DNA vaccines are ideal candidates for global vaccination purposes because they are
inexpensive and easy to manufacture on a large scale such that even people living in low …

Chimeric receptor T cells (CAR-T) can effectively cure leukemia; however, there are two
limitations: a complicated preparation process ex vivo and cytokine release syndrome …

Combining the bio-therapeutics with chemotherapeutic drugs can assist in augmenting the
therapeutic standards by increasing the efficacy and decreasing the toxicity. Hence, in the …

Lipid nanoparticles (LNPs) can be used as delivery vehicles for nucleic acid biotherapeutics.
In fact, LNPs are currently being used in the Pfizer/BioNTech and Moderna COVID-19 …

Nanoparticles have been widely used for nonviral gene delivery. Recently, cationic hybrid
nanoparticles consisting of two different materials were suggested as a promising delivery …

Cell-derived nanovesicles (CDNs) have been recently investigated as novel drug delivery
systems (DDSs), due to the preservation of key features from the cell membrane of their …

Gene therapy offers an alternative and promising avenue to lung cancer treatment. Here, we
used dibenzocyclooctyne (DBCO)‐branched primers to construct a PTEN gene nanovector …

The aim of the present work was to produce a cationic solid lipid nanoparticle (SLN) as non-
viral vector for protein delivery. Cationic SLN were produced by double emulsion method …

Purposes The objective of this study is to develop a versatile gene carrier based on
lipopeptides capable of delivering genetic material into target cells with minimal cytotoxicity …

In the last few years, our research group has focused on the design and development of
plasmid DNA (pDNA) based systems as devices to be used therapeutically in the biomedical …