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doi: 10.4158/EP161365.GL

This includes transparent reporting of synthesis conditions, purification steps, surface chemistry, size and charge data, PLQY, and biological testing protocols, alongside in vitro and in vivo dosing regimens with validated positive and negative controls [174]

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Kramr EA, Armtrong DL, Ikeda S, Wayner MJ, Harding JW, et al

Timing Cycles Around Clearance Windows For competition athletes, ensure ample clearance time between your last injection and potential testing

And that didn't happen until liposomal technology emerged in the late 1990s