Results 11 to 20 of about 21,694,813 (356)

Contribution of Nanotechnologies to Vaccine Development and Drug Delivery against Respiratory Viruses

open access: yesPPAR Research, 2021
According to the Center for Disease Control and Prevention (CDC), the coronavirus disease 2019, a respiratory viral illness linked to significant morbidity, mortality, production loss, and severe economic depression, was the third-largest cause of death ...
Mahdi Ftouh   +5 more
doaj   +1 more source

Human organs-on-chips for disease modelling, drug development and personalized medicine

open access: yesNature reviews genetics, 2022
The failure of animal models to predict therapeutic responses in humans is a major problem that also brings into question their use for basic research.
D. Ingber
semanticscholar   +1 more source

Conversion of Aquaculture Waste into Biomedical Wealth: Chitin and Chitosan Journey

open access: yesAdvances in Materials Science and Engineering, 2022
Biowaste originating from aquaculture sector represents a potential feedstock to produce value-added substances and materials like chitin and chitosan. They are the long chain polymers of N-acetylglucosamine polymers with huge industrial and biomedical ...
Jerrine Joseph   +8 more
doaj   +1 more source

Anti-tuberculosis treatment strategies and drug development: challenges and priorities

open access: yesNature Reviews Microbiology, 2022
Despite two decades of intensified research to understand and cure tuberculosis disease, biological uncertainties remain and hamper progress. However, owing to collaborative initiatives including academia, the pharmaceutical industry and non-for-profit ...
V. Dartois, E. Rubin
semanticscholar   +1 more source

Long-term stability predictions of therapeutic monoclonal antibodies in solution using Arrhenius-based kinetics

open access: yesScientific Reports, 2021
Long-term stability of monoclonal antibodies to be used as biologics is a key aspect in their development. Therefore, its possible early prediction from accelerated stability studies is of major interest, despite currently being regarded as not ...
Drago Kuzman   +5 more
doaj   +1 more source

Alzheimer's disease drug development pipeline: 2022

open access: yesAlzheimer's & Dementia, 2022
Alzheimer's disease (AD) represents a global health crisis. Treatments are needed to prevent, delay the onset, slow the progression, improve cognition, and reduce behavioral disturbances of AD.
J. Cummings   +6 more
semanticscholar   +1 more source

Intranasal drug delivery: opportunities and toxicologic challenges during drug development

open access: yesDrug Delivery and Translational Research, 2021
Over the past 10 years, the interest in intranasal drug delivery in pharmaceutical R&D has increased. This review article summarises information on intranasal administration for local and systemic delivery, as well as for CNS indications.
Lea-Adriana Keller   +2 more
semanticscholar   +1 more source

Ranking mAb–excipient interactions in biologics formulations by NMR spectroscopy and computational approaches

open access: yesmAbs, 2023
Excipients are added to biopharmaceutical formulations to enhance protein stability and enable the development of robust formulations with acceptable physicochemical properties, but the mechanism by which they confer stability is not fully understood ...
Chunting Zhang   +11 more
doaj   +1 more source

Structural and functional properties of SARS-CoV-2 spike protein: potential antivirus drug development for COVID-19

open access: yesActa Pharmacologica Sinica, 2020
Coronavirus disease 2019 is a newly emerging infectious disease currently spreading across the world. It is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Yuan Huang   +4 more
semanticscholar   +1 more source

Review: Role of Model-Informed Drug Development Approaches in the Lifecycle of Drug Development and Regulatory Decision-Making

open access: yesPharmaceutical Research, 2022
Model-informed drug development (MIDD) is a powerful approach to support drug development and regulatory review. There is a rich history of MIDD applications at the U.S. Food and Drug Administration (FDA).
R. Madabushi   +4 more
semanticscholar   +1 more source

Home - About - Disclaimer - Privacy