Publications by authors named "A R CURRERI"

There is preliminary evidence that the anticonvulsant medication Zonisamide (ZON) may be an effective, well-tolerated treatment for alcohol use disorder (AUD). However, further evaluation of its efficacy for treating patients with AUD is needed, and much remains unknown about ZON's therapeutic mechanisms. The present study aimed to evaluate the efficacy and tolerability of ZON in a double-blind, placebo-controlled, randomized trial.

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Cellular hitchhiking is an emerging strategy for the control of adoptively transferred immune cells. Hitchhiking approaches are primarily mediated by adhesion of nano and microparticles to the cell membrane, which conveys an ability to modulate transferred cells local drug delivery. Although T cell therapies employing this strategy have progressed into the clinic, phagocytic cells including dendritic cells (DCs) are much more challenging to engineer.

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Article Synopsis
  • mRNA is being explored as a treatment for various diseases, but traditional lipid nanoparticles (LNPs) used for delivery can cause safety and efficacy issues due to systemic exposure.
  • A new delivery system using a deep eutectic solvent (cholinium malonate) enables precise control over mRNA expression levels at the injection site, allowing for a 68% increase in local muscle expression while reducing unwanted liver expression by 72%.
  • This innovative approach enhances existing LNP formulations without needing complex lipid redesign, improving the targeted delivery of mRNA for potential medical applications.
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Ribonucleic acid (RNA) therapeutics are being actively researched as a therapeutic modality in preclinical and clinical studies. They have become one of the most ubiquitously known and discussed therapeutics in recent years in part due to the ongoing coronavirus pandemic. Since the first approval in 1998, research on RNA therapeutics has progressed to discovering new therapeutic targets and delivery strategies to enhance their safety and efficacy.

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Proteins are among the most common therapeutics for the treatment of diabetes, autoimmune diseases, cancer, and metabolic diseases, among others. Despite their common use, current protein therapies, most of which are injectables, have several limitations. Large proteins such as monoclonal antibodies (mAbs) suffer from poor absorption after subcutaneous injections, thus forcing their administration by intravenous injections.

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