Based on the data reported in many publications mentioning the drug loading of mesoporous silica nanoparticles (MSNs) since the drug precipitate as a crystalline form and requires separation. That was so confusing, and I want to discuss if this test is an actual test or a myth.
We have here a three mentioned scenarios
1- Measuring drug loading without washing MSNs after solvent evaporation or deposition or incipient witness method. So, why we measure drug loading, actually the drug loading efficiency should be 100%, and if there is a decrease in the drug content, that means only one thing "the preparation method was messy or inadequate preparation."
2- Measuring drug loading after washing with ethanol is inaccurate because ethanol will dissolve depending on drug solubility. Also, ethanol can dissolve amorphous and crystalline drugs, so there is no preferential separation.
3- Measuring drug loading after washing with water or water containing a minimum amount of ethanol. In this method, the drug is dissolved to the limit of drug solubility in water or the water-ethanol mixture.
..........................................
-What is useful to do with crystalline form is to measure the degree of crystallinity in loaded mesoporous silica.
-If there is a washing method you can suggest to separate crystalline form efficiently out of the loaded carrier, please discuss it.