Related Experiment Video
Updated: Apr 12, 2026

09:58
Preparation and In Vitro Characterization of Magnetized miR-modified Endothelial Cells
Published on: May 2, 2017
8.1K
Nanocarriers in gene therapy: a review
Journal of Biomedical Nanotechnology
|May 23, 2015
Summary
Nanocarriers offer a promising alternative to viral vectors for gene therapy, improving efficacy and reducing side effects. Further research is needed to overcome challenges for successful clinical application of these nanomaterials.
Area of Science:
- Biomedical Engineering
- Molecular Biology
- Nanotechnology
Background:
- Gene therapy is evolving beyond DNA delivery to include RNA-based therapeutics.
- Viral vectors, while effective, present significant safety and cost concerns.
- Non-viral vectors, particularly nanocarriers, are emerging as safer and more efficient alternatives.
Purpose of the Study:
- To review the advancements and applications of nanocarriers in gene therapy.
- To discuss the limitations and challenges associated with nanomaterial-based gene delivery.
Main Methods:
- Review of current literature on nanocarrier development for gene therapy.
- Analysis of various nanocarrier types (liposomes, nanoparticles, dendrimers, etc.).
- Evaluation of advantages and disadvantages of viral versus non-viral gene delivery systems.
Main Results:
- Nanocarriers demonstrate distinct characteristics and potential for enhanced gene therapy efficacy.
- Various nanocarrier platforms, including liposomes and nanoparticles, are detailed.
- Viral vectors exhibit limitations such as immunogenicity, carcinogenicity, poor specificity, and high cost.
Conclusions:
- Nanocarriers represent a viable alternative to viral vectors for gene therapy.
- Addressing current challenges is crucial for the successful clinical translation of nanocarrier-based gene delivery.
- Continued research into nanomaterials is essential for advancing gene therapy applications.
Related Concept Videos
Gene Therapy
28.2K
Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be...
28.2K
Gene Therapy
4.8K
4.8K
Site-Targeted Drug Delivery Systems: Polymeric Carriers
125
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...
125
Microorganisms in Medicine and Therapeutics
1.4K
Microorganisms play a fundamental role in vaccine development, gene therapy, and therapeutic production. Their biological properties are harnessed to advance medicine and public health. Beyond immunization, microorganisms contribute to gut health, antibiotic synthesis, and genetic disease treatment.Live Attenuated and Inactivated VaccinesLive attenuated vaccines, such as the measles, mumps, and rubella (MMR) vaccine, utilize weakened forms of pathogens to closely resemble natural infections.
1.4K

