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Blood scarcity is one of the main causes of healthcare disruptions worldwide, with blood shortages occurring at an alarming rate. Over the last decades, blood substitutes has aimed at reinforcing the supply of blood, with several products (e.g., hemoglobin-based oxygen carriers, perfluorocarbons) achieving a limited degree of success. Regardless, there is still no widespread solution to this problem due to persistent challenges in product safety and scalability. In this Review, we describe different advances in the field of blood substitution, particularly in the development of artificial red blood cells, otherwise known as engineered erythrocytes. We categorize the different strategies into natural, synthetic, or hybrid approaches, and discuss their potential in terms of safety and scalability. We identify synthetic engineered erythrocytes as the most powerful approach, and describe erythrocytes from a materials engineering perspective. We review their biological structure and function, as well as explore different methods of assembling a material-based cell. Specifically, we discuss how to recreate size, shape, and deformability through particle fabrication, and how to recreate the functional machinery through synthetic biology and nanotechnology. We conclude by describing the versatile nature of synthetic erythrocytes in medicine and pharmaceuticals and propose specific directions for the field of erythrocyte engineering.
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http://dx.doi.org/10.1002/adfm.202315879 | DOI Listing |
Vaccines (Basel)
July 2025
Immunology and Vaccines Laboratory, Faculty of Natural Sciences, Autonomous University of Queretaro, Santiago de Queretaro 76230, Queretaro, Mexico.
: Bovine babesiosis, caused by the tick-borne apicomplexan parasite spp., is an economically significant disease that threatens the cattle industry worldwide. is the most pathogenic species, leading to high morbidity and mortality in infected animals.
View Article and Find Full Text PDFAppl Radiat Isot
August 2025
Unit of Research in Radiation Biology & Environmental Radioactivity (URRBER), P.G & Research Department of Zoology, The New College (Autonomous), Affiliated to University of Madras, Chennai, Tamil Nadu, 600 014, India. Electronic address:
Radioprotection is a critical necessity in modern society, where synthetic drugs are currently the most prevalent agents used. However, natural compounds are gaining attention as promising radioprotectors due to their reduced adverse effects on human health. This study aims to explore the potential of natural compounds to replace the synthetic radioprotective drug, amifostine.
View Article and Find Full Text PDFWiley Interdiscip Rev Nanomed Nanobiotechnol
August 2025
Department of Pharmaceutical Sciences and Health Outcomes, The Ben and Maytee Fisch College of Pharmacy, The University of Texas at Tyler, Tyler, Texas, USA.
Nanoparticles (NPs) made up of cellular components such as extracellular vesicles (EVs) with a biomimetic outlook have emerged as a revolutionary approach in nanomedicine, providing significant benefits for targeted drug administration, immunotherapy, monitoring therapeutic response, and diagnostic applications. Utilizing the distinctive characteristics of natural cell membranes, membrane proteins, and cellular contents, these biomimetic NPs acquire essential biological functions from their source and biogenesis, including immune evasion, extended circulation, and target recognition, rendering them optimal candidates for therapeutic applications. This review offers a comprehensive examination of the methodologies of EVs infused with synthetic NP systems with the goal of overcoming their respective shortcomings.
View Article and Find Full Text PDFMol Ther Nucleic Acids
September 2025
Department of Bacterial and Parasitic Diseases, WRAIR-AFRIMS, Bangkok 10400, Thailand.
poses significant challenges to malaria control due to its relapsing nature. This study explores the immunogenicity and efficacy of nucleoside-modified mRNA-lipid nanoparticle (LNP) vaccines targeting the . circumsporozoite protein (PvCSP).
View Article and Find Full Text PDFBioorg Chem
August 2025
Department of Pharmacology, Pharmacotherapy and Toxicology, Faculty of Pharmacy, Medical University of Sofia, "Dunav" Str, № 2, 1000 Sofia, Bulgaria.
The strategic application of drug repurposing and repositioning in the design of hybrid molecules represents a promising alternative in contemporary drug discovery. Recent studies have highlighted the anticancer activity of ciprofloxacin derivatives, attributing this effect primary to their capacity to inhibit DNA topoisomerase II. In silico ADME profiling of C3-modyfied ciprofloxacin analogues, have further identified their role as potential P-glycoprotein inhibitors.
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