Here is the blurb I wrote in response to customer question regarding Magsil and Spinosin, @TheFire210 …The last lines in parentheses contains the kind of answer you seek, I believe.
General recommendations for MagSil PR:
Solvent should be non-polar (e.g., an alkane, such as n-heptane), NOT alcohol.
Use 10X MagSil PR weight to contaminated cannabinoid product weight… I.e., 10g MagSil to 1g distillate.
Use MagSil PR in a column, typically as (normal phase) chromatography stationary phase, rather than as a simple filtration medium. It is best to use MagSil PR as the 2nd to last step in your pesticide remediation protocol… The last step is pH equilibration of the product by washing with pure distilled water (with NaCl, then without), until the pH of the pure water after washing is the same as it was before washing. This pH is normally 6.2 to 6.8 at typical room temperatures.
I can say with a high degree of certainty that MagSil should be an effective stationary phase in the retention of spinosoids due to its polarity, structure and effective pH (when in contact with water or molecules of opposing effective pH character, like spinosoids). Also, this effect would be best employed in combination with mobile phase (solvent) of normal (straight chain) alkanes, like n-butane (C4) to n-heptane (C7)… so it is suitable for BHO systems with in-line CRC (color remediation chromatography) columns, probably those with increasingly polar & effectively acidic media layers in the direction of flow (for example, Alumicel B or MagSil on top, then the other of the two, then Silica gel, then Alumicel N, then Alumicel A, then acid-activated clay and/or charcoal like T-41).