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en rouge) et de la GSH (en bleu) sous excitation laser continue En haut : image d'une culture cellulaire marquée par des particules GSH (a) en début d'excitation, (b) après 10 min d'excitation laser intense. En bas : évolution de la fluorescence et de la GSH en fonction du temps, p.20 ,
En haut : spectres d'excitation laser à différentes longueurs d'onde (A) 720 nm nm et (D) 970 nm et spectres d'émission GSH correspondants En bas : images de cellules HTB-182 avec agent de contraste fluorescent (en rouge) exposés à des nanocristaux GSH (en bleu) La ligne du bas correspond aux mêmes images avec uniquement le signal de GSH ,
détection de marqueurs (ou SHRIMPS, acronyme anglais pour Second Harmonic Radiation IMaging ProbeS) de 300 nm sous une épaisseur de 120 µm d'un tissu de queue de souris ,
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(a) échantillon de sang en lumière blanche, (b) en lumière blanche et détection GSH et (c) GSH uniquement, p.32 ,
(a) et (b) Marqueurs GSH présents dans les germes. (c) Marqueurs dans une pousse, p.33 ,
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en rouge) et I Z (en bleu) en fonction de la polarisation incidente ? pour une solution de pNA, p.43 ,
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En encart) Diagramme DRX (Co, K?) des nanopoudres obtenues par centrifugation des échantillons A, B, C et D. F représente le diagramme de référence (ICSD 154674) de l'iodate de fer, Evolution du signal HRS en fonction du temps pour une microémulsion à W=6, [AOT]=0,2 M, [IO ? 3 ]=0,3 M et, p.97 ,
une suspension de BFO. (b) Comportement exponentiel de l'intensité HRS en fonction de la concentration, p.112 ,
Les tailles en intensité obtenues par DLS sont respectivement de 218 nm, 191 nm, 445 nm et 420 nm pour les suspensions de KNbO 3 , LiNbO 3 A, LiNbO 3 B et KTP. Les distributions considérées sont de type log-normale, p.84 ,