Formulation of Silk Fibroin-based Single Polymeric Floating Microspheres for Sustained Release of Lafutidine

被引:2
|
作者
Pantwalawalkar, Jidnyasa [1 ]
Nangare, Sopan [2 ]
机构
[1] Bharati Vidyapeeth Coll Pharm, Dept Pharmaceut, Kolhapur, Maharashtra, India
[2] HR Patel Inst Pharmaceut Educ & Res, Dept Pharmaceut, Shirpur, Maharashtra, India
关键词
Lafutidine; Silk fibroin; Microsphere; Floating drug delivery; Sustained release; DRUG-DELIVERY; SYSTEMS;
D O I
10.5530/ijper.56.2.59
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Purpose: The present study was aimed at the formulation of lafutidine-loaded silk fibroinbased floating microspheres (LAFU-SF-Microspheres) for the site-specific sustained release of the drug. Materials and Methods: Briefly, the single polymeric system comprising SF was selected to prepare LAFU-SF-Microspheres by employing the emulsion solvent evaporation method. Subsequently, the obtained LAFU-SF-Microspheres were assessed analysis, and accelerated stability study. Results: The particle size and zeta potential of the LAFU-SF-Microsphere were found to be 2.3-6.8 mu m and -21.93mV respectively whilst % EE and % DC of LAFU-SF-Microspheres were found to be 86.83 +/- 3.46% and 93.89 +/- 3.98% respectively. Moreover, it demonstrated the adequate angle of repose (26.50 +/- 1.06 degrees) and Carr's Compressibility Index (CI) confirming the excellent flow properties. In view of the floating profile, LAFU-SF-Microspheres showed floating lag time (FLT) between 9-13sec and total floating time (TFT) more than 12hr. Moreover, the % buoyancy was found to be 97.62 +/- 4.78%. LAFU-SF-Microspheres showed in-vitro % drug release up to 92.41 +/- 4.29% adopting the first-order model. The FTIR indicated successful incorporation of LAFU in LAFU-SF-Microspheres. The DSC and PXRD indicated the disrupted crystallinity of LAFU in LAFU-SF-Microspheres. The SEM images of microspheres displayed spherical shapes with smooth textures. Conclusion: SF microspheres can be fruitfully applied for customized floating and release patterns of drugs with distinct solubility classes.
引用
收藏
页码:396 / 404
页数:9
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