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Jurnal Farmasi Galenika (Galenika Journal of Pharmacy)
Published by Universitas Tadulako
ISSN : 24427284     EISSN : 24428744     DOI : https://doi.org/10.22487/j24428744
Core Subject : Health, Science,
Biochemistry, Genetics & Molecular Biology Chemistry Health Professions Immunology & microbiology Medicine & Pharmacology
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (E-ISSN: 2442-8744) (p-ISSN: 2442-7284), is an open access journal (print and e-journal) focusing on the scientific works in the field of Pharmacy and Pharmaceutical Science. The articles of this journal are published every six months, that is March and October (2 issues per year). This journal is developed by Department of Pharmacy, Faculty of Mathematics and Natural Science, Tadulako University and has been identified in Crossref with the DOI Number : 10.22487/j24428744. Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) has been accredited by Kemenristekdikti as Sinta 3 starting from Volume 5 No 1 2019.
Arjuna Subject : Pharmacology, Toxicology and Pharmaceutics - Ilmu Farmasi
Articles 10 Documents
 1 
Search results for , issue "Vol. 9 No. 1 (2023): (March 2023)" : 10 Documents clear
The Effect of Kersen (Muntingia calabura) Fruit Extract Addition to The Yogurt Antibacterial Activity on Escherichia coli: Pengaruh Penambahan Ekstrak Buah Kersen (Muntingia calabura) Terhadap Aktivitas Antibakteri Yogurt Terhadap Escherichia coli Annisa Krisridwany; Putri Ayu Lestari; Aji Winanta; Sabtanti Harimurti; Vella Lailli Damarwati
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.15799

Abstract

Background: Yogurt, completed with lactic acid bacteria, can inhibit the growth of Escherichia coli. The flavonoids, tannin, and saponin of the Muntingia calabura L. plant showed antibacterial activity. Objectives: The present study aims to observe the effect of the addition of Muntingia calabura L. fruit extract to yogurt on the activity of Escherichia coli. Material and Methods: The study was an experimental study with the treatment of addition of Muntingia fruit extract infusion with various concentrations (12.5 %, 25%, 50%, 75%, and 100% with three times replications) to the cow-milk-based yogurt. The staining reagents were used for the phytochemical screening. The mixed muntingia yogurt (MMY) was then centrifuged to obtain supernatant. The antibacterial activity was tested using the disc diffusion method by observing the diameter of the inhibition zone. Plain yogurt was used for the negative control and Cefotaxime for the positive control. Results: In Muntingia fruit extract, flavonoids, tannin, steroid, phenol, and saponin have been observed. The MMY showed antibacterial activity toward E. coli as indicated by the various diameter of inhibition zones of 5.03± 2.66 mm, 4.95± 0.39 mm, 5.68± 0.84 mm, 8.02± 1.45 mm, and 15.73± 1.60 mm for the Muntingia addition concentration of 12.5 %, 25%, 50%, 75%, and 100%, respectively. The diameter of the inhibition zone of negative control was 3.95 mm, while positive control was 45.60 mm. Conclusions: The addition of Muntingia calabura L. fruits extracts to yogurt at concentrations of 75% and 100% could inhibit the growth of E. coli bacteria as categorized for medium and strong inhibitory, respectively.
The Use of Ambon Banana Starch (Musa paradisiaca var. sapientum L.) as a New Binder in Tablet Formulation : Penggunaan Pati Pisang Ambon (Musa paradisiaca var. sapientum L.) Sebagai Bahan Pengikat Baru Dalam Formulasi Tablet Ikhwatun Mutmainnah; Santi Sinala; Sisilia TR Dewi
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.15917

Abstract

Background: Synthetic materials are commonly used as binders in tablet formulations, this causes the price of tablets to be more expensive. For this reason, new discoveries are sought that can replace synthetic materials by utilizing materials from nature. One of the binders that comes from natural ingredients and is easily obtained is the Ambon Banana Starch (Musa paradisiaca var. sapientum (L.)). Objectives: This study was conducted to determine the physical characteristics of paracetamol tablets from Ambon banana starch (Musa paradisiaca var. sapientum L.) as a binder. Materials and Methods: Paracetamol tablets were compressed using the wet granulation method by adding a binder in the form of Ambon banana starch mucilago. The consentration of Ambon banana starch used was Formula I (15%), Formula II (17.5%) and Formula III (20%). Evaluation of the physical characteristics of the preparation is determined through the parameters of granule testing and tablet testing. Results: Formulation I, II, and III have met the requirements for the granule test. Meanwhile, in tablet testing, the results of size uniformity test, weight uniformity test, hardness test, and disintegration time test met the requirements for all formulations. However, in the friability test, Formula I (15%) did not meet the requirements with a value of 2.07% (requirement <1%), while formulas II and III had met the requirements. Conclusions: This study showed that Ambon banana starch can be used as a binder in tablet formulation.
Safety assessment of statin-drug interaction effects in cardiology outpatient in Teaching Hospital at Surabaya: Penilaian keamanan efek interaksi obat statin pada pasien kardiovaskular rawat jalan RS Pendidikan di Surabaya Ana Khusnul Faizah; Amitasari Damayanti; Nani Wijayanti Dyah Nurrahman
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.15985

Abstract

Background: HMG-CoA inhibitors, more commonly known as statins, are lipid-lowering agents that have benefits in cardiovascular therapy. Statins are associated with two significant side effects that are asymptomatic elevations of liver enzymes and myopathy. Myopathy is the most likely to occur when statins are prescribed with other drugs. Objectives: To evaluate the effect of drug interactions between statins and concomitant drugs in outpatient cardiovascular patients. Methods: This study conducted in a prospective cohort. Drug interactions was checked by using lexicomp drug interactions software and patient’s complaints were taken through interviews. Results: There were 69 patients included in this study as sample. A total of 16 patients received atorvastatin, and 53 patients received simvastatin. More than half of sample (59%) showed statin-drug interactions. The most drug interactions were severe (41%), followed by moderate (22%) and mild (10%). The most interacting drugs were amlodipine and diltiazem. Based on the results of interview, there were no complaint of myopathy felt by patient. Conclusion: The effects of drug interactions still need to be considered even though the patients did not complain myopathy. Several factors can determine the impact of drug interactions that is not experienced by the patients.
Transfersome as Topical Drug Delivery: Formulation and Characterization: Transfersome sebagai Pengiriman Obat Topikal: Formulasi dan Karakterisasi Nur Zakiyah Darajat; Anis Chaerunisaa; Marline Abdassah
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.16030

Abstract

A transdermal delivery system is a non-invasive delivery system that provide a controlled therapeutic effect. However, this system has a barrier that is the outermost layer of the skin, so that only part of the drug can be administered via the transdermal route. The use of the vesicular system as a carrier for drugs or active substances is a solution for transdermal delivery systems to be able to pass through the skin barrier. One of the vesicular systems that can overcome this problem is transfersome. Displacement is elastic and can change shape by squeezing itself to pass through smaller-than-sized pores. In addition, transfersomes can encapsulate drugs or active substances that are amphiphilic, and have permeation ability than conventional liposomes. This review article aims to explain the definition and general description of transfersomes, their mechanism of action, methods of preparation and characterization, and their recent application in drug delivery using the vesicular transfersome system.
The Antigangrene Activity of Transdermal Patch of Insulin Leaves (Smallanthus Sonchifolius) to Diabetic Gangrene on White Rats: Aktivitas Antigangren Patch Transdermal Daun Insulin (Smallanthus sonchifolius) terhadap Gangrene Diabetik pada Tikus Putih Lucia Hendriati; Fecky Fernando Fredericktho; Iwan Sahrial Hamid; Teguh Widodo; Suryo Kuncorojakti
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.16076

Abstract

Background: Diabetic gangrene is a chronic complication of diabetes mellitus caused by neuropathy, blood vessel disorders, and infection by Staphylococcus aureus. S.sonchifolius leaves contains flavonoid as hypoglycemic agents and sesquiterpene lactones as antibacterial. Unfortunately, oral administration of S. sonchifolius leaves infusion causes kidney toxicity. Objective: The aimed of the study was to determine the effectiveness of the transdermal patch of S. sonchifolius leaves ethanol extract on gangrene wound healing with macroscopic parameters and neoangiogenesis of gangrenous wounds in white rats that have been induced by diabetes mellitus. Material and Methods: This study used 4 treatment groups: positive control (Bevalex® cream), negative control (patch without S. sonchifolius leaves extract), F1 (S. sonchifolius leaves patch without enhancer), and F2 (S. sonchifolius leaves patch with Tween 60 as enhancer). The dose of S. sonchifolius leaves given was 400 mg/kg BW. Alloxan-induced diabetic rat feet were injected with S. aureus to form gangrene. Observations were made on the 7th and 14th days. Results: Based on the Wagner-Meggit scale on macroscopic observations, administration of a transdermal patch of S. sonchifolius leaves accelerates gangrene healing. The statistical results of neoangiogenesis on the 7th and 14th days showed a significant difference (p<0.05) between the positive control, F1, and F2 to the negative control. F2 showed the highest angiogenesis on day 7 (114.00 ± 5,00) and 14 (161.00 ± 5.29) compared to all groups. Tween 60 as enhancer increase the number of angiogenesis. Both F1 and F2 did not show a significant difference to the positive control. Conclusion: S. sonchifolius leaves ethanol extract patch accelerated the diabetic gangrene healing process based on macroscopic and neoangiogenesis observation on the 7th and 14th days. Toxicity examination in white rats are needed before clinical study in human.
Vitamin C elicits protection against cylophosphamide-induced nephrotoxicity in rat animal model: Vitamin C Memproteksi Terhadap Nefrotoksisitas Yang Diinduksi Siklofosfamid Pada Hewan Model Tikus Alifah Dwi Yulianti; Yulia Yusrini Djabir; Prihantono Prihantono
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.15992

Abstract

Background: Cyclophosphamide (CPD) causes renal cell toxicity due to its toxic metabolites. Objectives: This study aimed to evaluate the nephroprotective effect of vitamin C at 125 mg/kgBW, 250 mg/kgBW, and 500 mg/kgBW doses based on the biomarker level of urea, creatinine, parameter of urinalysis and renal histopathology. Material and Methods: The experimental animals consisted of 25 rats (Rattus norvegicus) that were divided into 5 treatment groups: healthy control, placebo (water for injection + CPD 250mg/kgBB), and 3 vitamin C treatment groups (125, 250, or 500 mg/kgBW + CPD 250mg/kgBB). Results: The results of blood biomarker, urine analysis, and histopathological analysis showed that CPD induced nephrotoxicity characterized by an increase in urea levels from 21.79 mg/l to 156.65 mg/l, creatinine from 0.375 to 0.717 mg/l, urine protein from 0 to 2.7, with histopathological damage scores from mild to severe (scores 1-3). In the treatment groups, the average damage score was 1-2 (mild score). However, of the three doses used, only the 500 mg/kg dose had significantly improved biomarkers compared to the placebo group, including the urea, creatinine, and urine protein levels, as well as histopathological scores (p<0.05). Conclusions: Vitamin C at a dose of 250 mg/kgBW was able to prevent the increase of urea, creatinine, and urine protein levels, however, a higher dose (500 mg/kg) was required to provide optimal protection against renal structural damage caused by cyclophosphamide.
Direct Medical Costs and Accordance of INA-CBG's Claims on Covid-19 Patients at Anutapura Hospital: Biaya Medis Langsung dan Kesesuaian Klaim Tarif INA-CBG’s pada Pasien Covid-19 di RSU Anutapura Muhamad Rinaldhi Tandah; Khusnul Diana; Arya Dibyo Adisaputra; Shella Monica; Fatimah Azzahrah
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.16073

Abstract

Background: The pandemic Covid-19 has had an impact on various aspects of life, both socially and economically. One of the government's responsibilities is in financing the treatment of Covid-19 patients, which is stated in the Decree of the Minister of Health of the Republic of Indonesia Number HK.01.07/MENKES/5673/2021 regarding technical instructions for claiming the cost of Covid-19 services. Objectives: This study aimed to determine the average direct medical costs and according to the INA-CBGs rates for Covid-19 patients and the effect of length of stay, severity and comorbidities on the total cost from a hospital perspective. Material and Methods: This study was an observational descriptive study, used a sample of patients diagnosed with Covid-19 inpatients at Anutapura Hospital Palu in 2020. The sample was used 134 patients, who met the inclusion and exclusion criteria. The data collected includes patient characteristics, direct medical costs (consultation fees, visits, rooms, medical procedures, medical devices, examinations and drugs) and INA-CBGS rates. Results: the Covid-19 patients were hospitalized for 14 days (65.67%) with severe severity (92.54%), patients without comorbidities (comorbidities) (74.63%) and included in the group with INA-CBGs code was A-4-13-III (92.54%). The average direct medical cost of the patient was Rp. 5,371,333, with the largest cost being the room fee, which was 32.57% of the total cost. The average INA-CBG's tariff was Rp. 123,019,851. Conclusions: The INA-CBGs tariff was higher than direct medical costs with a difference of Rp. 117,648,518. The results of the linear regression test, it was found that there was a partial or simultaneous effect between length of hospitalization, severity and incidence of comorbidities on total direct medical costs.
Optimization of Soya Phosphatidylcholine and Tween 80 As A Preparation of Diclofenac Sodium Transfersome Vesicles Using Design-Expert: Optimasi Fosfatidilkolin Kedelai dan Tween 80 Sebagai Penyusun Vesikel Transfersom Natrium Diklofenak Menggunakan Design- Expert Wa Ode Sitti Zubaydah; Rina Andriani; Suryani Suryani; Astrid Indalifiani; Sitti Raodah Nurul Jannah; Devi Hidayati
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.16085

Abstract

Background: Diclofenac sodium is a non-steroidal anti-inflammatory drug (NSAID) widely prescribed for inflammation and pain. However, when used orally, diclofenac sodium has poor bioavailability because it undergoes first-pass metabolism in the liver, so only about 50% of the drug reaches systemic circulation. Therefore, the transdermal delivery system, in this case, transfersome nanovesicles, was chosen as an alternative to overcome these problems. Transfersome is a lipid vesicle with the best deformability in penetrating the skin layer among other nanovesicles. Transfersomes consist of active substances, phospholipids, surfactants, and other ingredients. The composition of phosphatidylcholine as a phospholipid and tween 80 as a surfactant is a variable that can affect the optimization of the transfersome formula. Therefore, the ratio of phospholipids and surfactants should be varied to obtain the most stable transfersome formula with high drug entrapment efficiency. Optimization as an approach to get the best combination of a formula can be done in a more efficient way using software called Design-Expert. This software is used to help carry out experimental designs, such as determining the optimum formula for a preparation. Objectives: This study aims to determine the ratio of soya phosphatidylcholine as a phospholipid and tween 80 as a surfactant in the optimum formula of diclofenac sodium transfersome vesicles using Design-Expert and to determine the characteristics of the resulting transfersome vesicles. Material and Methods: Optimizing the transfersome Diclofenac Sodium formula using the factorial design 22 with soya phosphatidylcholine and tween 80 factors, particle size response, and entrapment efficiency. The thin layer hydration method carried out the process of making diclofenac sodium transfersome. Results: The results obtained from this study, namely the optimum formula based on Design-Expert, obtained a ratio of soya phosphatidylcholine and tween 80 of 4.5%: 0.5%. The results of the characterization of the optimum formula obtained a particle size of 224.3 nm, a zeta potential of -57.1 mV, and entrapment efficiency of 99.85%. Conclusions: The results of the characterization of the diclofenac sodium transfersome have met the specifications required for each test.
Inhibition of HMG-CoA Reductase Activity by Kersen Leaves (Muntingia calabura L.) to Prevent Hypercholesterolemia: Inhibisi HMG-CoA Reduktase Menggunakan Ekstrak Daun Kersen (Muntingia calabura L) Untuk Mencegah Hiperkolesterolemia Tien Tien; Nishar Rakhman Ardiansyah; Carla Wulandari Sabandar; Laode Kardin; Pranita Aritrina
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.16086

Abstract

Background: Hypercholesterolemia is a condition of total cholesterol level >200 mg/dL and LDL >130 mg/dL. HMG-CoA (3-hydroxy-3-ethylglutaryl-coenzyme A) reductase is an enzyme that has a role in cholesterol biosynthesis. Hence, inhibition of this enzyme led to the decrement of cholesterol level. The extract of Kersen leaves (Muntingia calabura L.) is known to contain flavonoids, terpenoids, steroids, tannins, phenolic, and alkaloids. Flavonoids work by inhibiting the HMG-CoA reductase activity, so that mevalonate cannot be formed and thus decrease the cholesterol synthesis. Objectives: The present study aimed to determine the effect of Kersen leaves extract (M. calabura L.) in inhibiting the HMG-CoA reductase activity in vitro. Material and Methods: The study is a true experimental study with a post-test-only control group design. The independent variables were ethanol, methanol, and n-hexane extracts of Kersen leaves. Moreover, the percentage inhibition of the enzyme was the dependent variable. The test was conducted in vitro using UV-Vis spectrophotometry with pravastatin as a positive control. Results: The inhibitory effects of ethanol, methanol, n-hexane extracts of Kersen leaves, and pravastatin towards HMG-CoA reductase activity were 85.56%, 59.75%, 92.03%, and 99.58%, respectively. Post Hoc One-Way ANOVA showed that the p-values of pravastatin with ethanol, methanol, and n-hexane extracts were 0.687, 0.048, and 0.931, respectively. The n-hexane and ethanol extracts were potent for inhibiting the enzyme activity (p>0.05) comparable to pravastatin. Conclusion: The n-hexane and ethanol extracts of Kersen leaves could serve as a natural source of HMG-CoA reductase inhibitor to prevent hypercholesterolemia.
Antifertility Effect of Sirih Leaf (Piper betle L.) Ethanol Extract on Male Wistar Rats Spermatogenesis: Efek Antifertilitas Ekstrak Etanol Daun Sirih (Piper betle L.) Pada Spermatogenesis Tikus Wistar Jantan Melviana Lubis; Widia Syahfitri
Jurnal Farmasi Galenika (Galenika Journal of Pharmacy) (e-Journal) Vol. 9 No. 1 (2023): (March 2023)
Publisher : Universitas Tadulako

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22487/j24428744.2023.v9.i1.16029

Abstract

Background: Currently, there are still very limited male contraceptive options. The ideal male contraceptive is still needed and ideally has the characteristics of having sufficient effectiveness, fully reversible and safe for long-term use. Several studies have been conducted to explore Piper betle as a contraceptive. Objectives: This study aims to examine the effect of 96% ethanol extract of sirih leaf (Piper betle L.) in reducing rat spermatogenesis quality, which includes the number, concentration, motility and morphology of male rat sperm. Material and Methods: This study used a posttest design with 28 white male rats. The rats were divided into four groups, each consisting of 7 rats. Group I was a control group. The test groups were group II, III, IV, and V, and each received an ethanolic extract of Piper betle leaves with various dosages of 200, 400, and 800 mg/kg body weight (BW), respectively, for 30 days. On day 31, all mice were sacrificed and analyzed for sperm count and concentration, sperm motility and sperm morphology. Results: The administration of 96% Piper betle leaves ethanol extract (PBEE) decreased the number and concentration of rats sperm, decreased progressive sperm motility and reduced the proportion of normal morphological rat sperm. PBEE at 800 mg/kg BW dose showed the greatest decreasing effect among all doses (p = 0.01). Conclusions: PBEE has contraceptive ability with a mechanism to reduce sperm count and concentration, sperm motility and sperm morphology.

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