Pharmacology and Pharmacy (PHR)

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Pharmacology and Pharmacy (PHR)

Section Information

Pharmacology and Pharmacy focuses on the study of drugs, their mechanisms of action, therapeutic uses, safety profiles, and the science of medication development and delivery. It covers interactions between drugs and biological systems, aiming to optimize treatment outcomes and minimize adverse effects.

Modern research in this field includes pharmacodynamics, pharmacokinetics, toxicology, clinical pharmacology, drug formulation, biotechnology-based therapies, and personalized medicine. Advances in drug delivery systems, nanotechnology, pharmacogenomics, and computational modeling continue to shape therapeutic innovation.

This section publishes experimental studies, clinical research, reviews, and case reports addressing drug development, therapeutic strategies, pharmaceutical technology, medication management, and emerging trends in pharmacological science.

Scope
  • Pharmacodynamics and Drug Mechanisms
    • Cellular and molecular mechanisms of drug action
    • Receptor interactions, signaling pathways, and dose–response relationships
    • Therapeutic targets for emerging diseases
    • Experimental models for pharmacological research
  • Pharmacokinetics and Drug Metabolism
    • Absorption, distribution, metabolism, and excretion of drugs
    • Drug–drug interactions and metabolic pathways
    • Modeling, simulation, and individualized dosing
    • Bioavailability, bioequivalence, and therapeutic monitoring
  • Clinical Pharmacology and Therapeutics
    • Rational prescribing and therapeutic decision-making
    • Adverse drug reactions and pharmacovigilance
    • Special population dosing including pediatric and geriatric care
    • Pharmacogenomics and personalized treatment approaches
  • Pharmaceutical Technology and Drug Formulation
    • Design and development of drug dosage forms
    • Controlled-release systems and nanotechnology-based delivery
    • Stability, compatibility, and quality assessment of formulations
    • Innovation in oral, parenteral, transdermal, and inhalation products
  • Biopharmaceutics and Pharmacokinetic Modeling
    • Drug absorption and physiological barriers
    • In vitro–in vivo correlations and predictive modeling
    • Transporters, enzymes, and regulatory factors
    • Advanced computational tools in drug design
  • Toxicology and Safety Evaluation
    • Mechanisms of drug toxicity and organ-specific effects
    • Preclinical safety testing and risk assessment
    • Environmental and occupational toxicology
    • Antidotes, detoxification strategies, and monitoring
  • Pharmacy Practice and Medication Management
    • Community, clinical, and hospital pharmacy services
    • Medication adherence, counseling, and therapeutic monitoring
    • Drug distribution systems and regulatory frameworks
    • Patient safety, stewardship programs, and quality improvement
  • Biotechnology, Biologics, and Advanced Therapeutics
    • Monoclonal antibodies, vaccines, and cell-based therapies
    • Gene therapy, RNA-based treatments, and targeted therapeutics
    • Bioprocessing, formulation, and stability challenges
    • Regulatory and clinical considerations for biologics
Editorial Board

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Topical Advisory Panel

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Papers Published

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