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BioWorld - Sunday, May 10, 2026
Home » Topics » Drug design, drug delivery and technologies, BioWorld Science

Drug design, drug delivery and technologies, BioWorld Science
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Drug Design, Drug Delivery & Technologies

Ordaōs and Nonexomics establish mini-protein research collaboration

Sep. 29, 2022
Ordaōs Bio and Nonexomics LLC have established a proof-of-concept research collaboration to create customized mini-proteins.
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Illustration of scientist cutting DNA with scissors.
Drug Design, Drug Delivery & Technologies

CRISPR activation mouse model can turn on previously silenced genes

Sep. 28, 2022
By Tamra Sami
Researchers at the Walter and Eliza Hall Institute of Medical Research (WEHI) in Melbourne, Australia, have developed a new genome editing technique than can activate any gene, including those that have been silenced, allowing new drug targets and causes of drug resistance to be explored.
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Concept art for blood sugar.
Endocrine/Metabolic

EASD 2022: Sugar-scarfing muscle could treat type 2 diabetes

Sep. 22, 2022
By Mar de Miguel
A simple injection of muscle tissue could control glucose in patients with type 2 diabetes (T2D). Genetic modification of skeletal muscle and subsequent intramuscular implantation could increase blood sugar absorption and become an effective and long-lasting treatment for this pathology. “We took mice satellite cells and we genetically altered to overexpress GLUT4,” Hagit Shoyhet, researcher at the Levenberg lab of stem-cell and tissue engineering, Technion (Israel), said at the European Association for the study of Diabetes (EASD) 58th Annual Meeting.
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Synthetic biology

Angiogenesis and tissue regeneration through synthetic cell growth factors

Sep. 21, 2022
By Mar de Miguel
Synthetic cells (SCs) armed with recombinant growth factors could contribute to tissue regeneration and healing by promoting angiogenesis. This technology opens the door to its application in other therapies such as transplants that require the remodeling or formation of new blood vessels. In addition, they mark the way to produce intracorporeal biological drugs or the inhibition of the angiogenesis process itself when it comes to blocking the irrigation of a tumor.
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Liver organoid
Drug Design, Drug Delivery & Technologies

Emulate launches new AAV transduction application for Liver-Chip

Sep. 20, 2022
Emulate Inc. has launched a new adeno-associated virus (AAV) transduction application for the Liver-Chip that enables gene therapy researchers to test the delivery efficiency and safety of AAV vectors in a validated, human-relevant model of the liver and get results in weeks.
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Drug Design, Drug Delivery & Technologies

Combination strategy enables brain-specific kinase inhibition

Sep. 15, 2022
By Anette Breindl
Using a two-drug combination, researchers at the University of California at San Francisco (UCSF) have been able to achieve brain-specific inhibition of several kinases.
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Drug Design, Drug Delivery & Technologies

Bioengineered multifunctional exosomes evoke cancer immunity

Sep. 14, 2022
By Mar de Miguel
The design of genetically modified exosomes that combine multiple targets killed cancer cells and conferred immunity against them. Scientists at the University of Southern California (USC) applied bioengineering techniques to introduce up to four antitumor functions in the same type of extracellular vesicles and destroy EGFR-positive triple-negative breast cancer (TNBC) tumor cells.
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3D reconstructions of images of HIV vaccine
HIV/AIDS

Experimental HIV vaccine protects macaques against infection

Sep. 13, 2022
By Mar de Miguel
A new vaccine that uses the native-like HIV-1 envelope (Env) trimer CH505 and a Toll-like receptor (TLR) 7/8 agonist adjuvant, successfully evaluated in macaques, generated potent polyclonal neutralizing antibodies (nAbs) and a high protection against the infection of the homologous simian-human immunodeficiency virus (SHIV).
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Illustration of pill being analyzed
Drug Design, Drug Delivery & Technologies

Fuzionaire collaborates with McGill to create silicon-based drug candidates

Sep. 2, 2022
Fuzionaire Inc. has established a collaborative research agreement with McGill University to leverage the company's proprietary alkali metal catalyst platform in creating novel heterocyclic, biologically active, silicon-containing scaffolds and new silicon-based drug candidates.
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Native E. coli can be used for intestinal transgene delivery to potentially treat human diseases

Aug. 16, 2022
Live bacterial therapeutics (LBTs) that engraft in the gut and provide persistent beneficial functions to the host have emerged as a promising strategy against a wide range of diseases.
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