TY - JOUR
T1 - Development and characterisation of cellulose based electrospun mats for buccal delivery of non-steroidal anti-inflammatory drug (NSAID)
AU - Nazari, Kazem
AU - Kontogiannidou, Eleni
AU - Ahmad, Rita Haj
AU - Gratsani, Aggeliki
AU - Rasekh, Manoochehr
AU - Arshad, Muhammad Sohail
AU - Sunar, Burde Suheyla
AU - Armitage, David
AU - Bouropoulos, Nikolaos
AU - Chang, Ming Wei
AU - Li, Xiang
AU - Fatouros, Dimitrios G.
AU - Ahmad, Zeeshan
PY - 2017/5/1
Y1 - 2017/5/1
N2 - In this study conventional electrospinning (ESp) was used to prepare a series of buccal films containing indomethacin (INDO, a nonsteroidal anti-inflammatory drug), Ethocel (10), hydroxypropylmethylcellulose (HPMC) and Tween® 80 at various concentrations. The films were characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM), fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Drug release behaviour was assessed in vitro (buffer pH 6.8). SEM revealed film morphology and mean fibre diameter was dependent on the process formulation. INDO was encapsulated in the amorphous state once electrospun as evidenced from DSC and XRD studies. The presence of other excipients within fibrous matrices was confirmed using FTIR and Raman spectroscopy. Loading and release of INDO from filamentous structures was influenced by formulation composition; indicating potential to ‘fine-tune’ dosage forms. Given that ESp is a one-step preparation method and operational at ambient conditions; an attractive route for engineering tailored film type dosage forms is presented. This is a valuable approach for optimizing dosage forms as needed in a single step for various age groups.
AB - In this study conventional electrospinning (ESp) was used to prepare a series of buccal films containing indomethacin (INDO, a nonsteroidal anti-inflammatory drug), Ethocel (10), hydroxypropylmethylcellulose (HPMC) and Tween® 80 at various concentrations. The films were characterized using scanning electron microscopy (SEM) and atomic force microscopy (AFM), fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Drug release behaviour was assessed in vitro (buffer pH 6.8). SEM revealed film morphology and mean fibre diameter was dependent on the process formulation. INDO was encapsulated in the amorphous state once electrospun as evidenced from DSC and XRD studies. The presence of other excipients within fibrous matrices was confirmed using FTIR and Raman spectroscopy. Loading and release of INDO from filamentous structures was influenced by formulation composition; indicating potential to ‘fine-tune’ dosage forms. Given that ESp is a one-step preparation method and operational at ambient conditions; an attractive route for engineering tailored film type dosage forms is presented. This is a valuable approach for optimizing dosage forms as needed in a single step for various age groups.
KW - Buccal delivery
KW - Electrospinning
KW - Fibres
KW - In vitro studies
KW - Indomethacin
UR - http://www.scopus.com/inward/record.url?scp=85015053809&partnerID=8YFLogxK
U2 - 10.1016/j.ejps.2017.02.033
DO - 10.1016/j.ejps.2017.02.033
M3 - Article
C2 - 28249823
AN - SCOPUS:85015053809
SN - 0928-0987
VL - 102
SP - 147
EP - 155
JO - European Journal of Pharmaceutical Sciences
JF - European Journal of Pharmaceutical Sciences
ER -