Author(s):
T. Anusha, R. Swetha Sri
Email(s):
sweety.rss@gmail.com
DOI:
10.52711/2349-2988.2024.00016
Address:
T. Anusha1, R. Swetha Sri2*
1Research Student, Department of Quality Assurance, Sarojini Naidu Vanitha Pharmacy Maha Vidyalaya, Osmania University, Tarnaka – 500071, Secunderabad, Telangana, India.
2Assistant Professor, Department of Quality Assurance, Sarojini Naidu Vanitha Pharmacy Maha Vidyalaya, Osmania University, Tarnaka – 500071, Secunderabad, Telangana, India.
*Corresponding Author
Published In:
Volume - 16,
Issue - 2,
Year - 2024
ABSTRACT:
A new UV spectrophotometric technique was developed and validated for Darunavir API by using oral film. The drug was analyzed using a UV spectrophotometric technique, and its linearity, accuracy, precision, and robustness were determined by ICH guidelines. Acetonitrile was the solvent used, and 263nm was shown to be the wavelength. R2=0.9989 shows that the method was linear in the range of 2 to 16µg/ml. Method precision was carried out and RSD was found to be 0.933. The accuracy values obtained from testing at three levels were 99.8, 100.7, and 99.4 in (50,100,150%). The residues are collected using the swab sample technique on a 10cm2 stainless steel plate. To collect the residue, swab sticks are used to stripe the SS plate in three directions: horizontally, vertically, and diagonally. Forced Degradation studies were conducted for API and Synthetic mixture at various conditions and the % degradation was recorded. The proposed method was used for the synthetic mixture of Darunavir API which has its application in formulating OSD. An assay of oral films was done which obeys the beers lambert law in the concentration of 3.27µg/ml. Recovery studies gave statistical confirmation and support for the analysis's conclusions
Cite this article:
T. Anusha, R. Swetha Sri. Derivative UV Spectroscopic Cleaning Method Development and Validation of Darunavir API incorporated into Dissolving Oral Film. Research Journal of Science and Technology. 2024; 16(2):107-4. doi: 10.52711/2349-2988.2024.00016
Cite(Electronic):
T. Anusha, R. Swetha Sri. Derivative UV Spectroscopic Cleaning Method Development and Validation of Darunavir API incorporated into Dissolving Oral Film. Research Journal of Science and Technology. 2024; 16(2):107-4. doi: 10.52711/2349-2988.2024.00016 Available on: https://rjstonline.com/AbstractView.aspx?PID=2024-16-2-1
REFERENCES:
1. Jamakhandi CM, Godambe RD, Kumbhar PS. Development of Spectrophotometric and fluorometric methods for estimation of darunavir using the QbD Approach. Int. J of Current Pharmaceutical Research. 2017; 10(1): 13-19.
2. Mohammad AS et al. Optimization of UV Spectrophotometric Method for the estimation of Darunavir in Bulk Drugs and Tablet Formulation. International Journal of Pharmaceutical Sciences and Nanotechnology. 2016; 9(4): 3345-3348.
3. Patel PS. Development and validation of UV- Spectrophotometric and RP-HPLC methods for estimation of luliconazole in bulk and gel formulation. World Journal of Pharmacy and Pharmaceutical Sciences. 2019; 8(7): 709-729.
4. Varsha Tegeli, Avinash Birajdar, Varsha Tegeli, Avinash Birajdar. UV Spectrophotometric Method Development and Validation of Darunavir in Bluk and Solid Dosage Form. Research Journal of Pharmacy and Technology. 2021:14(6), 3262-4.
5. R. Swetha Sri, S. Jaya Sri, M. Sumakanth. Quantitative Estimation of Vanillin content in various brands of Vanilla Flavored Custard Powder by Conductometry. Research Journal of Science and Technology. 2024; 16(1): 6-0.
6. Raj, P.; Rao, R.; Mukherjee, P.B.; Sarvanan, V.S.; Natesan, Gopal; Kalyankar, Tukaram; Shivakumar, T. UV-Spectrophotometric determination of esomeprazole in tablet dosage forms. Asian Journal of Chemistry. 2007; 3250-2.
7. Syeda Kulsum, Ayesha Naz, Abdul Rehman, Abdul Bari, Mohammed Salman, Shayestha Jabeena and Samreen Akhter. Analytical Method Development and Validation for Simultaneous Estimation of Naproxen and Esomeprazole in Pharmaceutical Dosage Forms. Journal of Pharmaceutical Research International. 2022; 34(51B): 46-50.
8. M. Mukkanti Eswarudu, A. Lakshmana Rao, K. Vijay. Bioanalytical RP-HPLC Method for Simultaneous Quantification of Rivaroxaban and Ticagrelor in Spiked Human Plasma: Validation and Stability. Research Journal of Pharmacy and Technology. 2023; 16(6): 2741-6.
9. Girishchandra R. Mandake, Indrajit S. Patil, Omkar A Patil, Manoj M. Nitalikar, Shriniwas K Mohite. UV Spectroscopy Analysis and Degradation Study of Rivaroxaban. Asian J. Res. Pharm. Sci. 2018; 8(2): 57-60.
10. Arpitha Sunny, C. Sreedhar, T. Srinivas Rao, Akkama. H.G, Asmita Mahapatra. Development of New Analytical Method and Validation For Quantitation of Estimation of Rivaroxaban in Formulation and Bulk Drug. IJSRE. 2017; 5(5): 6469-6478.
11. Hetal Jebaliya, Batuk Dabhi, Madhavi Patel, Yashwantsinh Jadeja, and Anamik Shah. Stress Study and Estimation of a Potent Anticoagulant Drug Rivaroxaban by a Validated HPLC Method, Technology Transfer to UPLC. JCPR. 2015; 7(10): 65-74.