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Tag Archives: LOD

RP-HPLC Method Development and Validation for the Simultaneous Estimation of Oxycodone and Naltrexone in Pharmaceutical Dosage Form

Ch. Sravani Phanithavya*, K.N. Maneesha, M. Sreenivasulu, Y. Prapurna Chandra Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur (V&P), Muthukur (M), SPSR Nellore District–524 346 Abstract The aim of this study is to develop and validate a new RP-HPLC method for the Simultaneous Estimation of Oxycodone and Naltrexone in Pharmaceutical Dosage Form. The estimation of Oxycodone and Naltrexone was ... Read More »

Develop a new, simple, fast, rapid, accurate, efficient and Reproducible RP-UPLC Method for the Simultaneous analysis of Metformin and Saxagliptin

A. Srikanth*, G. Srikanth1, Shaik afroz begum2, Machiraju Sai Kalyan3 *Associate Professor, Dept. of Pharmaceutical Analysis Vasavi institute of pharmaceutical sciences, Kadapa. 1Assistant Professor, Dept. of Pharmaceutics, Vasavi institute of pharmaceutical sciences, Kadapa. 2Assistant Professor, Dept of Pharmaceutical Chemistry, Vasavi institute of pharmaceutical sciences, Kadapa. 3Student, Department of Pharmaceutical Analysis, Vasavi institute of pharmaceutical sciences, Kadapa. Abstract Introduction: Metformin decreases ... Read More »

Analytical Method Development and Validation for Pirfenidone (Anti-Fibrotic) in bulk drug and dosage form

Katikala Dharmendra*, Dr. C. Sreedhar, T. Sreenivasa Rao, Rikshaya Tamang, Meghnath Chaudhary, Mohamed adam Department of Pharmaceutical Analysis, Karnataka College of Pharmacy, #33/2,Thirumenahalli,Hegde Nagar main road, Bangalore – 560064, KA. India. A B S T R A C T Pirfenidone, 5-methyl-1-phenyl-2-(1H)-pyridine is a novel Anti-fibrotic agent approved for mild to moderate Idiopathic pulmonary fibrosis (IPF).  Isocratic reverse phase high performance ... Read More »

Analytical Method Development and Validation for the Estimation of Ceritinib by RP-HPLC Method in Bulk and Pharmaceutical Dosage Form

Krishna Reddy*, K. Pranaya, K. Babu, MA. Tanjeema, N. Ravi kumar, Udayasri Bomma Institute of Pharmacy, Khammam, Telangana, India A B S T R A C T The chromatographic conditions were successfully developed for the separation of Ceritinib by using Kromosil C18 4.5×150 mm 5.0 µm, flow rate was 0.8ml/min, and mobile phase ratio was 65:35% v/v methanol: water, detection ... Read More »

Analytical Method Development and Validation for the Estimation of Pantoprazole by RP-HPLC Method in Bulk and Pharmaceutical Dosage Form

Y. Krishna Reddy*, D. Ramesh, D. Kowshik, E. Manisha, K. Manisha, G. Kiranmayi    Bomma Institute of Pharmacy, Khammam, Telangana, India A B S T R A C T The chromatographic conditions were successfully developed for the separation of Pantoprazole by using thermosil C18 4.5×150 mm 5.0 µm, flow rate was 0.8ml/min, mobile phase ratio was 65:35% v/v methanol:water, detection ... Read More »

Analytical Method Development and Validation for the Simultaneous Estimation of Telmisartan and Hydrochlorothiazide by UV-Spectrophotometric Method in Bulk and Tablet Dosage Form

L. Kanaka Lakshmi*, S. Harshini, Dr. Vasudha Bakshi, D. Sireesha, Akiful Haque Deparment of Pharmaceutical Analysis, School of Pharmacy, Anurag Group of Institutions, Ghatkesar, Ranga Reddy, Telangana-501301, India.  A B S T R A C T The Spectroscopic method was successfully developed for the separation of Hydrochlorothiazide and Telmisartan by using as solvent methanol, detection wavelength were at 271nm and ... Read More »

Development of a new UV/Visible Spectophotometric and HPLC methods for simultaneous estimation of Metformin and Sitagliptin

Md. Salmasultana1, Asish Bhaumik*2, Hiroshima Kumari3, P. Lavanya4, A. Uma5, T. Haritha6 1,3,4Department of Pharmaceutical Analysis, Teja College of Pharmacy, Kodad, Nalgonda-508206, Telangana, India. 2,5,6Department of Pharmaceutical Chemistry, Teja College of Pharmacy, Kodad, Nalgonda-508206, Telangana, India. A B S T R A C T The main aim and objective of the present research work was to develop a new UV/VISIBLE ... Read More »

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