收藏切换
Application of Polyethylene Oxide in Mirabegron Extended-Release Tablets
收藏切换
PDF
Ruyi WANG, Zhiyong DU, Feng XIONG, Yingjun CAI, Liuang HUANG, Hao GAO, Tingting XIA
Chinese Pharmaceutical Journal | 2024, 59(10) : 921 - 928
Less
收藏切换
Chinese Pharmaceutical Journal | 2024, 59(10): 921-928
Application of Polyethylene Oxide in Mirabegron Extended-Release Tablets
Full
Ruyi WANG, Zhiyong DU, Feng XIONG, Yingjun CAI, Liuang HUANG, Hao GAO, Tingting XIA
Affiliations
  • Pharma Solution, Danisco Biotech (Shanghai) Limited Company, Shanghai 200335, China
Published: 2024-05-22 doi: 10.11669/cpj.2024.10.009
Outline
收藏切换

OBJECTIVE To investigate the impact of polyethylene oxide (PEO, POLYOXTM), penetration additives, and butylated hydroxytoluene (BHT) on tablet properties and drug release of mirabegron extended release (ER) tablets and provide some ideas of formulating polyethylene oxide based ER tablets for the formulators. METHODS Single-factor-experiment was applied to investigate the impact of formulation components on drug release of mirabegron ER tablets. Different molecular weight (MW), series of particle size and use level of polyethylene oxide, three types of penetration additives (PEG 8000, PEG 4000 and lactose) and several use levels of butylated hydroxytoluene (BHT) were investigated. RESULTS Mirabegron ER tablets formulated with polyethylene oxide WSR N60K at 28% use level got statistically equivalent drug release with marketed mirabegron ER tablets. Higher MW and higher use level of polyethylene oxide led to slower drug release, while lower MW and lower use level led to faster drug release. Particle size of polyethylene oxide WSR N60K did not significantly affect mirabegron drug release. The tablets using either polyethylene glycol (PEG 8000 or 4000) or lactose as penetration additives could achieve equivalent drug release as marketed mirabegron ER tablets. The blend of polyethylene oxide WSR 301 and N12K at ratio of 35∶65 has the same viscosity with polyethylene oxide WSR N60K and led to statistically similar drug release. CONCLUSION Formulation of polyethylene oxide based mirabegron ER tablets are robust.

POLYOXTM  /  extended release tablet  /  mirabegron  /  butylated hydroxytoluene
Ruyi WANG, Zhiyong DU, Feng XIONG, Yingjun CAI, Liuang HUANG, Hao GAO, Tingting XIA. Application of Polyethylene Oxide in Mirabegron Extended-Release Tablets[J]. Chinese Pharmaceutical Journal, 2024 , 59 (10) : 921 -928 . DOI: 10.11669/cpj.2024.10.009
Year 2024 volume 59 Issue 10
PDF
145
62
Cite this Article
BibTeX
Article Info
doi: 10.11669/cpj.2024.10.009
  • Receive Date:2023-02-13
  • Online Date:2025-11-25
  • Published:2024-05-22
Article Data
Affiliations
History
  • Received:2023-02-13
Affiliations
    Pharma Solution, Danisco Biotech (Shanghai) Limited Company, Shanghai 200335, China
References
Share
https://castjournals.cast.org.cn/joweb/zgyxzz/EN/10.11669/cpj.2024.10.009
Share to
QR

Scan QR to access full text

Cite this article
BibTeX
Citations
表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏
  • BibTeX
  • EndNote
  • RefWorks
  • TxT