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Electrostatic spraying for fine-tuning particle dimensions to enhance oral bioavailability of poorly water-soluble drugsopen access

Authors
Kim, Jung SukCheon, SeunghyunWoo, Mi RanWoo, SanghyunChung, Jee-EunYoun, Yu SeokOh, Kyung TaekLim, Soo-JeongKu, Sae KwangNguyen, Bao LocKim, Jong OhJin, Sung GiuChoi, Han-Gon
Issue Date
Oct-2024
Publisher
Shenyang Pharmaceutical University
Keywords
Electrostatic spray drying; Oral antitumor efficacy; Oral bioavailability; Particle size distribution; Poorly water-soluble drug; Regorafenib
Citation
Asian Journal of Pharmaceutical Sciences, v.19, no.5, pp 1 - 14
Pages
14
Indexed
SCIE
SCOPUS
Journal Title
Asian Journal of Pharmaceutical Sciences
Volume
19
Number
5
Start Page
1
End Page
14
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/120719
DOI
10.1016/j.ajps.2024.100953
ISSN
1818-0876
Abstract
While spray-drying has been widely utilized to improve the bioavailability of poorly water-soluble drugs, the outcomes often exhibit suboptimal particle size distribution and large particle sizes, limiting their effectiveness. In this study, we introduce electrostatic spraying as an advanced technology tailored for poorly water-soluble drugs, enabling the fabrication of nanoparticles with fine and uniform particle size distribution. Regorafenib (1 g), as a model drug, copovidone (5 g), and sodium dodecyl sulfate (0.1 g) were dissolved in 200 ml ethanol and subjected to conventional-spray-dryer and electrostatic spray dryer. The electrostatic spray-dried nanoparticles (ESDN) showed smaller particle sizes with better uniformity compared to conventional spray-dried nanoparticles (CSDN). ESDN demonstrated significantly enhanced solubility and rapid release in water. In vitro studies revealed that ESDN induced apoptosis in HCT-116 cells to a greater extent, exhibiting superior cytotoxicity compared to CSDN. Furthermore, ESDN substantially improved oral bioavailability and antitumor efficacy compared to CSDN. These findings suggest that ESD shows potential in developing enhanced drug delivery systems for poorly water-soluble drugs, effectively addressing the limitations associated with CSD methods. © 2024
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