4434 4443 10.1016/j.bmc.2016.07.048 27480027 · DOI
- [192]Jin Y.J. Lin C.C. Lu T.M. Li J.H. Chen I.S. Kuo Y.H. Ko H.H. Chemical constituents derived from Artocarpus xanthocarpus as inhibitors of melanin biosynthesis Phytochemistry 2015 117 424 435 10.1016/j.phytochem.2015.07.003 26188915 · DOI
- [193]Yamahara M. Sugimura K. Kumagai A. Fuchino H. Kuroi A. Kagawa M. Itoh Y. Kawahara H. Nagaoka Y. Iida O. Callicarpa longissima extract, carnosol-rich, potently inhibits melanogenesis in B16F10 melanoma cells J. Nat. Med. 2016 70 28 35 10.1007/s11418-015-0933-5 26267810 · DOI
- [194]Mustapha N. Bzéouich I.M. Ghedira K. Hennebelle T. Chekir-Ghedira L. Compounds isolated from the aerial part of Crataegus azarolus inhibit growth of B16F10 melanoma cells and exert a potent inhibition of the melanin synthesis Biomed. Pharmacother. 2015 69 139 144 10.1016/j.biopha.2014.11.010 25661350 · DOI
- [195]Nam J.H. Nam D.Y. Lee D.U. Valencene from the rhizomes of Cyperus rotundus inhibits skin photoaging-related ion channels and UV-induced melanogenesis in B16F10 melanoma cells J. Nat. Prod. 2016 79 1091 1096 10.1021/acs.jnatprod.5b01127 26967731 · DOI
- [196]Jin K.S. Lee J.Y. Hyun S.K. Kim B.W. Kwon H.J. Juniperus chinensis and the functional compounds, cedrol and widdrol, ameliorate α-melanocyte stimulating hormone-induced melanin formation in B16F10 cells Food Sci. Biotechnol. 2015 24 611 618 10.1007/s10068-015-0080-5 · DOI
- [197]de Freitas M.M. Fontes P.R. Souza P.M. William Fagg C. Neves Silva Guerra E. de Medeiros Nobrega Y.K. Silveira D. Bazzo Y.F. Simeoni L.A. Homem-de-Mello M. Extracts of Morus nigra L. leaves standardized in chlorogenic acid, rutin and isoquercitrin: Tyrosinase inhibition and cytotoxicity PLoS ONE 2016 11 e0163130 e0163154 10.1371/journal.pone.0163130 27655047 PMC5031429 · DOI
- [198]Kanlayavattanakul M. Lourith N. Chaikul P. Jasmine rice panicle: A safe and efficient natural ingredient for skin aging treatments J. Ethnopharmacol. 2016 193 607 616 10.1016/j.jep.2016.10.013 27721049 · DOI
- [199]Lourith N. Kanlayavattanakul M. Chingunpitak J. Development of sunscreen products containing passion fruit seed extract Braz. J. Pharm. Sci. 2017 53 1 8 10.1590/s2175-97902017000116116 · DOI
- [200]Sallam A. Mira A. Ashour A. Shimizu K. Acetylcholine esterase inhibitors and melanin synthesis inhibitors from Salvia officinalis Phytomedicine 2016 23 1005 1011 10.1016/j.phymed.2016.06.014 27444345 · DOI
- [201]Srisayam M. Weerapreeyakul N. Barusrux S. Kanokmedhakul K. Antioxidant, antimelanogenic, and skin-protective effect of sesamol J. Cosmet Sci. 2014 65 69 79 24797023
- [202]Diwakar G. Rana J. Saito L. Vredeveld D. Zemaitis D. Scholten J. Inhibitory effect of a novel combination of Salvia hispanica (chia) seed and Punica granatum (pomegranate) fruit extracts on melanin production Fitoterapia 2014 97 164 171 10.1016/j.fitote.2014.05.021 24909999 · DOI
- [203]Lourith N. Kanlayavattanakul M. Chaikul P. Chansriniyom C. Bunwatcharaphansakun P. In vitro and cellular activities of the selected fruits residues for skin aging treatment An. Acad. Bras. Ciências 2017 89 577 589 10.1590/0001-3765201720160849 28538817 · DOI
- [204]Patel P.D. Mohan G.C. Bhattacharya T. Patel R.A. Tsoukas M. Pediatric laser therapy in pigmented conditions Am. J. Clin. Dermatol. 2019 20 647 655 10.1007/s40257-019-00449-3 31134589 · DOI
- [205]Xie X.Y. Fu G.L. Yang Q. Zeng Y. Ke H. Lu J.J. Yi H. Clinical Efficacy of 755 nm Laser Treatment of Lip Mucosal Pigmentation in Children with Peutz–Jeghers Syndrome Dermatol. Ther. 2023 2023 8020443 8020447 10.1155/2023/8020443 · DOI
- [206]Nunez J.H. Strong A.L. Comish P. Hespe G.E. Harvey J. Sorkin M. Levi B. A Review of Laser Therapies for the Treatment of Scarring and Vascular Anomalies Adv. Wound Care 2023 12 68 84 10.1089/wound.2021.0045 35951024 · DOI
- [207]Purohit S.J. Tharmavaram M. Rawtani D. Prajapati P. Pandya H. Dey A. Niosomes as cutting edge nanocarrier for controlled and targeted delivery of essential oils and biomolecules J. Drug Deliv. Sci. Technol. 2022 73 103438 10.1016/j.jddst.2022.103438 · DOI
- [208]Sharma S. Vashist S. Lamba A.K. Arora S. Novel Strategies in the Treatment of Acne: A Review Int. J. Pharm. Investig. 2022 12 123 128 10.5530/ijpi.2022.2.23 · DOI
- [209]Yonekawa Y. Thomas B.J. Thanos A. Todorich B. Drenser K.A. Trese M.T. Capone Jr A. The cutting edge of retinopathy of prematurity care: Expanding the boundaries of diagnosis and treatment Retina 2017 37 2208 2225 10.1097/IAE.0000000000001719 28541957 · DOI
- [210]Al Qarqaz F. Al-Yousef A. Skin microneedling for acne scars associated with pigmentation in patients with dark skin J. Cosmet. Dermatol. 2018 17 390 395 10.1111/jocd.12520 29543377 · DOI
- [211]Ziaeifar E. Ziaeifar F. Mozafarpoor S. Goodarzi A. Applications of microneedling for various dermatologic indications with a special focus on pigmentary disorders: A comprehensive review study Dermatol. Ther. 2021 34 e151 e159 10.1111/dth.15159 34657363 · DOI
- [212]Lima E.V.A. Lima M.M.D.A. Miot H.A. Induction of pigmentation through microneedling in stable localized vitiligo patients Dermatol. Surg. 2020 46 434 435 10.1097/DSS.0000000000001846 30893180 · DOI
- [213]Ahmed N.A. Mohammed S.S. Fatani M.I. Treatment of periorbital dark circles: Comparative study of carboxy therapy vs chemical peeling vs mesotherapy J. Cosmet. Dermatol. 2019 18 169 175 10.1111/jocd.12536 29767467 · DOI
- [214]Sarkar R. Arsiwala S. Dubey N. Sonthalia S. Das A. Arya L. Gokhale N. Torsekar R.G. Somani V.K. Majid I. Chemical peels in melasma: A review with consensus recommendations by Indian pigmentary expert group Indian J. Dermatol. 2017 62 578 584 10.4103/ijd.IJD_490_17 29263530 PMC5724304 · DOI
- [215]Kadry M. Tawfik A. Abdallah N. Badawi A. Shokeir H. Platelet-rich plasma versus combined fractional carbon dioxide laser with platelet-rich plasma in the treatment of vitiligo: A comparative study Clin. Cosmet. Investig. Dermatol. 2018 11 551 559 10.2147/CCID.S178817 PMC6231433 30510437 · DOI
- [216]Mohamad N.E. ELgameel R.M. Mohamed M.H. Comparative study between the effectiveness of plasma skin regeneration versus micro-needling in the treatment of striae distensae J. Cosmet. Dermatol. 2022 21 4545 4553 10.1111/jocd.14751 35037365 · DOI
200 of 203 shown
- Authors
- Thawabteh, A. M., Jibreen, A., Karaman, D., Thawabteh, A., & Karaman, R.
- Affiliations
- Al-Quds University (PS)
- Research and Development Department, Beit Jala Pharmaceutical Co., Ltd., Beit Jala 97300, Palestine
- University of Basilicata (IT)
- Corresponding author
- Karaman, Rafik
- Venue
- Molecules
- Publisher
- MDPI AG
- Published
- 2023-06-18
- Volume
- 28
- Issue
- 12
- Pages
- 4839
- ISSN
- 1420-3049 (ISSN-L)
- PMC
- PMC10304091
- OpenAlex
- W4381149249
- Cited by
- 233
- References
- 225
- Citations by year
- 2026: 66 · 2025: 87 · 2024: 72 · 2023: 7
- FWCI
- 7.53
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecules (publishedVersion, cc-by)
- Preprints.org (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
- Health Sciences › Medicine › Dermatology › Dermatologic Treatments and Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Melanoma and MAPK Pathways
- Keywords
- skin pigmentation, melanogenesis, hyperpigmentation, hypopigmentation, albinism, melasma, vitiligo, Addison's disease, post-inflammatory hyperpigmentation, tyrosinase inhibitors, antioxidants, herbal medicine, marine-derived compounds, UV exposure, drug-induced pigmentation
- MeSH terms
- Humans, Melanins, Skin, Skin Pigmentation, Monophenol Monooxygenase, Hyperpigmentation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review