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[双氯芬酸钠脉冲释放微丸的研究]

[Studies on diclofenac sodium pulsatile release pellets].

作者信息

Guo Tao, Zheng Chun-li, Song Hong-tao, Sui Yin, Dang Da-sheng, Sun Xue-hui

机构信息

Department of Pharmacy, General Hospital of Shenyang Military Region, Shenyang 110016, China.

出版信息

Yao Xue Xue Bao. 2003 Sep;38(9):707-10.

Abstract

AIM

To investigate the preparation of diclofenac sodium pulsatile release pellets (DS-PRP), the release in vitro and the pharmacokinetics of the drug.

METHODS

Diclofenac sodium (DS) core pellets prepared by extrusion-spheronization technology were coated in a mini-fluidized bed spray coater with swelling material as the inner coating swelling layer and ethylcellulose aqueous dispersion as the outer coating controlled layer. The effects of formulation and medium on pulsatile release of DS were investigated under release rate test. Pharmacokinetic and bioavailability study in eight human subjects were performed by HPLC method.

RESULTS

The delayed-release time and release rate of DS from DS-PRP were influenced obviously by the swelling material, the concentration of SDS in medium, the coating level of the inner swelling layer and the outer controlled layer. In vitro, the delayed-release time T0.1 was 3.1 h, and the pulsed-release time T0.1-0.2 was 1.2 h. In vivo, the delayed-release time Tlag was 2.8 h, and the bioavailability was (91 +/- 12)%.

CONCLUSION

The release of drug from DS-PRP was shown to be in pulsed way both in vitro and in vivo.

摘要

目的

研究双氯芬酸钠脉冲释放微丸(DS-PRP)的制备、体外释放及药物的药代动力学。

方法

采用挤出滚圆法制备双氯芬酸钠(DS)空白丸芯,在微型流化床包衣机中以膨胀材料为内层包衣膨胀层、乙基纤维素水分散体为外层包衣控释层进行包衣。在释放度试验条件下考察处方和介质对DS脉冲释放的影响。采用高效液相色谱法对8名健康受试者进行药代动力学和生物利用度研究。

结果

DS-PRP中DS的延迟释放时间和释放速率受膨胀材料、介质中十二烷基硫酸钠浓度、内层膨胀层和外层控释层包衣量的影响显著。体外,延迟释放时间T0.1为3.1小时,脉冲释放时间T0.1-0.2为1.2小时。体内,延迟释放时间Tlag为2.8小时,生物利用度为(91±?12)%。

结论

DS-PRP在体内外均呈现脉冲式释药。

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