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NANOmedX: Future of Drug Delivery

USD $59.00 USD $249.00Price range: USD $59.00 through USD $249.00

Aim: The aim of the NANOmedX workshop is to illuminate the game-changing role of nanotechnology in drug delivery. By fostering knowledge exchange and collaboration, the workshop empowers participants to leverage nanomedicine’s potential for precise and effective therapies, bridging the gap between research and real-world applications to advance patient care.

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SKU: NSTC004 Category: Tags: , , ,

Aim

NANOmedX: Future of Drug Delivery trains participants to understand and design next-generation drug delivery systems using nanomedicine principles—from material selection and formulation to targeting strategies, characterization, and translational thinking. You will learn how nano-enabled carriers improve stability, biodistribution, controlled release, and therapeutic index, while also understanding safety, manufacturing, and regulatory fundamentals.

Program Objectives

  • Understand Modern Drug Delivery: Why conventional delivery fails and how nanocarriers solve key limitations.
  • Learn Nanocarrier Platforms: Liposomes, polymeric nanoparticles, micelles, dendrimers, SLNs/NLCs, and inorganic systems.
  • Targeting & Release Design: Passive vs active targeting, stimuli-responsive release, and controlled delivery strategies.
  • Formulation Know-How: Encapsulation, loading, stability, surface functionalization, and scale-up considerations.
  • Characterization Skills: Size, charge, morphology, release kinetics, and basic in vitro performance testing.
  • Safety & Translation: Toxicity basics, immunogenicity, biodistribution, quality-by-design, and regulatory overview.
  • Hands-on Application: Build a capstone nanomedicine delivery concept with a complete design rationale.

Program Structure

Module 1: Why the Future Needs Smarter Drug Delivery

  • Limitations of conventional dosage forms: instability, off-target toxicity, low bioavailability.
  • Drug delivery goals: enhance efficacy, reduce side effects, improve patient compliance.
  • Biological barriers: mucus, cell membranes, RES clearance, BBB (conceptual).
  • Where nanomedicine fits: precision delivery, controlled release, and combination therapies.

Module 2: Nanomedicine Fundamentals for Drug Delivery

  • Core concepts: size effects, surface chemistry, corona formation, and interaction with biology.
  • Key design parameters: size, PDI, zeta potential, hydrophobicity, ligand density.
  • Drug properties vs carrier choice: solubility, stability, permeability, and dose constraints.
  • Formulation strategy map: from therapeutic objective to carrier platform selection.

Module 3: Nanocarrier Platforms (What to Use and When)

  • Lipid systems: liposomes, SLNs, NLCs—advantages and use cases.
  • Polymer systems: PLGA-type concepts, polymeric NPs, micelles, nanogels.
  • Dendrimers and supramolecular carriers (intro-level).
  • Inorganic and hybrid systems: silica, gold, iron oxide (conceptual + safety considerations).

Module 4: Loading, Encapsulation & Stability Design

  • Encapsulation approaches: physical entrapment, adsorption, conjugation (concepts).
  • Drug loading vs encapsulation efficiency—how to interpret results.
  • Stability: aggregation, leakage, oxidation/hydrolysis; storage and lyophilization basics.
  • Surface modification: PEGylation concepts, charge tuning, ligand attachment.

Module 5: Targeting Strategies & Triggered Release

  • Passive targeting: EPR effect and its real-world constraints (balanced view).
  • Active targeting: antibodies, peptides, aptamers, small-molecule ligands.
  • Stimuli-responsive delivery: pH, enzymes, redox, temperature, light, magnetic triggers.
  • Designing release profiles: burst vs sustained release and application matching.

Module 6: Characterization Toolkit for Nanomedicine

  • Size and distribution: DLS concepts, PDI interpretation, common artifacts.
  • Surface charge: zeta potential meaning and limitations.
  • Morphology: TEM/SEM basics; when imaging is necessary.
  • Drug release kinetics and data interpretation; basic fitting concepts (intro).

Module 7: Biological Evaluation (In Vitro to In Vivo Thinking)

  • Cell uptake and trafficking concepts; endosomal escape basics.
  • Biocompatibility and cytotoxicity screening: what tests show (and don’t show).
  • Protein corona, immune recognition, and clearance pathways (conceptual).
  • Translational challenges: biodistribution, PK/PD, and dosage form constraints.

Module 8: Manufacturing, Scale-Up, Quality & Regulatory Basics

  • Scale-up realities: reproducibility, batch variability, sterility, and stability.
  • Quality-by-Design (QbD) mindset for formulation development (intro).
  • CMC basics: critical quality attributes (CQAs) and critical process parameters (CPPs).
  • Regulatory overview: safety packages, characterization expectations, and documentation.

Final Project

  • Design a nano-enabled drug delivery strategy for a chosen indication (cancer, infection, CNS, inflammation, etc.).
  • Select the carrier platform and justify based on drug + biological barrier constraints.
  • Define targeting/release approach, characterization plan, and safety considerations.
  • Deliverables: concept note + formulation plan + characterization checklist + risk/translation notes.

Participant Eligibility

  • Students and professionals in Biotechnology, Pharmacy, Nanotechnology, Biomedical Engineering, Chemistry, Materials Science
  • Researchers working in formulation, drug delivery, cancer biology, infectious diseases, or biomaterials
  • R&D professionals in pharma/biotech seeking a structured understanding of nanomedicine delivery systems
  • Anyone with a life-science background aiming to enter nanomedicine and advanced therapeutics

Program Outcomes

  • Platform Understanding: Ability to select suitable nanocarrier types for specific drugs and use cases.
  • Design Thinking: Confidence in designing targeting and release strategies with realistic constraints.
  • Characterization Literacy: Ability to interpret common nanomedicine characterization results correctly.
  • Translation Awareness: Understanding of safety, scale-up, and regulatory expectations at a foundation level.
  • Portfolio Deliverable: A capstone nanomedicine design proposal that you can showcase.

Program Deliverables

  • Access to e-LMS: Full access to course materials, templates, and reference readings.
  • Nanomedicine Toolkit Pack: Carrier selection matrix, loading/release planning sheets, characterization checklist.
  • Case Studies: Nano-delivery examples (lipid/polymer/inorganic) and design trade-offs.
  • Hands-on Project Support: Guided capstone review and feedback.
  • Final Assessment: Certification after assignments + capstone submission.
  • e-Certification and e-Marksheet: Digital credentials provided upon successful completion.

Future Career Prospects

  • Nanomedicine / Drug Delivery Research Associate
  • Formulation Scientist (Nano-formulations)
  • Drug Product Development Associate
  • Translational Nanotechnology Associate
  • Regulatory/CMC Support Associate (Nanomedicine)

Job Opportunities

  • Pharma & Biotech Companies: Advanced formulation, targeted therapeutics, delivery platform R&D.
  • CDMOs & Formulation Labs: Nano-formulation development, optimization, characterization, tech transfer.
  • Academic & Research Institutes: Nanomedicine design, biomaterials research, translational programs.
  • Hospitals & Clinical Research Teams: Translational evaluation support (non-clinical R&D roles).
  • HealthTech Startups: Rapid prototyping of delivery systems and proof-of-concept studies.
Category

E-LMS, E-LMS+Videos, E-LMS+Videos+Live Lectures

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Certification

  • Upon successful completion of the workshop, participants will be awarded a Certificate of Completion, validating their skills and knowledge in advanced AI ethics and regulatory frameworks. This certification can be added to your LinkedIn profile or shared with employers to demonstrate your commitment to ethical AI practices.

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