Related Experiment Video
Updated: Jun 17, 2026

07:53
Encapsulation of Cancer Therapeutic Agent Dacarbazine Using Nanostructured Lipid Carrier
Published on: April 26, 2016
Multifunctional core-shell polymeric nanoparticles for transdermal DNA delivery and epidermal Langerhans cells
Po-Wei Lee1, Sheng-Hsiang Hsu, Jin-Sheng Tsai
1Department of Chemical Engineering, National Tsing Hua University, Hsinchu, Taiwan 30013, ROC.
Biomaterials
|December 26, 2009
Summary
This study presents a novel core-shell nanoparticle for DNA immunization, enabling gene delivery to skin Langerhans cells (LCs). The nanoparticles track LC migration and gene expression in lymph nodes, showing potential for immunotherapy.
Area of Science:
- Immunology
- Nanotechnology
- Biomedical Engineering
Background:
- Skin's immune reactivity makes it a prime site for DNA immunization.
- Antigen-presenting cells like Langerhans cells (LCs) are abundant in the skin.
- Efficient DNA delivery systems are crucial for effective DNA immunization.
Purpose of the Study:
- To develop a multifunctional core-shell nanoparticle system for transdermal DNA delivery.
- To utilize nanoparticles for tracking Langerhans cell migration and gene expression.
- To explore the potential of this system in immunotherapy and vaccine development.
Main Methods:
- Fabrication of core-shell nanoparticles with a PLGA core (loaded with quantum dots) and a glycol chitosan shell (adsorbed with reporter gene).
- Transdermal delivery of nanoparticles into the epidermis using a gene gun.
- Characterization of nanoparticles using fluorescence spectrophotometry, TEM, EDX, and XRD.
- In vivo assessment in a mouse model to evaluate transfection, migration, and gene expression.
Main Results:
- Nanoparticles confirmed to have a core-shell structure with quantum dots in the core.
- pH-dependent surface charge of nanoparticles facilitated intracellular DNA release.
- Successful transfection of DNA into epidermal Langerhans cells (LCs) via gene gun delivery.
- Demonstrated migration of transfected LCs and reporter gene expression in skin-draining lymph nodes.
Conclusions:
- The developed core-shell nanoparticle system is effective for transdermal DNA delivery and immunization.
- The system allows for ultrasensitive monitoring of Langerhans cell migration and gene expression.
- This technology holds significant potential for advancing immunotherapy and vaccine development.
More Related Videos
Related Concept Videos
Site-Targeted Drug Delivery Systems: Polymeric Carriers
Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
Transdermal Drug Delivery Systems
Transdermal drug delivery systems (TDDS) enable the controlled release of drugs across the skin into systemic circulation. They are particularly advantageous for drugs with short half-lives or narrow therapeutic indices, as they maintain consistent plasma concentrations and reduce the risk of subtherapeutic or toxic levels.TDDS are categorized into monolithic, reservoir, and mixed systems. Monolithic systems embed the drug in a polymer matrix, where diffusion governs release. Reservoir systems...
Modified-Release Drug Delivery Systems: Site-Targeted
Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.

