FORMULATION AND CHARACTERIZATION OF LINEZOLID LOADED EUDRAGIT RS 100 POLYMERIC NANOPARTICLES

被引:2
|
作者
Shaji, Jessy [1 ]
Kumbhar, Monika [1 ]
机构
[1] Prin KM Kundnani Coll Pharm, Dept Pharmaceut, Mumbai 400005, Maharashtra, India
关键词
Tuberculosis; Linezolid; Polymeric nanoparticle; Double emulsion solvent evaporation; OPTIMIZATION;
D O I
10.13040/IJPSR.0975-8232.10(4).1944-52
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tuberculosis (TB) is an alluring affliction caused predominantly by Mycobacterium tuberculosis bacteria. A stumbling block in the conventional treatment of TB is the occurrence of multiple drug resistance (MDR) followed by high dose requirement, subsequent intolerance & severe toxicity. Nanoparticulate-based drug therapy has significant potency in the treatment of TB. In this present study, Linezolid loaded Eudragit RS 100 polymeric nanoparticles (LZD-PNPs) were developed and characterised for the treatment of TB. Double emulsion solvent evaporation method was selected to incorporate LZD into Eudragit RS 100. Differential scanning calorimetry (DSC), Fourier Transfer Infrared spectroscopy (FT-IR) studies were done to assess drug-polymer compatibility and to indicate absence of incompatibility. Particle size analysis was carried out to measure the mean particle size of the LZD-PNPs and was found to be at 47nm-119nm (+/- 26 to 41 SD) which indicated the polydispersity of the formulation. Zeta potential analysis of the sample was found to be -32 to -41mv, indicating its physicochemical stability. The Entrapment efficiency of LZD-PNPs ranged between 75.56% to 80.42%. Optimization of the LZD-PNPs was done by response surface analysis (Design Expert 11.0.5.0 software State Ease, Inc., Minneapolis, MN). The above data suggest that linezolid loaded Eudragit RS 100 polymeric nanoparticle were successfully formulated by double emulsion solvent evaporation method and characterized for effective delivery of MDR TB.
引用
收藏
页码:1944 / 1952
页数:9
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