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2
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本文引用的文献

1
Cyclodextrins as pharmaceutical solubilizers.环糊精作为药物增溶剂
Adv Drug Deliv Rev. 2007 Jul 30;59(7):645-66. doi: 10.1016/j.addr.2007.05.012. Epub 2007 May 29.
2
Immediate release of poorly soluble drugs from starch-based pellets prepared via extrusion/spheronisation.通过挤出/滚圆法制备的淀粉基微丸中难溶性药物的速释。
Eur J Pharm Biopharm. 2007 Nov;67(3):715-24. doi: 10.1016/j.ejpb.2007.04.014. Epub 2007 Apr 29.
3
Elucidation of spheroid formation with and without the extrusion step.
AAPS PharmSciTech. 2007 Feb 9;8(1):10. doi: 10.1208/pt0801010.
4
Use of chitosan-alginate as alternative pelletization aid to microcrystalline cellulose in extrusion/spheronization.壳聚糖-海藻酸盐作为微晶纤维素在挤出/滚圆法中替代制粒助剂的应用。
J Pharm Sci. 2007 Sep;96(9):2469-84. doi: 10.1002/jps.20855.
5
Optimization and scale-up of a fluid bed tangential spray rotogranulation process.流化床切向喷雾旋转制粒工艺的优化与放大
Int J Pharm. 2007 Apr 20;335(1-2):54-62. doi: 10.1016/j.ijpharm.2006.11.022. Epub 2006 Nov 12.
6
Cyclodextrins and their pharmaceutical applications.环糊精及其药物应用。
Int J Pharm. 2007 Feb 1;329(1-2):1-11. doi: 10.1016/j.ijpharm.2006.10.044. Epub 2006 Nov 9.
7
Development of starch-based pellets via extrusion/spheronisation.通过挤出/滚圆法制备淀粉基微丸
Eur J Pharm Biopharm. 2007 Apr;66(1):83-94. doi: 10.1016/j.ejpb.2006.08.015. Epub 2006 Sep 5.
8
Feasibility of eliminating premixing for the production of pellets in a rotary processor.在旋转处理器中消除颗粒生产预混合步骤的可行性。
Pharm Dev Technol. 2006;11(2):159-65. doi: 10.1080/10837450600561240.
9
Use of kappa-carrageenan as alternative pelletisation aid to microcrystalline cellulose in extrusion/spheronisation. I. Influence of type and fraction of filler.κ-卡拉胶作为微晶纤维素在挤出/滚圆造粒法中的替代制粒助剂的应用。I. 填料类型和比例的影响
Eur J Pharm Biopharm. 2006 May;63(1):59-67. doi: 10.1016/j.ejpb.2005.10.002. Epub 2005 Dec 2.
10
Use of kappa-carrageenan as alternative pelletisation aid to microcrystalline cellulose in extrusion/spheronisation. II. Influence of drug and filler type.κ-卡拉胶作为微晶纤维素在挤出/滚圆法中替代制粒助剂的应用。II. 药物和填充剂类型的影响。
Eur J Pharm Biopharm. 2006 May;63(1):68-75. doi: 10.1016/j.ejpb.2005.10.003. Epub 2005 Dec 1.

β-环糊精在制备具有改善溶解性能的崩解性微丸中的应用。

The use of beta-cyclodextrin in the manufacturing of disintegrating pellets with improved dissolution performances.

作者信息

Zema Lucia, Palugan Luca, Maroni Alessandra, Foppoli Anastasia, Sangalli Maria Edvige, Gazzaniga Andrea

机构信息

Istituto di Chimica Farmaceutica e Tossicologica "P. Pratesi", Università degli Studi di Milano, viale Abruzzi 42, 20131 Milan, Italy.

出版信息

AAPS PharmSciTech. 2008;9(2):708-17. doi: 10.1208/s12249-008-9106-0. Epub 2008 Jun 4.

DOI:10.1208/s12249-008-9106-0
PMID:18523889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2976967/
Abstract

It has recently been highlighted that the release behavior of pellets containing microcystalline cellulose (MCC) as the spheronizing agent may be impaired by the lack of disintegration. Although alternative spheronizing excipients have been proposed, their overall advantages have not thoroughly been assessed. In the present work, the possible use of beta-cyclodextrin (betaCD) was therefore explored for the manufacturing of pellets with a potential for effective disintegration and immediate release of poorly soluble active ingredients. MCC/betaCD powder formulations containing no drug or model drugs with different water solubility, able to form inclusion compounds with the employed cyclodextrin, were pelletized by agglomeration in rotary fluid bed equipment. By applying successive statistical experimental designs, the most critical formulation and operating parameters were identified and optimal manufacturing processes were ultimately set up. High yields of pellets provided with satisfactory physical-technological characteristics were obtained using powder formulations with up to 80% betaCD. Based on dissolution testing results, the suitability of betaCD for the preparation of disintegrating MCC-containing pellets with improved dissolution performance was finally demonstrated.

摘要

最近有研究强调,以微晶纤维素(MCC)作为滚圆剂的微丸,其释放行为可能会因缺乏崩解性而受到影响。尽管已经提出了替代滚圆辅料,但它们的总体优势尚未得到充分评估。因此,在本研究中,探讨了β-环糊精(βCD)在制备具有有效崩解潜力且能立即释放难溶性活性成分的微丸中的可能应用。不含药物或含有不同水溶性模型药物(能够与所用环糊精形成包合物)的MCC/βCD粉末制剂,通过在旋转流化床设备中团聚造粒。通过应用连续的统计实验设计,确定了最关键的制剂和操作参数,并最终建立了最佳生产工艺。使用βCD含量高达80%的粉末制剂,可获得具有令人满意的物理技术特性的高产率微丸。基于溶出度测试结果,最终证明了βCD适用于制备具有改善溶出性能的含MCC崩解微丸。