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What is the definition of method development by hplc?
Method development is a process amenable to continuous improvement
What is rs-hplc?
"RS-HPLC method" means "Related Substance HPLC Method".
What has the author Sukwinder Kaur Gill written?
Sukwinder Kaur Gill has written: 'Development of a method for the determination of chlortetracycline (CTC) in a three component mixture (Microfac) by HPLC'
Why is anthracene is used for calibration of hplc?
Anthracene is used as a calibration standard in High Performance Liquid Chromatography (HPLC) because it has a well-defined retention time and peaks in the UV-visible spectrum, making it easy to detect and quantify. Its consistent behavior helps in determining retention times, resolving power, and column efficiency during method development and troubleshooting in HPLC.
How you can select buffer in hplc according to pka value?
In HPLC, you can select a buffer based on its pKa value to achieve better separation of analytes by controlling pH of the mobile phase. Choose a buffer with a pKa value close to the desired pH for the separation, as this ensures the buffer will be most effective in maintaining stable pH. Selecting a buffer with a pKa within ± 1 unit of the desired pH is a commonly used guideline in HPLC method development.
In hplc validation according to ich guidelines loq is 10 times of sn ratio but you are doing 6times of it is there any guidelines from you?
'Actually for LOQ precision there is no guidelines, but LOQ definition is to be actually quantified with accuracy and precision. That,s why to conform the precision we are injecting six times and find the rsd less than 10%. It shows that LOQ is able to quantify with accuracy and precision
Why reproducibility is important in hplc?
Reproducibility in HPLC ensures that results can be consistently obtained when the experiment is repeated, leading to reliable data. It allows for verification of results by other researchers and ensures the accuracy and reliability of the method. Reproducibility is crucial for validating the robustness of the HPLC method and for ensuring that results are accurate and can be trusted.
How you find out Pka value of organic compound for HPLC method develoment?
If you can't find it in the literature it can be determined experimentally by titration.
Why the pH of buffer is not changes in robustness of validation of hplc method?
it must change by (+- 0.3) to have control in pH meter error
How do you estimate Serratiopeptidase in Pharmaceutical products Is there a HPLC method available?
To estimate Serratiopeptidase in pharmaceutical products, HPLC (High-Performance Liquid Chromatography) is a commonly used method. A validated HPLC method can separate and quantify Serratiopeptidase in a sample, providing accurate results for quality control purposes in pharmaceutical analysis. It is essential to use appropriate standards and optimize chromatographic conditions for this analysis.
What is assay by HPLC?
Assay by HPLC refers to using high-performance liquid chromatography (HPLC) as a technique to quantify the presence and concentration of a specific compound or analyte in a sample. HPLC separates and analyzes components within a mixture based on their interactions with the mobile and stationary phases, allowing for accurate measurement of analyte concentrations. It is commonly used in pharmaceutical, environmental, and food industries for quality control purposes.
What is difference between specificity and selectivity in hplc method validation?
Specificity refers to the ability of an analytical method to accurately measure the analyte of interest in the presence of potential interfering substances. Selectivity, on the other hand, refers to the ability of the method to only detect the analyte of interest while ignoring any other components present in the sample. Both are important parameters in HPLC method validation to ensure accurate and reliable results.
