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DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 29Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK PHARMA at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution

Thursday, 17 March 2016

Dr. Vandana Arora Sethi

Head of the Department at School of Pharmacy, Lloyd Institute of Management & Technology

links

vandana.sethi@gmail.com
https://www.facebook.com/vandana.sethi.9619

https://in.linkedin.com/in/dr-vandana-arora-sethi-48a84118

Experience

Reader

Lloyd Institute of Management & Technology

August 2006 – Present (9 years 8 months)

Lecturer

Allana College of Pharmacy

August 2005 – July 2006 (1 year)

Research Analyst

Smart Analyst

April 2005 – August 2005 (5 months)

Research Associate

Ranbaxy Research Laboratories

2002 – 2003 (1 year)

Education

Delhi University

M.Pharm., Pharmaceutics, First- Gold medalist

1995 – 2001

Activities and Societies: Debates and Anchoring

(Open)1 honor or award

National Institute of Medical Sciences

Doctor of Philosophy (Ph.D.), Pharmaceutical Sciences
Honors & Awards

LG Trophy for the Best Outgoing student

Delhi Government
August 2001

Sai Medha Award for the best student
September 1995

Best Teacher Award
October 2009
Cite this article as:

Vandana Arora Sethi, Abdul W. Siddiqui, Govind Mohan, Development and Evaluation of Niosomal Formulation of Famciclovir, Asian Journal of Pharmaceutical Technology & Innovation, 03 (13); 2015. www.asianpharmtech.com
Development and Evaluation of Niosomal Formulation of Famciclovir

Vandana Arora Sethi*¹, Abdul W. Siddiqui², Govind Mohan³

1,3    Department of Pharmacy, NIMS University, Jaipur Rajasthan
2       Department of Pharmacy, Mangalayatan University, Aligarh U.P.

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ABSTRACT
Niosomes are one of the best and most effective among these carriers system.               Because of the presence of hydrophilic, lipophilic and amphiphilic moieties in the structure, these niosomes can accommodate various drug molecules with a wide range of solubility. So, these may act as a depot, releasing the drug in a defined manner. Rationale behind the present study is to improve the oral bioavailability of Famciclovir by preparing niosomes. Encapsulation of Famciclovir in lipophilic vesicular structure may be expected to enhance the dissolution, oral absorption and prolong the existence of the drug in the systemic circulation. The niosomal dispersions were formulated using various combinations of cholesterol and spans. The formulations were evaluated in-vitro and in-vivo and compared with the marketed preparation of Famciclovir.

Key-words: liposomes, niosomal dispersion, famciclovir, in vivo study.

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Corresponding Author: * Vandana Arora Sethi, Department of Pharmacy, NIMS University, Jaipur, Rajasthan, India. Mob.no. +919873250790
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