Design and Development of Matrix Diffusion Control Transdermal Drug Delivery System for Antiemetic Drug

Author:

Nagdev Sanjay1,Agrawal Omprakash2,Md. Usman Rageeb3

Affiliation:

1. Ph.d Scholar, School of Pharmacy, Madhyanchal Professional University, Ratibad, Bhopal (M.P)

2. Professor, School of Pharmacy, Madhyanchal Professional University, Ratibad, Bhopal, (M.P)

3. Associate Professor, Smt. S.S. Patil College of Pharmacy, Chopda (Maharashtra)

Abstract

Delivery of drugs into the systemic circulation via transdermal drug delivery system is well known. Transdermal drug delivery system is one of the most reliable and convenient delivery system for the delivery across skin. The aim of this research project is to develop a matrix diffusion control transdermal therapeutic system that combines the drug Ramosetron hydrochloride with an amount of hydrophilic and hydrophobic polymers using a solvent extraction method. Ramosetron hydrochloride is a highly potent drug and has an extended duration of action ad minor side effects despite the severity that it undergoes hepatic pass metabolism and therefore the purpose of this study was to prepare a transdermal patch for Ramosetron hydrochloride for the treatment of chemotherapy induced nausea and vomiting (Anti-emetic action) and evaluate it for various parameters.

Publisher

A and V Publications

Subject

Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Reference27 articles.

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2. Solanki S, Patel K, Patel J, Patel M, Patel J. Transdermal Drug Delivery Systems: A Review. Research Journal of Pharmacy and Technology.2012; 5(6): 757-763.

3. Chien Y. Development of transdermal drug delivery systems. Drug development and industrial pharmacy. 1987; 13(4): 589-651. https://doi.org/10.3109/03639048709105212

4. Misra A. Transdermal drug delivery. Controlled and novel drug delivery, 1st ed. New Delhi: CBS Publishers and Distributors. 1997; 100-29.

5. Chien Y, Patani G. Transdermal drug delivery devices: system design and composition. Encyclopedia of Pharmaceutical Technology. 1999; 18: 309-337.

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