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New investigation of distribution imaging and content uniformity of very low dose drugs using hot-melt extrusion method

Authors
Park, Jun-BomKang, Chin-YangKang, Wie-SooChoi, Han-GonHan, Hyo-KyungLee, Beom-Jin
Issue Date
Dec-2013
Publisher
ELSEVIER
Keywords
Hot-melt extrusion; Low dose drugs; Distribution imaging; Content uniformity; Coumarin-6; Thermosensitive polymers
Citation
INTERNATIONAL JOURNAL OF PHARMACEUTICS, v.458, no.2, pp.245 - 253
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume
458
Number
2
Start Page
245
End Page
253
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/25934
DOI
10.1016/j.ijpharm.2013.10.027
ISSN
0378-5173
Abstract
The content uniformity of low dose drugs in dosage forms is very important for quality assurance. The aim of this study was to prepare uniformly and homogeneously distributed dosage forms of very low-dose drugs using twin screw hot-melt extrusion (HME) and to investigate the distribution of drugs using instrumental analyses. For the feasibility of HME method, a very low amount of coumarin-6, a fluorescent dye, was used to visualize distribution images using confocal laser scanning microscope (CLSM). Limaprost, tamsulosin and glimepiride were then used as low-dose model drugs to study the applicability of HME for content uniformity and distribution behaviors. Hydrophilic thermosensitive polymers with low melting point, such as Poloxamer188 and polyethylene glycol (PEG) 6000, were chosen as carriers. The melt extrusion was carried out around 50 degrees C, at which both carriers were easily dissolved but model drugs remained in solid form. The physicochemical properties of the hot-melt extrudates, including differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD) and Fourier transform infrared spectroscopy (FT-IR), were measured. Content uniformity of the drugs was also checked by HPLC. CLSM imaging showed that model drugs were well distributed throughout the hot-melt extrudate, giving better content uniformity with low batch-to-batch variations compared with simple physical mixtures. DSC, PXRD and FT-IR data showed that there was no interaction or interference between model drugs and thermosensitive polymers. The current HME methods could be used to prepare uniformly distributed and reproducible solid dosage forms containing very low dose drugs for further pharmaceutical applications. (C) 2013 Elsevier B.V. All rights reserved.
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