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Preparation and Evaluation of Fenofibrate Self-microemulsifying Drug Delivery System
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Jiangwei LÜ1, Jingjing JIANG1, Wei CHEN1, Xueying ZHAO1, Wenjun ZHANG1, *, Youpeng QU2
Chinese Pharmaceutical Journal | 2024, 59(24) : 2343 - 2353
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Chinese Pharmaceutical Journal | 2024, 59(24): 2343-2353
Preparation and Evaluation of Fenofibrate Self-microemulsifying Drug Delivery System
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Jiangwei LÜ1, Jingjing JIANG1, Wei CHEN1, Xueying ZHAO1, Wenjun ZHANG1, *, Youpeng QU2
Affiliations
  • 1 School of Pharmacy, Harbin University of Commerce, Harbin 150076, China
  • 2 School of Life Science and Technology, Harbin Institute of Technology, Harbin 150080, China
Published: 2024-12-22 doi: 10.11669/cpj.2024.24.007
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OBJECTIVE In order to improve the solubility and dissolution of the insoluble drug fenofibrate (FNB) optimize, the prescription of the self-microemulsifying drug delivery system (SMEDDS) was optimized and its quality was evaluated. METHODS The prescription composition and proportion range of SMEDDS were determined by the solubility experiment, compatibility test and pseudoternary phase diagram. Star point design-response surface methodology was used to further optimize the formulation of fenofibrate self-microemulsifying drug delivery system (FNB-SMEDDS) by using solubility, average particle size and polydispersity index (PDI) as evaluation indicators. The physical and chemical properties, and preliminary stability of FNB-SMEDDS were evaluated. RESULTS The optimal prescription of FNB-SMEDDS was ethyl oleate (EO) 22.86% as oil phase, polyoxyethylene (40) hydrogenated castor oil (cremophor RH40) 51.07% as surfactant, diethylene glycol monoethyl ether (transcutol HP) 26.07% as co-surfactant. The obtained FNB-SMEDDS was uniform and transparent. The FNB-SMEDDS was self-emulsified in water with average particle size of (39.29±0.45) nm, PDI of (0.11±0.01), Zeta potential of (-7.7±0.9) mV, drug loading rate of 15 mg·g-1, encapsulation rate of (95.11±0.26)%, and emulsification time of (56.03±1.65) s. Stability experiments showed that after being stored at room temperature in the dark for 30 days, there was no significant change in its index components and appearance properties, indicating good stability. Compared with FNB API, FNB-SMEDDS significantly improved the in vitro dissolution of FNB. The cumulative release rates in water, pH 1.2 hydrochloric acid solution and pH 6.8 phosphate buffer solution for 120 min were (97.68±0.61)%, (92.23±4.07)% and (93.65±2.25)%, respectively. CONCLUSION FNB-SMEDDS has good appearance, high emulsification efficiency. It can significantly improve in vitro dissolution of the drug, and is expected to improve the in vivo bioavailability of FNB.

fenofibrate  /  self-microemulsifying drug delivery system  /  pseudoternary phase diagram  /  central composite design-response surface methodology  /  quality evaluation  /  dissolution
Jiangwei LÜ, Jingjing JIANG, Wei CHEN, Xueying ZHAO, Wenjun ZHANG, Youpeng QU. Preparation and Evaluation of Fenofibrate Self-microemulsifying Drug Delivery System[J]. Chinese Pharmaceutical Journal, 2024 , 59 (24) : 2343 -2353 . DOI: 10.11669/cpj.2024.24.007
Year 2024 volume 59 Issue 24
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doi: 10.11669/cpj.2024.24.007
  • Receive Date:2024-02-28
  • Online Date:2025-11-13
  • Published:2024-12-22
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  • Received:2024-02-28
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    1 School of Pharmacy, Harbin University of Commerce, Harbin 150076, China
    2 School of Life Science and Technology, Harbin Institute of Technology, Harbin 150080, China
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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
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