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可视化卡马西平在有无辅料存在的水悬浮液中的转化:使用扫描电子显微镜和拉曼显微镜的单晶研究

Visualizing the conversion of carbamazepine in aqueous suspension with and without the presence of excipients: a single crystal study using SEM and Raman microscopy.

作者信息

Tian F, Sandler N, Gordon K C, McGoverin C M, Reay A, Strachan C J, Saville D J, Rades T

机构信息

School of Pharmacy, University of Otago, Dunedin, New Zealand.

出版信息

Eur J Pharm Biopharm. 2006 Nov;64(3):326-35. doi: 10.1016/j.ejpb.2006.05.014. Epub 2006 Jun 3.

Abstract

Visual observations of the hydration process of single carbamazepine (CBZ) crystals in water and in various excipient solutions [(1% w/v) - hydroxypropyl cellulose (HPC), poly(vinyl pyrrolidone) (PVP), sodium carboxymethylcellulose (CMC) at pH 7.5 and 3.0, and polyethylene glycol (PEG)] using scanning electron microscopy (SEM) are reported in this paper. Raman microscopy was used to confirm the chemical structures of the unconverted CBZ and the CBZ dihydrate (DH) needles. It was found that defect structures were a more important driving force than the nature of crystal faces for the initiation of the hydration, but face differences became obvious after 6 h immersion. The biggest crystal face grown from methanol, (100), was the slowest one to be covered with DH needles. A comparison of the molecular arrangements along the three crystal faces [(100), (010) and (001)] was carried out using crystal structure visualization software, and fewer polar groups exposed on the (100) face than on the (001) and (010) faces were found, explaining the comparatively weak interaction of the (100) face with water during hydration. Furthermore, investigation of the influence of excipients on the hydration of CBZ showed that both HPC and PVP strongly inhibited conversion, and no conversion of CBZ to DH was found after 18 h immersion in water. PEG and CMC (pH 7.5) were less potent inhibitors than HPC and PVP, and DH needles were observed on all the faces except the (100) face after 18 h immersion. No conversion was detected for the crystal immersed in CMC solution at pH 3.0. This is likely to be caused by the decreased polarity of CMC in water at pH 3.0 (pKa,cmc = 4.3), and thus a higher surface adsorption of CMC to the CBZ crystals in dispersion. The influence of excipients on the conversion of CBZ observed in this study agreed well with our previous quantitative studies using Raman spectroscopy. In this study, visual observation using electron microscopy has been demonstrated to be a unique and powerful tool to improve our understanding of polymorphic conversions of CBZ in aqueous suspension.

摘要

本文报道了利用扫描电子显微镜(SEM)对卡马西平(CBZ)单晶在水和各种辅料溶液[(1% w/v)-羟丙基纤维素(HPC)、聚乙烯吡咯烷酮(PVP)、pH 7.5和3.0的羧甲基纤维素钠(CMC)以及聚乙二醇(PEG)]中的水合过程进行的视觉观察。拉曼显微镜用于确认未转化的CBZ和CBZ二水合物(DH)针状晶体的化学结构。研究发现,对于水合作用的起始,缺陷结构比晶面性质是更重要的驱动力,但浸泡6小时后晶面差异变得明显。从甲醇中生长出的最大晶面(100)是被DH针状晶体覆盖最慢的晶面。使用晶体结构可视化软件对沿三个晶面[(100)、(010)和(001)]的分子排列进行了比较,发现(100)面上暴露的极性基团比(001)和(010)面上少,这解释了水合过程中(100)面与水的相互作用相对较弱的原因。此外,对辅料对CBZ水合作用影响的研究表明,HPC和PVP都强烈抑制转化,在水中浸泡18小时后未发现CBZ向DH的转化。PEG和CMC(pH 7.5)是比HPC和PVP效力较弱的抑制剂,浸泡18小时后,除了(100)面外,在所有晶面上都观察到了DH针状晶体。在pH 3.0的CMC溶液中浸泡的晶体未检测到转化。这可能是由于pH 3.0(pKa,cmc = 4.3)时CMC在水中的极性降低,因此CMC在分散体中对CBZ晶体的表面吸附更高。本研究中观察到的辅料对CBZ转化的影响与我们之前使用拉曼光谱进行的定量研究结果非常吻合。在本研究中,已证明使用电子显微镜进行视觉观察是一种独特而强大的工具,有助于我们更好地理解CBZ在水悬浮液中的多晶型转化。

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