Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Intrinsically Chiral Excimers: Water-Compatible Trityl-Based Nanoparticles as Tailored Dual Emitters of Circularly Polarized Luminescence in the Vis or NIR Regions.

Small (Weinheim an der Bergstrasse, Germany)·2026
Same author

Luminescent Trityl-based Diradicaloids: A Theoretical and Experimental Assessment of Charge-Resonance in Low-Lying Excited States.

Chemistry (Weinheim an der Bergstrasse, Germany)·2025
Same author

Activating Thermoplastic Polyurethane Surfaces with Poly(ethylene glycol)-Based Recombinant Human α-Defensin 5 Monolayers for Antibiofilm Activity.

ACS applied bio materials·2025
Same author

Targeted nanoliposomes to improve enzyme replacement therapy of Fabry disease.

Science advances·2024
Same author

3D Printing as a Strategy to Scale-Up Biohybrid Hydrogels for T Cell Manufacture.

ACS applied materials & interfaces·2024
Same author

Nanothermometer Based on Polychlorinated Trityl Radicals Showing Two-Photon Excitation and Emission in the Biological Transparency Window: Temperature Monitoring of Biological Tissues.

Small methods·2023

Related Experiment Video

Updated: Mar 13, 2026

Solid Lipid Nanoparticles SLNs for Intracellular Targeting Applications
08:19

Solid Lipid Nanoparticles SLNs for Intracellular Targeting Applications

Published on: November 17, 2015

18.7K

Lipid-based nanovesicles for nanomedicine.

N Grimaldi1, F Andrade2, N Segovia2

  • 1Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus Universitari de Bellaterra, 08193, Cerdanyola del Vallès, Spain. vecianaj@icmab.es ventosa@icmab.es and Nanomol Technologies SA, Módul de Recerca B, Campus Universitari de Bellaterra, 08193, Cerdanyola del Vallès, Spain.

Chemical Society Reviews
|October 11, 2016
PubMed
Summary

New non-liposomal lipid-based nanovesicles (L-NVs) offer advantages over traditional liposomes for drug delivery. Compressed fluid technologies show promise for scalable L-NV production, advancing nanomedicine towards clinical applications.

More Related Videos

Preparation and Characterization of Nanoliposomes for the Entrapment of Bioactive Hydrophilic Globular Proteins
11:30

Preparation and Characterization of Nanoliposomes for the Entrapment of Bioactive Hydrophilic Globular Proteins

Published on: August 31, 2019

25.5K
Formulating and Characterizing Lipid Nanoparticles for Gene Delivery using a Microfluidic Mixing Platform
09:41

Formulating and Characterizing Lipid Nanoparticles for Gene Delivery using a Microfluidic Mixing Platform

Published on: February 25, 2021

25.7K

Related Experiment Videos

Last Updated: Mar 13, 2026

Solid Lipid Nanoparticles SLNs for Intracellular Targeting Applications
08:19

Solid Lipid Nanoparticles SLNs for Intracellular Targeting Applications

Published on: November 17, 2015

18.7K
Preparation and Characterization of Nanoliposomes for the Entrapment of Bioactive Hydrophilic Globular Proteins
11:30

Preparation and Characterization of Nanoliposomes for the Entrapment of Bioactive Hydrophilic Globular Proteins

Published on: August 31, 2019

25.5K
Formulating and Characterizing Lipid Nanoparticles for Gene Delivery using a Microfluidic Mixing Platform
09:41

Formulating and Characterizing Lipid Nanoparticles for Gene Delivery using a Microfluidic Mixing Platform

Published on: February 25, 2021

25.7K

Area of Science:

  • Nanomedicine and advanced drug delivery systems.
  • Focus on lipid-based nanovesicles (L-NVs) for therapeutic applications.

Background:

  • Liposomes, the first generation of L-NVs, are established drug carriers but face challenges like poor stability and high production costs.
  • Non-liposomal L-NVs represent a newer generation with potential to overcome liposome limitations.

Approach:

  • Review of diverse L-NVs, emphasizing novel non-liposomal designs.
  • Exploration of current and cutting-edge L-NV production methods, particularly compressed fluid technologies.
  • Discussion of L-NV applications and future perspectives in nanomedicine.

Key Points:

  • Non-liposomal L-NVs offer enhanced properties compared to traditional liposomes.
  • Compressed fluid technologies are highlighted as a scalable and efficient production method.
  • L-NVs show significant potential for clinical translation and market entry.

Conclusions:

  • Non-liposomal L-NVs are poised to advance nanomedicine by addressing limitations of current liposomal formulations.
  • Scalable production methods like compressed fluid technology are crucial for the successful transition of L-NVs from research to market.
  • Further development and clinical evaluation are necessary to fully realize the potential of this new generation of nanovesicles.