<?xml version="1.0" encoding="UTF-8"?><Articles><Article><id>137</id><JournalTitle>DESIGN, FORMULATION AND EVALUATION OF OFLOXACIN NANOPARTICLES</JournalTitle><Abstract>The aim of this study was to formulate and evaluate the ofloxacin nanoparticles to improve the therapeutic efficacy of
ofloxacin by loading in nanoparticle drug delivery system. Nanoparticles are especially designed to release the drugs in the
vicinity of the target tissue. Nanoparticles are solid colloidal particles with diameter ranging from 1-1000 nm. Ofloxacin
nanoparticles was prepared by emulsion polymerization method by using Eudragit S-100 polymer as a continuous phase for
four different ratios such as (Drug: Polymer) (1:1), (1:2), (1:3) and (1:4). The formulated nanoparticles was evaluated for
external morphological studies using scanning electron microscope, Drug content, invitro release studies and IR spectral
analysis. In IR study reveals that more in no major shifting as well as non less of functional groups peak between the drug,
polymer and drug loaded nanoparticles. The invitro release study showed that the formulation ratio (1:1) gives the better
sustained effect over 96.54 % of drug was released at 8 hours. This study conclude that the ofloxacin nanoparticles are suitable
candidates to produce good antibiotic prolong action.</Abstract><Email>subbupharm@gmail.com</Email><articletype>Research</articletype><volume>3</volume><issue>5</issue><year>2012</year><keyword>Ofloxacin,Nanoparticles,Eudragit S-100,Emulsion Polymerization,In vitro evaluation</keyword><AUTHORS>L.Subramanian,V.Ganesan,N.Venkateshan, P.Solairaj</AUTHORS><afflication>Periyar Maniammai University, Thanjavur, Tamilnadu, India.,Erode College of Pharmacy, Erode, Tamilnadu, India.,Sankaralingam Bhuvaneshwari College of Pharmacy, Sivakasi, Tamilnadu, India.,Sankaralingam Bhuvaneshwari College of Pharmacy, Sivakasi, Tamilnadu, India.</afflication></Article></Articles>