UJI EFEKTIFITAS BEBERAPA SENYAWA SEBAGAI PENINGKAT PENETRASI TERHADAP LAJU DIFUSI KRIM ASAM KOJAT TIPE MINYAK DALAM AIR SECARA IN VITRO
DOI:
https://doi.org/10.30595/pji.v10i1.773Abstract
ABSTRAK Bahan peningkat penetrasi merupakan zat tambahan yang membantu difusi obat melewati stratum korneum. Tujuan dari penelitian ini adalah untuk mengetahui efek penggunaan propilenglikol, DMSO, dan isopropil miristat dengan berbagai konsentrasi sebagai peningkat penetrasi dalam proses difusi asam kojat secara in vitro. Krim asam kojat dibuat dengan variasi konsentrasi propilenglikol, DMSO, dan isopropil miristat masing–masing 1%, 2%, 4%, dan 8% serta tanpa peningkat penetrasi. Pengujian stabilitas krim meliputi organoleptis, penentuan tipe emulsi, pH, dan viskositas. Uji difusi dengan alat sel difusi Frans menggunakan membran kulit tikus (Rattus novergicus) dan difusi asam kojat dalam cairan kompartemen reseptor pada interval waktu 0, 15, 30, 45, 60, 75, 90, 105, dan 120 menit diukur dengan menggunakan spektrofotometer UV. Hasil uji stabilitas menunjukkan tidak ada perubahan sebelum dan sesudah penyimpanan dipercepat tehadap organoleptis, penentuan tipe emulsi, dan pH tetapi viskositas berbeda sangat signifikan akibat variasi bahan dan konsentrasi peningkat penetrasi. Dari formula krim asam kojat yang mengandung DMSO 8%, propilen glikol 1%, isopropil miristat 8% yang diformulasi dapat dikategorikan stabil secara fisik dan paling efektif dibanding formula lainnya. Kata kunci: peningkat penetrasi, laju difusi, asam kojat. ABSTRACT Penetration of an enhancer is an additive that assist the diffusion of the drug through the stratum corneum. The purpose of this study was to determine the effect propylene glycol, DMSO, and with various concentrations of isopropyl myristate as penetration enhancers in the diffusion process of kojic acid in vitro. Kojic acid cream made with various concentration propylene glycol, DMSO, and isopropyl myristate, 1%, 2%, 4%, and 8% respectively, well as no penetration enhancers. Tests include organoleptic stability of cream, determining the emulsion type, pH, and viscosity. Diffusion test with tool diffusion frans cells using mouse skin membrane (Rattus novergicus) and diffusion in the liquid compartment kojic acid receptors on the time interval 0, 15, 30, 45, 60, 75, 90, 105, and 120 min were measured by using UV spectrophotometer. Stability test results showed there was no change before and after accelerated storage on organoleptic, determination of the type of emulsion viscosity and pH but differ significantly due to variations in ingredients and concentrations of penetration enhancers. Of kojic acid cream formula containing 8% DMSO, 1% propylene glycol, isopropyl myristate 8% which can be categorized formulated physically stable and most effective formula than the others. Key words: penetration enhancers, the rate of diffusion, kojic acid.References
Jellinek, J.S., 1970. Formulation and function of cosmetic., London: wilwy Interscience.
Balsam, M.S., Sagarin, E., 1972. Cosmetic science technology. Volume 1. New York: John Wiley and Sons.
Majeed, M., 2008. Anatomi fisiologi kulit. Jakarta: Sabinsa Corporation.
Ahmad, V.U., Ullah, F., Hussain J., Faroog, U., Zubair, M., Khan, M.T., Choudhary, M.I., 2004. Tyrosinase inhibitors from Rhododendron collettianum and their structure-activity relationship (SAR) studies. Chem Pharm Bull., 52(12):1458–1461.
Serra-Baldrich, E., Tribo, M.J., Camarasa, J.G., 1998. Allergic contact dermatitis from kojic acid. Contact Dermatitis, 39(2):86-87.
Lachman, L., Lieberman, H.A., Kanig, J.L. 1970, The theory and practice of industrial pharmacy Philadelphia: Lea & Febiger.
Popli, H., Sharma, S.N., 1990. Evaluation of sustained release formulations. The Eastern Pharmacist, Januari:75-79.
Downloads
Published
How to Cite
Issue
Section
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution 4.0 International License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).