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Formulation and Physical Characterization of Essential Oil Bangle (Zingiber cassumunar Roxb.) Nanoemulsion Gel Purwanto, Ungsari Rizki Eka; Sholikhah, Mar’atus; Munisih, Siti
Journal of Science and Technology Research for Pharmacy Vol 1 No 1 (2021)
Publisher : Universitas Negeri Semarang

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.15294/jstrp.v1i1.43500

Abstract

Background: Bangle rhizome (Zingiber cassumunar Roxb) essential oil as long been used by Indonesian and often used by postpartum women, as a treatment for abdominal obesity. The formulation of bangle essential oil into topical preparations has not been widely reported. So far, bangle essential oil is not available in pharmaceutical dosage form. The users immediately apply essential oil to the abdominal area and previous study showed that the terpinene-4-ol only diffused 0,39% from 2 mg/cm2 of Bangle essential oil through skin membrane. The development of topical bangle essential oil is necessary to increase the effectiveness of the delivery of active substances through the skin and the comfort of the user. In order to increase the penetration of the terpinen-4-ol, the Bangle essential oil was formulated in the form of a nanoemulsion and then the nanoemulsion was dispersed into a gel base to increase user convenience. Aim: The aim of the present study was to investigate the potential of nanoemulsion formulations for Bangle essential oil and to know the optimum the composition of surfactants and cosurfactants in nanoemulsion system. This study also aims to determine the effect of base gel used in the nanoemulsion gel formulation on the appropriate physical properties. Method: The pre-emulsion was made beforehand with oil and a mixture of surfactant and cosurfactant. With the help of a Design Expert® ver. 10.0.1 software, component of sufactant and co-surfactant were optimized. The design formula was divided into seven nanoemulsion formulas with a ratio of Polysorbate 80: PEG 400, F1 (1: 8), F2 (8: 1), F3 (6,25: 2,75), F4 (8: 1), F5 (1: 8), F6 (1: 8), F7 (4,5: 4,5). The optimum consentration of Polysorbate 80 as surfactant and PEG 400 as co-surfactants in Bangle essential oil nanoemulsion was analyzed using simplex lattice design methode. The optimal formula was further evaluated for its distribution, droplet size, and zeta potential. Distilled water was used as the aqueous phase in nanoemulsion. The amount of aqueous phase: the amount of pre-emulsion is 9 : 1. The optimum nanoemulsion formula then dispersed in carbophol hydrogel to be nanoemulsion gel. Physical characterization of Bangle nanoemulsion gel like a pH, adhesion power, spreadability, viscosity before and after cycling test had been investigated. Result: The optimum composition of surfactant Tween 80 and co-surfactan PEG 400 was 7.659: 1.34. The results showed that the optimal formula with 2% Bangle Essential Oil Loaded in Nanoemulsion had the Z-average 95,2 nm with Index Polidispersity 0,176 and Zeta Potensial -0,1 mV. Bangle Nanoemulsion-Gel had a homogenous organoleptic, spreadability in 6,69 + 0.85 cm, adhesion power in 2.14 + 0.29 seconds, viscosity 5969 + 32.03 cps, and pH 6,58 + 0,29. Conclusion: Bangle Essential Oil Nanoemulsion-Gel formulation has the good physical characteristics and potentially be used as topical dosage forms. A further study is needed to determine the effectiveness of the treatment of abdominal obesity by topical administration of this preparation.
FUCOIDAN NANOENCAPSULATION FROM BROWN ALGAE (Sargassum polycystum) AS A POTENTIAL MARINE IMMUNOMODULATORY AGENT Purwanto, Ungsari Rizki Eka; Ikasari, Endang Diyah; Bagiana, I Kadek; Kusmita, Lia; Trisnayanthi, Ni Nyoman Ayu Indah; Mudianta, I Wayan; Prasetijo, Rahmadi
Jurnal Ilmiah Farmako Bahari Vol 15, No 1 (2024): Jurnal Ilmiah Farmako Bahari
Publisher : Faculty of Mathematic and Natural Science, Garut University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.52434/jifb.v15i1.3207

Abstract

The quest for better and more effective treatments has encouraged the search for therapies derived from natural sources to obtain effective immune therapy, considering that several pandemics have arisen caused by viruses. Developing fucoidan from brown algae in drug encapsulation as an immunomodulator could be more promising. This study aimed to produce nanoencapsulation loaded with fucoidan-purified extract from brown algae and to evaluate the influence of nanoencapsulation formulation on the immunomodulatory activity of fucoidan. Fucoidan was obtained from brown algae and extracted by hot aqueous, followed by ethanol purification. Nanoencapsulation of fucoidan purified extract was prepared using the ionic gelation method. The carbon clearance method was carried out for the immunomodulatory activity test of the nanoencapsulation of fucoidan purified extract. Nanoencapsulation of fucoidan purified extract with the optimum composition of maltodextrin 9.9% and S-TPP 0.1% (1:5) resulted in particle size of 715.4 nm, zeta potential -0.1 mV, pH 7.54, transmittance 97.54%+0.08, and entrapment efficiency 89.94%+0.17. The carbon clearance test showed that the nanoencapsulation of fucoidan was a strong immunostimulant with a phagocytosis index of 1.65. The development of nanoencapsulation could increase the phagocytosis index of fucoidan purified extracts from brown algae. Further molecular studies are needed to demonstrate the molecular activity of this preparation as an immunomodulator.
OPTIMIZATION SUSTAINED RELEASE TABLET FUCOIDAN PURIFIED EXTRACT FROM BROWN SEAWEED (Sargassum polycystum) AS IMMUNOMODULATOR Ikasari, Endang Diyah; Wulansari, Endang Dwi; Purwanto, Ungsari Rizki Eka
Medical Sains : Jurnal Ilmiah Kefarmasian Vol 9 No 4 (2024)
Publisher : Sekolah Tinggi Farmasi Muhammadiyah Cirebon

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37874/ms.v9i4.1310

Abstract

Fucoidan is a sulfate polysaccharide compound that is widespread in the sea, especially in brown algae. Previous fucoidan pharmacokinetics studies have shown that fucoidan nanoparticles have the effect of increasing the immunomodulatory ability of fucoidan, but fucoidan consumed orally has a half-life in plasma of about 3 hours so that to reduce the amount of fucoidan supplement use in a day, fucoidan can be formulated into sustained release tablet preparations. The purpose of this study was to determine the optimal composition of Na. Alginate and HPMC as polymers in sustained-release tablet preparations containing purified fucoidan from brown seaweed to produce tablets with characteristics that meet the compendial requirements of the Indonesian Pharmacopoeia and can maintain fucoidan release in plasma with only one consumption per day to improve user compliance. Fucoidan extraction from brown seaweed was carried out using hot extraction. Purified fucoidan tablets were prepared by the Simplex Lattice Design method using Design Expert version 10.1. The concentration of Na. Alginate and HPMC used as much as 2–5% with 8 formulas, which were then printed on a tablet printing tool. The optimum formula was tested as an immunomodulator in mice with parameters for lymph weight, phagocytosis index, and stimulant index. Optimum formula for Na. alginate: HPMC (3.252:3.748%) with flow speed 8.552 g/sec, compressibility 15,648%, hardness 3.726 kg, friability 0.044%, MC 3.296, Crushing time 21.34 minutes, Q15 34.608%, Q45 34.824%. The optimum formula for the immunomodulatory effect had a significant effect on the lymph weight of mice.