What are the reasons for mass balance failure during forced degradation

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Pharma Growth Hub

Pharma Growth Hub

Күн бұрын

What are the reasons for mass balance failure during forced degradation

Пікірлер: 23
@Dileeppharma
@Dileeppharma 2 жыл бұрын
"You did a great job! sir what a informative presentation."
@rahulkulkarni3037
@rahulkulkarni3037 3 жыл бұрын
Fantastic explanation 👏 Sir
@pankajshah1084
@pankajshah1084 3 жыл бұрын
Nice video sir, very clear voice and clarity, one day you will cross 1M subscribers.
@chandrasekhar-kr2uu
@chandrasekhar-kr2uu 2 жыл бұрын
Really very informative tnx ...
@sambhajimasal928
@sambhajimasal928 3 жыл бұрын
This is wonderful ❤
@visweswararao8049
@visweswararao8049 3 жыл бұрын
Sir, you gave clear all probable reasons to get variation in mass balance. Can please explain about analytical qbd
@rahulgunjal663
@rahulgunjal663 3 жыл бұрын
Sir kindly make video on CAD detector method development in hplc.
@vivekghosh7364
@vivekghosh7364 3 жыл бұрын
Please tell us about the different techniques to check peak purity other than purity angle and threshold or with mass spectroscopic method.
@krish_krish354
@krish_krish354 3 жыл бұрын
For analytical calculation which guidelines chapter have to see. Can you refer
@sbshaikh30
@sbshaikh30 2 жыл бұрын
How to overcome these mass balance issues??.. Plz explain
@ghadahalharbi1814
@ghadahalharbi1814 2 жыл бұрын
Sir please what is your reference? I have looked on ICH Q1E and I don’t find it
@anushapulipati2642
@anushapulipati2642 3 жыл бұрын
Can u please tell me the Different types of RS method,in which case to we go for the diluted standard method,and area normalisation method,and impurity vs impurity method..
@krish_krish354
@krish_krish354 3 жыл бұрын
How to do alkali forced degradation Sample with alkali solution added and kept in oven for degradation time or diluent also added and kept in oven for degradation study. Can you explain sir
@ambikapanda409
@ambikapanda409 3 жыл бұрын
Sir can u tell me about metal degradation,like with cupper and iron
@buddepumohanarao8309
@buddepumohanarao8309 3 жыл бұрын
Sir if degradation impurity have no chromphorcity then what to do for identification.
@suriyasuriya-xt7dt
@suriyasuriya-xt7dt Жыл бұрын
For Api assay method ,force degradation study will be conduct🧐🧐🧐
@mitalipereira446
@mitalipereira446 3 жыл бұрын
In case of higher mass balance where aduct is formed with main ingredient, what do we expect about peak purity, is it passing or failing?
@pharmagrowthhub3083
@pharmagrowthhub3083 3 жыл бұрын
If aduct yields single peak and if there are no co-eluting peaks- you should not have any issues with peak purity
@sachinsawant6932
@sachinsawant6932 3 жыл бұрын
Degradent peak RRF value consider as 1
@buddepumohanarao8309
@buddepumohanarao8309 3 жыл бұрын
Sir in case of degradation impurity is co eluting with main peak then peak purity is fail.then how to it justfied
@pharmagrowthhub3083
@pharmagrowthhub3083 3 жыл бұрын
You will not be able to justify co-eluting peak with principal compound. You need to revise method to separate out co-eluting peak from principal peak.
@naceranaci4139
@naceranaci4139 Жыл бұрын
0:34
@p.sangameshgoud8487
@p.sangameshgoud8487 3 жыл бұрын
Plz tell RRF calculation
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