From Chairman's Desk

Suresh Nagpal

doi:10.18579/jpcrkc/2010/9/1/79465

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Journal of Pharmaceutical Research

DOI: 10.18579/jpcrkc/2010/9/1/79465

Year: 2010, Volume: 9, Issue: 1, Pages:

Original Article

From Chairman's Desk

Suresh Nagpal

This work is licensed under a Creative Commons Attribution 4.0 International License.

Abstract

No Abstract.

Year: 2010, Volume: 9, Issue: 1

Original Article Formulation and Evaluation of Fast Dissolving Oral Dosage Forms Containing Dietary Supplements

Formulation and Evaluation of Fast Dissolving Oral Dosage Forms Con...

Background: Dysphagia is a common issue across all age groups, particularly with solid dosage forms. The development ...

Original Article Quantification and Validation of a HPLC-UV Method for Simultaneous Analysis of Nitrosoamine Impurities (NDMA, NDEA and NDIPA) in Losartan

Quantification and Validation of a HPLC-UV Method for Simultaneous ...

Impurity profiling is an important aspect in drug therapy for its safety and efficacy. The study of impurities of sar...

Original Article A Prospective Interventional Study on Quality of Life in Tuberculosis Patients

A Prospective Interventional Study on Quality of Life in Tuberculos...

BACKGROUND: Tuberculosis (TB) is one of the oldest infections known toaffect humans and in spite of the new treatment strategie...

Original Article A Review on Drug Interactions in Oral Hypoglycemic Drugs by Mechanism of Cytochrome P450 Enzyme Inhibition

A Review on Drug Interactions in Oral Hypoglycemic Drugs by Mechani...

Purpose: Drug interaction is a phenomenon that has to be thoroughly investigated in order to avoid adverse effects. This review...

Stability Indicating RP-HPLC Method for Determination and Validation of Lurasidone HCL in Bulk and Pharmaceutical Dosage Forms

Original Article Stability Indicating RP-HPLC Method for Determination and Validation of Lurasidone HCL in Bulk and Pharmaceutical Dosage Forms

Stability Indicating RP-HPLC Method for Determination and Validatio...

Objective:To develop and validate a simple, selective, rapid and stability indicating reverse phase high performance liquid chr...

Original Article Stock Assessment of Co-Trimoxazole Tablets in HIV/AIDS Program of Kebbi State, Nigeria

Stock Assessment of Co-Trimoxazole Tablets in HIV/AIDS Program of K...

Purpose: This research was aimed at determining the inventory level of Co-Trimoxazole tablets used in the HIV/AIDS program of K...

Original Article A Validated RP HPLC Method for the Determination of Moprolol in Bulk and Tablet Dosage Form

A Validated RP HPLC Method for the Determination of Moprolol in Bul...

A validated reverse phase high performance liquid chromatographic method (RP-HPLC) has been developed for the estimation of mop...

Quantitative Determination of Duloxetine Hydrochloride in Pharmaceutical formulation by UV-Spectrophotometry and First Order Derivative Methods

Original Article Quantitative Determination of Duloxetine Hydrochloride in Pharmaceutical formulation by UV-Spectrophotometry and First Order Derivative Methods

Quantitative Determination of Duloxetine Hydrochloride in Pharmaceu...

Two methods, 'UV- Spectrophotometric' and 'First order derivative' methods have been developed for determination of Duloxetine ...

A Self Emulsifying Drug Delivery System (SEDDS) for Nisoldipine: Characterization, Dissolution and Conversion into Solid Sedds

Original Article A Self Emulsifying Drug Delivery System (SEDDS) for Nisoldipine: Characterization, Dissolution and Conversion into Solid Sedds

A Self Emulsifying Drug Delivery System (SEDDS) for Nisoldipine: Ch...

Poorly soluble drugs such as nisoldipine offer challenges in developing a drug product with adequate bioavailability. The objec...

Original Article Synthesis, Physical Characterization and In Silico Study of Novel Schiff Base

Synthesis, Physical Characterization and In Silico Study of Novel S...

Now a days treatment of infectious diseases is a challenging issue faced by the medical community. There are bunch of...

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