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Penetapan Kadar Betametason Valerat Pada Sediaan Krim betametasone 0,1 % Secara Kromatografi Cair Kinerja Tinggi Indriati Indriati; Ferdinan Jalung; Herviza Wulandary Pane
Journal of Pharmaceutical and Sciences JPS Volume 6 Nomor 4 (2023)
Publisher : Fakultas Farmasi Universitas Tjut Nyak Dhien

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36490/journal-jps.com.v6i4.287

Abstract

Background; Medicine is used as a support in the world of health. Medicine is a material intended for use in establishing diagnoses, preventing, reducing, eliminating, curing diseases or symptoms of diseases, injuries or bodily and spiritual disorders in humans or animals, beautifying the body or parts of the human body. Objective; To validate the method of determining the level of Betamethasone Valerate using HPLC with stationary phase C18 and mobile phase methanol: water that meets the requirements of the method validation test including precision, accuracy, selectivity, linearity and sensitivity. Methods; This research is a type of Quasy Experimental research with a Pretest Posttest Nonequivalent Control Group design, namely in this design the experimental group and control group are not randomly selected, in other words this design is carried out before and after treatment. Results; The determination of levels is carried out after the method to be used has been proven valid after going through the validation test processes. The determination of levels was carried out on the five face cream samples as much as 3 totolan in each sample. The results of the level determination test showed that the five samples did not contain betamethasone valerate and triamcinolone acetonide. Conclusion; The KLT-densitometry method used to quantify the content of topical corticosteroids in Betamethasone 0.1% cream tested has met the validation parameters of ICH and AOAC includes accuracy, precision, specificity, linearity, LOD, LOQ.
Uji Aktivitas Antipiretik Ekstrak Daun Bidara (Ziziphus Spina Christi L) Terhadap Mencit Jantan (Mus Musculus) Ferdinan Jalung; Mila Febrina Rindayani; Meity Christiani
Journal of Pharmaceutical and Sciences JPS Volume 6 Nomor 4 (2023)
Publisher : Fakultas Farmasi Universitas Tjut Nyak Dhien

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.36490/journal-jps.com.v6i4.289

Abstract

Background; Indonesia has thousands of types of plants spread across various regions. The existing biodiversity can be used as raw material for modern and traditional medicines. Indonesian people have long known and used traditional medicine to treat various diseases. The increasingly expensive price of modern medicine on the market is one reason to explore the use of traditional medicine again. Many types of medicinal plants in Indonesia have been used as raw materials for medicine, some of these plant species have even been clinically tested for their phytochemical content, efficacy and safety of use. Objectives; To find out that bidara leaf extract (Ziziphus spina-christi L.) has antipyretic activity. Method; This type of research is experimental research.Extraction is carried out to filter out polar compounds so 60% ethanol liquid is used. Results; From the results of research that has been carried out, it was found that the average difference in temperature reduction between time and fever temperature was from 30 minutes to 120 minutes. For doses of 100 mg/30 g, 150 mg/30 g BW of mice, 200mg/30 g BW of mice, NaCMC and Paracetamol at 30 minutes respectively were 0.27, 0.37, 0.44, 0 .04 and 0.8oC. For doses of 100 mg/30 g, 150 mg/30 g BW of mice, 200 mg/30 g BW of mice, NaCMC and Paracetamol at 60 minutes respectively were 0.6, 0.67, 0.94, 0.07 and 1.47oC. For doses of 100 mg/30 g, 150 mg/30 g BW of mice, 200 mg/30 g BW of mice, NaCMC and Paracetamol at 90 minutes respectively were 1.04, 1, 1.24, 0, 07 and 2.1oC. Conclusion; Bidara leaf extract (Ziziphus spina-christi L.) has antipyretic activity in mice. Bidara leaf extract (Ziziphus spina-christi L.) which has antipyretic activity is at a dose of 100 mg, 150 mg and 200 mg/30 grams of body weight for mice.