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INDONESIA
Indonesian Journal of Pharmaceutical Science and Technology
Published by Universitas Padjadjaran
ISSN : 23561971     EISSN : 2406856X     DOI : -
Core Subject : Health, Science,
Computer Science & IT Medicine & Pharmacology
Jurnal Sains dan Teknologi Farmasi Indonesia (IJPST) adalah publikasi ilmiah pada seluruh aspek Sains dan Teknologi Farmasi. Jurnal ini diterbitkan 3 kali setahun untuk menyediakan forum bagi apoteker, dan profesional kesehatan lainnya untuk berbagi praktik terbaik, meningkatkan jaringan kerja dan pendekatan yang lebih kolaboratif dalam Sains dan Teknologi Farmasi.
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Articles 7 Documents
 1 
Search results for , issue "Vol 10, No 2 (2023)" : 7 Documents clear
Formulation And Effectiveness Test of Tansdermal Patch of Ethanol Extract of Ginger (Zingiber officinale Rosc. Var Amarum) As Antiemetic Arini Syarifah; Shintia L. Charisma; Nabila Nabila; Inas Kanina
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.36518

Abstract

Shogaol and gingerol, compounds in ginger, can act as antiemetic. Ginger extract was formulatedby patch transdermal to increase the effectiveness of therapy and to minimize the side effects. Inthis study, maceration with ethanol 96% was used as extraction method and phytochemical screeningwas carried out to the extract to identfy the exctracted compounds. The formulation of transdermalpatch used matrix method with ginger extract concentrations of 0,5 gr (F1), 1 gr (F2), and 1,5 gr (F3).Evaluation of patch was carried out by organoleptic test, patch weight, thickness, tensile strength,elongation at break, modulus young, moisturizer test, and folding endurance. Effectiveness test usedwistar mice by observed the pica response and a decreasing in kaolin consumption. The yield of theextract obtained was 6,46% and it contained essential oils, flavonoids, steroids, and polyphenols. Thebest patch characteristics of the concentration was F3 with a patch weight of 0,39 gr, thickness 0,23mm, tensile strength 1,32 N/mm2, elongation at break 129,52%, young's modulus 0,96 mPa, humidity1,32%, and folding endurance >200 times. F3 was also the most effective formulation with 6%response of pica and 93,11% of decreasing in kaolin consumption observed in day 9. In conclusion, F3can reduce nausea and vomiting.
Nano-extract of Acalypha hispida Increased Cu,Zn-SOD Antioxidant in Pancreas of Diabetic Rat Siti Sa'diah; Hamzah Alfarisi; Tutik Wresdiyati; Berry Juliandi
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.37981

Abstract

Nanotechnology has rapidly grown in various research fields to treat oxidative stress in diabetes,including medicine and phytomedicine. Previous research showed that Acalypha hispida has strongantioxidant activity in vitro and anti-hyperglycemic activity in vivo. However, the size reductionin the crude extract should be applied to decrease the doses and increase the efficacy. The researchobjective was to evaluate the nano-extract of A. hispida leaves on Cu,Zn-SOD antioxidant content inthe pancreas of diabetic rats. The analysis of Cu,Zn-SOD antioxidant content was carried out usingimmunohistochemistry. Cu,Zn-SOD content of pancreas in diabetic rats (DMC) was significantlylower than in normal rats (NLC). The antioxidant content of Cu,Zn-SOD in MET, CAH, NAH3, andNAH6 groups was significantly higher than in the DMC group of the pancreas of diabetic rats. Nanoextractof A. hispida showed a better effect in increasing Cu,Zn-SOD antioxidant content than crudeextract. The result concluded that nano-extract of A. hispida leaves increased Cu,Zn-SOD antioxidantcontent in the pancreas of diabetic rats.
Activity of Kersen (Muntingia calabura L.) and Kasturi (Mangifera casturi Kosterm.) Extract as Afrodisiac Karunita Ika Astuti; Aristha N. Putri; Revita Saputri; Ika P. Sari; Teuku N.S. Sulaiman
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.37862

Abstract

Kasturi (Mangifera casturi Kosterm.) is a typical plant of South Kalimantan, and Kersen (Muntingiacalabura L) contains flavonoids and steroids was empirically used for aphrodisiac. However, nopreclinical trials using that extracts. This research to test the aphrodisiac activity to optimal dose isobtained and the possibility of a synergistic or toxic effect if the two extracts are combined. Thestudy aimed to determine of secondary metabolites and the aphrodisiac effect of extracts. The testused a completely randomized design into 8 groups. Parameters measured were frequency approach(introduction), riding (climbing), and mating (coitus). The results showed the Kasturi have of flavonoid,Steroid, and Phenol. Kersen extract have contained saponins, phenol, flavonoid, steroid. Kersen extract200 mg/kg BW dose shows the highest rather than the others. The combination of kersen and kasturiextracts of 100 mg/kgBW and 200 mg/kg BW doses did not show better effect when compared to asingle dose. It can be concluded that the aphrodisiac activity in the combination of kersen and kasturiextracts tends not synergis.
Molecular Docking of Red Betel Leaf Bioactive Compounds (Piper crocatum) as Lipoxygenase Inhibitor Fernanda Chairunisa; Mega Safithri; Dimas Andrianto; Rini Kurniasih; Riyan Alifbi Putera Irsal
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.38934

Abstract

Degenerative diseases occurred due to several risk factors that are directly related to inflammationwhich affected several diseases such as coronary heart disease (CHD) and diabetes. One of theinflammatory causative agents is leukotrienes produced by the lipoxygenase enzyme (LOX) so thatit takes anti-inflammatory drugs made from herbal plants. Red betel leaf (Piper crocatum) potentiallyinhibited the lipoxygenase enzyme because it contains potential phytochemical compounds suchas alkaloids, flavonoids, eugenol, saponins, and tannins. This research aimed to test the inhibitionof active compounds from extract and fractions of red betel leaves that have the best inhibition forlipoxygenase enzymes causing malondialdehyde formed through molecular docking simulations. Thisresearch used lipoxygenase enzyme as receptor (PRB code: 4NRE), C8E as natural ligand and activecompound from extract and fractions of red betel leaves as a ligand. The highest inhibition regarded toNandrolone phenylpropionate and Sofalcone ligand with -10.4 kcal/mol and -9.1 kcal/mol of affinityenergy. Amino acid residues that played a role in ligand and receptor interaction were HIS373 andHIS378. The receptor structure with the best ligands was declared stable based on molecular dynamicssimulations.
Evaluation of Antioxidant Activity of Vernonia amygdalina Leaves and Its Flavonoid-Phenolic Content Muammar Fawwaz; Mamat Pratama; Musafira Musafira; Indira Wahab; Rina Iriani; Aminah Aminah; Andi Trihadi Kusuma; Muhammad Ikhlas Arsul
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.41617

Abstract

Bitter leaf, Vernonia amygdalina (VA), is used in various alternative medicine in several countries,including Indonesia. This study aims to evaluate the antioxidant activity of VA leaves by three differentin vitro methods. The antioxidant activity was evaluated by radical scavenging of 1,1-diphenyl-2-picryl-hydrazyl (DPPH), ferric reducing antioxidant power (FRAP), and cupric reducing antioxidantcapacity (CUPRAC). The antioxidant capacity by FRAP and CUPRAC methods were expressed asmg of quercetin equivalents (QE) per g extract (mgQE/g) and mg of ascorbic acid equivalents (AAE)per g extract (mgAAE/g), respectively. All methods were measured by UV-Visible spectrophotometryat maximum wavelength. The results exhibited that VA leaves ethanolic extract contains flavonoidphenolic.The VA leaves ethanolic extract has an antioxidant activity by scavenging the DPPH methodwith the half inhibition concentration (IC50) was 8,22 μg/mL. The antioxidant capacity of VA leavesethanolic extract by FRAP and CUPRAC methods was 21,03 mgQE/g and 160,64 mgAAE/g extract,respectively. The VA leaves ethanolic extract has a powerful antioxidant potency which might correlateto the flavonoid-phenolic content in the extract.
Formulation and Characterization Liposome of Oxcarbazepine Dina Permata Wijaya; Budi Untari; Herlina Herlina; Putri Siti Rahayu
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.33707

Abstract

Oxcarbazepine (OXC) was used as first line therapy or additional therapy for treatment of partialand secondary of seizures. The penetration of OXC into nasal mucosa can be enhanced by formingliposome. This research has the aim to prepare and characterize iposome laoding OXC. The OXCliposome formula was composed by using soya lechitin and cholesterol with various amount usingthin film hydration method. Characterization by determining the encapsulation efficiency (%EE), pH,viscosity, particle size, polydispersity of index, zeta potential, and in vitro release. The liposome ofOXC was also analyzed for its stability based on heating-coling cycle method. The proportion of bestformula was obtained at the amount of cholesterol of 42,11 mg yield %EE of 92,63%, pH of 8,47,viscosity of 1,10 cP, and decreased amount of OXC in stability test of 0,34%. The results of particlediameter were 579 nm, polydispersity index (PDI) of 0,34, and zeta potential of -99,38 mV. The in vitrorelease of the liposome of OXC was studied and compared with OXC. The result of in vitro releaseliposome OXC (F2) ahowed increase (62,26%) than (41,97%).
Formulation of Blush On Cream from Hibiscus Sabdariffa (L.) Flower Extract Tubagus Akmal; Yenni P. Tanjung; Yudhea Afrizki
Indonesian Journal of Pharmaceutical Science and Technology Vol 10, No 2 (2023)
Publisher : Indonesian Journal of Pharmaceutical Science and Technology

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24198/ijpst.v10i2.41875

Abstract

Natural dyes have become more popular as a result of the harmful and carcinogenic effects of syntheticdyes. Anthocyanins are natural dyes that are widely used to replace synthetic dyes and can also act asantioxidants that can be found in rosella (Hibiscus sabdarrifa L.). This study aimed to obtain blushon cream from rosella flower extract (RFE) with olive oil and to determine the effect of olive oilconcentration on the evaluation results. The blush on cream was made in 3 formula, F1 (13,5%),F2 (15,5%), and F3 (17,5%). The cream was evaluated for 28 days in room temperature (15–30⁰C)which included organoleptic, pH, homogeneity, spreadability, adhesion, cream type, and viscosity.The results of the evaluation of RFE blush on cream with olive oil showed that F1, F2, and F3 metthe requirements for evaluating the preparation for organoleptic tests, pH, homogeneity, spreadability,adhesion, cream type, and viscosity. Variations concentration of olive oil gave no significant effect(p>0,05) on the organoleptic, pH, homogeneity, spreadability, and cream type and had significant effect(p<0,05) on the adhesion and viscosity test. The findings demonstrate that RFE can be made in blushon cream formulations with olive oil as emollients.

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