A historical review of brain drug delivery

WM Pardridge - Pharmaceutics, 2022 - mdpi.com
The history of brain drug delivery is reviewed beginning with the first demonstration, in 1914,
that a drug for syphilis, salvarsan, did not enter the brain, due to the presence of a blood …

Intracellular delivery by membrane disruption: mechanisms, strategies, and concepts

MP Stewart, R Langer, KF Jensen - Chemical reviews, 2018 - ACS Publications
Intracellular delivery is a key step in biological research and has enabled decades of
biomedical discoveries. It is also becoming increasingly important in industrial and medical …

Advances in non-viral DNA vectors for gene therapy

CL Hardee, LM Arévalo-Soliz, BD Hornstein… - Genes, 2017 - mdpi.com
Uses of viral vectors have thus far eclipsed uses of non-viral vectors for gene therapy
delivery in the clinic. Viral vectors, however, have certain issues involving genome …

Emerging therapeutic approaches for cystic fibrosis. From gene editing to personalized medicine

I Pranke, A Golec, A Hinzpeter, A Edelman… - Frontiers in …, 2019 - frontiersin.org
An improved understanding of the cystic fibrosis (CF) transmembrane conductance regulator
(CFTR) protein structure and the consequences of CFTR gene mutations have allowed the …

Dry powder pharmaceutical biologics for inhalation therapy

RYK Chang, MYT Chow, D Khanal, D Chen… - Advanced Drug Delivery …, 2021 - Elsevier
Therapeutic biologics such as genes, peptides, proteins, virus and cells provide clinical
benefits and are becoming increasingly important tools in respiratory medicine. Pulmonary …

Evidence suggesting absence of mitochondrial DNA methylation

M Mechta, LR Ingerslev, O Fabre, M Picard… - Frontiers in …, 2017 - frontiersin.org
Methylation of nuclear genes encoding mitochondrial proteins participates in the regulation
of mitochondria function. The existence of cytosine methylation in the mitochondrial genome …

Inorganic nanomaterial‐mediated gene therapy in combination with other antitumor treatment modalities

G Lin, RA Revia, M Zhang - Advanced functional materials, 2021 - Wiley Online Library
Cancer is a genetic disease originating from the accumulation of gene mutations in a
cellular subpopulation. Although many therapeutic approaches have been developed to …

An insight into non-integrative gene delivery approaches to generate transgene-free induced pluripotent stem cells

KK Haridhasapavalan, MP Borgohain, C Dey, B Saha… - Gene, 2019 - Elsevier
Over a decade ago, a landmark study that reported derivation of induced Pluripotent Stem
Cells (iPSCs) by reprogramming fibroblasts has transformed stem cell research attracting …

Delivering the CRISPR/Cas9 system for engineering gene therapies: Recent cargo and delivery approaches for clinical translation

RA Foley, RA Sims, EC Duggan, JK Olmedo… - … in Bioengineering and …, 2022 - frontiersin.org
Clustered Regularly Interspaced Short Palindromic Repeats associated protein 9
(CRISPR/Cas9) has transformed our ability to edit the human genome selectively. This …

Effects of circular DNA length on transfection efficiency by electroporation into HeLa cells

BD Hornstein, D Roman, LM Arévalo-Soliz… - PloS one, 2016 - journals.plos.org
The ability to produce extremely small and circular supercoiled vectors has opened new
territory for improving non-viral gene therapy vectors. In this work, we compared transfection …