Journal of Pharmaceutical and Sciences https://journal-jps.com/new/index.php/jps <p>Thank you for visiting the Journal of Pharmaceutical and Sciences (e-ISSN: 2656-3088). It is with great pleasure that the first issue of the JJournal of Pharmaceutical and Sciences is released to the academic world, which is intended to accommodate the needs of researchers to publish their work. The Faculty of Pharmacy at Tjut Nyak Dhien University publishes this journal. This journal's publisher is dedicated to advancing research and knowledge in the pharmaceutical, science, and health fields. Articles that have been published can be accessed and downloaded online by the public (open-access journal). Manuscripts can be submitted to the Journal of Pharmaceutical and Sciences in Indonesian and English. The Journal of Pharmaceutical and Life Sciences has been accredited by the Directorate General of Higher Education, Ministry of Research, Technology, and Higher Education, Republic of Indonesia. With a SINTA accreditation rating of 4. Certificate No. 164/E/KPT/2021 (<a href="https://drive.google.com/file/d/1Uc_FFB7Pi9qAophB2f5Ggghw7BNCA-wu/view">download Certificate</a>).</p> <p><strong>Journal Migration</strong></p> <p>As of January 1, 2023, Volume 6 number 1, the Journal of Pharmaceutical and Sciences has migrated to a new website at <a href="https://journal-jps.com/new">https://journal-jps.com/new</a>. While the old version (volume 1 to volume 5) can still be accessed as usual at the URL: <a href="https://lama.journal-jps.com">https://lama.journal-jps.com</a> or <a href="https://journal-jps.com/index.php/jps/issue/archive">https://journal-jps.com/index.php/jps/issue/archive</a>.</p> <p><a href="https://journal-jps.com/new/index.php/jps/about/submissions"><strong>Submit your manuscript via the new website</strong></a></p> Fakultas Farmasi Universitas Tjut Nyak Dhien en-US Journal of Pharmaceutical and Sciences 2656-3088 Review of Potential Activities of Sambiloto Herbs, Meniran Herbs, and Kumis Kucing Leaves in the Management of Diabetic Neuropathy: A Narrative Review https://journal-jps.com/new/index.php/jps/article/view/940 <p>Diabetic neuropathy is one of the most common microvascular complications among patients with diabetes mellitus, characterized by damage to peripheral nerves due to persistently high blood sugar levels, excessive oxidation and inflammation. Conventional treatments are often not effective enough in comprehensively addressing this problem, so strategies using medicinal plants are emerging as promising options. This study aims to review the potential pharmacological activities of three medicinal plants, namely sambiloto (Andrographis paniculata), meniran (Phyllanthus niruri), and cat's whisker (Orthosiphon aristatus), in the treatment of diabetic neuropathy. This study was conducted using the Narrative Review method with a literature search of two databases PubMed and ScienceDirect with an interval of publication years 2016-2026. A total of 16 articles were selected. The three types of plants showed significant pharmacological properties, including as antioxidants, anti-inflammatory, hypoglycemic, and neuroprotective. Sambiloto functions through andrographolide compounds that inhibit the NF-κB pathway and increase Nrf2 antioxidant activity. Meniran has an effect in lowering blood glucose levels and increasing the performance of antioxidant enzymes. Cat whisker plays a role in glucose control, kidney care, and inflammation in the system. The results of this study are expected to provide an overview of additional therapies in overcoming diabetic neuropathy through the workings of Sambiloto, meniran, and cat's whiskers have complementary potential. The combination of these three plants offers a diverse approach, but further research is needed to assess synergistic effects, safety, and the most appropriate formulation as a modern herbal treatment.</p> Anita Purnama Sari Elza Sundhani Retno Wahyuningrum Copyright (c) 2026 Anita Purnama Sari , Elza Sundhani , Retno Wahyuningrum https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-03 2026-05-03 1115 1123 10.36490/journal-jps.com.v9i2.940 The Integrating Precision Genomic Strategies and Islamic Ethical Perspectives in Stunting Prevention: Focus on the Growth Hormone-IGF-1 Pathway https://journal-jps.com/new/index.php/jps/article/view/1320 <p>Stunting remains one of the major chronic nutritional problems in Indonesia. The national prevalence of stunting has decreased from 37.2% in 2013 to 19.8% in 2024; however, this figure is still above the World Health Organization threshold (&lt;20%) and has not yet reached the national target of 14%. The interaction of nutritional, environmental, and genetic factors influences stunting. Genetic variations within the Growth Hormone–Insulin-like Growth Factor One pathway play a significant role in regulating linear growth in children; disruptions in this pathway can increase vulnerability to stunting. In addition, the majority of Indonesia's population adheres to Islam, making religious values a strategic potential for strengthening health interventions. This review article examines the integration of scientific approaches, focusing on genetics and Islamic values, in stunting prevention by highlighting polymorphisms in the IGF1, IGF1R, and GHR genes and their relevance to the principles of maqāsid al-sharī‘ah, particularly hifz al-nasl (protection of lineage). The analysis is conducted using a descriptive-analytical approach based on recent scientific literature and Islamic references, including the Qur’an, prophetic traditions, and scholarly exegesis. The findings indicate a strong alignment between scientific approaches and Islamic teachings, including the importance of adequate nutrition during pregnancy, exclusive breastfeeding, consumption of lawful, nutritious food, genetic screening efforts consistent with the values of divine decree, and vitamin D supplementation to support Insulin-like Growth Factor One levels. This integration has the potential to enhance community acceptance of stunting-prevention programs, strengthen moral and spiritual motivation, and support the achievement of national stunting-reduction targets. Thus, an approach that combines precise genomics and Islamic values may serve as a contextual and sustainable strategy in shaping a generation that is healthy, intelligent, and spiritually resilient.</p> Hifdzil Qur’ani Nasywa Khoirun Nisa Pramudya Pratama Ahsanal Kasasiah Jekmal Malau Copyright (c) 2026 Hifdzil Qur’ani , Nasywa Khoirun Nisa , Pramudya Pratama , Ahsanal Kasasiah , Jekmal Malau https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-03 2026-05-03 1132 1144 10.36490/journal-jps.com.v9i2.1320 Comparison of Antioxidant Activity of Flavonoid Compounds From (Moringa Oleifera L.) Leaf Extract Using Uv-Vis Spectrophotometry Method https://journal-jps.com/new/index.php/jps/article/view/677 <p>The bioactive compounds found in moringa leaves (<em>Moringa oleifera</em> L.) can function as natural antioxidants to protect cells from damaging free radicals. The purpose of this study is to ascertain the antioxidant activity of moringa leaves according to the type of solvent, analyze the relationship between antioxidant capacity and concentration of active compounds, and determine the best solvent. Extraction was carried out using ethanol, methanol, and aquades solvents, followed by testing antioxidant activity using UV-Vis spectrophotometry method on DPPH radicals. The content of phenols, flavonoids, and tannins in the extract was measured to understand their contribution to antioxidant activity Based on the results of the study, the extract containing ethanol solvent showed the most powerful antioxidant activity, with an IC50 value of 103.98 ppm. In conclusion, the type of solvent has a significant effect on the antioxidant activity of moringa leaves, with ethanol solvents being the most effective option. This research strengthens the potential of moringa leaves as a natural source of antioxidants that can be utilized for applications in the pharmaceutical and health fields, although further research is needed to optimize extraction techniques and the development of moringa oleifera leaf-based product</p> Puteri Rahma Maharani Izmi Haura Syahida Munir Alinu Mulki Copyright (c) 2026 Puteri Rahma Maharani, Izmi Haura Syahida , Munir Alinu Mulki https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-06 2026-05-06 1177 1183 10.36490/journal-jps.com.v9i2.677 The Effect of Menopause on the Cardiovascular System https://journal-jps.com/new/index.php/jps/article/view/1556 <p>Menopause is the permanent cessation of menstruation for 12 consecutive months without any underlying pathological cause. This occurs due to ovarian follicular atresia, which leads to the cessation of estrogen production. The menopausal transition begins 5 to 10 years before menstruation ceases. During menopause, estrogen levels decline, leading to biological changes in the body, such as an increase in total cholesterol, low-density lipoproteins (LDL), triglycerides, and apolipoprotein B, as well as a decrease in high-density lipoprotein (HDL), an increase in visceral fat, and the development of metabolic syndrome. Various characteristics of menopause have been evaluated in relation to cardiovascular disease (CVD) risk, including age at menopause onset, type and stage of menopause, endogenous estradiol levels, and menopause-related symptoms. These factors have been found to be associated with CVD risk, with the highest risk occurring in women with ovarian failure and relatively early menopause. Women with early menopause (aged 40–44 years) have a hazard ratio of 1.55 (95% CI: 1.38–1.73) for coronary artery disease events compared to women with menopause at age 50–54 years. Women with premature ovarian failure tend to have a shorter life expectancy compared to those who experience late menopause, primarily due to an increased risk of cardiovascular disease.</p> Guadelupe Maria Melisa Wiriadinata Dewa Ayu Agus Sri Laksemi Copyright (c) 2026 Guadelupe Maria Melisa Wiriadinata, Dewa Ayu Agus Sri Laksemi https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-08 2026-05-08 1184 1191 10.36490/journal-jps.com.v9i2.1556 The Impact of Telemedicine on Patient Satisfaction Levels in Several Developed and Developing Countries: A Systematic Review https://journal-jps.com/new/index.php/jps/article/view/1404 <p>Telemedicine is a telecommunication technology in healthcare that has expanded rapidly, especially during COVID-19. Its implementation varies between developed and developing countries, raising questions about its impact on patient satisfaction and the factors influencing it. This study aims to evaluate the impact of telemedicine on patient satisfaction across developed and developing countries and to identify key factors influencing satisfaction to inform improvements in telemedicine delivery models. The systematic review was conducted using PubMed, Scopus, and Web of Science databases. The search utilized keywords related to telemedicine and patient satisfaction. The inclusion criteria focused on peer-reviewed articles published between 2020 and 2025, resulting in 14 studies (seven from developed countries and seven from developing countries) being analyzed. Data were extracted and synthesized following the PRISMA guidelines. The analysis identified 14 eligible studies. The findings indicate that telemedicine generally has a positive impact on patient satisfaction, with high satisfaction levels reported across various settings. For example, studies from Sweden and India reported that approximately 78-93% of patients expressed satisfaction or willingness to reuse the telemedicine service. However, several challenges were identified, particularly in developing countries such as Indonesia and the Philippines, including service costs, limited digital infrastructure, and low technological literacy</p> Salsabilla Dyah Puspitasari Anna Wahyuni Widayanti Susi Ari Kristina Copyright (c) 2026 Salsabilla Dyah Puspitasari , Anna Wahyuni Widayanti , Susi Ari Kristina https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-08 2026-05-08 1192 1204 10.36490/journal-jps.com.v9i2.1404 Rosemary (Rosmarinus officinalis) Phytochemicals as Prevention of Collagen Degradation and Wrinkle Formation: a Literature Review https://journal-jps.com/new/index.php/jps/article/view/1486 <p>of the most visible manifestations. Aging disrupt the balance between collagen synthesis and degradation, leading to fragmentation of collagen fibers and loss of skin elasticity. Natural phytochemicals have gained increasing attention as potential agents for preventing or delaying skin aging due to their antioxidant and anti-inflammatory properties. Rosemary (<em>Rosmarinus officinalis</em>) contains a variety of bioactive compounds with potential dermatological benefits. Major phytochemicals identified in rosemary include phenolic acids such as rosmarinic acid, diterpenes such as carnosic acid and carnosol, as well as flavonoids and volatile terpenoids. These compounds have demonstrated strong antioxidant activity and the ability to modulate molecular pathways associated with skin aging. Evidence from in vitro studies suggests that rosemary phytochemicals can reduce reactive oxygen species (ROS) production, suppress inflammatory signaling pathways, and inhibit the expression of MMPs involved in collagen degradation. Emerging clinical evidence, particularly from oral supplementation studies, also suggests improvements in skin elasticity, wrinkle depth, and oxidative stress biomarkers, supporting the translational potential of rosemary phytochemicals in human skin. Available evidence supports the potential application of rosemary-derived compounds in dermatological and cosmeceutical formulations aimed at preventing collagen degradation and wrinkle formation. This literature review summarizes current evidence on the phytochemical composition of rosemary and the molecular mechanisms through which its bioactive compounds may contribute to the prevention of skin aging.</p> Nyoman Ledy Trisna Parimartha Dewa Ayu Agus Sri Laksemi Copyright (c) 2026 Nyoman Ledy Trisna Parimartha , Dewa Ayu Agus Sri Laksemi https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-08 2026-05-08 1205 1219 10.36490/journal-jps.com.v9i2.1486 Advanced Drug Delivery Systems: Nano-Formulation Challenges of Poorly Water-Soluble Phytochemicals https://journal-jps.com/new/index.php/jps/article/view/1537 <p>The poor water solubility and low oral bioavailability of various phytochemical compounds (BCS Classes II and IV) continue to be major obstacles in the development of modern therapeutics, despite their remarkable therapeutic potential. This narrative review critically evaluates the use of nanoscale drug delivery systems to overcome the biopharmaceutical limitations of hydrophobic phytochemicals and pinpoints key challenges in clinical translation and industrial-scale production. The review provides a comprehensive analysis of the latest literature on the effectiveness of nanotechnology-based physicochemical modifications, including solid lipid nanoparticles (SLNs), nanostructured lipid carriers (NLCs), nanosuspensions, polymeric micelles, liposomes, and phytosomes. The review's results indicate that nano-carrier engineering significantly enhances solubility, avoids first-pass metabolic degradation, and enables targeted delivery. Specifically, nanoformulations have proven effective at penetrating the dense matrix of the tumor microenvironment (TME) in cancer therapy, crossing the blood-brain barrier (BBB) in neurodegenerative diseases, and protecting drugs from stomach acid in infectious and metabolic conditions. However, the transition toward commercialization is hindered by issues of long-term physicochemical stability (e.g., lipid polymorphic transitions) and challenges in standardizing botanical raw materials. These issues affect the reproducibility of large-scale production, ultimately delaying the availability of these promising therapies to patients in need. In conclusion, while nanoformulations offer transformative solutions for overcoming phytochemical biological barriers, standardizing protocols, innovating green synthesis, and fostering interdisciplinary collaboration are essential for overcoming scalability barriers and preparing these innovations for clinical application.</p> Juliana Palungan Rona Hawa Kamilah Moh. Firmansah Sima Asmara Dewa Marya Mahardika Putri Winda Wahyu Setya Rahmah M Iman Tarmizi Thaher Copyright (c) 2026 Juliana Palungan, Rona Hawa Kamilah , Moh. Firmansah , Sima Asmara Dewa Marya Mahardika Putri, Winda Wahyu Setya Rahmah , M Iman Tarmizi Thaher https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-08 2026-05-08 1220 1238 10.36490/journal-jps.com.v9i2.1537 Relationship Between Delta Like Ligand 1 (DLL-1) Levels in Serum and Cerebrospinal Fluid (CSF) with The Severity of Tuberculosis Meningitis https://journal-jps.com/new/index.php/jps/article/view/1514 <p>Tuberculous meningitis (TBM) is an infection caused by <em>Mycobacterium tuberculosis</em> (M.tb) affecting the meninges, characterized by high morbidity rates. The prognosis of TBM is partially determined by clinical severity, classified according to the British Medical Research Council (BMRC) scale. Delta Like Ligand 1 (DLL-1) is a transmembrane protein that plays a role in the formation of lipid cells, which are essential for the survival, virulence, and defense of M.tb against the host immune system. DLL-1 expression can be induced by the stimulation of M.tb cell walls in response to the human immune system. This study aims to analyze the correlation between DLL-1 levels in the serum and cerebrospinal fluid (CSF) with the clinical severity of TBM patients. A cross-sectional study was conducted involving 30 TBM patients treated at M. Djamil Central General Hospital, Padang, from October 2025 to January 2026. Serum and CSF DLL-1 levels were measured using the enzyme-linked immunosorbent assay (ELISA) method, while TBM severity was assessed based on the BMRC criteria. Data analysis was performed using SPSS version 26.0 with a significance level of p &lt; 0.05. The results of the analysis showed no significant difference in serum DLL-1 levels (p = 0.129) or CSS DLL-1 levels in relation to the severity of TBM (p = 0.097).</p> Abdul Razak Syarif Indra Restu Susanti Yuliarni Syafrita Reno Bestari Gunawan Septa Dinata Copyright (c) 2026 Abdul Razak, Syarif Indra, Restu Susanti, Yuliarni Syafrita, Reno Bestari, Gunawan Septa Dinata https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-03 2026-05-03 1124 1131 10.36490/journal-jps.com.v9i2.1514 Nephroprotective Effectiveness Test of Coffee Fruit Extract (Coffea arabica L.) Against Histopathological Features and Inflammatory Markers in Gentamicin-Induced Mice https://journal-jps.com/new/index.php/jps/article/view/1354 <p>Gentamicin is an aminoglycoside antibiotic widely used in the treatment of severe bacterial infections; however, its clinical application is limited due to nephrotoxic effects. Gentamicin-induced nephrotoxicity is closely associated with oxidative stress and inflammatory responses, which contribute to tubular damage and renal dysfunction. Coffee fruit (<em>Coffea arabica</em> L.) contains various bioactive compounds, including phenolics, flavonoids, and polyphenols, which exhibit antioxidant and anti-inflammatory activities and may provide renal protection. This study aimed to evaluate the nephroprotective effectiveness of coffee fruit extract against gentamicin-induced kidney injury in rats based on histopathological features and inflammatory markers. This experimental in vivo study used male Wistar rats divided into five groups: normal control, gentamicin control, and gentamicin combined with coffee fruit extract at doses of 100, 200, and 400 mg/kg body weight. Gentamicin was administered intraperitoneally to induce nephrotoxicity, while the extract was given orally for 14 days. Serum interleukin-6 (IL-6) levels were measured using enzyme-linked immunosorbent assay, and kidney tissues were examined histopathologically using hematoxylin–eosin staining. The results showed that gentamicin significantly increased serum IL-6 levels and caused moderate renal histopathological damage. Administration of coffee fruit extract significantly reduced IL-6 levels at doses of 200 and 400 mg/kg body weight (p&lt;0.05) and improved renal histopathological features in a dose-dependent manner, with the highest dose showing the most pronounced protective effect. In conclusion, coffee fruit extract demonstrates nephroprotective potential against gentamicin-induced renal injury by reducing inflammatory responses and improving kidney histopathology.</p> Anas Tasya Glori Br Ginting Asyrun Alkhairi Lubis Refi Ikhtiari Copyright (c) 2026 Anas Tasya Glori Br Ginting , Asyrun Alkhairi Lubis , Refi Ikhtiari https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-04 2026-05-04 1145 1155 10.36490/journal-jps.com.v9i2.1354 Formulation and Antioxidant Activity of Old Coconut Water Syrup (Cocos nucifera L) and Red Fruit Extract (Pandanus conoideus L) Using the DPPH Method https://journal-jps.com/new/index.php/jps/article/view/1496 <p><strong>Background:</strong> Mature coconut water (<em>Cocos nucifera</em> L.) has the potential as a health drink but is often discarded as waste. Red fruit (<em>Pandanus conoideus</em> L.) is an endemic plant of Papua that is rich in antioxidants. The combination of both is expected to produce a beneficial herbal syrup preparation. <strong>Objective:</strong> To formulate a combination syrup of mature coconut water and red fruit extract and to determine its antioxidant activity using the DPPH method. <strong>Methods:</strong> Red fruit extract was obtained by maceration using 96% ethanol. Phytochemical screening was performed on both ingredients. The syrup was prepared with the addition of sugar, citric acid, vanilla, and CMC. Physical evaluation included organoleptic, homogeneity, pH, viscosity, and clarity tests. Antioxidant activity was tested using the DPPH method at a wavelength of 517 nm using a UV-Vis spectrophotometer. <strong>Results:</strong> Phytochemical screening showed that mature coconut water contains alkaloids, while red fruit extract contains flavonoids, tannins, saponins, and alkaloids. The syrup evaluation met SNI requirements: organoleptic (reddish-orange color, characteristic odor, sweet taste), homogeneous, pH 5–6, viscosity 250 mPa·s, and clear. The IC50 values of the syrup in three consecutive replicates were 550.34 μg/mL, 2282.3 μg/mL, and 2863.4 μg/mL, which are classified as weak antioxidant activity (IC50 &gt; 200 ppm). <strong>Conclusion:</strong> The combination syrup of mature coconut water and red fruit extract exhibits weak antioxidant activity but meets the physical quality standards of the preparation. This preparation has the potential to be developed as a herbal health drink.</p> Siti Mun Muhliza Ahmad Ratih Arum Astuti A.M. Muslihin Copyright (c) 2026 Siti Mun Muhliza Ahmad , Ratih Arum Astuti , A.M. Muslihin https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-06 2026-05-06 1156 1167 10.36490/journal-jps.com.v9i2.1496 In Vitro Study : Antifungal Activity of Coffea canephora Peel and Leaf Extracts Against Candida albicans https://journal-jps.com/new/index.php/jps/article/view/1456 <p><em>Candida albicans </em>is a major cause of invasive candidiasis with high morbidity and mortality rates, and it has shown increasing resistance to antifungal agents. The objective of this research to evaluate the antifungal activity of <em>Coffea canephora </em>peel and leaf extract against <em>Candida albicans </em>in vitro by determining the Minimum Inhibitory Concentration (MIC). Robusta coffee peel and leaves were extracted using maceration with 96% ethanol, followed by phytochemical screening and antifungal activity testing using the broth dilution method. Phytochemical screening revealed the presence of alkaloids, phenolic-tannins, flavonoids, saponins, and terpenoids, while steroid were not detected. Based on the antifungal activity test conducted separately, both extracts had the same MIC value at a concentration of 12,5%. Statistical analysis using One Way ANOVA demonstrated a significant difference among treatment groups (p&lt;0,05). The antifungal activity of the extract is presumed to be associated with phenolic compounds, such as chlorogenic acid and caffeine, which may act through disruption of cell membrane integrity and inhibition of ergosterol synthesis. These finding suggest that <em>Coffea canephora </em>peel and leaf extract has the potential to be further developed as an antifungal agent, especially in topical formulations, but further toxicity tests and in vivo tests are required.</p> Mastuti Widianingsih Yesi Afrida Aini Copyright (c) 2026 Mastuti Widianingsih , Yesi Afrida Aini https://creativecommons.org/licenses/by-nc-sa/4.0 2026-05-06 2026-05-06 1168 1176 10.36490/journal-jps.com.v9i2.1456