Sciences of Pharmacy
Open Access Journal

Sciences of Pharmacy

p-ISSN: 2830-7046
e-ISSN: 2830-7259
DOI: 10.58920/sciphar
sciphar@etflin.com (Managing Editor)
Preclinical and clinical drug developmentDrug deliveryPharmaceutical formulationPharmacodynamicsPharmacokineticsDrug metabolismPharmacogeneticsGene-based therapyCell-based therapyProtein-based therapyDrug classesDrug nomenclatureDrug-drug interactionAdverse drug reactionDrug toxicityPharmacovigilancePharmacoepidemiologyPharmacoeconomicsClinical pharmacy

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Volume 3 Issue 2

Showing 5 Articles

RESEARCH ARTICLE

  • research article

    Larvicidal Activity of Red Betel Leaves (Piper ornatum) Ethanolic Extract Against Mosquito Larvae

    Amelia Soyata, Khoirunnisa Khoirunnisa, Sabda Wahab

    Larvae are the initial carriers of dengue hemorrhagic fever (DHF) and culex, making them significant in disease transmission. Excessive chemical larvicides pose serious risks to human health, thus driving the development of biological alternatives like red betel leaf extract. This study aimed to assess the efficacy of red betel leaf extract in larval control. Using 300 larvae, concentrations of 5%, 6%, and 7% were tested with three replicates over 24 h. The bioassay involved placing the larvae into a plastic container filled with the extract. It was found that ethanol extract from Piper ornatum leaves contained alkaloids, tannins, saponins, flavonoids, and terpenoids. After 24 h, results revealed 83% mortality at 5%, 98% at 6%, and 100% at 7% of extract concentration. Consequently, the 7% concentration showed the fastest efficacy in killing mosquito larvae (100% in 50 min). The LC50 value, representing the concentration at which 50% of larvae are killed, was determined to be 0.04%. Additionally, the LT50 value, indicating the time required to kill 50% of larvae (based on the LC50 value), was found to be 3.34 hours. In conclusion, red betel leaf extract demonstrated promising larvicidal activity against mosquito larvae. Future research is anticipated to prove its safety via in vitro and in vivo test.

    Sciences of Pharmacy

    13 Jun 2024
    5 pages
  • research article

    Effect of Combination of Porang and Moringa Flour on Blood Glucose Levels and Body Weight in Rats

    Dian Ratih Laksmitawati, Umi Marwati, Fauzia Noprima Okta, Citra Prastuti Partana

    Porang tuber is rich in fiber and low in calories of carbohydrates. Moringa oleifera leaf has a high protein and a low content of lipids. Obesity and diabetes mellitus are the risk factors of cardiovascular disease, also known as cardiovascular disease risk factors. Combining of porang and moringa as feed can increase nutrition without causing weight gain. This study aims to determine these two materials as antidiabetic and antiobesity agents. The samples are porang tuber, a combination of porang tuber and M. oleifera leaves, a combination of M. oleifera leaves and wheat flour, wheat flour, and standard feed of mice. The parameters tested in this study are analysis of macronutrients of feed, loss of weight of mice, average consuming feed in 28 days, and reduction of blood glucose with a glucometer. The results obtained are a combination of porang tuber and moringa had a low contain carbohydrates and a high contain lipids and protein, can reduction in body weight of 21%, the lowest consumption of feed, and the lowest fasting and postprandial blood glucose levels compared to the other feeds. A combination of porang and moringa can be an antidiabetic and antiobesity agent.

    Sciences of Pharmacy

    2 Apr 2024
    7 pages
  • Bioactive Compounds of Rosa canina L. and Their Effect on Tumor Necrosis Factor-α and Interleukin-1β Activity in Diabetes-Induced Rats
    research article

    Bioactive Compounds of Rosa canina L. and Their Effect on Tumor Necrosis Factor-α and Interleukin-1β Activity in Diabetes-Induced Rats

    İlayda Sezin YALÇINKAYA, Onur AKTAN, Leyla AÇIK, Gülnihal KULAKSIZ ERKMEN, NILUFER VURAL, Sibel KAYMAK, Yiğit Can ATEŞ

    The ethnopharmacological significance of Rosa canina, or dog rose, transcends diverse cultures, with traditional applications in treating various diseases. This study investigates the potential pharmacological application of R. canina for diabetes treatment, aiming to assess its antidiabetic properties through in vitro, in vivo, and in silico analyses targeting pro-cytokines. Biochemical profiling utilizing HPLC, and phenolic content analyses were conducted to reveal the antioxidant properties of R. canina. In diabetic rats, root extracts influenced the expression of TNF-α and IL-1β, with an exploration of DNA-binding and protective activities. DPPH scavenging and iron chelating activities were measured, identifying significant IC50 values. The chromatographic analysis identified various compounds, with Kaempferol 3-O-glucoside and Rutin exhibiting high inhibitory activity against TNF-alpha. In silico analyses highlighted inhibitory activities by molecular docking against TNF-α and IL-1β (PDB IDs 2AZ5 and 9ILB, respectively) and their drug potential based on ADMET properties. The obtained results have demonstrated a significant decrease in blood glucose levels in mice through the reduction of TNF-α and IL-1β mediated diabetic processes, facilitated by the R. canina extract. In conclusion, this study exploring the effects of R. canina extracts on diabetic rats have provided valuable insights into its potential therapeutic benefits. The observed reductions in blood glucose levels, improvements in lipid profiles, and modulation of antioxidant activity highlight its promising role in managing diabetes-related complications. Further research is warranted to elucidate the underlying mechanisms and optimize the dosage regimens for harnessing the full therapeutic potential of R. canina extracts in diabetes management.

    Sciences of Pharmacy

    2 May 2024
    15 pages
  • research article

    Nanosuspension Formula of Curcuma xanthorriza Rhizome Dry Extract: Impact of Tween 80-PEG 400 Ratio

    Moch Futuchul Arifin, Elza Shafira, Yuslia Noviani, Yesi Desmiaty, Fauzia Noprima Okta

    Our previous research investigated nanosuspension using the ionic gelation method with a 2:1 ratio of chitosan to sodium tripolyphosphate (TPP) and 0.44% Curcuma xanthorriza rhizome extract. The results indicated an unstable nanosuspension with a particle size of 399.3 nm, a polydispersity index of 0.60, and an entrapment efficiency of 73.37%. This study aims to develop a nanosuspension using Tween 80-PEG 400 to improve the characteristics and dissolution at pH 6.8. Curcuma rhizome was macerated with 96% ethanol and dried using a spray dryer. The nanosuspension formulation was designed using a 22 factorial design with Tween 80 (0.1%-0.4%) and PEG 400 (0.1%-0.4%) as factors, and the formulation was analyzed using Minitab 18. The dissolution of the optimum formulation was tested. The best formulation, comprising 0.1% Tween 80 and 0.4% PEG 400, provided a spherical shape, a particle size of 111.26 nm, a polydispersity index of 0.27, a zeta potential of 30.77 mV, an entrapment efficiency of 84.30%, and a desirability value of 0.9058. The release of curcumin at pH 6.8 after 180 minutes was 37.85% ± 0.1375 with a DE180 of 83.60% ± 0.1457. The 22 factorial design proved effective for enhancing formulation attributes. Based on the result obtained, it can be concluded that the best formulation contains 0.1% Tween 80 and 0.4% PEG 400, with zero-order release kinetics and a diffusion mechanism.

    Sciences of Pharmacy

    10 Jun 2024
    8 pages
  • research article

    Characterization, In Silico Antimalarial, Antiinflammatory, Antioxidant, and ADMET Assessment of Neonauclea excelsa Merr.

    Neksumi Musa, Mubarak Muhammad Dahiru, Enoch Buba Badgal

    In our study, we identified the phytoconstituents and carried out antimalarial, anti-inflammatory, antioxidant, and ADMET assessments of Neonauclea excelsa. The phytochemicals were detected and quantified followed by identification via GC-MS. The antimalaria, anti-inflammatory, and antioxidant assessments were done by molecular docking (MD) and molecular dynamics simulation (MDS) while ADMET by ADMET predictions. Saponins (27.33% ±1.20) and terpenes (8.33% ±0.73) were detected while alkaloids, steroids, glycosides, and flavonoids were absent. Exactly 29 compounds were identified with squalene being the most abundant (32.41%). Compound II exhibited the lowest BA (-6.4 kcal/mol) and Ki (20.12 µM), interacting with dihydrofolate reductase-thymidylate synthase. IV exhibited the lowest respective BA and Ki interacting with Plasmodium falciparum hexose transporter protein 1 (-6.2 kcal/mol and 28.20 µM), cyclo-oxygenase-2 (-7.2 kcal/mol and 5.21 µM), and myeloperoxidase (-7.4 kcal/mol and 3.71 µM). Compound VII had the lowest respective BA and Ki interacting with inducible nitric oxide synthase (-8.0 kcal/mol and 1.35 µM), xanthine oxidase (-7.2 kcal/mol and 5.21 µM), and cytochrome p450 21A2 (-7.0 kcal/mol and 7.30 µM). The MDS showed various cluster mobilities and residue fluctuations up to 5.26, 2.96, 5.10, 3.51, 5.02, 4.65, and 6.18 Å for dihydrofolate reductase-thymidylate synthase, P. falciparum hexose transporter protein 1, inducible nitric oxide synthase (INOS), cyclo-oxygenase-2 (COX2), xanthine oxidase (XO), cytochrome p450 21A2, and myeloperoxidase, respectively. Additionally, these compounds demonstrated good pharmacological properties with minimal toxicity. Conclusively, the identified compounds might be significant contributors to the antimalarial, anti-inflammatory, and antioxidant activity of N. excelsa and are good sources of novel antimalarial, anti-inflammatory, and antioxidant drugs.

    Sciences of Pharmacy

    8 May 2024
    16 pages

Journal Key Facts

Publishing Fee (APC)

IDR 1,100,000

Open Access License

CC BY 4.0

Language

English

Abstracting & Indexing
SintaCAS

Overview

Sciences of Pharmacy (SciPhar) is an international, peer-reviewed open-access journal of pharmacy published by ETFLIN. We offer a platform and place for researchers and intellectuals, especially the youth, to share their insights and works. SciPhar accepts original article, reviews, mini-review, book-review, technical note, case report, case series, clinical trial, opinion/perspective, conference proceeding, and pictorial essay. Author may submit or suggest another type of scientific manuscript. Sciphar publishes 4 issues a year. Sciences of Pharmacy is affiliated with Faculty of Pharmacy, Universitas Islam Sultan Agung.

Current Issue

Latest Articles

Recently published research articles, review papers, and technical notes from the current volume of the journal.

  • research article

    Antiprostatic Activities of Hippocratea africana Root Extract and Fractions Against Testosterone-Induced Benign Prostatic Hyperplasia in Rats

    Jude Efiom Okokon, Daniel Ekeleme, Grace Emmanuel Essien

    Hippocratea africana (Willd. ) Loes. ex Engl. (Celastraceae) syn. Loeseneriella africana (Willd. ) N. Hallé root which is used as medicine traditionally to treat various diseases by the Ibibios was investigated for antiprostatic effect against testosterone-induced benign prostatic hyperplasia (BPH). The dried root powder was cold extracted in 50% ethanol and the extract dissolved in distilled water and partitioned with dichloromethane (DCM) to obtain DCM and aqueous fractions of H. africana root. BPH was induced in groups of male rats (n=5) using testosterone propionate (3 mg/kg). Based on previously determined median lethal dose, the root extract and fractions of H. africana (200-600 mg/kg) were investigated for effects on prostate weight and histology, prostate sensitive antigen (PSA), testosterone levels, lipid profile, oxidative stress markers, semen analysis and testis histology of rats with testosterone propionate induced BPH. Finasteride (5 mg/kg) was used as standard drug. The root extract/fractions were found to cause significant (p < 0.05 - 0.01) decreases in PSA and testosterone levels, reductions in prostate and testis weights, improvement of semen volume and health, elevations of antioxidant enzymes (SOD, CAT, GPX) and molecule (GSH) and also reduced MDA level. These results suggest that the root extract and fractions of H. africana possess antiprostatic potentials against testosterone-induced BPH in rats which may be due to the antioxidant activities of its phytochemical constituents.

    Sciences of Pharmacy

    8 Jun 2026
    14 pages
  • review

    Genetic Polymorphism of N-acetyltransferase 2 (NAT2) among Patients with Tuberculosis: A Scoping Review of the Indonesian Studies

    Oki Nugraha Putra, Sylvia Rizki Ramadhani, Yulistiani Yulistiani, Julaeha Julaeha, Affan Yuniar Nur Hidayatullah

    The distribution of N-acetyltransferase-2 (NAT2) genetic polymorphisms varies across ethnic groups among Indonesian TB patients. This review aimed to provide a comprehensive understanding of the prevalence of NAT2 genetic polymorphisms and their association with DILI and isoniazid pharmacokinetics in Indonesian TB patients. A scoping review was conducted by searching Google Scholar, Scopus, and PubMed in accordance with PRISMA guidelines for scoping review (PRISMA-ScR). We retrieved 668 studies from three databases and we enrolled 12 studies for final analysis. Eleven studies reported on adult TB patients and one study on pediatric TB patients. Overall, the available evidence suggests that the slow acetylator phenotype is relatively common among TB patients in Indonesia, although its distribution varies across regions and ethnic groups. The NAT2*6 polymorphism was frequently observed among TB patients with a slow acetylator phenotype. TB patients with slow acetylation exhibited higher serum concentrations of isoniazid, which were significantly associated with an increased risk of DILI. No studies reported an association between NAT2 genetic polymorphisms or acetylation status and treatment outcomes among TB patients. This review confirms substantial variation in NAT2 genetic polymorphisms across studies in Indonesia. TB patients with a slow acetylator phenotype appear to have a greater risk of developing DILI compared with those with intermediate or fast acetylator phenotypes.  Information on acetylator status may identify patients at higher risk of hepatotoxicity, particularly those with the slow acetylator phenotype. Therefore, integrating NAT2 pharmacogenetics into clinical practice may predict hepatotoxicity and optimize tuberculosis therapy.

    Sciences of Pharmacy

    21 Apr 2026
    9 pages
  • research article

    Green-Synthesized Silver Nanoparticles Using Erythrina subumbrans Leaf Extract: Optimization and Antibacterial Activity

    Indri Maharini, Karen Putri Utami, Lilis Rachmawati, Fitrianingsih Fitrianingsih, Puspa Dwi Pratiwi

    The high prevalence of acne and increasing antibiotic resistance necessitate the development of sustainable antimicrobial agents. This study investigated the green synthesis of silver nanoparticles (AgNPs) using Erythrina subumbrans (Hassk.) Merr. leaf extract as a natural bioreductant and stabilizer. The primary objective was to optimize the synthesis process and evaluate the antibacterial efficacy of the resulting nanoparticles specifically against Propionibacterium acnes. Physicochemical and structural characterization were performed using spectroscopic and microscopic techniques to confirm the formation and stability of the nanoparticles. The results successfully demonstrated the synthesis of crystalline, nanoscale AgNPs with plant-derived functional groups facilitating their stabilization. Analytical data indicated a relatively uniform particle size distribution, spherical morphology, and favorable surface characteristics, suggesting high suitability for biomedical integration. Significantly, the synthesized AgNPs exhibited potent antibacterial activity against P. acnes. The underlying mechanism of action is attributed to the disruption of bacterial cell membranes, induction of intracellular reactive oxygen species, and subsequent interference with vital cellular functions. Utilizing E. subumbrans extract offers an eco-friendly, cost-effective, and sustainable alternative to conventional chemical synthesis, reducing the reliance on toxic reagents. These findings highlight the significant potential of plant-mediated AgNPs as innovative antimicrobial agents for dermatological applications. This research provides a robust foundation for the advancement of nanotechnology-based topical treatments. Consequently, further investigation into pharmaceutical formulation development, comprehensive safety assessments, and clinical efficacy trials is highly recommended to establish E. subumbrans-mediated silver nanoparticles as viable therapeutic solutions for managing acne and other skin-related infections in the future.

    Sciences of Pharmacy

    21 Apr 2026
    11 pages
  • research article

    Physico-Chemical Characterisation and Determination of Luteolin Content of Red Pidada (Sonneratia Caseolaris L.) Leaf Extract

    Eka Siswanto Syamsul, Dwi Lestari, Dachriyanus Dachriyanus, Supomo Supomo

    Red Pidada (Sonneratia caseolaris L.) leaves are widely used in traditional medicine, particularly for skin care and treatment of minor ailments. This study aimed to characterise the powdered leaf material and determine luteolin content of the ethanolic leaf extract. Dried leaf powder was extracted by maceration using ethanol. The powdered material was characterised through macroscopic and microscopic evaluations, as well as determining physicochemical parameters including water-soluble extractive value, ethanol-soluble extractive value, moisture content, total ash, and acid-insoluble ash. Furthermore, metabolite profiling of the extract was conducted using high-resolution liquid chromatography–mass spectrometry (HR-LCMS) to identify constituents. Luteolin content was quantified using thin-layer chromatography (TLC) densitometry on silica gel 60 F254 plates with a mobile phase of n-hexane:ethyl acetate (2:3). Macroscopically, the leaves were oval to elongated, with rounded to blunt apices, entire margins, pinnate venation, and dark-green colour. Microscopic examination revealed upper and lower epidermal tissues, stomata, and vascular bundles. The powdered leaves exhibited a bitter taste. The water-soluble and ethanol-soluble extractive values were 11% and 16%, respectively, while moisture content, total ash, and acid-insoluble ash were 8.8%, 8.12%, and 0.47%. HR-LCMS analysis produced 38 tentative compound matches, including luteolin. Under specified conditions, TLC-densitometry showed an Rf value of 0.54 for luteolin, with a mean amount of 3.849 µg. These findings provide baseline physicochemical and phytochemical data for standardisation of S. caseolaris L. leaf extract for future research applications and quality control purposes in pharmaceutical and herbal product development to ensure consistency safety and efficacy across batches.

    Sciences of Pharmacy

    28 Apr 2026
    7 pages
  • research article

    Natural Antidepressant Candidate from Cassia alata L. Ethanolic Extract: Behavioral (TST-FST) Evidence in Mice

    Kristina Srirahayu Damaiyanti Putri, Juwita Rosalia Sintia Nabella, Nily Su’aida, Karina Erlianti

    Cassia alata L. is a medicinal plant containing various secondary metabolites with reported neuroactive properties. This study aimed to evaluate the antidepressant-like behavioral effects of the ethanolic extract of C. alata leaves in mice using acute behavioral despair tests. Male mice (n = 5 per group) were orally administered ethanolic extract of C. alata leaves at doses of 100, 200, and 400 mg/kg body weight. A sub-acute stress exposure protocol using the Tail Suspension Test was applied, and antidepressant-like activity was subsequently evaluated using the Forced Swimming Test, with immobility time at T2 as the primary outcome measure. Amitriptyline served as the standard drug. Data were analyzed using one-way ANOVA followed by Tukey’s HSD post hoc test (p < 0.05). Chemical profiling was performed using LC–MS/MS. One-way ANOVA revealed a significant difference in immobility time among groups (F (4,20) = 21.465, p < 0.001). Post hoc analysis showed that all extract-treated groups exhibited significantly lower immobility times compared to the negative control (p < 0.05). The highest dose (400 mg/kgBW) was not significantly different from amitriptyline (p > 0.05), while lower doses showed intermediate effects. LC–MS/MS analysis tentatively identified 17 compounds, including flavonoid derivatives, luteolin, and anthraquinones. Under present experimental conditions, the ethanolic extract of C. alata leaves exhibited antidepressant-like behavioral activity in acute animal models. These findings are limited to short-term behavioral observations and do not establish clinical efficacy, safety, or underlying mechanisms. Further studies are required to clarify pharmacological relevance and translational potential of this extract for future preclinical and clinical investigations.

    Sciences of Pharmacy

    10 Jun 2026
    10 pages