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本文引用的文献

1
An effect of cellulose crystallinity on the moisture absorbability of a pharmaceutical tablet studied by near-infrared spectroscopy.采用近红外光谱法研究纤维素结晶度对药物片剂吸湿性的影响。
Appl Spectrosc. 2014;68(6):625-32. doi: 10.1366/13-07273.
2
Near-infrared imaging analysis of cellulose tablets by a band position shift.通过谱带位置移动对纤维素片剂进行近红外成像分析。
Appl Spectrosc. 2009 Aug;63(8):974-7. doi: 10.1366/000370209788964584.
3
PCA-CR analysis of dissolution profiles. A chemometric approach to probe the polymorphic form of the active pharmaceutical ingredient in a drug product.溶出曲线的主成分分析-聚类分析。一种用于探究药品中活性药物成分多晶型的化学计量学方法。
Int J Pharm. 2009 Aug 13;378(1-2):187-93. doi: 10.1016/j.ijpharm.2009.05.037. Epub 2009 May 27.
4
Multiple perturbation two-dimensional correlation analysis of cellulose by attenuated total reflection infrared spectroscopy.
Appl Spectrosc. 2009 May;63(5):501-6. doi: 10.1366/000370209788346977.
5
Evaluation of a novel sugar coating method for moisture protective tablets.用于防潮片剂的新型糖包衣方法的评估
Int J Pharm. 2007 May 24;336(2):319-28. doi: 10.1016/j.ijpharm.2006.12.015. Epub 2006 Dec 16.
6
Use of a glutaric acid cocrystal to improve oral bioavailability of a low solubility API.使用戊二酸共晶体提高低溶解度活性药物成分的口服生物利用度。
Pharm Res. 2006 Aug;23(8):1888-97. doi: 10.1007/s11095-006-9032-3.
7
Measurement of density variations in tablets using X-ray computed tomography.
Int J Pharm. 2004 Mar 1;271(1-2):215-24. doi: 10.1016/j.ijpharm.2003.11.022.
8
Salt form selection and characterization of LY333531 mesylate monohydrate.LY333531甲磺酸盐一水合物的盐型选择与表征
Int J Pharm. 2000 Apr 5;198(2):239-47. doi: 10.1016/s0378-5173(00)00350-1.
9
Effect of crystallinity of microcrystalline cellulose on the compactability and dissolution of tablets.微晶纤维素的结晶度对片剂可压性和溶出度的影响。
Eur J Pharm Biopharm. 1999 May;47(3):225-30. doi: 10.1016/s0939-6411(98)00102-7.
10
Effect of moisture sorption on tabletting characteristics of spray dried (15% amorphous) lactose.水分吸附对喷雾干燥(15%无定形)乳糖压片特性的影响。
Pharm Res. 1994 Sep;11(9):1233-8. doi: 10.1023/a:1018973923831.

微晶纤维素结晶度对片剂亲水性以及片剂中活性药物成分乙酰水杨酸水解的影响。

The effect of microcrystalline cellulose crystallinity on the hydrophilic property of tablets and the hydrolysis of acetylsalicylic acid as active pharmaceutical ingredient inside tablets.

作者信息

Awa Kimie, Shinzawa Hideyuki, Ozaki Yukihiro

机构信息

Analytical Research and Development Laboratories, Sumitomo Dainippon Pharma Co., Ltd., Osaka, Japan,

出版信息

AAPS PharmSciTech. 2015 Aug;16(4):865-70. doi: 10.1208/s12249-014-0276-7. Epub 2015 Jan 14.

DOI:10.1208/s12249-014-0276-7
PMID:25583304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4508302/
Abstract

The crystal structures of active pharmaceutical ingredients and excipients should be strictly controlled because they influence pharmaceutical properties of products which cause the change in the quality or the bioavailability of the products. In this study, we investigated the effects of microcrystalline cellulose (MCC) crystallinity on the hydrophilic properties of tablets and the hydrolysis of active pharmaceutical ingredient, acetylsalicylic acid (ASA), inside tablets by using tablets containing 20% MCC as an excipient. Different levels of grinding were applied to MCC prior to tablet formulation, to intentionally cause structural variation in the MCC. The water penetration and moisture absorbability of the tablets increased with decreasing the crystallinity of MCC through higher level of grinding. More importantly, the hydrolysis of ASA inside tablets was also accelerated. These results indicate that the crystallinity of MCC has crucial effects on the pharmaceutical properties of tablets even when the tablets contain a relatively small amount of MCC. Therefore, controlling the crystal structure of excipients is important for controlling product qualities.

摘要

活性药物成分和辅料的晶体结构应严格控制,因为它们会影响产品的药学性质,进而导致产品质量或生物利用度的改变。在本研究中,我们以含有20%微晶纤维素(MCC)作为辅料的片剂为对象,研究了MCC结晶度对片剂亲水性以及片剂中活性药物成分乙酰水杨酸(ASA)水解的影响。在片剂制备前,对MCC进行不同程度的研磨,以有意造成MCC的结构变化。通过更高程度的研磨,随着MCC结晶度的降低,片剂的水渗透性和吸湿性增加。更重要的是,片剂中ASA的水解也加速了。这些结果表明,即使片剂中MCC含量相对较少,MCC的结晶度对片剂的药学性质也有至关重要的影响。因此,控制辅料的晶体结构对于控制产品质量很重要。