janoshik
Subscriber
I assume the client has a reason to protect the email there, so no. You can ask them to have the client name anonymized and share the full report.
Follow along with the video below to see how to install our site as a web app on your home screen.
Note: This feature may not be available in some browsers.
i understand. appreciate it.I assume the client has a reason to protect the email there, so no. You can ask them to have the client name anonymized and share the full report.
We don't use standalone UV, but HPLC.Hello, where can I found such information. how is GH tested by you. for example when you test GH vials do you consider that there are other excipients, do you consider interference factor? like some protective substances like for example glycin or trehalose (both of these substances have UV absorption peaks. These two interfering factors should be eliminated) and so one were added.
I know that HPLC is used for testing (Because HPLC usually uses ultraviolet detectors for detection), because there could be excipients contains like glycine as a protective agent and others. This glycine has strong unexpected absorption, and HPLC needs to be manually excluded when processing report scores. Excipients cannot be counted as magazines for points.We don't use standalone UV, but HPLC.
Cheers
The very point of HPLC is so that there is no interference, because you separate the components such as glycine in time, far away from the compounds of interest, such as GH and GH related impurities.I know that HPLC is used for testing (Because HPLC usually uses ultraviolet detectors for detection), because there could be excipients contains like glycine as a protective agent and others. This glycine has strong unexpected absorption, and HPLC needs to be manually excluded when processing report scores. Excipients cannot be counted as magazines for points.
So again my question is do you consider interference factor when count purity of GH in your tests or count as GH sample has only manitol for example or concider it is pure GH?
I prefer to stay on the safe side with my claims.Without getting too in the weeds from stats standpoint, @janoshik quotes his HPLC method as 5% margin of error (one sided hence +/- 5?) .
Code:https://www.janoshik.com/details/
This is why you have both labs report the results of 10 replicates haha. Everyone would be very enlightened by the distribution.
Exciting.
Postscript: would be useful for both labs to share their method RSV (relative standard deviation) based on internal work.
Fantastic. N = ? here. How many reps?I prefer to stay on the safe side with my claims.
View attachment 278293
We do multiplicates and I have RSD for this particular sample available.
know that HPLC is used for testing (Because HPLC usually uses ultraviolet detectors for detection
It's HPLC-DAD gradient methods, some details are here:
The very point of HPLC is so that there is no interference, because you separate the components such as glycine in time, far away from the compounds of interest, such as GH and GH related impurities.
I think you are using wrong terms to ask your question due to language barrier and mean whether the excipients are counted into impurities, which they are not.
Not only mannitol, trehalose or other saccharides don't show on UV at all, the excipients that show are not counted among the impurities.
...only one stupid enough to count glycine used as an excipient as an impurity is @Dr JIM
know that HPLC is used for testing (Because HPLC usually uses ultraviolet detectors for detectionIt's HPLC-DAD gradient methods, some details are here:
"only mannitol, trehalose or other saccharides don't show on UV at all"so you claim that glycin .... don't show on UV at all?
no it doesn't in the region that GH is commonly detected at.so you claim that trehalose don't show on UV at all?
Please, don't be arrogant enough to attempt to school me when you are clueless.I think you also in fact has barrier maybe not in language but while asking your laborants,
I said we don't use standalone UV, which is a different machine to HPLC with UV detection, that lacks the separation component of chromatography, thus is susceptible to interference from other UV absorbing compounds, which is something you've mistakenly talked about due to your lack of mastery of English lanugauge, I didn't say we don't use UV/DAD for detection on our HPLC.because when I asked about UV absorption peaks you did not understand and I needed to remind you that HPLC usually uses ultraviolet detectors for detection
Shame on me, but just two. When they come so close together, the statistical probability of both of them being way off is so low there's no reason to keep going. Don't think we've ever had to go above 6.Fantastic. N = ? here. How many reps?
Thanks.
"only mannitol, trehalose or other saccharides don't show on UV at all"
Does glycine sound like a saccharide to you?
no it doesn't in the region that GH is commonly detected at.
exactly, this is why I recommend to ask laborants more before replyI think you are trying to lead a discussion that is above both your chemistry and language skillset and thus is of no benefit to either of us, so please, cease such attempts.
You are either really really really stupid or an intentional troll.
Shame on me for giving you a benefit of doubt.
I'm leaning towards the second as you are a new account that blocked its profile immediately unpon registering, so I will kindly request that you sod off.