V Kiran Kumar, N Appala Raju, Namratha Rani, JVLN Seshagiri Rao, T Satyanarayana
V Kiran Kumar1, N Appala Raju2*, Namratha Rani2, JVLN Seshagiri Rao3 and T Satyanarayana2
1Dept. of Pharma. Chem., Sree Chaitanya Institute of Pharmaceutical Sciences, LMD.Colony, Karimnagar-505527.AP.
2Dept. of Pharma. Chem., Sultan-Ul-Uloom College of Pharmacy, Mount Pleasant, Road 3, Banjara Hills, Hyderabad-500034.
3University College of Pharmaceutical Sciences, Andhra University, Visakhapatnam. AP.
* Corresponding Author
Volume - 2,
Issue - 1,
Year - 2009
A simple, precise, rapid and accurate reverse phase HPLC method developed for the estimation of Paclitaxel in
Parenterals dosage form. A Unison US C18, 250x4.6 mm i.d, 5 m partical size, with mobile phase consisting of
Methanol and 0.02 M potassium dihydrogen phosphate in water (pH 2.5 adjusted with o-phosphoric acid) in the ratio of
80:20 v/v was used. The flow rate was 1 ml/min and the effluents were monitored at 225 nm. The retention time was
4.978 min. The detector response was linear in the concentration of 15-180 mcg/ml. The respective linear regression equation being Y= 46411.83x+29.2578. The limit of detection and limit of quantification was 0.03 and 0.09 mcg/ml respectively. The percentage assay of Paclitaxel was 99.09 %. The method was validated by determining its accuracy, precision and system suitability. The results of the study showed that the proposed RP-HPLC method is simple, rapid, precise and accurate, which is useful for the routine determination of Paclitaxel in bulk drug and in its pharmaceutical dosage form.
Cite this article:
V Kiran Kumar, N Appala Raju, Namratha Rani, JVLN Seshagiri Rao, T Satyanarayana. The Estimation of Paclitaxel in Parenterals by RP-HPLC. Asian J. Research Chem. 2(1): Jan.-March, 2009;Page 90-92.