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-19 L, a 260 nM liposome solution will encapsulate a fraction of the total ap; 0.08 as determined by the product of the per liposome times the total number of liposome particles in solution.
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Note that both the green and red traces have the same initial slope, that is, the samples in contact with DOPC have the same initial Stern-Volmer fluorescence quenching constant
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Briefly, immobilization involved (a) the functionalization of glass coverslips with Vectabond reagent, (b) the covalent tethering of a 100/1 PEG (MW 5000)/biotin-PEG (MW 5000) mixture to the coverslip surface, (c) the assembly of a flow chamber, (d) a 10 min incubation of a streptavidin solution and (e) a 3-4 min incubation of the 5 pM liposome solution under study followed by a steady flow of buffer solution to remove all non-immobilized liposomes and non-encapsulated MPS-PPV.
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Briefly, immobilization involved (a) the functionalization of glass coverslips with Vectabond reagent, (b) the covalent tethering of a 100/1 PEG (MW 5000)/biotin-PEG (MW 5000) mixture to the coverslip surface, (c) the assembly of a flow chamber, (d) a 10 min incubation of a streptavidin solution and (e) a 3-4 min incubation of the 5 pM liposome solution under study followed by a steady flow of buffer solution to remove all non-immobilized liposomes and non-encapsulated MPS-PPV.
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