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Nanobiotechnology in Drug Delivery and Diagnostics Course

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

This one-month Nanobiotechnology program offers insights into the applications of nanotechnology in drug delivery and diagnostics. Participants will explore the design of nanomaterials for targeted therapies, diagnostics, and personalized medicine, preparing for careers in nanomedicine.

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Aim

This course explores how nanobiotechnology enables advanced drug delivery and diagnostic systems, combining nanomaterials, biomolecules, and bioengineering principles to improve targeting, sensitivity, and therapeutic performance. Participants will learn nanoparticle classes (lipid nanoparticles, polymeric nanoparticles, inorganic nanostructures), surface functionalization, controlled release strategies, and how nano-enabled diagnostics (biosensors, imaging agents, lab-on-chip concepts) are designed and evaluated. The program emphasizes mechanistic understanding, characterization, safety-by-design, translational constraints, and responsible communication—without providing wet-lab protocols or clinical treatment advice. The course culminates in a capstone where learners create a Nano-Enabled Delivery + Diagnostics Blueprint for a selected disease area or point-of-care need.

Program Objectives

  • Nanobiotech Foundations: Understand how nanoscale properties influence biological interactions and performance.
  • Nanocarrier Platforms: Learn major delivery systems (lipid, polymer, inorganic, hybrid) and their tradeoffs.
  • Targeting & Controlled Release: Understand passive/active targeting and stimuli-responsive release concepts.
  • Nano-Diagnostics: Explore biosensor and imaging concepts enabled by nanomaterials.
  • Characterization Literacy: Learn what key measurements mean (size, zeta potential, loading, stability, sensitivity).
  • Safety & Translation: Understand toxicity considerations, regulatory awareness, and scale-up constraints.
  • Evidence-Based Design: Learn how to define KPIs, compare baselines, and communicate results responsibly.
  • Hands-on Outcome: Create an end-to-end blueprint for a nano-enabled therapeutic/diagnostic concept.

Program Structure

Module 1: Introduction to Nanobiotechnology in Medicine

  • Why nanoscale matters: surface area, transport, cellular uptake, and bio-distribution concepts.
  • Key applications: targeted delivery, controlled release, imaging contrast, and point-of-care diagnostics.
  • Translational constraints: stability, manufacturability, cost, and regulatory expectations (overview).
  • Defining success: efficacy signals, safety signals, and measurable design KPIs.

Module 2: Biological Barriers and Targeting Principles

  • Barriers to delivery: bloodstream stability, immune clearance, tissue penetration, and cellular uptake.
  • Passive vs active targeting: size effects, microenvironment concepts, ligand targeting overview.
  • Protein corona and bio-identity: how surfaces influence biological behavior (conceptual).
  • Design tradeoffs: targeting vs toxicity, stability vs release, and circulation time vs clearance.

Module 3: Nanocarriers for Drug Delivery (Platforms and Tradeoffs)

  • Lipid-based systems: liposomes and lipid nanoparticles (LNPs) overview and use-cases.
  • Polymeric nanoparticles: biodegradable polymers, micelles, and nanogels (conceptual).
  • Inorganic nanostructures: gold, silica, iron oxide—key properties and safety considerations (overview).
  • Hybrid systems: combining materials for multi-functional delivery and imaging.

Module 4: Controlled Release and Stimuli-Responsive Systems

  • Release mechanisms: diffusion, degradation, and triggered release (high-level).
  • Stimuli triggers: pH, temperature, enzymes, redox environment, and light (conceptual).
  • Designing for kinetics: burst release vs sustained release and how to evaluate profiles.
  • Practical limitations: variability across patients/tissues and robustness requirements.

Module 5: Surface Functionalization and Bioconjugation Concepts

  • Why surface chemistry matters: stability, targeting, stealth, and biocompatibility.
  • Ligands and targeting moieties: antibodies, peptides, aptamers (conceptual overview).
  • PEGylation and alternatives: circulation time and immune interactions (overview).
  • Quality concerns: batch consistency, binding performance, and long-term stability.

Module 6: Nano-Enabled Diagnostics and Biosensing

  • Diagnostics landscape: lab-based vs point-of-care; sensitivity/specificity and limit-of-detection concepts.
  • Nano-biosensors: plasmonics, electrochemical nanointerfaces, and fluorescence enhancement concepts.
  • Lab-on-chip concepts: microfluidics overview and integration with nano-sensing.
  • Sample-to-answer workflow thinking: sample prep constraints and usability.

Module 7: Nano-Imaging and Theranostics (Conceptual)

  • Imaging modalities overview: MRI/CT/optical/ultrasound and how nano-agents can enhance contrast.
  • Theranostics concept: combining therapy + diagnostics for feedback-driven interventions.
  • Signal interpretation: background noise, biodistribution effects, and quantification challenges.
  • Safety-by-design: dose, clearance pathways, and long-term considerations.

Module 8: Characterization, Stability, and Quality-by-Design (QbD)

  • Key characterization metrics: size distribution (DLS), morphology (TEM/SEM), surface charge (zeta), and concentration.
  • Drug loading and encapsulation efficiency concepts; release profile measurement logic.
  • Stability: aggregation, leakage, oxidation, and storage condition effects.
  • QbD mindset: critical quality attributes (CQAs) and control strategies (overview).

Module 9: Translation, Safety, and Regulatory Awareness

  • Toxicity considerations: immune responses, off-target accumulation, and material-specific risks (overview).
  • Manufacturing scale-up: reproducibility, sterile processing awareness, and supply chain constraints.
  • Regulatory landscape awareness: documentation, validation, and risk management mindset.
  • Responsible communication: differentiating concept validation vs clinical readiness.

Final Project

  • Create a Nano-Enabled Drug Delivery and Diagnostics Blueprint for a selected application.
  • Include: unmet need, target biology (high-level), platform choice, design KPIs, characterization plan, safety considerations, and translational roadmap.
  • Example projects: nanoparticle delivery concept for an antimicrobial strategy, nano-biosensor concept for early biomarker detection, theranostic design blueprint, or a point-of-care nano-enabled diagnostic workflow for a community health setting.

Participant Eligibility

  • Students and professionals in Biotechnology, Biomedical Engineering, Nanotechnology, Chemistry, Pharmacy, or related fields.
  • Researchers interested in drug delivery, biosensors, diagnostics, and translational nanomedicine.
  • Industry professionals exploring nano-enabled platforms for R&D and product development.
  • Basic knowledge of biology/chemistry is helpful but not required.

Program Outcomes

  • Platform Understanding: Ability to compare nanocarrier and nano-diagnostic platforms and select based on constraints.
  • Design Thinking: Ability to define measurable KPIs and build an evidence-based design rationale.
  • Characterization Literacy: Understanding of key measurements and how they link to performance and safety.
  • Translation Awareness: Understanding scale-up, quality, and regulatory considerations in nano-enabled products.
  • Portfolio Deliverable: A complete blueprint suitable for academic review, grant planning, or early-stage product scoping.

Program Deliverables

  • Access to e-LMS: Modules, case studies, and design worksheets.
  • Design Toolkit: Platform selection matrix, KPI definition template, characterization plan template, and safety-by-design checklist.
  • Case Exercises: Carrier selection tradeoff task, diagnostics sensitivity/specificity planning, and stability risk assessment worksheet.
  • Project Guidance: Mentor feedback for the final blueprint refinement.
  • 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
  • Bio-Nano Diagnostics & Biosensing Associate
  • Nanomaterials Characterization & QA Associate
  • Translational R&D Associate (Nano-Enabled Therapeutics)
  • Biomedical Product Innovation Associate

Job Opportunities

  • Biotech & Pharma R&D: Drug delivery research, formulation, and translational development teams.
  • Diagnostics & MedTech: Biosensor R&D, point-of-care development, and validation support roles.
  • Nanotechnology Companies: Nano-enabled materials and healthcare platform development.
  • Research Institutes & Universities: Nanobiotech labs working on delivery systems and advanced diagnostics.
  • Innovation Labs & Startups: Early-stage nano-enabled therapeutics and diagnostic product development.
Category

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

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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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