I made Plga peptide Nanoparticles . Before lypholization when I do DLS then 2 peaks are visibl but the background peak is only less than 1 percent then I centrifuge it at 600 rpm for 2 minute and then I take the supernatant and discard the debris / pellet then again I do DLS now I get 1 peak only and good results . Then when I do DLS after lypholization again it's showing 2 peaks . Why this is so ? I dissolved the peptide nps uniformly with distilled water but even then it's showing 2 peaks

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