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Effect of Drug-Polymer Interaction on Drug Particle Size in Crystalline Solid Dispersion
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Yong ZHANG1, Qiuli YAN2, Wenchuan YANG2, Haiying YAN2, Chunhui HU1, *
Chinese Pharmaceutical Journal | 2024, 59(14) : 1320 - 1330
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Chinese Pharmaceutical Journal | 2024, 59(14): 1320-1330
Effect of Drug-Polymer Interaction on Drug Particle Size in Crystalline Solid Dispersion
Full
Yong ZHANG1, Qiuli YAN2, Wenchuan YANG2, Haiying YAN2, Chunhui HU1, *
Affiliations
  • 1 State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University, Xining 810001, China
  • 2 Medical College, Qinghai University, Xining 810001, China
Published: 2024-07-22 doi: 10.11669/cpj.2024.14.008
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OBJECTIVE To prepare crystallinesolid dispersion(CSD)with ketoconazole (KET) and sorafenib (SOR) as model drugs and poloxamer188 (P188) as carrie, improve the dissolution rate of drug by reducing the drug particle size in vitro and discuss the mechanism of intermolecular interaction on drug particle size regulation. METHODS The drug-P188-CSD was prepared by rotary evaporation method. The intermolecular interaction and crystallization kinetics of drug-P188 in CSD were studied by solubility parameter method (SP), differential scanning calorimetry (DSC) and polarizing microscope (POM). Then the crystal domain size of drug in CSD preparation was measured by powder X-ray diffraction (PXRD). Finally, the solubilization effect of CSD preparation on insoluble drugs was evaluated by dissolution in vitro. RESULTS SP and DSC results showed that in CSD, the two model drugs interacted with P188, and the interaction between SOR and P188 was more significant. The results of POM and PXRD showed that the interaction of drug-P188 would inhibit the crystallization of P188 and reduce the drug particle size by comprehensively regulating the nucleation rate and growth rate of the drug crystal. At the same time, the stronger the interaction force, the stronger the inhibition effect on P188, and the greater the reduction of drug particle size in CSD. The results of dissolution in vitro showed that CSD preparation can effectively improve the dissolution of the drug. The smaller the particle size, the greater the percentage cumulative dissolution rate. CONCLUSION The stronger the interaction between drug and P188 in CSD, the greater the reduction in drug particle size, and the more significant the solubilization effect.

intermolecular interaction  /  crystalline solid dispersion  /  drug particle size  /  in vitro dissolution
Yong ZHANG, Qiuli YAN, Wenchuan YANG, Haiying YAN, Chunhui HU. Effect of Drug-Polymer Interaction on Drug Particle Size in Crystalline Solid Dispersion[J]. Chinese Pharmaceutical Journal, 2024 , 59 (14) : 1320 -1330 . DOI: 10.11669/cpj.2024.14.008
Year 2024 volume 59 Issue 14
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doi: 10.11669/cpj.2024.14.008
  • Receive Date:2023-02-13
  • Online Date:2026-01-14
  • Published:2024-07-22
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  • Received:2023-02-13
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    1 State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University, Xining 810001, China
    2 Medical College, Qinghai University, Xining 810001, 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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