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 单克隆抗体应对最终药物的生产,配制,递送和稳定性方面的挑战 407条(本栏目收费,不能显示细节,电话13136136841)
oxidation mechanism,51,62 51 62 
physical degradation,67,77 67 77 
Stability-indicating assays development,103,105 103 105 
Stainless steel needles,157,159 157 159 
Standard capillary electrophoresis instrumentation,167 167 
Static light scattering (SLS),136,172,174 136 172 174 
Sterile water for injection (SWFI),178,181 178 181 
Stokes,165 165 
Storage modulus (G′),169 169 
Subcutaneous (SC),2,3,71 2 3 71 
administration,131 131 
analytical tools for high-concentration formulation development,136 136 
bioavailability of high-concentration mAb formulation,135,136 135 136 
challenge of formulating,131,132 131 132 
impact on delivery due to high viscosity,132,134 132 134 
manufacturing impact of high-concentration SC formulations,134,135 134 135 
infusion devices,153,155 153 155 
Sugars as lyoprotectants,115,117 115 117 
Surface plasmon resonance (SPR),29 29 
Surface-active agents,110,111 110 111 
Surfactants,110,111 110 111 
Tangential flow filtration (TFF),134,135,139,140 134 135 139 140 
Target product profile (TPP),1 1 
Tert-Butylhydroperoxide (TBHP),54,56 54 56 
Tertiary structure,68,69 68 69 
Thawing,75,77 75 77 
Tissue plasminogen activator (tPA),20 20 
Glass capillary viscometry,165,166 165 166 
Hagen Poiseuille equation,132,167,168 132 167 168 
Halozyme technology,148,150 148 150 
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