Author(s): Bharani Pandilla, K. Chitra, C. N. Nalini, Ashok P.

Email(s): bharaniashok@gmail.com

DOI: 10.52711/0974-360X.2021.00376   

Address: Bharani Pandilla1*, K. Chitra2, C. N. Nalini1, Ashok P.
1Department of Pharmaceutical Analysis, C. L. Baid Metha College of Pharmacy, Chennai, Tamil Nadu, India.
2Department of Pharmaceutical Chemistry, Sri Ramachandra Institute of Higher Education and Research (Deemed to be university), Chennai, Tamil Nadu, India.
*Corresponding Author

Published In:   Volume - 14,      Issue - 4,     Year - 2021


ABSTRACT:
A simple, rapid, accurate and economical method has been developed for the quantification of droxidopa by UPLC. The chromatographic system was equipped with Phenomenex column C18 (50mm x 3.0mm, 3µ) as stationary phase and UV detector at 235nm, in conjunction with a mobile phase of buffer: methanol (25:75 % v/v ratio) at a flow rate of 1.0mL/min. Linearity was observed over the concentration range of 100-300µg/mL for droxidopa. The droxidopa peak eluted at 0.35 min. The recovery of Droxidopa was found to be 100.17% - 100.63% respectively. Statistical techniques were employed for the validation of precision, linearity, accuracy, robustness and ruggedness and can be applied for routine analysis. Validation revealed that the developed method was specific, accurate, precise, reliable, robust, reproducible and suitable for the routine quantitative analysis.


Cite this article:
Bharani Pandilla, K. Chitra, C. N. Nalini, Ashok P. Method Development and Validation of Droxidopa by RP-UPLC. Research Journal of Pharmacy and Technology. 2021; 14(4):2125-8. doi: 10.52711/0974-360X.2021.00376

Cite(Electronic):
Bharani Pandilla, K. Chitra, C. N. Nalini, Ashok P. Method Development and Validation of Droxidopa by RP-UPLC. Research Journal of Pharmacy and Technology. 2021; 14(4):2125-8. doi: 10.52711/0974-360X.2021.00376   Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-4-52


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