» Authors » N S Chandrashekar

N S Chandrashekar

Explore the profile of N S Chandrashekar including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 6
Citations 26
Followers 0
Related Specialties
Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Chandrashekar N, Shobha Rani R
Indian J Pharm Sci . 2010 Apr; 70(1):94-6. PMID: 20390089
Skin of an average adult body covers a surface of approximately 2 m2 and receives about one-third of the blood circulating through the body. The transdermal route of administration cannot...
2.
Chandrashekar N, Prasanth V
Asian Pac J Cancer Prev . 2008 Nov; 9(3):437-40. PMID: 18990017
The aim of the present study was formulate and clinically evaluate 5-fluorouracil (5-FU) transdermal patches. Cytotoxicity was measured by exposing cell suspensions to increasing concentrations of drug from 10-100 microg/ml...
3.
Chandrashekar N, Shobha Rani R
J Mater Sci Mater Med . 2008 Jul; 20 Suppl 1:S189-94. PMID: 18592348
Microprocessor controlled transdermal delivery of anticancer drugs 5-Fluorouracil (5-FU) and 6-Mercaptopurine (6-MP) was developed and in vitro evaluation was done. Drugs were loaded based on the pharmacokinetics parameters. In vitro...
4.
Chandrashekar N, Hiremath S
Biol Pharm Bull . 2008 Apr; 31(4):656-61. PMID: 18379058
Using skin as a port for systemic drug administration, transdermal drug delivery has expanded greatly over the last two decades. Our aim was to formulate the single layer drug-in-adhesive transdermal...
5.
Chandrashekar N, Hiremath S
Recent Pat Anticancer Drug Discov . 2008 Jan; 2(3):235-9. PMID: 18221066
The purpose of this study was to determine the permeation of the hydrophilic compound 5-fluorouracil through human epidermal membranes, Ehrlich Ascites Carcinoma (EAC) cells were used as a model cell...
6.
Chandrashekar N, Shobha Rani R
J BUON . 2007 Dec; 12(4):529-34. PMID: 18067212
Purpose: The purpose of this study was to fabricate monolithic 5-fluorouracil (5-FU) transdermal patch with microprocessor- controlled iontophoretic delivery, to evaluate the pharmacodynamic effects on Dalton's lymphoma ascites (DLA) induced...