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Contact Name
Harry Noviardi
Contact Email
harry.noviardi@gmail.com
Phone
+622518323819
Journal Mail Official
lppm@sttif.ac.id
Editorial Address
Jl. Kumbang No.23, Bogor, Jawa Barat, 16151
Location
Kota bogor,
Jawa barat
INDONESIA
Jurnal Farmamedika (Pharmamedica Journal)
ISSN : 25026011     EISSN : 26864487     DOI : https://doi.org/10.47219/ath
Core Subject : Health, Science,
Jurnal Farmamedika dikelola oleh Lembag Penelitian dan Pengabdian Masyarakat, Sekolah Tinggi Teknologi Industri dan Farmasi Bogor. Frekuensi penerbitan jurnal sebanyak 2 kali dalam satu tahun pada bulan Juni dan Desember. Kategori tulisan berupa hasil penelitian dari peneliti maupun akademisi dalam bidang Kimia Bahan Alam, Analisis Farmasi, Farmakologi dan Toksikologi, Kimia Medicinal, Biologi Molekular dan Bioteknologi, Farmakoterapi, Farmasi Klinis, Farmasetika dan Teknologi Farmasi, Biologi Farmasi, Manajemen Farmasi, Farmakoekonomi.
Articles 6 Documents
Search results for , issue "Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)" : 6 Documents clear
UJI ANTIOKSIDAN EKSTRAK PIGMEN KAROTENOID DAN SITRULIN PADA KULIT BUAH BLEWAH (Cucumis melo L.) SECARA IN VITRO (METODE DPPH) Antonius Padua Ratu; Nadia Fahmi Silabi; Padmono Citroreksoko
Jurnal Farmamedika (Pharmamedika Journal) Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)
Publisher : Sekolah Tinggi Teknologi Industri dan Farmasi Bogor

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (937.027 KB) | DOI: 10.47219/ath.v1i1.39

Abstract

Antioxidants stabilize free radicals with a complete the lack of electrons from free radicals and inhibiting the chain reaction of free radical formation. The purpose this research is to determine the amount of the antioxidant potential of the cantaloupe skin extracts and the effect of different test result of pigment carotene and citrulline in skin cantaloupe extracts to the extraction stage. Cantaloupe skin with drying and without drying treatment is gradually extracted using three solvents (petroleum ether-acetone-water). The highest antioxidant activity shown by extracts water without drying treatment (667.30 mg / L), which was significantly different (P <0.05) with acetone and petroleum ether (996.65 and 2368.26 mg / L). Treatment with drying only on petroleum ether extract (1607.28 mg / L), which provides activity compared with acetone and water (2871.54 and 2290.75 mg / L). However, cantaloupe skin extract antioxidant activity was lower compared with β-carotene and vitamin C. Treatment without drying also give the highest pigments carotenoid shown by extracts aceton (β-caroten 11,32 mg/L, lycopene 0,29 mg/100g) and level of citrulline in water extracts (29,91 mg/L). The difference of effect in simplisia treatment and solvent on the activity of antioxidants and pigments carotenoid levels were significantly different (P <0.05), whereas the levels of citrulline in the simplisia treatment was not significantly different for solvent acetone and significantly different (P <0.05) for solvent petroleum ether and water.
KARAKTERISASI NANOVESIKEL TRANSFERSOM SEBAGAI PEMBAWA “RUTIN” DALAM PENGEMBANGAN SEDIAAN TRANSDERMAL Devi Ratnasari; Effionora Anwar
Jurnal Farmamedika (Pharmamedika Journal) Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)
Publisher : Sekolah Tinggi Teknologi Industri dan Farmasi Bogor

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (832.094 KB) | DOI: 10.47219/ath.v1i1.40

Abstract

Transdermal become the alternative to deliver low solubility compound and low bioavalibility when given orally. Rutin is a flavonoid compound are found in watermelon and citrus. Rutin shows a low absorption when administered orally so the alternative is given in the transdermal route. A variety of approaches taken to increase the penetration of transdermal, one with nanovesikel carrier system. Transfersome is nanovesicle 200-300 nm sized composed of phospholipids, surfactants and water to increase penetration in trasndermal route. This study was to characterization transfersome containing rutin. The result show the size of transfersome < 150 nm, polydispersity index about 0.1 to 0.3, zeta potential less than -30 mV and entrapment efficiency > 80%.
POTENSI EKSTRAK AIR DAUN ALPUKAT(Persea americana M.) SEBAGAI DIURETIKPADA TIKUS PUTIH JANTAN Triyani Sumiati; Ferry Effendi; Muhamad Sofyan Iskandar
Jurnal Farmamedika (Pharmamedika Journal) Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)
Publisher : Sekolah Tinggi Teknologi Industri dan Farmasi Bogor

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (747.051 KB) | DOI: 10.47219/ath.v1i1.41

Abstract

Diuretics is a substance that can stimulate of urine output. The content of flavonoid compunds contained in water extracts of avocado leaves have a diuretic activity. Testing is done withgiving a water extract of avocado leaves per oral to 30 male rats strain (Sparague-Dawley) with weight 200 grams were divided into 6 groups. Frequency of urination with water extract of avocado leaves 5 % , 10 % , 15 % and 20 % respectively which is 2 , 5 , 9 and 20 times with observation for 3 hours. Furosemide tablets urination frequency was 25 times over 3 hours. The result showed that the water extract of avocado leaves 20% have diuretic activity is equivalent to Furosemide tablets at a dose of 7.2 mg / 200 mg BB in male rats.
EVALUASI KEJADIAN INTERAKSI OBAT PADA PASIEN RAWAT INAP GERIATRI PENDERITA GAGAL JANTUNG Siti Mariam
Jurnal Farmamedika (Pharmamedika Journal) Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)
Publisher : Sekolah Tinggi Teknologi Industri dan Farmasi Bogor

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (488.006 KB) | DOI: 10.47219/ath.v1i1.42

Abstract

An interaction occurs when the effects of a drug changed by the presence of other drugs, herbal medicine, food, drinks or other chemical agents in the environment. Drug interactions considered clinically important when the resulting increase or decrease the toxicity and effectiveness of the drugs that interact, especially when it comes to drugs with narrow safety margin (low terapheutic window). Genesis interactions may occur in patients taking two or more drugs. Interaction incident may occur in patients taking two or more drugs. The use of many drugs that often occur in geriatric patients, who suffer from degenerative diseases such as hypertension, diabetes mellitus, dyslipidemia, osteoarthritis and cardiovascular disease. Research conducted retrosfektif using medical records (MR) geriatric patients suffering from heart failure who are hospitalized in the Betha Medika Hospital in Sukabumi period March-April 2016. Retrieved 70 patients, 45% male and 54% female. Morbidities highest of 10 comorbidities with most patients is Hypertension Heart Disease (PJH). Drud interaction occur between: spironolactone, digoxin, amlodipine, bisoprolol with other drugs medicine drug classes heart failure and comorbid disease drug interactions with the number of events is different.
PERBANDINGAN INHIBISI α-MANGOSTIN, β-MANGOSTIN, DAN γ-MANGOSTIN TERHADAP PROTEIN AKT-KINASE PADA SEL KANKER PANKREAS SECARA MOLECULAR DOCKING Harry Noviardi; Armi Wulanawati; Muhamad Sholehuddin Malik Ibrohim
Jurnal Farmamedika (Pharmamedika Journal) Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)
Publisher : Sekolah Tinggi Teknologi Industri dan Farmasi Bogor

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (983.16 KB) | DOI: 10.47219/ath.v1i1.43

Abstract

The mangosteen pericarp contains a class of compounds called xanthones, including α-mangostin, β-mangostin, and, γ-mangostin. Mangosteen products have become popular natural medicine. cancer is a malignant tumor types are particularly deadly caused by proliferative effects to inhibit apoptosis cell. Akt protein is considered to be the key downstream effector of reducing apoptosis. This study aims to determine the ratio of the potential of α-mangostin, β-mangostin, γ-mangostin as inhibitors of Akt protein of pancreatic cancer cells by the Gibbs free energy (ΔG), inhibition constants, hydrogen interactions. The computationally study using molecular docking method.Based on the analysis docking, γ-mangostin provides the potential for better inhibition than gemcitabine.
POTENSI ENZIM TRANSGLUTAMINASE SEBAGAI GEL PENYEMBUH LUKA STADIUM II PADA AYAM RAS JANTAN Sitaresmi Yuningtyas; Winugroho; Abdul Ghoni
Jurnal Farmamedika (Pharmamedika Journal) Vol 1 No 1 (2016): Jurnal Farmamedika (Pharmamedica Journal)
Publisher : Sekolah Tinggi Teknologi Industri dan Farmasi Bogor

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (702.933 KB) | DOI: 10.47219/ath.v1i1.44

Abstract

The transglutaminase (EC 2.3.2.13) is an enzyme that catalyses an acyl transfer reaction of the γ-carboxiamide groups glutamine residues in proteins, peptides and various primary amines. Enzyme transglutaminase helps to stabilized the fibrin monomer during the process of blood clotting. This research was to determine the activities of the wound healing process stage II in male broilers given the transglutaminase enzyme sample gels. In this researchgel formulationmadeenzymetransglutaminase1%, 3%, 5% and7%. Transglutaminaseenzymegelpreparationorganoleptictestandhomogeneity test. Furthermore,thegel formulationapplied to themalebroilersownwoundsstage II. Transglutaminaseenzymegel formulationhad ahomogeneoustexture, white, odorlesstypicalenzymetransglutaminase, andhad apH rangefrom 6.2 to 6.7. The percentagereduction inwoundlength ofstage IIinmalebroilersbyenzymetransglutaminaseperfomedgel1%, 3%, 5% , 7% and Bioplacenton® gel (positive control) were 80.54%, 99.00%, 99.67%, 87.25%, and 99.33% respectively. Based on analysis statisticsofANOVA, percentage reduction inwoundlength ofstage IIby treatment withtransglutaminasepreparationgel5% higher and significantly differentcompared totreatmentwithBioplacenton®(positive control). Hence, transglutaminaseenzymepreparations5% gelcanact as awound healerstage IIinmalebroilers.

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