By following + or - 2 pH to the pKa value
Common types of buffers used for HPLC include phosphate buffers, acetate buffers, citrate buffers, and ammonium acetate buffers. These buffers help to maintain the pH of the mobile phase, stabilize analytes, and provide consistent elution profiles. It's important to choose the right buffer based on the pH requirements of the analytes being analyzed.
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.
mixture of enantiomers can be separated by HPLC
Yes, melamine can be detected by HPLC (High Performance Liquid Chromatography). HPLC is a common analytical technique used to separate and quantify compounds in a mixture, including melamine. Detection methods such as UV-Vis spectroscopy or mass spectrometry can be used in conjunction with HPLC to identify and quantify melamine accurately.
GC can give very resolved sharp peaks with short run time compared to hplc. additionally, there is less compatibility issue in setting an MS up to a GC than HPLC
Nothing will happen
Buffer concentration can affect retention time in HPLC by influencing the pH of the mobile phase, which can in turn impact interactions between the analyte and stationary phase. Higher buffer concentrations can alter the ionization state of the analyte, leading to changes in its retention time. Additionally, buffer concentrations can also affect peak shape and resolution in the chromatogram.
it must change by (+- 0.3) to have control in pH meter error
Yes.
Common types of buffers used for HPLC include phosphate buffers, acetate buffers, citrate buffers, and ammonium acetate buffers. These buffers help to maintain the pH of the mobile phase, stabilize analytes, and provide consistent elution profiles. It's important to choose the right buffer based on the pH requirements of the analytes being analyzed.
the same guidelines for method validation
column ----250mm 4.6mm L1 flow rate.--- 1ml/minute wavelength-- 195nmInjection Volume 10ul temperature ambent Buffer Preprations Take 600ml distilled water adjust pH 2.5 with phosphric acid take 500mg 1-pentane sulphonic sodium salt. add 100ml distilled watere after disolved of sodium salt Mobile Phase Ratio. Buffer 7: acetronitrile 3 (Buffer 700ml:Acetronitrile 300ml)
NP-HPLC is "Normal Phase" HPLC, wherein the solvents used are less polar than the substrate in the HPLC column (e.g. using hexane or dichloromethane with a silica HPLC column). RP-HPLC is "Reverse-Phase" HPLC, wherein the solvents used are more polar than the substrate in the HPLC column (e.g. using Water and Methanol with a octadecylsilane (ODS or C18) column).
If you can't find it in the literature it can be determined experimentally by titration.
why RT was shifting & how to RT calculation in HPLC
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.
mixture of enantiomers can be separated by HPLC