DEVELOPMENT OF GEL DOSAGE FORM OF ETHYL ACETATE EXTRACT OF MANGOSTEEN RIND
(Garcinia mangostana L.)
Abstract
Abstract Alpha-mangostin is a xanthonoid compound contained in mangosteen rind (Garcinia mangostana L.) and has an
antibacterial effect against Staphylococcus aureus, the bacterium that causes acne. In this study, mangosteen rind extract is
formulated in a gel dosage form. This study aimed to determine the optimum formula, the physical and chemical properties as
well as the optimum formula release profile of the gel dosage form of mangosteen rind extract.
The mangosteen rind extract gel formula consists of viscolam, propylene glycol, glycerin, microcare®, ethyl acetate extract of
mangosteen rind, and distilled water. The formula was optimized by varying the concentrations of viscolam (2% and 5%),
propylene glycol (5% and 20%) and glycerin (2% and 15%) using a factorial experimental design program called Design Expert
7.0.0. The 8 formulas were developed into gel dosage form and the physical and chemical properties were then evaluated. The
evaluation tests include viscosity, dispersive power, and pH tests. The evaluation results were processed using the Design Expert
7.0.0 program to determine the optimum formula.
The results of the analysis showed the optimum formula of gel dosage form of mangosteen rind extract with viscolam percentage
of 4.97%, propylene glycol of 9.91%, glycerin of 12.23%, microcare® of 0.3%, TEA (q.s), ethyl acetate extract of mangosteen
rind of 1%, and distilled water of 45%. The evaluation results of the physical and chemical properties of the gel optimum
formula revealed the viscosity of 2,345 cps, dispersive power of 6.59 cm, and pH of 6.74. Alpha-mangostin release test on the
optimum formula revealed a flux value of 41.327 ?g/cm2/t1/2. From these results, it is concluded that the optimum formula has
met the physical and chemical characteristics of a good gel.
Downloads
References
[1] Koh, J.J., et al., 2013. Rapid Bacterial Action of Alpha-Mangostin
Againts MRSA As An Outcome of Membrane Targeting. Biochimica
et Biophysica. pp. 834-844.
[2] Dachriyanus, R. Agustina and R. Andayani. 2014. Development and
Validation of Thin-Layer Chromatographic Method for
Determination of α–mangostin in Young Pericarp, Ripe Pericarp and
Bark Extract of Garcinia mangostana L. using TLC-Densitometry. J.
Res. Pharm. Sci. 5(4): 294-298
[3] Draelos, Z.D. and L.A. Thaman. 2006. Cosmetic Formulation of Skin
Care Product. New York: Taylor & Francis Group. P. 377.
JHSM UNUD Journals, p-ISSN: e-ISSN:
32
[4] Ansel, H.C. 2008. Pengantar Bentuk Sediaan Farmasi Edisi 4.
Translator: Farida Ibrahim. Jakarta: UI Press.
[5] Lieberman, H. A. 1997. Pharmaceutical Dosage Form: Disperse
Sytems, Vol. 1. New York: Marcell Dekker Inc.
[6] Budiputra, D.K. 2013. “Pengembangan Formula dan Karakterisasi
Nanoemulsi dan Nanosuspensi Kurkumin dalam Bentuk Gel untuk
Rute Transdermal” (Master’s thesis). Bogor: Institut Teknologi
Bandung.
[7] Rita Corp. 2007. Viscolam AT 100EF. Material Safety Data Sheet.
USA.
[8] Sukmawati, N.M.A. 2013. “Formulasi dan Evaluasi Sediaan Masker
Wajah Gel Peel Off dari Ekstrak Etanol 96% Kulit Buah Manggis
(Garcinia mangostana L.)” (undergraduate thesis). Denpasar:
Universitas Udayana
[9] Melani, H. D., T. Purwanti, and W. Soeratri. 2005. Korelasi Kadar
Propilenglikol dalam Basis Dan Pelepasan Dietilammonium
Diklofenak Dari Basis Gel Carbopol ETD 2020. Majalah Farmasi
Airlangga, 5(1): 1-6.
[10] Martin, A., J. Swarbrick, and A. Cammarata. 1993. Farmasi Fisik:
Dasar-dasar Farmasi Fisik dalam Ilmu Farmasetik. Third Edition.
Translator: Yoshita. Jakarta: UI-Press. pp. 1124-1187.
[11] Berko, S., et al. 2014. Monitoring of Skin Penetration and
Absorption with a New in Vivo Experimental Model. Farmacia,
62(6): 1157-1163.
[12] Dwiastuti, R. 2010. Pengaruh Penambahan CMC (Carboxymethyl
Cellulose) sebagai Gelling Agent dan Propilen Glikol sebagai
Humektan dalam Sediaan Gel Sunscreen Ekstrak Kering Polifenol
Teh Hijau (Camellia sinensis L). Jurnal Penelitian. 13(2): 227-228.
[13] Garg, A., D. Aggarwal, S. Garg, and A.K. Sigla. 2002. Spreading of
Semisolid Formulation. USA: Pharmaceutical Technology. pp. 84-
104.