Wednesday , 15 August 2018

Tag Archives: Validation

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

V. Haribaskar*, M. Sukanya, B. Kumar, M. Gobinath, Ramesh Dhani Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Nellore, Andhra Pradesh, India A B S T R A C T The Present work was to develop a simple, fast, accurate, precise, reproducible, Reverse Phase High Performance Liquid Chromatographic Method for simultaneous estimation of Valsartan and Sacubitril in pure drug ... Read More »

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

V. Hari Baskar*, V. Pushpalatha, M. Gobinath, Ramesh Dhani Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Nellore, Andhra Pradesh, India A B S T R A C T The Present work was to develop a simple, fast, accurate, precise, reproducible, Reverse Phase High Performance Liquid Chromatographic Method for simultaneous estimation of Acetaminophine and Oxycodone in pure drug form. ... Read More »

Development and Validation of RP-HPLC Method for the Estimation of Sitagliptin Phosphate in Bulk and Its Tablet Dosage Form

I. Arulraj1, P. Vembu2 and A. Chenthilnathan1* 1Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli – 627 012, Tamil Nadu, India. 2Bafna Pharmaceuticals Limited, Grantlyon village, Chennai – 600 052, Tamil Nadu, India. A B S T R A C T A simple and sensitive reversed-phase liquid chromatographic method has been developed and validated for the estimation of Sitagliptin phosphate ... Read More »

Development and Validation of a Stability Indicating RP-HPLC Method for the Determination of Piroxicam in Pharmaceutical Dosage Form

A. Chandra Prabha1, M. Sankar2 and A. Chenthilnathan1* 1Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli–627012, Tamil Nadu, India. 2Caplin Point Laboratories Ltd., Gummidipoondi, Chennai–601201, Tamil Nadu, India A B S T R A C T A stability-indicating RP-HPLC was developed and validated for the determination of Piroxicam in bulk and its injection dosage form. The separation was carried out ... Read More »

Analytical Method Development and Validation for Apixaban by RP-HPLC

Md. Abdul Majeed*1, Dr.K.Vijaya1, B. Anitha2 1Department of Pharmaceutical Analysis, Monad Univeristys, Hapur, Rajasthan, India 2SARC (Scientific and Applied Research Center), Hyderabad, Telangana, India A B S T R A C T A simple and precise RP-HPLC method was developed for the determination of Apixaban dosage form the chromatographic separation was achieved on an Zorbax Bonus RP (250 X 4.6mm) ... Read More »

Method Development and Validation by RP-HPLC for the Simultaneous Estimation of Cinacalcet and Maxacalcitol in Tablet Dosage Form

N. Usha*, M. Gobinath, V. Hari Baskar, Ramesh Dhani, A. Soniya Department of Pharmaceutical Analysis, Ratnam Institute of Pharmacy, Pidathapolur, Muthukur, SPSR Nellore, A.P, India.  A B S T R A C T A Simple, selective, accurate, precise and linear RP-HPLC method was developed subsequently validated for estimation of cinacalcet in bulk & tablet dosage form. Gradient elution at a ... Read More »

Simultaneous Spectroscophotomertic Estimation of Moxifloxacin Hydrochloride and Imatinib Mesylate

Hiyashree Rajkhowa, Nayan Pradhan*, Hemant Giri, Bhupendra Shrestha Department of Pharmaceutical Analysis and Quality Assurance, Himalayan Pharmacy Institute, Majhitar, East Sikkim, India  A B S T R A C T A simple, accurate, and precise spectrophotometric method was developed for the simultaneous estimation of moxifloxacin hydrochloride (MOX) and imatinib mesylate (IMA). MOX and IMA solution were simultaneously determined at their ... Read More »

Method Development and Validation of Nebivolol by RP-HPLC

Naga Jyothi. C*, Gummi Vishwanth, P. Sunitha Pharmaceutical Analysis and Quality Assurance,   JNTUH, Kukutpally, Hyderabad, India A B S T R A C T An isocratic reversed-phase high performance liquid chromatographic method was established for the estimation of Nebivolol in tablet dosage form. The chromatographic conditions were successfully developed for the estimation of Nebivolol by using Develosil C18 column (150×4.6mm, ... Read More »

Analytical Method Development and Validation for Simultaneous Estimation of Ambroxol HCL and Levocetrizine in Its Bulk and Dosage Form by RP-HPLC

R. Vivek*, Dr. T. Rama Mohan Reddy, Dr. V. Uma Maheswara Rao Department of Pharmaceutical Analysis and Quality Assurance, CMR College of Pharmacy, Medchal, Hyderabad, Rangareddy, India A B S T R A C T A simple Reverse phase liquid chromatographic method has been developed and subsequently validated for simultaneous determination of Levocetirizine and Ambroxol HCl in combination. The separation ... Read More »

Analytical Method Development and Validation for Simultaneous Estimation of Albendazole and Ivermectin Tablet of Dosage Form by RP-HPLC

B. Saidulu*, G. Usha Sree, Dr. V. Uma Maheswara Rao Department of Pharmaceutical Analysis and Quality Assurance, CMR College of Pharmacy, Medchal, Hyderabad, Rangareddy, India A B S T R A C T A reverse phased liquid chromatography (LC) method was developed and validated for simultaneous estimation of albendazole and ivermectin in tablet dosage form. The isocratic LC analysis was ... Read More »

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