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Electrostatic spraying for fine-tuning particle dimensions to enhance oral bioavailability of poorly water-soluble drugs
被引:4
|作者:
Kim, Jung Suk
[1
]
Cheon, Seunghyun
[1
]
Woo, Mi Ran
[1
]
Woo, Sanghyun
[1
]
Chung, Jee-Eun
[1
]
Youn, Yu Seok
[2
]
Oh, Kyung Taek
[3
]
Lim, Soo-Jeong
[4
]
Ku, Sae Kwang
[5
]
Nguyen, Bao Loc
[6
]
Kim, Jong Oh
[6
]
Jin, Sung Giu
[7
]
Choi, Han-Gon
[1
]
机构:
[1] Hanyang Univ, Coll Pharm, Ansan 15588, South Korea
[2] Sungkyunkwan Univ, Sch Pharm, Suwon 440746, South Korea
[3] Chung Ang Univ, Coll Pharm, Seoul 156756, South Korea
[4] Sejong Univ, Dept Biosci & biotechnol, Seoul 143747, South Korea
[5] Daegu Haany Univ, Coll Korean Med, Dept Anat & Histol, Gyongsan 38610, South Korea
[6] Yeungnam Univ, Coll Pharm, Gyongsan 712749, South Korea
[7] Dankook Univ, Dept Pharmaceut Engn, Cheonan 31116, South Korea
基金:
新加坡国家研究基金会;
关键词:
Electrostatic spray drying;
Poorly water-soluble drug;
Regorafenib;
Particle size distribution;
Oral bioavailability;
Oral antitumor efficacy;
REGORAFENIB;
D O I:
10.1016/j.ajps.2024.100953
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
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. (c) 2024 Shenyang Pharmaceutical University. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
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