Arjun Sony

Naproxen is a non-steroidal anti-inflammatory drug (NSAID) commonly used for the reduction of mild to moderate pain, fever, inflammation and stiffness caused by conditions such as osteoarthritis, rheumatoid arthritis, psoriatic arthritis, gout, ankylosing spondylitis, injury, menstrual cramps, tenditis, bursitis and the treatment of primary dysmenorrheal. The reason behind incorporation of Naproxen in Niosomes as this non-ionic surfactants vesicles offer several advantages over other drug carriers like liposome with respect to its biocompatibility, simple and controllable preparation, their capacity to carry large amount of drug, commercially availability, capable of entrapping hydrophilic and hydrophobic drug, cheaper in cost, any special condition not require for the use of the surfactant. The niosome system which achieves the site specific delivery of drug with controlled release kinetics of drug in predictable manner. Before this preparation, prior preparations had been made known as Pro-niosomes with Cholesterol, Surfactant, and Ethanol which later on converting to Niosomes. 

  The task of developing immediate release tablet is accomplished by using a suitable diluents and super-disintegrants. Faster disintegration of the tablet administrated orally minimizes absorption time and improves its bioavailability in less time. Immediate Release tablet of Antibiotic drug is formulated using dry granulation using super disintegrant croscarmellose sodium. Azithromycin is Antibiotic drug is used to treat STDs due to Chlamydia and gonorrhea, community-acquired pneumonia, pelvic inflammatory disease, pediatric otitis media and pharyngitis, and Mycobacterium avium complex (MAC) in patients with advanced HIV disease. One of the important studies included in the present investigation is of study on process parameter effect on performance of the Immediate Release tablets. The effect of selected process parameters on critical properties of immediate release (IR) tablets were studied, like effect of disintegration time, friability, dissolution profile.   Key words: Immediate release, Azithromycin, Croscarmellose sodium