
About the Journal
ABOUT THE JOURNAL
Pharmacology & Toxicology Research (PTR) (ISSN 2349-4581) is a peer-reviewed Indexed Journal. The journal is dedicated to publishing high-quality research in Clinical Pharmacology, Medical Pharmacology, Experimental Pharmacology, Clinical Toxicology, Medical Toxicology, and Applied Toxicological Sciences. This journal is committed to publishing comprehensive research articles, critical reviews, case reports, mini-reviews, and short communications exclusively within the realms of Toxicology & Pharmacology.
AREAS OF PUBLICATION
- Clinical and Medical Pharmacology
Clinical Pharmacology, Medical Pharmacology, General Pharmacology, Experimental Pharmacology, Applied Pharmacology, Translational Pharmacology, Molecular Pharmacology, Cellular Pharmacology, Biochemical Pharmacology, Systemic Pharmacology, Clinical Pharmacotherapeutics, Rational Drug Use, Evidence-Based Pharmacotherapy, Personalized Medicine, Precision Pharmacology.
- Pharmacokinetics and Pharmacodynamics
Pharmacokinetics, Pharmacodynamics, Clinical Pharmacokinetics, Drug Absorption, Drug Distribution, Drug Metabolism, Drug Excretion, Drug Bioavailability, Bioequivalence Studies, Drug–Drug Interactions, Drug–Food Interactions, Therapeutic Drug Monitoring, Population Pharmacokinetics, Pharmacokinetic–Pharmacodynamic Modelling.
- Clinical and Medical Toxicology
Clinical Toxicology, Medical Toxicology, General Toxicology, Experimental Toxicology, Applied Toxicology, Human Toxicology, Acute and Chronic Poisoning, Drug Overdose, Poisoning Diagnosis and Management, Antidote Therapy, Drug-Induced Toxicity, Toxicological Emergencies, Toxicological Risk Assessment.
- Drug Safety and Pharmacovigilance
Pharmacovigilance, Drug Safety Monitoring, Adverse Drug Reactions, Adverse Drug Events, Medication Errors, Drug-Induced Organ Injury, Post-Marketing Surveillance, Pharmacoepidemiology, Drug Utilization Studies, Drug Safety Assessment, Medication Safety, Benefit–Risk Assessment.
- Organ-Specific Pharmacology and Toxicology
Cardiovascular Pharmacology, Neuropharmacology, Psychopharmacology, Renal Pharmacology, Hepatic Pharmacology, Respiratory Pharmacology, Gastrointestinal Pharmacology, Endocrine Pharmacology, Reproductive Pharmacology, Immunopharmacology, Cardiovascular Toxicology, Neurotoxicology, Hepatotoxicity, Nephrotoxicity, Pulmonary Toxicology, Immunotoxicology, Reproductive and Developmental Toxicology.
- Drug Discovery and Development
Drug Discovery, Drug Design, Medicinal Chemistry, Pharmaceutical Chemistry, Drug Development, Preclinical Drug Evaluation, Experimental Therapeutics, Computational Drug Discovery, Molecular Docking, Structure–Activity Relationships, Drug Screening, Novel Therapeutic Agents, Drug Repurposing, Drug Delivery Systems, Nanopharmacology, Nanotoxicology.
- Clinical Trials and Therapeutic Research
Clinical Trials, Randomized Controlled Trials, Clinical Drug Evaluation, Therapeutic Efficacy Studies, Comparative Drug Studies, Clinical Research Methodology, Bioequivalence Trials, Post-Marketing Clinical Studies, Drug Treatment Outcomes, Clinical Pharmacotherapy, Therapeutic Guidelines, Real-World Evidence Studies.
- Molecular Pharmacology and Pharmacogenomics
Molecular Pharmacology, Cellular Pharmacology, Pharmacogenetics, Pharmacogenomics, Toxicogenomics, Drug Receptor Biology, Receptor Pharmacology, Signal Transduction, Molecular Drug Targets, Gene–Drug Interactions, Epigenetic Pharmacology, Systems Pharmacology, Proteomics, Metabolomics.
- Environmental, Occupational and Chemical Toxicology
Environmental Toxicology, Occupational Toxicology, Industrial Toxicology, Chemical Toxicology, Pesticide Toxicology, Heavy Metal Toxicity, Environmental Pollutants, Toxic Chemical Exposure, Environmental Health Risk Assessment, Ecotoxicology, Food Toxicology, Cosmetic Toxicology, Toxicological Biomarkers.
- Herbal, Natural Product and Traditional Medicine Pharmacology
Herbal Pharmacology, Phytopharmacology, Ethnopharmacology, Natural Product Pharmacology, Medicinal Plant Research, Herbal Drug Evaluation, Phytochemical Toxicology, Herbal Drug Safety, Traditional Medicine Pharmacology, Nutraceutical Pharmacology, Natural Product Drug Discovery, Herb–Drug Interactions.
- Antimicrobial and Cancer Pharmacology
Antimicrobial Pharmacology, Antibiotic Pharmacology, Antiviral Pharmacology, Antifungal Pharmacology, Antiparasitic Pharmacology, Antimicrobial Resistance, Cancer Pharmacology, Oncopharmacology, Anticancer Drug Development, Cancer Chemotherapy, Targeted Therapy, Immunotherapeutic Agents, Chemotherapy-Induced Toxicity.
- Regulatory Pharmacology and Toxicological Sciences
Regulatory Toxicology, Regulatory Pharmacology, Drug Regulatory Affairs, Pharmaceutical Safety Evaluation, Toxicological Testing Methods, Good Laboratory Practices, Good Clinical Practices, Toxicity Testing, Genotoxicity, Mutagenicity, Carcinogenicity, Reproductive Safety Assessment, Drug Approval and Regulatory Compliance.
ABSTRACTING & INDEXING
- Google Scholar
- Crossref
ARCHIVING INFORMATION
- Zenodo - A Universal Repository in OpenAIRE’s Hosted by CERN, Funded by European Commission
- Internet Archive
- PKP Preservation Network - Public Knowledge Project
FOLLOWING CATEGORIES OF MANUSCRIPTS ARE CONSIDERED FOR PUBLICATION
- Review Article
- Research Article
- Case Study
- Clinical Trial
- Community Case Study
- Data Report
- Opinion
- Commentary
- News & Highlights
- Mini Review
- Short Research Communication
- Letter to the Editor
- Methods & Protocols
- Book Review
- Negative Results
- Clinical Debate
- Clinical Images
- Innovations: Technology of The Future, Hypothesis & Clinical Trail Protocols
ETHICAL STANDARDS
Statement of Human and Animal Rights
In the research work where, human subjects or material were involved, all authors should clearly declare that entire experiment work was done as per ethical standards of the responsible committee on human experimentation (both institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000 and 2008. In case of animal experiments, authors should clearly reveal that all experimental procedures were done according to institutional and national guidelines for animal care and laboratory use.
Statement of Informed Consent
Patients have a right to privacy that should not be infringed without informed consent. Identifying information, including patients' names, initials, or hospital numbers, should not be published in written descriptions, photographs, and pedigrees unless the information is essential for scientific purposes and the patient (or parent or guardian) provides written informed consent for publication. Authors should also identify individuals who provide writing assistance and disclose the funding source for this assistance. Identifying details should be omitted if they are not essential. Complete anonymity is difficult to achieve; however, informed consent should be obtained if there is any doubt. For example, masking the eye region in photographs of patients is inadequate to ensure anonymity. If identifying characteristics are altered to protect the patient, such as in genetic pedigrees, authors should guarantee that alterations do not distort scientific meaning.
Publication Ethics and Publication Malpractice Statement
Editor’s responsibilities
Editors are responsible for taking the decision to publish a submitted manuscript on the basis of quality, originality, scope and relevance. Editor and editorial staff will maintain the necessary confidentiality of the manuscript and will not use it for any other purpose.
Reviewer’s responsibilities
Reviewers should screen the manuscript for various quality parameters and provide the relevant comments to the editors, which helps them in decision making. Reviewers must carefully check the literature citation, writing quality, experiment setup and scientific relevance of results. A special emphasis will be given on plagiarism checking of manuscript. Reviewers will also maintain the necessary confidentiality of the manuscript and will not use it for any other purpose. Conflicts of interest regarding collaboration with authors of submitted manuscript must be disclosed to the editor, and then excluded from the review process.
Author’s responsibilities
Manuscript submitted to our journal should not be published in any other journal, and also not currently under consideration by another journal. The manuscript must be approved by all the co-authors for their scientific contents and submission for publication in the journal.
Authors should provide the details of their experimental work so that others may replicate the experiments. Authors should prepare their raw data and submit it to editors/reviewers upon request.
Any kind of fraud or unethical practices like Fabrication/ Falsification of Data, Plagiarism, Unacceptable Author Contribution, Citation Manipulation, Concurrent Submissions, and Redundant Publications are totally unacceptable. All authors must give a clear statement that no unethical practices are involved in this research work. All authors have a responsibility to disclose the conflicts of interests and financial support for work, if any.
After publication of the manuscript, if any error is found in research work, the chief-editor should be immediately informed. After deep discussion with the research team, the manuscript will be corrected or even withdrawn.
Literature source for ethical standard:
- Committee on Publication Ethics (COPE). Code of Conduct and Best-Practice Guidelines for Journal Editors.
- Graf C, Wager E, Bowman A, Fiack S, Scott-Lichter D, Robinson A. Best Practice Guidelines on Publication Ethics: a publisher's perspective. Int J Clin Pract Suppl. 2007 Jan;61(152):1-26.
- International Committee of Medical Journal Editors. Uniform Requirements for Manuscripts Submitted to Biomedical Journals: Writing and Editing for Biomedical Publication. 2006.
- American Psychological Association. Ethical Principles of Psychologists and Code of Conduct, Section 8 ‘Research and Publication’.
- American Chemical Society. Ethical Guidelines.