Strategies for delivering therapeutics across the blood–brain barrier
GC Terstappen, AH Meyer, RD Bell… - Nature Reviews Drug …, 2021 - nature.com
Achieving sufficient delivery across the blood–brain barrier is a key challenge in the
development of drugs to treat central nervous system (CNS) disorders. This is particularly …
development of drugs to treat central nervous system (CNS) disorders. This is particularly …
[HTML][HTML] Manufacturing challenges and rational formulation development for AAV viral vectors
A Srivastava, KMG Mallela, N Deorkar… - Journal of pharmaceutical …, 2021 - Elsevier
Adeno-associated virus (AAV) has emerged as a leading platform for gene delivery for
treating various diseases due to its excellent safety profile and efficient transduction to …
treating various diseases due to its excellent safety profile and efficient transduction to …
SARS-CoV-2 crosses the blood–brain barrier accompanied with basement membrane disruption without tight junctions alteration
L Zhang, L Zhou, L Bao, J Liu, H Zhu, Q Lv… - Signal transduction and …, 2021 - nature.com
SARS-CoV-2 has been reported to show a capacity for invading the brains of humans and
model animals. However, it remains unclear whether and how SARS-CoV-2 crosses the …
model animals. However, it remains unclear whether and how SARS-CoV-2 crosses the …
Adeno-associated virus (AAV) as a vector for gene therapy
MF Naso, B Tomkowicz, WL Perry III, WR Strohl - BioDrugs, 2017 - Springer
There has been a resurgence in gene therapy efforts that is partly fueled by the identification
and understanding of new gene delivery vectors. Adeno-associated virus (AAV) is a non …
and understanding of new gene delivery vectors. Adeno-associated virus (AAV) is a non …
Variants of the adeno-associated virus serotype 9 with enhanced penetration of the blood–brain barrier in rodents and primates
The development of gene therapies for the treatment of diseases of the central nervous
system has been hindered by the limited availability of adeno-associated viruses (AAVs) that …
system has been hindered by the limited availability of adeno-associated viruses (AAVs) that …
[HTML][HTML] The GPI-linked protein LY6A drives AAV-PHP. B transport across the blood-brain barrier
Efficient delivery of gene therapy vectors across the blood-brain barrier (BBB) is the holy
grail of neurological disease therapies. A variant of the neurotropic vector adeno-associated …
grail of neurological disease therapies. A variant of the neurotropic vector adeno-associated …
Overcoming the blood–brain barrier. challenges and tricks for CNS drug delivery
LA Bors, F Erdő - Scientia Pharmaceutica, 2019 - mdpi.com
Treatment of certain central nervous system disorders, including different types of cerebral
malignancies, is limited by traditional oral or systemic administrations of therapeutic drugs …
malignancies, is limited by traditional oral or systemic administrations of therapeutic drugs …
Fantastic AAV gene therapy vectors and how to find them—random diversification, rational design and machine learning
Parvoviruses are a diverse family of small, non-enveloped DNA viruses that infect a wide
variety of species, tissues and cell types. For over half a century, their intriguing biology and …
variety of species, tissues and cell types. For over half a century, their intriguing biology and …
Blood–brain barrier: emerging trends on transport models and new-age strategies for therapeutics intervention against neurological disorders
The integrity of the blood–brain barrier (BBB) is essential for normal central nervous system
(CNS) functioning. Considering the significance of BBB in maintaining homeostasis and the …
(CNS) functioning. Considering the significance of BBB in maintaining homeostasis and the …
Viral vectors for neural circuit mapping and recent advances in trans-synaptic anterograde tracers
Viral tracers are important tools for neuroanatomical mapping and genetic payload delivery.
Genetically modified viruses allow for cell-type-specific targeting and overcome many …
Genetically modified viruses allow for cell-type-specific targeting and overcome many …