用电喷雾法将伊曲康唑装入介孔二氧化硅以提高溶解度

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Charitini Volitaki, Andrew Lewis, Duncan Q M Craig, Asma Buanz
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引用次数: 0

摘要

介孔二氧化硅颗粒(MSPs)是一种潜在的载体,可通过物理方式稳定所负载药物的无定形性质,从而提高水溶性差药物的表观溶解度和溶解速率。在制备此类系统时,人们认识到装载方法对药物的物理状态和性能有着至关重要的影响。迄今为止,利用电喷雾将药物装入介孔二氧化硅的研究非常有限。在本研究中,我们进一步探讨了这种方法的使用,特别是作为生产无定形和高药物负载介孔二氧化硅的一种手段;研究包括调查药物负载和介孔二氧化硅浓度对制剂性能和工艺的影响。为了评估电喷雾技术的相对有效性,研究人员将其与旋转蒸发技术(一种更广泛使用的负载技术)进行了比较。使用粉末 X 射线衍射(PXRD)和差示扫描量热法(DSC)评估了制剂中药物的物理状态。药物释放曲线是通过体外药物释放对比试验确定的。即使药物含量较高,电喷雾法也能成功制备出含有无定形药物的制剂。相反,在旋转蒸发法制备的低药物载量制剂中,伊曲康唑呈无定形状态,而在高载量制剂中,药物呈结晶状态。与纯净的伊曲康唑相比,除了旋转蒸发法制备的最高载药量(结晶)制剂外,其他所有制剂的药物释放率都提高了 10 倍。电喷雾法制备的伊曲康唑载量高达 30 毫克/毫升的制剂至少能保持六小时的过饱和状态。总之,这项研究的结果表明,电喷雾法能够制备出高负荷的无定形药物负载 MSP,并具有相关的良好释放特性。与标准旋转蒸发法的比较表明,电喷雾法对于生产较高负载量的无定形材料可能更为有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrospraying as a Means of Loading Itraconazole into Mesoporous Silica for Enhanced Dissolution.

Mesoporous silica particles (MSPs) have been investigated as potential carriers to increase the apparent solubility and dissolution rate of poorly water-soluble drugs by physically stabilising the amorphous nature of the loaded drug. In preparing such systems, it is recognized that the loading method has a critical impact on the physical state and performance of the drug. To date, there has been very limited investigation into the use of electrospraying for loading drugs into mesoporous silica. In this study, we further explore the use of this approach, in particular as a means of producing amorphous and high drug-loaded MSPs; the study includes an investigation of the effect of drug loading and MSP concentration on the formulation performance and process. A comparison with rotary evaporation, a more widely utilised loading technique, was conducted to assess the relative effectiveness of electrospraying. The physical state of the drug in the formulations was assessed using powder X-ray diffraction (PXRD) and differential scanning calorimetry (DSC). The drug release profiles were determined by a comparative in vitro drug release test. Electrospraying successfully produced formulations containing amorphous drug even at a high drug loading. In contrast, while itraconazole was present in amorphous form at the lower drug-loaded formulations produced by rotary evaporation, the drug was in the crystalline state at the higher loadings. The percentage of drug released was enhanced up to ten times compared to that of pure itraconazole for all the formulations apart from the highest loaded (crystalline) formulation prepared by rotary evaporation. Supersaturation for at least six hours was maintained by the formulations loaded with up to 30 mg/mL itraconazole produced by electrospraying. Overall, the results of this study demonstrate that electrospraying is capable of producing amorphous drug-loaded MSPs at high loadings, with associated favourable release characteristics. A comparison with the standard rotary evaporation approach indicates that electrospraying may be more effective for the production of higher loadings of amorphous material.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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