Polymer Drug Delivery Systems
Polymer drug delivery systems represent innovative strategies that utilize polymers as carriers for therapeutic agents, aiming to enhance drug efficacy, bioavailability, and minimize side effects. These systems are pivotal in the pharmaceutical field, garnering significant attention for their potential in achieving controlled drug release. Utilizing polymers as carriers for pharmaceutical agents, these systems are intricately designed to regulate drug release, ultimately improving efficacy, bioavailability, and minimizing side effects. Polymers can be customized to achieve specific drug release profiles, targeting mechanisms, and prolonged therapeutic effects. Available in diverse forms such as nanoparticles, micelles, and hydrogels, polymer drug delivery systems demonstrate versatility in a range of medical applications. Their role is vital in refining drug delivery precision and optimizing therapeutic outcomes. These systems are designed to enhance the efficacy, safety, and controlled release of drugs. Here are key aspects of polymer drug delivery systems:
- Biodegradable Polymers: Biodegradable polymers are a cornerstone of polymer drug delivery systems. These polymers break down into non-toxic byproducts, reducing the need for removal surgeries and minimizing long-term side effects.
- Polymeric Micelles: Amphiphilic block copolymers self-assemble into polymeric micelles, forming nanoscale structures. These micelles can encapsulate hydrophobic drugs, improving their solubility and bioavailability.
- Polymeric Nanofibers: Electrospinning techniques produce polymeric nanofibers that provide a high surface area for drug loading. These nanofibers are explored for applications in tissue engineering and wound healing.
- Responsive Polymers: Smart or responsive polymers undergo changes in their physicochemical properties in response to external stimuli such as temperature, pH, or enzyme activity. This property allows for triggered drug release at specific sites.
- Polymeric Implants: Biodegradable polymeric implants are designed to release drugs gradually over an extended period. These implants are often used for long-term treatment of chronic conditions.
- Polymer-Drug Conjugates: Conjugating drugs directly to polymers enhances their pharmacokinetic properties. Polymer-drug conjugates can improve drug stability, extend circulation time, and facilitate targeted delivery.
Title : Development of novel drug delivery pathways enabled by perillyl alcohol (NEO100), A monoterpene with multifaceted biomedical applications
Axel H Schonthal, University of Southern California, United States
Title : From marker to mechanism: Ligand discovery enables functional analysis of OR51E1, an ectopic olfactory receptor, in prostate cancer
Vladlen Slepak, University of Miami School of Medicine, United States
Title : Hepatotoxic botanicals-shadows of pearls
Consolato M Sergi, University of Alberta, Canada
Title : Tailored cellular environments to enable drug design
Lan Wang, Paretor LLC, United States
Title : Personalized and Precision Medicine (PPM) as a unique healthcare model based on design-inspired biotech- & biopharma-driven applications to secure the human healthcare and biosafety
Sergey Suchkov, N D Zelinskii Institute for Organic Chemistry of the Russian Academy of Sciences, InMedStar and Biona, Russian Federation
Title : Precision diagnostics: Effectiveness of innovative imaging technologies for early detection of lung cancers
Huiqin Yang, ICON Clinical Research Ltd, United Kingdom
Title : Principles and standards for managing healthcare transformation towards personalized, preventive, predictive, participative precision medicine ecosystems
Bernd Blobel, University of Regensburg, Germany
Title : Biocompatible synthesis of non crystalline iron oxide nanoparticles with stable colloidal properties
Lan Wang, Paretor LLC, United States
Title : Design and characterization of gum arabic buccal films for protein drug delivery
Krisztian Pamlenyi, University of Szeged, Hungary
Title : Hydrogen sulfide in sepsis: From bench to bedside
Madhav Bhatia, University of Otago, New Zealand