Author(s):
S. Marakatham, P. Shanmugapandiyan
Email(s):
nandhupharm@yahoo.co.in
DOI:
10.52711/0974-360X.2021.00708 
Address:
S. Marakatham1*, Dr. P. Shanmugapandiyan2
1Research Scholar, Department of Pharmacy, Prist University Deemed to be University, Thanjavur, Tamilnadu.
2Research Supervisor, Department of Pharmacy, Prist University Deemed to be University, Thanjavur, Tamilnadu.
*Corresponding Author
Published In:
Volume - 14,
Issue - 8,
Year - 2021
ABSTRACT:
A novel, simple and sensitive bioanalytical method was developed for estimation of Doravirine, Lamavudine and tenofovir disoproxil fumarate in human plasma with daclatasvir as internal standard. The method was developed using alliance HPLC using Phenomenex C18 (150mm x 4.6mm, 5m) column with mobile phase of 0.01N Potassium dihydrogen phosphate pH (3.5): Acetonitrile (60:40) at flow rate of 1.0ml/min. Detection wavelength was found to be 277nm. The linearity range for doravirine, lamuvidine and Tenfovir was 50-2000ng/ml, 125-5000ng/ml and 20-800ng/ml. Correlation coefficient was 0.999. The method was validated and stability study was carried out as per FDA guidelines.
Cite this article:
S. Marakatham, P. Shanmugapandiyan. Bioanalytical Method Development and Validation of Doravirine, Lamavudine and Tenofovir Disoproxil Fumarate using HPLC in Human Plasma. Research Journal of Pharmacy and Technology. 2021; 14(8):4087-1. doi: 10.52711/0974-360X.2021.00708
Cite(Electronic):
S. Marakatham, P. Shanmugapandiyan. Bioanalytical Method Development and Validation of Doravirine, Lamavudine and Tenofovir Disoproxil Fumarate using HPLC in Human Plasma. Research Journal of Pharmacy and Technology. 2021; 14(8):4087-1. doi: 10.52711/0974-360X.2021.00708 Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-8-14
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