STRATI Journal of Pharmaceutical Sciences and Drug Development

The journal aims to:

• Promote high-quality research and knowledge dissemination in pharmaceutical sciences and drug development.
• Facilitate interdisciplinary collaboration among drug discovery, formulation, pharmacokinetics, and regulatory sciences.
• Support innovation in drug design, delivery systems, and therapeutic strategies.
• Encourage research that addresses challenges in drug safety, efficacy, and patient adherence.
• Provide a forum for discussing emerging trends, technologies, and regulatory issues in pharmaceuticals.

The scope includes but is not limited to:

• Drug discovery and medicinal chemistry.
• Pharmacology and toxicology studies.
• Pharmaceutical formulation and drug delivery systems.
• Pharmacokinetics and pharmacodynamics.
• Biopharmaceutics and bioavailability studies.
• Clinical pharmacy and therapeutics.
• Regulatory affairs and quality assurance.
• Novel technologies in drug development and manufacturing.

Detailed Themes

The journal welcomes manuscripts on a broad range of topics including but not limited to:

Drug Discovery and Medicinal Chemistry

• Design and synthesis of novel therapeutic compounds
• Structure-activity relationships and molecular modeling
• Natural products and phytochemicals
• High-throughput screening and lead optimization

Pharmacology and Toxicology Studies

• Mechanisms of drug action and receptor pharmacology
• Preclinical toxicology and safety assessments
• Pharmacogenomics and personalized pharmacotherapy
• Drug interactions and adverse drug reactions

Pharmaceutical Formulation and Drug Delivery Systems

• Development of novel drug delivery platforms (e.g., nanoparticles, liposomes)
• Controlled release and targeted delivery systems
• Stability and compatibility studies
• Excipients and formulation optimization

Pharmacokinetics and Pharmacodynamics

• Absorption, distribution, metabolism, and excretion (ADME) studies
• Bioavailability and bioequivalence assessments
• Modeling and simulation of drug behavior
• Dose-response relationships

Biopharmaceutics and Bioavailability Studies

• In vitro and in vivo correlation studies
• Dissolution testing and method development
• Biowaivers and regulatory considerations
• Impact of formulation variables on bioavailability

Clinical Pharmacy and Therapeutics

• Clinical trials and evidence-based drug therapy
• Therapeutic drug monitoring and patient compliance
• Pharmacoeconomics and health outcomes research
• Medication management and optimization

Regulatory Affairs and Quality Assurance

• Regulatory guidelines and compliance
• Good manufacturing practices (GMP)
• Quality control and assurance in pharmaceutical production
• Pharmacovigilance and post-marketing surveillance

Novel Technologies in Drug Development and Manufacturing

• Use of AI and machine learning in drug design
• 3D printing of pharmaceuticals
• Continuous manufacturing and process analytical technology
• Biosimilars and biopharmaceuticals development

Send your paper to Email: strat.institute@gmail.com