%0 Journal Article
%T Optimization of High-Performance Liquid Chromatography Parameters for Purification of Oligonucleotide-A
%A Christina Perez
%A Mubeen Rani
%A Tuan Phan
%J American Journal of Analytical Chemistry
%P 39-50
%@ 2156-8278
%D 2022
%I Scientific Research Publishing
%R 10.4236/ajac.2022.132004
%X The modification of high-performance liquid chromatography parameters leads to a more effective oligonucleotide-A purification process. Using various experimental parameters such as buffer, concentration, and pH, a method for optimizing the purification of an oligonucleotide-A on a reverse-phase C18 column was created. To purify oligonucleotide-A, High-Performance Liquid Chromatography (HPLC), Ultraviolet-Visible Spectrophotometry (UV-Vis), Liquid Chromatography-Mass Spectrometry (LC-MS), and lyophilization were used. Chromatographic data were collected with a semi-prep HPLC system, quantified with the UV-Vis technique, and validated with the LC-MS method. The most optimized parameters found to obtain the purity of 93.0% are 40 mM triethylammonium bicarbonate (TEAB) buffer with pH 7, which is approximately 6.0% higher than the reported method of which the purity is 87.0%. However, the yield under these conditions was reduced by about 5%. The worst possible optimized settings that resulted in the lowest purity (84.0%) and yield (69.0%) are 10 mM ammonium acetate (NH<sub>4</sub>CH<sub>3</sub>CO<sub>2</sub>) with pH 7.
%K Purification
%K High-Performance Liquid Chromatography
%K Oligonucleotide-A
%K Dipotassium Phosphate
%K Triethylammonium Acetate
%K Triethylammonium Bicarbonate
%K Ammonium Acetate
%U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=115537