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Tag Archives: Lisinopril

Design and In-vitro Characterization of Lisinopril Retentive Floating Tablets

T. Jahnavi*, Bh. Sriswetha, D. Raghava, K. Nageswara Rao Department of Pharmaceutical Technology, K.G.R.L College of Pharmacy, Bhimavaram-534201, Andhra Pradesh, India A b s t r a c t Lisinopril is a potent, competitive inhibitor of angiotensin-converting enzyme (ACE), the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a ... Read More »

Development and Validation of New Analytical Method for the Simultaneous Estimation of Lisinopril and Amlodipine in Pharmaceutical Dosage Form by UV Spectrophotometry

Pavan Kumar.V*, P. Jyoshna, P. Nageena, E. Sandhya Mahalakshmi, K. Siva Kumar, A. Subha Jahnavi, A. Tharun Sai Department of Pharmaceutical Analysis, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati-517561      A B S T R A C T An elementary, valid, Speedy and decisive strategy was developed to determine Lisinopril and Amlodipine quantitatively in combined pharmaceutical dosage forms. The method was ... Read More »

Development and Validation of Micellar Electrokinetic Chromatographic Assay Method for Simultaneous Estimation of Antihypertensive Drugs in Pharmaceutical Formulations

A. Ramyasree1*, Dr. R. Sekar2 1NRI college of Pharmacy, Vijayawada, Andhra Pradesh 2Indian Institute of Chemical Technology (IICT), Hyderabad, Telangana A B S T R A C T A micellar electrokinetic capillary chromatographic (MEKC) method has been developed for the simultaneous determination of anti-hypertensive drugs amlodipine (AM) and lisinopril (LS) in pharmaceutical formulations. Analysis was performed in a 75 µm ... Read More »

Validated RP-HPLC Method Development for the Simultaneous Estimation of Lisinopril and Hydrochlorthiazide in Bulk and Pharmaceutical Dosage Form

Amarnath Mundra*, Harshini.S, Sireesha. D, Akifulhaque, Vasudha.B Department of Pharmaceutical Analysis and Quality assurance, Anurag group of institutions (Formerly Lalitha college of pharmacy), Hyderabad. A B S T R A C T A simple and cost effective RP-HPLC method is described for the determination of lisinopril and Hydrochlorothiazide in pure form and in pharmaceutical formulations. The drug was highly soluble ... Read More »

Formulation and Characterization of Bilayer Floating Tablets of Glipizide & Lisinopril

*Sheetal Buddhadev1, Raval Kashyap2, Dr. Sandip Buddhadev3  1Assistant Professor, Department of Pharmaceeutics, Noble Pharmacy College, Junagadh 2HOD, Department of QA, Noble Pharmacy College, Junagadh 3Associate Prof., Department of Dravyaguna, Government Ayurved College, Junagadh A B S T R A C T The purpose of the study is to prepare Bilayer floating tablets containing Glipizide as sustained release and Lisinopril as ... Read More »

Formulation and Evaluation of Sublingual Tablets of Lisinopril

D. Nirmala Kumari*, R. Jagadeesh Reddy, K. Divyavani, B. Saidamma Department Pharmaceutics, Mother Teresa Pharmacy College, Sathuapally, Khammam, Andhra Pradesh, India A B S T R A C T Lisinopril is the drug of choice in hypertension. Bioavailability of the drug is 25% of orally. However, its extensive first pass metabolism results in poor bioavailability. The objective of present research ... Read More »

Validated RP-HPLC Method for Simultaneous Estimation of Lisinopril and Hydrochlorothiazide in Combined Dosage forms

Author Details P. Nagaraju*, G. Indira Priyadarshini, SA. Bilal Ahmed and V. Siddhartha Department of Pharmaceutical Analysis, Hindu College of Pharmacy, Amaravathi Road, Guntur–522 002, Andhra Pradesh, India. Abstract A rapid and sensitive reverse phase high performance liquid chromatography (RP-HPLC) method has been developed for simultaneous estimation of Lisinopril and Hydrochlorothiazide. Chromatographic separation was achieved on reverse phase Agilent LC 1100 ... Read More »

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