I believe the HPLC device itself has a computer that is quite familiar with any equation that may apply HD!
(If you WOULD READ the procedure you would KNOW there was no assuming anything especially something as elementary as ensuring the volume comparisons WERE IDENTICAL, COL!)
The problem is quite simple really many are using in-vivo GH and IGF levels as the benchmark for how much each vial of GH should contain and extrapolating THOSE results to determine the validity of an HPLC assay.
This is classic bro science period, so much so that some have bought into this notion TT "blood levels" are more reliable than analytical in vitro testing!
Sorry fellas you've got it ass backwards a MS and HPLC were developed for the very reasons some suggest they are inaccurate, in vitro drug quantification.
It's amazing how some want to rewrite pharmacokinetic laws bc some UGL states they KNOW their GH has a HIGHER concentration (absent ANY analytical testing from what I see) than what THE STANDARD has revealed using a SUB-STANDARD assay such as GH OR IGF levels.
If GH and IGF analyses are so accurate then why oh why doesn't ANY pharmaceutical company use those tests as a
quantitative marker instead of the FDA MANDATED MS and HPLC?
That's the ticket let's determine the concentration of all drugs by FIRST slamming them into humans. Not that we should be concerned about protein binding, GFR, assay timing, influence of other drugs, body weight, half life or their quality bc it will all come out in the wash, absolutely luxurious!
(If you WOULD READ the procedure you would KNOW there was no assuming anything especially something as elementary as ensuring the volume comparisons WERE IDENTICAL, COL!)
The problem is quite simple really many are using in-vivo GH and IGF levels as the benchmark for how much each vial of GH should contain and extrapolating THOSE results to determine the validity of an HPLC assay.
This is classic bro science period, so much so that some have bought into this notion TT "blood levels" are more reliable than analytical in vitro testing!
Sorry fellas you've got it ass backwards a MS and HPLC were developed for the very reasons some suggest they are inaccurate, in vitro drug quantification.
It's amazing how some want to rewrite pharmacokinetic laws bc some UGL states they KNOW their GH has a HIGHER concentration (absent ANY analytical testing from what I see) than what THE STANDARD has revealed using a SUB-STANDARD assay such as GH OR IGF levels.
If GH and IGF analyses are so accurate then why oh why doesn't ANY pharmaceutical company use those tests as a
quantitative marker instead of the FDA MANDATED MS and HPLC?
That's the ticket let's determine the concentration of all drugs by FIRST slamming them into humans. Not that we should be concerned about protein binding, GFR, assay timing, influence of other drugs, body weight, half life or their quality bc it will all come out in the wash, absolutely luxurious!
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