barriers to liposomal gene delivery: from application site to the target

Authors

hamid r. moghimi school of pharmacy, shahid beheshti university of medical sciences, tehran, iran

mostafa saffari department of pharmaceutics, school of pharmacy, islamic azad university, tehran, iran

crispin r. dass school of pharmacy, faculty of health sciences, curtin university, perth 6845, australia

abstract

abstractgene therapy is a therapeutic approach to deliver genetic material into cells to alter their function in entire organism. one promising form of gene delivery system (dds) is liposomes. the success of liposome-mediated gene delivery is a multifactorial issue and well-designed liposomal systems might lead to optimized gene transfection particularly in vivo. liposomal gene delivery systems face different barriers from their site of application to their target, which is inside the cells. these barriers include presystemic obstacles (epithelial barriers), systemic barriers in blood circulation and cellular barriers. epithelial barriers differ depending on the route of administration. systemic barriers include enzymatic degradation, binding and opsonisation. both of these barriers can act as limiting hurdles that genetic material and their vector should overcome before reaching the cells. finally liposomes should overcome cellular barriers that include cell entrance, endosomal escape and nuclear uptake. these barriers and their impact on liposomal gene delivery will be discussed in this review.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Barriers to liposomal gene delivery: from application site to the target

AbstractGene therapy is a therapeutic approach to deliver genetic material into cells to alter their function in entire organism. One promising form of gene delivery system (DDS) is liposomes. The success of liposome-mediated gene delivery is a multifactorial issue and well-designed liposomal systems might lead to optimized gene transfection particularly in vivo. Liposomal gene delivery systems...

full text

Barriers to liposomal gene delivery: from application site to the target

AbstractGene therapy is a therapeutic approach to deliver genetic material into cells to alter their function in entire organism. One promising form of gene delivery system (DDS) is liposomes. The success of liposome-mediated gene delivery is a multifactorial issue and well-designed liposomal systems might lead to optimized gene transfection particularly in vivo. Liposomal gene delivery systems...

full text

Barriers to Liposomal Gene Delivery: from Application Site to the Target

Gene therapy is a therapeutic approach to deliver genetic material into cells to alter their function in entire organism. One promising form of gene delivery system (DDS) is liposomes. The success of liposome-mediated gene delivery is a multifactorial issue and well-designed liposomal systems might lead to optimized gene transfection particularly in vivo. Liposomal gene delivery systems face di...

full text

from linguistics to literature: a linguistic approach to the study of linguistic deviations in the turkish divan of shahriar

chapter i provides an overview of structural linguistics and touches upon the saussurean dichotomies with the final goal of exploring their relevance to the stylistic studies of literature. to provide evidence for the singificance of the study, chapter ii deals with the controversial issue of linguistics and literature, and presents opposing views which, at the same time, have been central to t...

15 صفحه اول

Niosomes from Preparation to Application in Drug Delivery

Introduction: In recent years, the treatment strategy for infectious and autoimmune diseases has significantly changed. Up to now, cancer treatment has been conducted on the basis of clinical and pathological methods. The most common cancer treatments is limited to chemotherapy, radiation therapy and surgery. However, cancer treatment is still not optimal. Common challenges for treatment of cer...

full text

Microglial Barriers to Viral Gene Delivery

In this issue of Neuron, Tufail et al. present an underlying mechanism for microglia-mediated elimination of virally transduced cells in the central nervous system. These findings could contribute to the development of improved gene therapies for various neurological disorders by exploring why microglia destroy viable cells following viral infection.

full text

My Resources

Save resource for easier access later


Journal title:
iranian journal of pharmaceutical research

جلد ۱۵، شماره Special Issue، صفحات ۳-۱۷

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023