The samples that we're using consist of a hydrophobic drug compound and a nanopolymer (PEG-siPMNT). We synthesized it by dialysis in DW as the following step: dissolve drug in DMF, then add the polymer and TEOS, mixed well. Following by loading into the dialysis bag. DW was changed in 4hr, 8hr, 12hr and 18hr. Collected samples were supposed to be a water soluble nanoformulated solution. Instead, we yieled a gel-like state (as shown).

We wanted to be clear on which factor caused the gelation. Many attemps before yield expected results, but the gelation has become more frequent from time to time.

Sorry for my terible English. We wish you a great day!

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