可药性                        
                
                                
                        
                            血脑屏障                        
                
                                
                        
                            体外                        
                
                                
                        
                            神经科学                        
                
                                
                        
                            药物发现                        
                
                                
                        
                            体内                        
                
                                
                        
                            药物输送                        
                
                                
                        
                            中枢神经系统                        
                
                                
                        
                            生物                        
                
                                
                        
                            计算生物学                        
                
                                
                        
                            纳米技术                        
                
                                
                        
                            生物信息学                        
                
                                
                        
                            材料科学                        
                
                                
                        
                            生物化学                        
                
                                
                        
                            基因                        
                
                                
                        
                            生物技术                        
                
                        
                    
            作者
            
                Snehal Raut,Aditya Bhalerao,Behnam Noorani,Luca Cucullo            
         
                    
        
    
            
            标识
            
                                    DOI:10.1007/978-1-0716-2289-6_2
                                    
                                
                                 
         
        
                
            摘要
            
            Traditional in vitro models can replicate many essential features of drug transport/permeability across the blood-brain barrier (BBB) but are not entirely projecting in vivo central nervous system (CNS) uptake. Species differences fail to translate experimental therapeutics from the research laboratory to the clinic. Improved in vitro modeling of human BBB is vital for both CNS drug discovery and delivery. High-end human BBB models fabricated by microfluidic technologies offer some solutions to this problem. BBB's complex physiological microenvironment has been established by increasing device complexity in terms of multiple cells, dynamic conditions, and 3D designs. It is now possible to predict the therapeutic effects of a candidate drug and identify new druggable targets by studying multicellular interactions using the advanced in vitro BBB models. This chapter reviews the current as well as an ideal in vitro model of the BBB.
         
            
 
                 
                
                    
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