共 33 条
Methotrexate-loaded porous polymeric adsorbents as oral sustained release formulations
被引:12
作者:
Wang, Xiuyan
[1
]
Yan, Husheng
[1
,2
]
机构:
[1] Nankai Univ, Coll Chem, Inst Polymer Chem, Key Lab Funct Polymer Mat,Minist Educ, Tianjin 300071, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
来源:
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
|
2017年
/
78卷
基金:
中国国家自然科学基金;
关键词:
Adsorption;
Drug delivery;
Oral formulation;
Porous polymeric adsorbent;
Sustained release;
ION-EXCHANGE-RESIN;
WEAK-INTERACTIONS;
ANTICANCER DRUGS;
DELIVERY-SYSTEMS;
ADSORPTION;
MICROSPHERES;
MICROPARTICLES;
MICROCAPSULES;
NANOPARTICLES;
COMPLEX;
D O I:
10.1016/j.msec.2017.04.136
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
082905 [生物质能源与材料];
100103 [病原生物学];
摘要:
Methotrexate as a model drug with poor aqueous solubility was adsorbed into porous polymeric adsorbents, which was used as oral sustained release formulations. In vitro release assay in simulated gastrointestinal fluids showed that the methotrexate-loaded adsorbents showed distinct sustained release performance. The release rate increased with increase in pore size of the adsorbents. In vivo pharmacokinetic study showed that the maximal plasma methotrexate concentrations after oral administration of free methotrexate and methotrexate-loaded DA201-H (a commercial porous polymeric adsorbent) to rats occurred at 40 min and 5 h post-dose, respectively; and the plasma concentrations decreased to 22% after 5 h for free methotrexate and 44% after 24 h for methotrexate-loaded DA201-H, respectively. The load of methotrexate into the porous polymeric adsorbents not only resulted in obvious sustained release, but also enhanced the oral bioavailability of methotrexate. The areas under the curve, AUC(0-24) and AUC(0-inf), for methotrexate-loaded DA201-H increased 33 and 7.7 times, respectively, compared to those for free methotrexate. (C) 2017 Elsevier B.V. All rights reserved.
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页码:598 / 602
页数:5
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