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BioWorld - Thursday, February 19, 2026
Home » Topics » Science » Drug design, drug delivery and technologies

Drug design, drug delivery and technologies
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Illustration of Toxoplasma gondii tachyzoites
Drug design, drug delivery & technologies

Parasite could deliver therapeutic proteins to the brain

Aug. 13, 2024
By Mar de Miguel
Infection or cure? Scientists from Tel Aviv University and the University of Glasgow genetically modified the Toxoplasma gondii to bring a protein inside neurons. The novelty of using a protozoan that can travel from the gut to parasitize the CNS contrasts with the possibility of causing a disease. The scientists are already working on how to avoid it.
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Illustration of HIV cell entry
HIV/AIDS

Treating HIV with defective, thieving HIV

Aug. 13, 2024
By Mar de Miguel
A strategy inspired by deficient HIV replication could be used as a treatment to reduce viral load in patients living with HIV and help control the pandemic of the retrovirus. Scientists from the University of California San Francisco want to use HIV against itself by using a parasitic version of the pathogen.
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Illustration of Toxoplasma gondii tachyzoites
Drug design, drug delivery & technologies

Parasite could deliver therapeutic proteins to the brain

Aug. 8, 2024
By Mar de Miguel
Infection or cure? Scientists from Tel Aviv University and the University of Glasgow genetically modified the Toxoplasma gondii to bring a protein inside neurons. The novelty of using a protozoan that can travel from the gut to parasitize the CNS contrasts with the possibility of causing a disease. The scientists are already working on how to avoid it.
Read More
pumpkinseed
Patents

Pumpkinseed reveals systems for label-free analyte detection

Aug. 2, 2024
By Simon Kerton
In Pumpkinseed Technologies Inc.’s first public patenting, the company’s co-founders describe their development of new proteomics platform that merges nanotechnology, biochemistry, silicon photonics and machine learning for high-resolution phenotyping to deliver new biological insights.
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Non-Hodgkin lymphoma cells in the blood flow
Cancer

Combining MALT1 and BCL2 inhibitors could block B-cell lymphomas

Aug. 1, 2024
Scientists from Abbvie Inc. and the Department of Lymphoma and Myeloma, University of Texas MD Anderson Cancer Center have discovered a new allosteric MALT1 inhibitor, ABBV-MALT1, for the treatment of certain types of diffuse large B-cell lymphoma (DLBCL).
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Illustration of brain in head highlighting the blood-brain barier.
Neurology/psychiatric

Montara secures seed funding for binary brain pharmacology

July 31, 2024
Montara Therapeutics Inc. has received $8 million seed financing from several investors to further its development of its ’binary pharmacology’ for diseases of the brain.
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RNA illustration
Drug design, drug delivery & technologies

Triastek, Biontech to collaborate on orally available RNA drugs

July 24, 2024
Triastek Inc. and Biontech SE have entered into a research collaboration and platform technology license agreement for the development of RNA therapeutics for oral delivery based on Triastek’s Melt Extrusion Deposition (MED) 3D printing technology.
Read More
transdermal patch
Patents

Wearable acoustic patch developed for transdermal drug delivery

July 23, 2024
By Simon Kerton
A team of researchers from the University of Northumbria filed for protection of a flexible transdermal patch taht uses surface acoustic wave  technology they believe offers distinct advantages over traditional transdermal patches.
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Model showing DNA methyltransferase (DNMT3) bound to DNA
Neurology/psychiatric

Epigenetic editor silences prion protein gene in the brain

July 22, 2024
Epigenetic silencing could prevent the production of proteins that cause pathologies. CHARM (coupled histone tail for autoinhibition release of methyltransferase), a DNA methylation-based editor, suppressed transcription of prion proteins in the brains of mice.
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Silhouette of child and brain
Genetic/congenital

Reactivation of UBE3A gene to treat Angelman syndrome

July 15, 2024
Epigenetic desilence of the paternal allele of the gene that causes Angelman syndrome (AS) could be used to treat this disease for which there are currently no approved therapies.
Read More
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