Abstract

ABSTRACT Flurbiprofen (FLB), a NSAID, widely used for preventing pain generally for arthritis or dental problems. In this study, FLB loaded chitosan microspheres were prepared by ionotropic gelation method. In this method, microspheres were formed by dropping chitosan solutions containing FLB into sodium alginate solutions including sodium tripolyphosphate (TPP). A variety of formulation parameters like drug:polymer ratio, drug concentration, polymer’s molecular weight, polymer concentration, pH and the concentration of TPP solutions, drying method and stirring time were analyzed. The dissolution studies were performed in a shaking water bath in pH 7.4 phosphate buffer saline (PBS) at 37 °C. Laser diffractometer was used for particle size analysis, and scanning electron microscope (SEM) was used for morphological properties. Drug loading and loading efficiency were calculated by using UV spectrophotometer. The particles obtained were spherical with 0.7-1.3 mm size range, and the loading efficiency was approximately 21-79%. The dissolution studies conducted revealed that drug:polimer ratio and the polymer type and concentration affected the drug release from microspheres. It was observed that increasing the polymer concentration, polymer’s molecular weight and TPP concentration decreased the FLB release from microspheres, which was according to Higuchi kinetics.

Highlights

  • Controlled release systems have been developed against the problems commonly associated with conventional dosage forms (Özalp, Özdemir, 2001; Özdemir, Şahin, 1997)

  • We studied the effect of parameters like molecular weight and concentration of chitosan, the concentration of TPP and the drug-polymer ratio on the encapsulation efficiency, size distribution, particle morphology, release behavior of the drug and release kinetics

  • Chitosan microspheres containing flurbiprofen were prepared by ionotropic gelation method (Bodmeier, Oh, Pramar, 1989)

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Summary

Introduction

Controlled release systems have been developed against the problems commonly associated with conventional dosage forms (dosage frequency, side effects etc) (Özalp, Özdemir, 2001; Özdemir, Şahin, 1997). One of these systems, implant systems, enables targeting in local applications, as well as improving the treatment effectiveness. Giving the active substance within a polymeric system to ensure controlled release or targeting has been quite widespread. Polymers used in implant systems, which are capable of controlled release, are categorized into two: synthetic and natural (Wood, 1980; Davis, Hunneyball, Ratcliffe, 1985; Bogdansky, 1990; Doppalapudi et al, 2014).

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