Preparation, Characterization and In Vitro Evaluation of Dirithromycin Loaded Eudragit (R) RS 100 Nanoparticles for Topical Application


Yenilmez E., YURTDAŞ KIRIMLIOĞLU G., ŞENEL B., BAŞARAN E.

LATIN AMERICAN JOURNAL OF PHARMACY, cilt.36, sa.11, ss.2203-2212, 2017 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 36 Sayı: 11
  • Basım Tarihi: 2017
  • Dergi Adı: LATIN AMERICAN JOURNAL OF PHARMACY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.2203-2212
  • Anahtar Kelimeler: dirithromycin, Eudragit (R) RS100, nanoparticle, spray drying, POLYMERIC NANOPARTICLES, VERAPAMIL HYDROCHLORIDE, RS100 NANOPARTICLES, DRUG-RELEASE, ANTIBIOTICS, DELIVERY, FORMULATIONS, SPECTROSCOPY, ACNE, NANO
  • Anadolu Üniversitesi Adresli: Evet

Özet

The purpose of the study was to formulate dirithromycin (DR) loaded Eudragit (R) RS 100 (ERS) nanoparticles for topical application and to analyze the physical and chemical characteristics and in vitro toxicity of the prepared formulations. The nanoparticles of DR with ERS were formulated by spray drying method. The characteristics of nanoparticles were revealed applying scanning electron microscopy, particle size analysis, zeta potential analysis, differential scanning calorimetry, Fourier transform infrared spectroscopy and proton nuclear magnetic resonance spectroscopy. The release rate of DR from drug/ polymer nanoparticles was investigated as well. Quantitative determination of cytotoxicity of the formulations was investigated on 3T3 mouse embryo fibroblast cell lines. Analyses of results revealed that nano-range sized self-cationic particles with relative spherical morphology were achieved by spray drying method. Nanoparticles displayed slowed release patterns in comparison with the drug powder as expected. With non-toxic properties and extended releases, DR loaded ERS nanoparticles seem to be a promising drug delivery systems for specific applications in the formulation of pharmaceuticals.