https://ajhponline.com/index.php/journal/issue/feed Asian Journal of Hospital Pharmacy 2026-01-21T14:09:36-05:00 Dr. G. V. Nagaraju editor@ajhponline.com Open Journal Systems <p><strong>Asian Journal of Hospital Pharmacy (<em>Asian Jour Hosp Phar</em>)</strong>&nbsp; &nbsp;is a double-blind Peer-Reviewed Quarterly open access international journal dedicated to the promotion of research Pharmaceutical sciences. We define Open Access journals as journals that use a funding model that does not charge readers or their institutions for access. The journal publishes Research articles, Review article, Case Reports, and Short communication from broad areas like Pharmacy practice,&nbsp; Clinical Pharmacy, Hospital Pharmacy, Pharmacotherapeutics Pharmacoepidemiology and Economics, Clinical Research, Pharmaceutics, Pharmacology, Pharmacognosy &amp; Phytochemistry, Pharmaceutical Chemistry, Pharmaceutical Biotechnology, Pharmaceutical Analysis,&nbsp; Pharmacogenomics, Medicinal Chemistry, Molecular Pharmacology, Novel drug delivery system, Nanotechnology, Analytical Chemistry, Organic Chemistry, Natural Chemistry, Polymer Sciences, and Biotechnology, etc.</p> <p><strong>Road Indexing:</strong> https://portal.issn.org/resource/ISSN/2583-0724</p> <p><strong>Open Access Policy</strong></p> <p>All the Published articles By the Asian Journal of Hospital Pharmacy (AJHP) are available Worldwide Under the Open Access Policy. As per the Budapest Open Access Initiative, Readers can Directly Access Published articles without paying any subscription or access fees. Readers are allowed to read, download, copy and distribute the full text of all published articles, and readers can Utilize the published article for Non-Commercial Purpose.</p> <p><strong>Data Preservation</strong></p> <p><strong>Asian Journal of Hospital Pharmacy (AJHP)</strong>Preserved all published data content in&nbsp;PORTICO</p> https://ajhponline.com/index.php/journal/article/view/111 Decontamination efficacy of hypochlorous acid water on cyclophosphamide and 5-fluorouracil residues 2026-01-21T14:09:36-05:00 Mayumi Nakaishi m55nakaishi@gmail.com Koki Takeda k-takeda@dwc.doshisha.ac.jp Asako Nishimura anishimu@dwc.doshisha.ac.jp Akiko Kiriyama akiriyam@dwc.doshisha.ac.jp Nobuhito Shibata nshibata@dwc.doshisha.ac.jp <p>Hypochlorous acid water (HAW) is widely used for disinfection in medical settings, yet its ability to decompose hazardous anticancer drug residues remains unclear. This study evaluated the decontamination efficacy of HAW on anticancer drugs by examining their decomposition kinetics, using sodium hypochlorite (NaClO) as a reference. Cyclophosphamide (CPA) and 5-fluorouracil (5-FU) were tested with 0.02% HAW, NaClO at 0.02%, 0.2%, and 2%, and ozone water. Decomposition kinetics were monitored, and cytotoxicity of drug–decontaminant mixtures was assessed using the MTT assay. HAW rapidly decomposed both drugs, with no detectable CPA after 5 minutes, while NaClO degraded CPA more slowly and showed concentration-dependent equilibrium for 5-FU. In the MTT assay, CPA mixed with either HAW or NaClO produced cytotoxic products, whereas 5-FU mixtures showed no cytotoxicity. These findings suggest that HAW is more effective than NaClO in decomposing CPA and 5-FU and could be a promising agent for removing anticancer drug residues, although the potential cytotoxicity of decomposition products should be considered when applying HAW for surface decontamination in clinical settings.</p> 2025-12-31T00:00:00-05:00 Copyright (c) 2026 Mayumi Nakaishi, Koki Takeda, Asako Nishimura, Akiko Kiriyama, Nobuhito Shibata https://ajhponline.com/index.php/journal/article/view/113 Comprehensive review on antimicrobial resistance: mechanisms, clinical challenges 2025-10-22T01:03:23-04:00 Devivara Prasad R ramiramireddyharshitreddy@gmail.com Harshith R ramiramireddyharshitreddy@gmail.com Balaji Prasad S ramiramireddyharshitreddy@gmail.com Jeevesh P ramiramireddyharshitreddy@gmail.com Manasa I ramiramireddyharshitreddy@gmail.com Sanjana K ramiramireddyharshitreddy@gmail.com Shakeela SK ramiramireddyharshitreddy@gmail.com <p>Antimicrobial resistance (AMR) poses a growing global health threat, necessitating a deeper understanding of its mechanisms and clinical implications. This review investigates three critical resistance phenomena: extended-spectrum β-lactamases (ESBLs) in gram-negative bacilli, penicillin-resistant Streptococcus pneumoniae (PRSP), and vancomycin-resistant enterococci (VRE). We synthesize clinical, microbiological, and molecular data from hospital outbreaks,surveillance programs to elucidate the evolutionary and epidemiological drivers of resistance. ESBL-producing Klebsiella pneumoniae and Escherichia coli emerged through plasmid-mediated gene transfer and transposon mobility, with hospital outbreaks linked to prolonged antibiotic use and invasive procedures. PRSP strains acquired mosaic genes encoding altered penicillin-binding proteins, retaining virulence despite resistance, while VRE outbreaks were fueled by van operon dissemination via plasmids, leading to high mortality rates. The study reveals convergent resistance mechanisms across pathogens, underscoring the limitations of current therapies. Moreover, it highlights the efficacy of carbapenems and β-lactam–β-lactamase inhibitors against ESBLs, the geographic variability of PRSP serotypes, and the urgent need for infection-control measures to curb VRE transmission. Our findings emphasize the necessity of multidisciplinary interventions, including antibiotic stewardship, vaccine development, and novel therapeutic strategies, to mitigate AMR's escalating impact. This research contributes a comprehensive analysis of resistance dynamics, offering actionable insights for clinicians, policymakers, and researchers to address one of the most pressing public health challenges of our time.</p> 2025-10-20T00:00:00-04:00 Copyright (c) 2025 https://ajhponline.com/index.php/journal/article/view/114 A review of over the counter medication safety, affordability, and prevalence 2025-10-30T01:48:25-04:00 Jahnavi Chitteti sribharathiyeddu@gmail.com Sribharathi Yeddu sribharathiyeddu@gmail.com Afroz Patan sribharathiyeddu@gmail.com Prapurna Chandra Yadala sribharathiyeddu@gmail.com <p>Over-the-counter (OTC) medications have become a cornerstone of modern self-care, allowing individuals to independently treat common ailments such as headaches, colds, and digestive discomfort without medical supervision. Their widespread availability offers substantial benefits—reducing unnecessary doctor visits, cutting healthcare costs, and empowering consumers to take control of their health. Globally, 60–80% of adults report using OTC products, with even higher rates in Europe and growing adoption across India and other low- and middle-income countries. Economic analyses show that every dollar spent on OTC drugs can save up to seven dollars in healthcare expenditure, highlighting their value to both individuals and health systems. However, the convenience of OTC access is coupled with significant risks. Misuse, accidental overdose, drug interactions, and inappropriate self-diagnosis contribute to adverse outcomes, particularly among vulnerable groups such as children, pregnant women, and the elderly. The misuse of antibiotics sold as OTC in some regions further fuels antimicrobial resistance—a major global health concern. Regulatory frameworks vary widely across countries, with strong safety controls in the US and Europe but substantial enforcement gaps in India and other developing markets. Education gaps also persist, as many users fail to read labels or underestimate potential side effects. This review evaluates the prevalence, benefits, risks, and regulatory challenges of OTC medication use. A balanced approach—strengthening regulation, enhancing pharmacist involvement, and improving public awareness—is essential to ensure that OTC drugs continue to support health without compromising safety.</p> 2025-10-28T00:00:00-04:00 Copyright (c) 2025 https://ajhponline.com/index.php/journal/article/view/119 Orphan diseases: bridging the global gaps in rare disease care andfuture priorities 2025-12-28T05:09:44-05:00 Sumalatha Borancha chandinimandepudi72@gmail.com Priyanka Tatikonda chandinimandepudi72@gmail.com Jyoshna Borancha chandinimandepudi72@gmail.com Subiya Maheen chandinimandepudi72@gmail.com Keerthija Reddy Kommidi chandinimandepudi72@gmail.com Tejasri Mahalaxmi Panala chandinimandepudi72@gmail.com Satyanarayana L chandinimandepudi72@gmail.com Lakshmi Chandini Mandepudi chandinimandepudi72@gmail.com <p>Orphan diseases are also referred as rare disease and these are medical conditionsthat effect a small portion of the population.They collectively effectmillions of individuals amongworldwide.Orphandisease is chronic,genetic, andlife-threatening, often demonstration&nbsp; early&nbsp; in life. Typically, fewer than 200,000 peoples in the United States, because of the limited&nbsp; count of patients, there is lack of financial support forpharmaceutical companies to invest&nbsp; in treatment development,and that leads in minimal therapeutic options&nbsp; and research, as a result,these orphan diseases are&nbsp; continuously unconsidered in drug development&nbsp; efforts. Inducesto the supportivepolicieslike the orphan&nbsp; drugs Act introduction. Examples of orphan disease&nbsp; types; genetic disorders, autoimmune diseases, rare cancer, metabolic disorders,&nbsp; infection disease. Characteristics of orphan disease which includeslowprevalence,high mortality&nbsp; and&nbsp; morbidity, complex and often unexplained and need for orphan&nbsp; drug&nbsp; development. This article delivers an overview of orphan&nbsp; disease, &nbsp;examples, treatment, impact on patients and families, challenges&nbsp; in treatment and&nbsp; diagnosis, future direction.</p> 2025-12-26T00:00:00-05:00 Copyright (c) 2025