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   1 nd 6-propionyl-2-(dimethylamino)naphthalene (Prodan).                                                
     2 esponse to the excited states of Laurdan and Prodan.                                                 
     3 new fluorophores are structurally related to Prodan.                                                 
     4 e significantly red-shifted when compared to Prodan.                                                 
     5 ity-sensitive emission comparable to that of PRODAN and displays high quantum yields in a range of so
  
     7 es N,N-dimethyl-6-propionyl-2-naphthylamine (prodan) and coumarin 153 (C153) in a series of toluene/d
     8 bumins, a hydrophobic fluorescent indicator (PRODAN), and a hydrophobic additive (deoxycholate) to de
     9 N), 6-propionyl-2-dimethylamino-naphthalene (PRODAN), and Lissamine rhodamine B 1,2-dihexadecanoyl-sn
    10 uorescent probes used (bis-pyrene, nystatin, prodan, and merocyanine) were chosen because they differ
  
  
  
  
    15 he 6-propionyl-2-(dimethylamino)naphthalene (Prodan) fluorescence spectra for both lipids are consist
  
  
  
    19 ent properties and partition coefficients of Prodan in model membranes of phosphatidylcholines and ph
    20 f 7HSAP1 with the solvatochromic fluorophore PRODAN indicated that the nanotubes could encapsulate sh
  
  
  
  
  
  
  
    28 s of 2-propionyl-6-dimethylaminonaphthalene (PRODAN) with twisted carbonyl groups were investigated a
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