cover
Contact Name
Giftania Wardani Sudjarwo
Contact Email
giftania.wardani@hangtuah.ac.id
Phone
+6285608362150
Journal Mail Official
jpst.journal@hangtuah.ac.id
Editorial Address
Jl. Arief Rahman Hakim No.150, Keputih, Kec. Sukolilo, Kota SBY, Jawa Timur 60111 Gedung F7 Prodi Farmasi Fakultas Kedokteran
Location
Kota surabaya,
Jawa timur
INDONESIA
Journal of Pharmacy Science and Technology
Published by Universitas Hang Tuah
ISSN : -     EISSN : 26140993     DOI : https://doi.org/10.30649/pst
Core Subject : Health,
The Journal of Pharmaceutical Science and Technology is a journal for scientific publications on all pharmaceutical aspects including pharmaceutical science (pharmaceutical technology, pharmaceutical chemistry, pharmaceutical biology, pharmacognosy, microbiology and pharmaceutical biotechnology), community pharmacy, clinical pharmacy until explore the potential of marine biota. This journal is published twice a year to provide a means for pharmacists and other health professionals to share research results to improve the science of pharmaceuticals. The Journal of Pharmaceutical Science and Technology is intended to present the best quality research articles in pharmaceutical science, community pharmacy and clinical pharmacy to become scientific guides in fields related to science and pharmaceutical technology. This journal is a peer-reviewed journal and publishes original research articles on all aspects of science and pharmaceutical technology. This journal accepts original articles as well as for other categories such as review articles and case reports for all aspects of pharmaceutical science, pharmacy clinics and community pharmacy.
Articles 48 Documents
GAMBARAN POLA TERAPI OBAT PASIEN GAGAL JANTUNG DI RSUP DR. M. DJAMIL PADANG PERIODE OKTOBER-DESEMBER 2023: Description of Drug Therapy Patterns for Heart Failure Patients at RSUP Dr. M. Djamil Padang October-December 2023 period elsa, elsa marsellinda; Aulia, Dea Suci
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 4 No. 1: Desember 2023
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v4i2.89

Abstract

ABSTRACT Heart failure is a complex clinical syndrome due to functional or structural ventricular dysfunction, resulting in symptoms of left ventricular dysfunction. The goal of treating heart failure is to reduce morbidity and mortality and prevent the worsening of heart disease. The purpose of this study was to describe the pattern of heart failure drug therapy at Dr. M.Jamil Padang Hospital. Data were collected retrospectively from the medical records of heart failure patients admitted to the cardiac ward. period October to December 2023 analyzed descriptively. Results: In this study, furosemide (31.29%) was followed by ramipril (21.09%) and candesartan (15.65%). The most common drug combination therapy was a combination of three drugs (32.14%), followed by a combination of two drugs (30.36%) and a combination of four drugs (22.32%). Conclusion: based on the results of the study, it can be concluded that the most widely used therapy is furosemide, ACEI, and ARB. The most common drug combination used for heart failure patients is ARB/ACEI and diuretics.
SKRINING FITOKIMIA DAN UJI POTENSI ANTIKANKER EKSTRAK METANOL KULIT BATANG (Rhizophora mucronata (Lamk.)) MENGGUNAKAN METODE BSLT (Brine Shrimp Lethality Test) Asniyah, Asniyah; Mahmiah, Mahmiah; Sudjarwo, Giftania Wardani
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 4 No. 1: Desember 2023
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v4i2.101

Abstract

Cancer is one of the leading causes of death in the world. The main therapies for cancer include surgery, chemotherapy, radiotherapy. However, the use of chemotherapy drugs can cause side effects such as hair loss, bone marrow suppression, drug resistance. Based on these side effects, this study conducted research on natural ingredients as an alternative to cancer treatment. Rhizophora mucronata can be used as an anticancer, where people in coastal areas or around mangrove forests use mangroves as medicinal plants, and are believed to have minimal side effects so that they can be developed as traditional medicines. In this study, analysis of phytochemical screening and anticancer potential tests of methanol extract of Rhizophora mucronata stem bark was carried out from Pamurbaya, Surabaya, East Java. In this study, the BSLT (Brine Shrimp Lethality Test) method was used to test the anticancer potential with the LC50 (Letal Concentration) value as a parameter. The results of phytochemical screening of the methanol extract of Rhizophora mucronata stem bark contain tannins, saponins, alkaloids, steroids, flavonoids, anthraquinones and polyphenols and have anticancer potential with an LC50 value of 120.8656 ppm which falls into the toxic category.
UJI AKTIVITAS ANTIOKSIDAN EKSTRAK AKAR BAKAU HITAM (Rhizophora mucronata (Lamk.)) DENGAN METODE DPPH (2,2-diphenyl-1-picrylhydrazyl) Sulistiorini, Indah; Mahmiah, Mahmiah; Sudjarwo, Giftania Wardan
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 4 No. 1: Desember 2023
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v4i2.102

Abstract

Indonesia is a country that has a variety of marine ecosystems that have a lot of potential, one of which is mangroves. Rhizophora mucronata is a species in the mangrove ecosystem in Indonesia. Rhizophora mucronata or black mangroves are plants that contain various kinds of compounds. Antioxidants play an important role in the prevention of degenerative diseases. This research is motivated by the presence of carcinogenic dangers caused by consuming synthetic antioxidants at high doses synthetic antioxidants can function as prooxidants which can increase oxidative stress and damage body cells, so it wants to explore the natural antioxidant potential of Rhizophora mucronata. Rhizophora mucronata root was chosen in this study because no one has examined the potential of this plant that grows in the Pamurbaya area, Surabaya - East Java as an antioxidant. This study aims to determine the content of secondary metabolites and antioxidant activity of the root extract of Rhizophora mucronata. In this study, the antioxidant activity test used the DPPH (2,2-diphenyl-1-picrylhydrazyl) method. The results showed that the antioxidant activity of the methanol extract of Rhizophora mucronata root had very weak antioxidant activity with an IC50 value of 2604.56 ppm. The antioxidant potential of the methanol extract of Rhizophora mucronata root has an IC value of 50 with a very weak antioxidant intensity
Beberapa sediaan tablet yang telah dimodifikasi dengan metode yang dapat meningkatkan kelarutan Sari, Aulia Permata; Rahmah, Azka Nurkhairiyah; Nurholisa, Neng Dera Siti; Andriani, Febby; Pahlevi, Muhamad Reza; Sutoro, Meylani
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 5 No. 1: Juli 2024
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v5i1.96

Abstract

Nowadays there are many pharmaceutical preparations, one of which is tablet preparation. Tablets are solid preparations containing medicinal ingredients with or without fillers. Modified preparation means that the pharmaceutical formulation has been changed from the standard or original formulation. Modification can be done for several purposes, such as increasing solubility, increasing bioavailability, regulating drug release, increasing stability, or improving other formulation properties. The purpose of this paper is to provide a perspective on the methods used to improve drug solubility, dissolution rate, and stability of active substances. The writing of this review article uses the research journal literature study method. The primary sources used have been published online through Google scholar by entering the keywords modified active substance, solid dispersion, tablet making methods that increase solubility, tablet dissolution. In this review, it was found that there are techniques that can be done such as co-amorphous, co-crystalline, nanoemulsifying, micronization, precipitation, melting, addition of crushing agents and factorial methods of adding binders to be the choice of scientists in developing pharmaceutical preparations with active ingredients that have poor BCS values.
P PENGARUH TERAPI ANTIKOAGULAN TERHADAP FAKTOR PEMBEKUAN DARAH PADA PASIEN DENGAN FIBRILASI ATRIAL Nurhayati, Maulida Aisshella; Lukiyono, Yauwan Tobing
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 5 No. 1: Juli 2024
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v5i1.98

Abstract

Atrial fibrillation (AF) is the most common type of cardiac arrhythmia and can increase the risk of ischemic stroke due to the formation of blood clots. Anticoagulant therapy plays an important role in preventing thromboembolic complications in patients with AF. This study aims to systematically review the effects of anticoagulant therapy on blood coagulation factors in AF patients. The literature review was conducted by searching and analyzing scientific publications available in electronic databases such as PubMed, Scopus, and the Cochrane Library. The keywords used included “atrial fibrillation,” “anticoagulant,” “blood coagulation factors,” and other related terms. The selected studies comprised observational research and clinical trials that evaluated the effects of anticoagulant therapy on blood coagulation factors in AF patients. After screening, 25 studies were included for analysis. Most studies indicated that warfarin therapy significantly inhibited the extrinsic blood coagulation pathway, as indicated by an increase in the international normalized ratio (INR) and a decrease in prothrombin activity. In contrast, direct oral anticoagulants (DOACs) such as apixaban, rivaroxaban, and dabigatran did not show significant effects on the measured coagulation factors. Therefore, regular monitoring of coagulation parameters, particularly INR, in patients receiving warfarin therapy is essential to ensure therapeutic effectiveness and safety.
itu OPTIMASI SEDIAAN NANOEMULGEL KOMBINASI TITANIUM DIOXIDE, ZINK OXIDE DAN NIACINAMIDE SEBAGAI SUN PROTECTION FACTOR PADA FORMULASI SUNSCREEN: Hasil Data Titanium Dioksida, Zink Oksida dan Niacinamide Rahmadani, Widya
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 5 No. 1: Juli 2024
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v5i1.305

Abstract

Excessive exposure to ultraviolet (UV) radiation can lead to various skin disorders, including premature aging, hyperpigmentation, and skin cancer, making the use of sunscreen an essential step in skin protection. Titanium dioxide and zinc oxide are physical sunscreen agents that work by reflecting and absorbing UV rays, while niacinamide serves as an antioxidant, anti-inflammatory agent, and skin barrier enhancer. The combination of these three ingredients in a nanoemulgel formulation has the potential to enhance UV protection efficacy while improving formulation characteristics. The optimization of nanoemulgel focuses on improving physical stability, SPF efficacy, and user comfort, which are influenced by particle size, surfactant selection, and homogenization methods. Nano-sized particles (<200 nm) of titanium dioxide and zinc oxide allow for more uniform skin coverage and reduce the white cast effect, while the nanoemulgel delivery system increases the bioavailability of active ingredients and prolongs UV protection duration. Studies have shown that combining titanium dioxide, zinc oxide, and niacinamide in a nanoemulgel significantly increases SPF compared to conventional formulations while providing additional benefits such as anti-inflammatory effects and improved formulation stability. The appropriate selection of oil and surfactant components also determines the viscosity, physical stability, and spreadability of the formulation. Therefore, nanoemulgel-based formulations represent an innovative approach to developing sunscreens that are more effective, stable, and user-friendly. Further studies through in vivo and clinical testing are necessary to ensure long-term safety and efficacy.
Identifikasi Identifikasi Fitokimia Daun Gandarusa (Justicia Gendarussa L.) Asal Kabupaten Pangkep: Analisis Kandungan Senyawa Aktif Menggunakan Metode Kromatografi dan Uji Fitokimia Ildayani, Ildayani; Ramadhani, Livia Ernesta; Sa’adah, Nur Lailatus; Apriliani, Ayu; Natasya, Natasya; Ikram, Nurul; Mutiara, Sitti Ayzah; Sari, Andi Aliya Meilana; Sahruni, Sahruni; Usman, Fityatun; Haryanto, Haryanto
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 5 No. 1: Juli 2024
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v5i1.395

Abstract

Gandarusa leaves (Justicia gendarussa L.) are recognized as medicinal plants rich in various active phytochemicals. Extraction was carried out using the maceration method with 96% ethanol, followed by evaporation with a rotary evaporator to obtain a concentrated extract. Fractionation was performed using liquid-liquid partitioning with n-hexane and ethyl acetate to separate compounds based on polarity. The results revealed the ethyl acetate fraction had the highest yield at 20.8%, followed by the n-hexane fraction at 20%. Phytochemical identification using thin-layer chromatography confirmed the presence of alkaloids, flavonoids, and steroids. UV-Vis spectrophotometry analysis showed the total flavonoid content reached 0.741 mg/L based on the quercetin standard curve. These findings highlight the potential of gandarusa leaves as a promising source of bioactive compounds for pharmaceutical development.
Stabilitas Membran Sel Eritrosit Ekstrak, Fraksi Kloroform, Etil Asetat dan Metanol Herba Patah Tulang (Euphorbia Tirucalli L.) Fika, Irma; Wirasti, Wirasti; Pambudi, Dwi Bagus; Waznah, Urmatul
JOURNAL OF PHARMACY SCIENCE AND TECHNOLOGY Volume 5 No. 1: Juli 2024
Publisher : Prodi Farmasi Fakultas Kedokteran Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/pst.v5i1.402

Abstract

Euphorbia tirucalli L. (patah tulang) contains secondary metabolites with potential anti-inflammatory activity. This study aimed to identify its bioactive compounds and evaluate erythrocyte membrane stabilization of the extract and fractions. Extraction was performed by maceration with 96% ethanol, followed by fractionation using chloroform, ethyl acetate, and methanol. Total flavonoid and phenolic contents were measured by UV-Vis spectrophotometry, while erythrocyte membrane stabilization was tested in vitro. Phytochemical screening revealed flavonoids, phenols, saponins, steroids, triterpenoids, and tannins. The phenolic content was 432.1 ± 99.4 mg/g in the extract, 1,057 ± 88.02 mg/g in the chloroform fraction, 254.4 ± 48.84 mg/g in the ethyl acetate fraction, and 643.2 ± 267.3 mg/g in the methanol fraction. The highest flavonoid content was found in the chloroform fraction (4.26 ± 0.12 mg/g), followed by the extract (3.63 ± 0.35 mg/g), ethyl acetate (3.56 ± 0.36 mg/g), and methanol (2.6 ± 0.03 mg/g). Membrane stabilization assays showed the extract provided the strongest protection (95.04%), followed by chloroform (89.51%), ethyl acetate (87.71%), and methanol (87.52%), approaching the positive control diclofenac sodium (90.59%). Kruskal-Wallis and Tukey tests indicated the ethanol extract at 100 μg/mL (p=0.997 >0.001) and chloroform fraction at 500 μg/mL (p=0.023 >0.001) were not significantly different from the control, while ethyl acetate and methanol fractions differed significantly (p<0.001). These results demonstrate that the ethanol extract and chloroform fraction possess the highest anti-inflammatory potential, supported by high phenolic and flavonoid levels and consistent statistical analysis.