https://www.wjpsonline.com/index.php/wjps/issue/feedWorld Journal of Pharmaceutical Sciences2025-10-17T12:57:58+00:00Editor-in-Chiefeditor@wjpsonline.comOpen Journal Systems<p><strong>The World Journal of Pharmaceutical Sciences (WJPS; Print ISSN: 2321-3310; Online </strong><strong>ISSN: 2321-3086)</strong> is an international, peer-reviewed monthly open-access journal published by Atom and Cell Publishers. The journal welcomes original research articles, review articles, short communications, mini-reviews, case reports, letter to the editor, guest editorial or commentaries and editorials of all aspects of pharmacy and pharmaceutical sciences.</p> <p><strong>Why publish with WJPS</strong></p> <p><strong>Impact Factor: 1.318</strong></p> <p><strong>Crossref DOI Assigned: 10.54037/WJPS</strong></p> <p><strong>Quick Quality Review: </strong>The journal has strong international team of editors and reviewers. Constructive reviews from renowned scientist and researcher at all editorial levels.</p> <p><strong>Rapid Decision and Publication:</strong> We guarantee a review of your manuscript by a panel of qualified experts within 15 days of submission. Authors that need a faster decision can request Fast Track review and get a response in 3-5 business days.</p> <p><strong>Indexing</strong>: Google Scholars; Advanced Science Index; Chemical Abstracts Service; Cosmos Impact Factor; CiteFactor; Directory of Research Journals Indexing; Eurasian Scientific Journal Index; Geneva Foundation for Medical Education and Research; Global Impact Factor; Index Copernicus; InfoBase Index; International Impact Factor Services; International Scientific Indexing; Open Academic Journals Index; Polish Scholarly Bibliography; Scholarsteer</p> <p><strong>Low Publication Fees:</strong> Comparable journals charge a huge sum for each accepted manuscript. WJPS only charges the fees necessary to recoup costs associated with running the journal.</p> <p>You may submit manuscripts online through following link <a href="https://wjpsonline.com/index.php/wjps/about/submissions" target="_blank" rel="noopener">https://wjpsonline.com/index.php/wjps/about/submissions</a> or as an email attachment to the following mail: editor.wjps@gmail.com</p>https://www.wjpsonline.com/index.php/wjps/article/view/1959ANALYTICAL METHOD DEVELOPMENT AND RAPID ANALYTICAL TECHNIC FOR SIMULTANEOUS ESTIMATION OF MONTELUKAST AND BILASTINE IN BULK AND PHARMACEUTICAL DOSAGE FORM BY USING RP-HPLC METHOD2025-10-17T12:47:20+00:00Dr. Subhas Sahoopolepraveen5577@gmail.com<p>A simple, Accurate, precise method was developed for the simultaneous estimation of the Bilastine and Montelukast in bulk and pharmaceutical dosage form. Chromatogram was run through Agilent C18 150 x 4.6 mm, 5mm. Mobile phase containing Buffer :Acetonitrile taken in the ratio 70:30 was pumped through column at a flow rate of 1.0 ml/min. Buffer used in this method was 0.01N Na2Hpo4 buffer. Temperature was maintained at 30°C. Optimized wavelength selected was 265.0 nm. Retention time of Bilastine and Montelukast were found to be 2.141 min and 2.605 min. %RSD of the Bilastine and Montelukast were and found to be 0.4% and 0.2% respectively. %Recovery was obtained as 99.47% and 99.55% for Bilastine and Montelukast respectively. LOD, LOQ values obtained from regression equations of Bilastine and Montelukast were 0.1, 0.03 and 0.03, 0.10 respectively. % Assay was obtained as 99.74% and 99.72% for Bilastine and Montelukast respectively. Regression equation of is Montelukast y = 45726x + 6306.9, y = 43360x + 810 of Bilastine.</p>2025-10-17T00:00:00+00:00Copyright (c) 2025 Dr. Subhas Sahoohttps://www.wjpsonline.com/index.php/wjps/article/view/1962RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS ESTIMATION OF TENEGLIPTIN AND REMOGLIFLOZIN IN BULK AND PHARMACEUTICAL DOSAGE FORM2025-10-17T12:57:58+00:00Dr. S. Srinivasa Raoharikas232@gmail.com<p>Simultaneous estimation of the Remogliflozin and Teneligliptin in pharmaceutical dosage form. Chromatogram was run through Discovery C18 250 x 4.6 mm, 5m. Mobile phase containing Buffer Ammonium acetate: Acetonitrile taken in the ratio 60:40 was pumped through column at a flow rate of 0.9 ml/min.. Temperature was maintained at 30°C. Optimized wavelength selected was 229 nm. Remogliflozin and Teneligliptin were eluted at 2.139 min and 2.176 min respectively. %RSD of the Remogliflozin and Teneligliptin were and found to be 0.6 and 0.7 respectively. %Recovery was obtained as 99.50% and 99.50% for Remogliflozin and Teneligliptin respectively. LOD, LOQ values obtained from regression equations of Remogliflozin and Teneligliptin were 0.11, 0.33 and 0.005, 0.014 respectively. Regression equation of Remogliflozin is y = 52813x + 14718, and y = 69817x + 586.95 of Teneligliptin.</p>2025-10-17T00:00:00+00:00Copyright (c) 2025 Dr. S. Srinivasa Raohttps://www.wjpsonline.com/index.php/wjps/article/view/1960HPLC-BASED METHOD DEVELOPMENT AND VALIDATION FOR QUANTIFICATION OF NIRMATRELVIR AND RITONAVIR IN COMBINATION THERAPY2025-10-17T12:54:25+00:00Dr. S. Srinivasa Raodaramanasa676@gmail.com<p>A simple, Accurate, precise method was developed for the simultaneous estimation of the Nirmatrelvir and Ritonavir in pharmaceutical dosage form. Chromatogram was run through Kromasil C18 250 x 4.6 mm, 5. Mobile phase containing Buffer 0.1% OPA : Acetonitrile taken in the ratio 60:40 was pumped through column at a flow rate of 1.0ml/min. Buffer used in this method was 0.1% OPA. Temperature was maintained at 30°C. Optimized wavelength selected was 240 nm. Nirmatrelvir and Ritonavir were eluted at 2.303 min and 2.783 min respectively. %RSD of the Nirmatrelvir and Ritonavir were and found to be 0.8 and 0.5 respectively. %Recovery was obtained as 99.63% and 99.70% for Nirmatrelvir and Ritonavir respectively. LOD, LOQ values obtained from regression equations of Nirmatrelvir and Ritonavir were 0.04, 0.13 and 0.01, 0.02 respectively. Regression equation of Nirmatrelvir is y = 92901x + 3504.3, and y = 116867x + 4632.7 of Ritonavir.</p>2025-10-17T00:00:00+00:00Copyright (c) 2025 Dr. S. Srinivasa Raohttps://www.wjpsonline.com/index.php/wjps/article/view/1961RP-HPLC METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS DETERMINATION OF PREGABALIN AND ETORICOXIB IN PHARMACEUTICAL FORMULATIONS2025-10-17T12:56:17+00:00Dr. S. Srinivasa Raoachonicalahari24@gmail.com<p>The simultaneous estimation of the Pregabalin and Etoricoxib in Tablet dosage form. Chromatogram was run through Agilent C18 150 mm (4.6 x 150mm, 5μm) Mobile phase containing Buffer 70% (Ammonium acetate ) :40% Acetonitrile was pumped through column at a flow rate of 1 ml/min. Temperature was maintained at 30°C. Optimized wavelength selected was 234.0 nm. Retention time of Pregabalin and Etoricoxib were found to be 2.233 min and 2.712 min. %RSD of the Pregabalin and Etoricoxib were and found to be 0.5 and 0.5 respectively. %Recovery was obtained as 100.06% and 99.81% for Pregabalin and Etoricoxib respectively. LOD, LOQ values obtained from regression equations of Pregabalin and Etoricoxib were 0.03, 0.09 and 0.02, 0.06 respectively. Regression equation of Pregabalin is y = 33728x + 2248.7, and y = 37618x + 3978.9 of Etoricoxib.</p>2025-10-17T00:00:00+00:00Copyright (c) 2025 Dr. S. Srinivasa Rao