Tyrosinase Inhibition from Green Tea (Camellia sinensis (L.) Kuntze) gel
Abstrak
Green tea (Camellia sinensis (L.) Kuntze) leaf has polyphenol substance that able to inhibit tyrosinase enzyme. Tyrosinase enzyme is one of the essential components that can be initiated melanin formation on the skin (melanogenesis). The natural inhibitory enzyme can be utilized in cosmetics and medicinal industries as depigmentation agent. Green tea leaf was formulated in the dosage form of a gel with carbomer 934 as a gelling agent. This study aimed to determine the optimum concentration of carbomer 934 on green tea leaf extract gel that has an inhibitory tyrosinase activity. This research used three carbomer 934 concentration, there was 0.5%, 0.75%, and 1% respectively. Which every formula was evaluated during six weeks involve organoleptic, homogeneity, viscosity, pH, centrifuge, and freeze-thaw test (during six cycles). The optimum formula was evaluated tyrosinase activity used a spectrophotometer-vis. The results showed that the great concentration of carbomer 934 was contained on the first formula, which has not phase separation and 49.62 ppm of IC50 value. This research showed that green tea leaf extract gel with 0,5% carbomer 934 prevented tyrosinase activity.
Keywords: Carbomer 934, gel, green tea leaf extract, inhibitory of tyrosinase
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Reddy SB, Vashi NA. Hyperpigmentation, Edited by: Dimitris Rigopoulos, Alexander C. Katoulis. Boca Raton: CRC Press; 2017.
Cayce KA, McMichael AJ, Feldman SR. Hyperpigmentation: an overview of the common afflictions. Dermatol Nurs. 2004; 16(5): 401-416.
Criton M, Le Mellay-Hamon V. Dimeric Cinnamoylamide Derivatives as Inhibitors of Melanogenesis. Biol. Pharm. Bull. 2011; 34(3): 420-425.
Alam MB, Bajpai VK, Lee J, Zhao P, Byeon JH, Ra JS, Majumder R, Lee JS, Yoon JI, Rather IA, Park YH, Kim K, Na M, Lee SH. Inhibition of melanogenesis by jineol from Scolopendra subspinipes mutilans via MAP-Kinase mediated MITF downregulation and the proteasomal degradation of tyrosinase. Scientific Reports. 2017; 7: 47858.
Abdel-Naser MB, Krueger-Krasagakis S, and
Krasagakis K. Hyperpigmentation, Edited by: Dimitris Rigopoulos, Alexander C. Katoulis. Boca Raton : CRC Press; 2017.
Sangsrichan S, Ting R. Antioxidation and Radical Scavenging Activities and Tyrosinase Inhibition of Fresh Tea Leaves, Camellia sinensis. Science Journal Ubon Ratchathani University. 2010; 1: 76-81.
Yashin A, Nemzer B, Combet E, Yashin Y. Determination of the Chemical Composition of Tea by Chromatographic Methods: A Review. Journal of Food Research. 2015; 4(3): 56-87.
Suhandi S, Jafar G. Kajian Pustaka Hidrogel Ekstrak Daun Teh Hijau (Camellia sinensis L.) sebagai Bleaching Skin pada Mata Panda (karya tulis ilmiah). Sekolah Tinggi Farmasi Bandung, Bandung; 2014.
Wardiyah S. Perbandingan Sifat Fisik Gel, Krim, dan Salep yang Mengandung Etil P-Metoksisinamat dari Ekstrak Rimpang Kencur (Kaempferia galanga L.) (skripsi). Jakarta: UIN Syarif Hidayatullah; 2015.
Langley CA, Dawn B. Pharmaceutical Compounding and Dispensing. Second Edition. UK: Pharmaceutical Press; 2012.
Thitimuta S, Pithayanukul P, Nithitanakool S, Bavovada R, Leanpolchareanchai J, and Saparpakorn P. Camellia sinensis L. Extract and Its Potential Beneficial Effects in Antioxidant, Anti-Inflammatory, Anti-Hepatotoxic, and Anti-Tyrosinase Activities. Molecules. 2017; 22(401): 1-14.
Rowe RC, Paul JS, Marian EQ. Handbook of Pharmaceutical Excipient (6th Ed). UK: Royal Pharmaceutical Society; 2009.
Madan J, Singh, R. Formulation and Evaluation of Aloe Vera Topical Gels. International Journal of Pharmaceutical Science. 2010; 2(2): 515-551.
Rahmi H, Ramadhan R, Radjab NS. Pengaruh Konsentrasi Natrium Alginat Terhadap Gel Ekstrak Daun Teh Hijau (Camellia Sinensis L.) Sebagai Inhibitor Tirosinase. PHARMACY. 2017; 14(2): 162–72.
Hanani E. Analisis Fitokimia. Jakarta: EGC; 2014.
Sharma B, Singh LR. Pharmaceutical gels for topical drug delivery: An overview. International Journal of Research in Pharmacy and Pharmaceutical Sciences. 2018; 3(2): 19-24.
Gupta PC. Physicists in Pharmaceutical Industry. PharmaTutor. 2014; 2(11): 75-76.
Mahardika H. Uji Penghambatan Tirosinase secara In Vitro serta Stabilitas Fisik dan Stabilitas Kimia Sediaan Krim yang Mengandung Asam Azelat (skripsi). Depok: Universitas Indonesia; 2012.
Indonesia Ministry of Health. Suplemen II Farmakope Herbal Indonesia. 1st Edition. Jakarta: Indonesia Ministry of Health; 2011.
Chang RK, Raw A, Lionberger R, Yu L. Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products. AAPS Journal. 2013; 15(1): 41-52.
Anwar E. Eksipien dalam Sediaan Farmasi: Karakterisasi dan Aplikasi. Jakarta: Dian Rakyat; 2012.
Bagci N, Bayindir ZS, Inal O, Altanlar N, Yuksel N. Development and In vitro Evaluation of Nifedipine Gel Formulations for Anorectal Applications. Current Drug Delivery. 2020; 17(2): 126 – 139.
Charissa M, Joshita D, Berna E. Uji Aktivitas Antioksidan dan Penghambatan Tirosinase serta Uji Manfaat Gel Ekstrak Kulit Batang Taya (Nauclea subdita) terhadap Kulit. Jurnal Kefarmasian Indonesia. 2016; 6(2): 98-107.
DOI: https://doi.org/10.24198/ijpst.v8i2.27145
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