Answer Posted / suneel kumar
There are so many reason important are as follows..
1. To Maintain the PH of mobile Phase.
2. Most of the Pharmaceutical Substances are get easily
separation in buffer compare to water.
3. Peak shape will be good with addition of Buffer.
Is This Answer Correct ? | 2 Yes | 1 No |
Post New Answer View All Answers
how you establish the LOQ?
what is the origin to prepare standard operating procedure
How to set specification of assay, fisdolution and related substances?
What is the calibration of uv process and preparation
What is control room temperature and which guide line says?
why glutent are detected in the rice cereal baby food product even manufacturer claimed that they are using rice and milk only?we have using ELISA to do the test,and rice supposed not containing any glutent,rite?We already repeat the test so many times and it still detected.just wondering where the glutent came from?
How to calculate coreletion coefficient
how pda detector works over uv?
on saturation solubility study data how we can find out the bcs class of drug?
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
what is mean by covalidation
How to know the estimated LOQ concentration in ppm
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
As per ICH related substances stability trend limit from initial to shelf life
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?