Author(s): Mohd. Majid, Richa Mishra, Brijesh Kunvar Mishra

Email(s): incessantguy@yahoo.com

DOI: Not Available

Address: Mohd. Majid*, Richa Mishra and Brijesh Kunvar Mishra
Technocrats Institute of Technology-Pharmacy, Anand Nagar, Bhopal, Madhya Pradesh, India
*Corresponding Author

Published In:   Volume - 2,      Issue - 2,     Year - 2009


ABSTRACT:
Paracetamol1, 2 is a non steroidal analgesic and antipyretic agent with minimal side effects. Chemically it is 4-hydroxy acetanilide. It is a potent antipyretic and equianalgesic with aspirin in therapeutic doses, commonly used in the conditions like headache, dysmenorrhoea. It is the most frequently prescribed antipyretic agent. It is white crystalline powder, freely soluble in ethanol (95%) and in acetone; sparingly soluble in water, very slightly soluble in dichloromethane and in ether. The drug suffers from poor bioavailability due to its poor aqueous solubility. Aqueous solubility plays and important role in the dissolution of drug in the gastrointestinal fluid. Various approaches for increasing the aqueous solubility of drugs have been reported in literature. The use of carriers as cosolvents is one such approach. The present study investigates the use of various carriers that can enhance the solubility of Paracetamol and improve its bioavailability.


Cite this article:
Mohd. Majid, Richa Mishra, Brijesh Kunvar Mishra. Effects of Various Carriers on the Solubility of Paracetamol. Research J. Pharm. and Tech.2(2): April.-June.2009,;Page 419-420.


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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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