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Characterization of nanoparticle uptake by endothelial cells
Jasmine Davda1, Vinod Labhasetwar
1Department of Pharmaceutical Sciences, College of Pharmacy, 986025 Nebraska Medical Center, Omaha, NE 68198-6025, USA.
International Journal of Pharmaceutics
|March 19, 2002
Summary
Biodegradable nanoparticles effectively target endothelial cells for drug and gene therapy. Studies show rapid uptake and cytoplasmic localization, confirming biocompatibility and potential for sustained therapeutic effects.
Area of Science:
- Biomaterials Science
- Cell Biology
- Drug Delivery Systems
Background:
- The endothelium plays a crucial role in biological systems, making it a key target for therapeutic interventions.
- Developing effective methods for delivering drugs or genes to endothelial cells is essential for various medical applications.
Purpose of the Study:
- To characterize the uptake of poly (DL-lactide-co-glycolide) nanoparticles by endothelial cells in vitro.
- To assess the influence of incubation time and nanoparticle concentration on cellular uptake.
- To evaluate the biocompatibility of these nanoparticles with endothelial cells.
Main Methods:
- Formulation of nanoparticles using poly (DL-lactide-co-glycolide) incorporating bovine serum albumin and 6-coumarin.
- Incubation of nanoparticles with endothelial cells in cell culture.
- Confocal microscopy to visualize nanoparticle localization within cells.
- Mitogenic assays to assess cellular viability and biocompatibility.
Main Results:
- Nanoparticle cellular uptake was dependent on incubation time and concentration.
- Confocal microscopy revealed rapid nanoparticle uptake and predominant cytoplasmic localization.
- Mitogenic studies confirmed the biocompatibility of the nanoparticles with endothelial cells.
Conclusions:
- Poly (DL-lactide-co-glycolide) nanoparticles are suitable for targeting endothelial cells.
- These nanoparticles can be used for localized delivery of therapeutic agents or genes.
- Endothelial cell-localized nanoparticles offer potential for sustained drug release and protection from degradation.