Salam. Sometimes I find in the articles quoting 3 SDV/b, sometimes 3.3 SDV/b, which formula is taken in general that of 3 or that of 3.3. what's the difference?
dear sir, thanks for the superb explanation. Where i can get this formula for residual calculations? Which regulatory document mentions the formula for residual calculations? I am unable to find out the regulatory reference for this calculation.
Thank you so much. I need some clarity, when I iniect blank, I will get very more than 1 peak response. I may have 2 to 5 areas, who can I handle that???. So if IAM looking at the impurities in my sample but when there is no impirity, no peak for impurity. How do I handle this?
Hello sir... according to ich guidelines loq value considered maximum 50% of our spec limit if our loq not stablish 50% or below spec limit than what will be do...?? Please suggest me sir...and explain what is the reason not stablish loq below 50%..
Sir please made a video for set the LOQ limit for 2 to 5 impurity present in sample having different uv Please made all clear about the method validation with the example it will be helpful for us
In case of AAS atomic absorption spectroscopy The linearity start from 0.1 ppm to 0.5 ppm (LOD) and the concentration fall below the 0.1 i.e 0.023 then What will be the result? Should we calculate this or not If not then what will be the result? If anyone have answer Plz let me know
Sir ur expalnation is very good but ihave a one doubt for blank mesurement method 1. We are inject blank solution or placebo 60 mesurements but the solutions not present in our analyte then how integrate peak and caliculate sddeviation
Hello Sir I got confused with how to compute the residuals especially the predictable response which you mentioned (mx + c). Kindly explain in detailed. And thank you in advance if you will notice my comment and query.
Residual formula: Observed Area - Predicted area Predicted area shall be calculated from the Regression curve Y=MX+C Example: the obtained area for the below conc. is stated below 1ppm - 400 2ppm - 800 3ppm - 1189 4 ppm - 1600 5 ppm - 1985 NOw plot a linearity plot to obtained ur regression equation. y = 397x + 3.8 from the above ontained value, now will calculate the residuals as stated below for 1ppm level: Y=397 (1)+3.8 Y=397+3.8 Y=400.8 So your residual is (Practical obtained area - predicted area from the regression line) Residual = 400 - 400.8 Residual = - 0.8 SO the observed residual for 1 ppm is -0.8. similarly the residual for other concentrations will be caluculated in the same way. Hope u got the answer.
Your explanation is very powerful and easily understand by anyone. Appreciate.
ur explanation was amazing and crystal clear, keep making the lectures to enrich knowledge
It was very informative & useful information and you explained ina detail so anyone can understand, Great ..Help
Thank you sir, Highly informative. Please put video for gradient method development in HPLC
Great sir,your explanation is very versatile 👌, useful for us.
When do you use the SD of the Y- intercept vs SS of regression line to find LOD?
Highly informative sir 👍🙏
Very Informative lecture😍
Good video. I see that the y-intercept is not used in the LOD calculations. Where does y intercept feature?
For LoQ S/N ratio is more than 10 reqired .
Any maximun limit for S/N ratio like if its found like 800 is it acceptable ...??
Great efforts
Salam.
Sometimes I find in the articles quoting 3 SDV/b, sometimes 3.3 SDV/b, which formula is taken in general that of 3 or that of 3.3.
what's the difference?
dear sir, thanks for the superb explanation. Where i can get this formula for residual calculations? Which regulatory document mentions the formula for residual calculations? I am unable to find out the regulatory reference for this calculation.
Thank you so much. I need some clarity, when I iniect blank, I will get very more than 1 peak response. I may have 2 to 5 areas, who can I handle that???. So if IAM looking at the impurities in my sample but when there is no impirity, no peak for impurity. How do I handle this?
Hi sir
Why In visual observation LOQ not determined .
Ple send the answer
Is there need of seprate calibration curves for QL and DL.
Why lod loq value are comming different through regression method
Which concentrations need to be selected while determine the lod and loq?can we go below 1 ppm too in the given example...
Hello sir... according to ich guidelines loq value considered maximum 50% of our spec limit if our loq not stablish 50% or below spec limit than what will be do...??
Please suggest me sir...and explain what is the reason not stablish loq below 50%..
Why the number 3 comes in the formula for LOD?
Sir please made a video for set the LOQ limit for 2 to 5 impurity present in sample having different uv
Please made all clear about the method validation with the example it will be helpful for us
What if the specification limit is below to the quantification limit then is that LOQ is valid?
How can I determine slope I'm Excel?
Very helpful sir, can we have a video about impurity method validation from protocol preparation to report generation?
Yes sir
In case of AAS atomic absorption spectroscopy
The linearity start from 0.1 ppm to 0.5 ppm (LOD)
and the concentration fall below the 0.1 i.e 0.023 then
What will be the result?
Should we calculate this or not
If not then what will be the result?
If anyone have answer
Plz let me know
Actual value and predictable value explain with another one more example in visible manner
Thank you👏🏼👏🏼👏🏼
Sir ur expalnation is very good but ihave a one doubt for blank mesurement method
1. We are inject blank solution or placebo 60 mesurements but the solutions not present in our analyte then how integrate peak and caliculate sddeviation
The response may be expected due to detector background noise and diluent or matrix effect...
Why we determined lod and loq??
Seperate curve for detection limit in that LOQ should not be added other linearity level can be added. Is it so
Slope can be better evaluated with a calibration curve comprising higher concentrations and LOQ conc need not be considered in it.
@@pharmagrowthhub3083 thank you sir
Thank you very much.
Sir what is maximum limit of impurity
can we get the PPT PDF plz
Thank you so much sir
You made video on related substances
Hello Sir I got confused with how to compute the residuals especially the predictable response which you mentioned (mx + c). Kindly explain in detailed. And thank you in advance if you will notice my comment and query.
Residual formula: Observed Area - Predicted area
Predicted area shall be calculated from the Regression curve
Y=MX+C
Example: the obtained area for the below conc. is stated below
1ppm - 400
2ppm - 800
3ppm - 1189
4 ppm - 1600
5 ppm - 1985
NOw plot a linearity plot to obtained ur regression equation.
y = 397x + 3.8
from the above ontained value, now will calculate the residuals as stated below for 1ppm level:
Y=397 (1)+3.8
Y=397+3.8
Y=400.8
So your residual is (Practical obtained area - predicted area from the regression line)
Residual = 400 - 400.8
Residual = - 0.8
SO the observed residual for 1 ppm is -0.8. similarly the residual for other concentrations will be caluculated in the same way.
Hope u got the answer.
@@rajeshgoud1274 why we are using y= 397x +3.8 ?? Plz let me know the ans
What is the real formula?
Super sir
can i get it in pdf
TQ Sir..
hi Can you explain more about how to ca the calculate the residuals, I'm confused about the formula
Tanks
Send me excel sheet sir plz.
Sir please make a vidio in hindi language for better understanding.then will be more grow your channel and views and gain subscribers.
you are not tell residual actual calculations properly
10.35 minutes can u explain a little elaborate with other example