Discuss the Advances in Micro fluidic Technologies for Efficient Blood Cell Separation.

Instruction Please follow the abstract I have provided to write the review article. Organize the microfluidic technologies for blood cell separation and include the latest advancements in the article. If you have an approach that is stronger than the abstract I have provided, please feel free to discuss any aspects you prefer from the original structure. The article should include a total of 3-4 tables or diagrams (at least one diagram). I don’t have any specific ideas for these at the moment, so please discuss any ideas you have for tables or diagrams with me before creating them. Additionally, please cite 30 to 50 references, preferably the latest ones. I have also uploaded a similar review article for your reference. Title: Advances in Microfluidic Technologies for Efficient Blood Cell Separation AbstractThe separation of blood cells using microfluidic devices has emerged as a critical technique in biomedical research and clinical diagnostics. This review provides a comprehensive overview of recent advancements in microfluidic technologies for blood cell separation, highlighting the principles of operation, design considerations, and performance metrics of various microfluidic platforms. Key methods, such as deterministic lateral displacement, hydrodynamic filtration, and dielectrophoresis, are discussed in detail. The review also explores innovative applications in disease diagnostics, personalized medicine, and the development of lab-on-a-chip systems. Challenges and future directions in the field are addressed, emphasizing the potential of microfluidic blood cell separation to revolutionize medical diagnostics and therapeutic monitoring. Reference review papers:1. Microfluidic Blood Separation: Key Technologies and Critical Figures of Merithttps://doi.org/10.3390/mi141121172. Recent advances in microfluidic technologies for separation of biological cellshttps://pubmed.ncbi.nlm.nih.gov/32797312/DOI: 10.1007/s10544-020-00510-7

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