ABSTRACT:
Clopidogrel, an adenosine diphosphate inhibitor derived from Ticlopidine, has not previously been quantified in simulated nasal fluid using a straightforward UV-spectrophotometric approach, as revealed in the existing literature. In this study, we established a simplified UV-spectrophotometric technique specifically for assessing Clopidogrel Bisulphate in simulated nasal fluid. The standard curve was constructed within the concentration range of 0.5 to 3µg/ml, and the method underwent comprehensive validation for accuracy, precision, robustness, and reproducibility. The absorption maxima were identified at 242nm, and the method exhibited excellent linearity within the concentration range of 0.5 to 3µg/ml, boasting a correlation coefficient of 0.996. The developed method proved its accuracy, with the mean recovery value closely approximating 95%. Additionally, the limit of detection (LOD) and limit of quantification (LOQ) were determined to be 0.193 and 0.6434, respectively. Overall, this newly devised and rigorously validated method stands out for its simplicity, accuracy, precision, cost-effectiveness, and reproducibility.
Cite this article:
Bhagyashree Kokate, Veena Belgamwar. Analytical profiling of Clopidogrel Bisulphate: A Method Development and Validation by UV-Spectrophotometer using Simulated Nasal Fluid. Research Journal of Pharmacy and Technology.2025;18(2):815-8. doi: 10.52711/0974-360X.2025.00120
Cite(Electronic):
Bhagyashree Kokate, Veena Belgamwar. Analytical profiling of Clopidogrel Bisulphate: A Method Development and Validation by UV-Spectrophotometer using Simulated Nasal Fluid. Research Journal of Pharmacy and Technology.2025;18(2):815-8. doi: 10.52711/0974-360X.2025.00120 Available on: https://rjptonline.org/AbstractView.aspx?PID=2025-18-2-52
9. REFERENCES:
1. Antypenko L, Gladysheva S, Vasyuk S. Development and validation of clopidogrel bisulphate determination in bulk by UV spectrophotometric method. Scripta Scientifica Pharmaceutica. 2016; 3(2): 25. Doi:10.14748/ssp. v3i2.1704
2. Zaazaa HE, Abbas SS, Abdelkawy M, Abdelrahman MM. Spectrophotometric and spectrodensitometric determination of Clopidogrel Bisulfate with kinetic study of its alkaline degradation. Talanta. 2009; 78(3): 874-884. Doi: 10.1016/ j.talanta.2008.12.064
3. Deshmukh PR, Gaikwad VL, Tamane PK, Mahadik KR, Purohit RN. Development of stability-indicating HPLC method and accelerated stability studies for osmotic and pulsatile tablet formulations of Clopidogrel Bisulfate. Journal of Pharmaceutical and Biomedical Analysis. 2019; 165: 346-356. Doi: 10.1016/ j.jpba.2018.12.020
4. Agrawal H, Kaul N, Paradkar AR, Mahadik KR. Stability indicating HPTLC determination of clopidogrel bisulphate as bulk drug and in pharmaceutical dosage form. Talanta. 2003; 61(5): 581-589. Doi:10.1016/s0039-9140(03)00364-3
5. Sharma S, Sharma JB, Bhatt S, Kumar M. Method Development and validation of UV spectrophotometric method for the quantitative estimation of curcumin in simulated nasal fluid. Drug Research. 2020; 70(08): 356-359. Doi:10.1055/a-1193-4655
6. Jain PS, Chaudhari AJ, Patel SA, Patel ZN, Patel DT. Development and validation of the UV-spectrophotometric method for determination of terbinafine hydrochloride in bulk and in formulation. Pharmaceutical Methods. 2011; 2(3): 198-202. Doi:10.4103/2229-4708.90364
7. Kaur P, Mandal UK. Development and Validation of a UV Spectrophotometric method of Mycophenolate mofetil useful at Preformulation stage of Microemulsion Formulation. Research Journal of Pharmacy and Technology. 2019; 12(10): 4777. Doi:10.5958/0974-360x.2019.00824.
8. Nath L, Laldinchhana N, Choudhury AD, Barakoti H, Devi CM. Development and validation of UV-VIS spectrophotometric method for estimation of amphotericin B. Research Journal of Pharmacy and Technology. 2020; 13(1): 55. Doi:10.5958/0974-360x.2020.00009.
9. N VL, Rao GK, Roja Rani B, Manasa K, V Bhavani Prasad. Development and validation of UV spectrophotometric method for the estimation of finasteride in tablets. International Journal of Pharma Sciences. 2013; 3(1): 123-125.
10. Maleque M, Hasan MD, Hossen F, Safi S. Development and validation of a simple UV spectrophotometric method for the determination of levofloxacin both in bulk and marketed dosage formulations. Journal of Pharmaceutical Analysis. 2012; 2(6): 454-457. Doi: 10.1016/j.jpha.2012.06.004
11. Karnakar N, Hechhu R, Amani P, Sri Tharun D, Nagaraju M, Saurabh Bodhgaya Sharma. Analytical method development and validation of diclofenac sodium by UV-visible spectroscopy using AUC method. The Journal of Rehabilitation Research and Development. 2020; 7(1): 20-24.
12. Sankar PR Sr, Swathi V, Srinivasa Babu P. Development and validation of novel UV and RP-HPLC methods for determination of cilnidipine (a new generation ca channel blocker) in pharmaceutical dosage form. International Journal of Pharmaceutical Sciences and Research. 2019; 4–4: 1886-1894. Doi:10.13040/IJPSR.0975-8232.10(4).1886-94