What are the reasons for mass balance failure during forced degradation

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  • Опубліковано 27 лис 2024

КОМЕНТАРІ • 23

  • @Dileeppharma
    @Dileeppharma 2 роки тому +1

    "You did a great job! sir what a informative presentation."

  • @rahulkulkarni3037
    @rahulkulkarni3037 2 роки тому +1

    Fantastic explanation 👏 Sir

  • @chandrasekhar-kr2uu
    @chandrasekhar-kr2uu 2 роки тому

    Really very informative tnx
    ...

  • @pankajshah1084
    @pankajshah1084 3 роки тому +2

    Nice video sir, very clear voice and clarity, one day you will cross 1M subscribers.

  • @visweswararao8049
    @visweswararao8049 3 роки тому +2

    Sir, you gave clear all probable reasons to get variation in mass balance.
    Can please explain about analytical qbd

  • @sambhajimasal928
    @sambhajimasal928 3 роки тому +1

    This is wonderful ❤

  • @rahulgunjal663
    @rahulgunjal663 3 роки тому +2

    Sir kindly make video on CAD detector method development in hplc.

  • @vivekghosh7364
    @vivekghosh7364 3 роки тому +1

    Please tell us about the different techniques to check peak purity other than purity angle and threshold or with mass spectroscopic method.

  • @ghadahalharbi1814
    @ghadahalharbi1814 2 роки тому

    Sir please what is your reference? I have looked on ICH Q1E and I don’t find it

  • @sbshaikh30
    @sbshaikh30 2 роки тому +1

    How to overcome these mass balance issues??.. Plz explain

  • @krish_krish354
    @krish_krish354 3 роки тому +1

    For analytical calculation which guidelines chapter have to see. Can you refer

  • @anushapulipati2642
    @anushapulipati2642 3 роки тому +1

    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 роки тому +1

    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

  • @buddepumohanarao8309
    @buddepumohanarao8309 3 роки тому +1

    Sir if degradation impurity have no chromphorcity then what to do for identification.

  • @ambikapanda409
    @ambikapanda409 3 роки тому

    Sir can u tell me about metal degradation,like with cupper and iron

  • @mitalipereira446
    @mitalipereira446 3 роки тому

    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 роки тому

      If aduct yields single peak and if there are no co-eluting peaks- you should not have any issues with peak purity

  • @suriyasuriya-xt7dt
    @suriyasuriya-xt7dt Рік тому

    For Api assay method ,force degradation study will be conduct🧐🧐🧐

  • @sachinsawant6932
    @sachinsawant6932 3 роки тому

    Degradent peak RRF value consider as 1

  • @naceranaci4139
    @naceranaci4139 Рік тому

    0:34

  • @buddepumohanarao8309
    @buddepumohanarao8309 3 роки тому +1

    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 роки тому

      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.

  • @p.sangameshgoud8487
    @p.sangameshgoud8487 3 роки тому

    Plz tell RRF calculation