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盐酸氨溴索微囊化速溶片的制备与评价

Preparation and evaluation of microencapsulated fast melt tablets of ambroxol hydrochloride.

作者信息

Jacob S, Shirwaikar A

机构信息

Department of Pharmaceutical Sciences, S. Bhagwan Singh (PG) Institute of Biomedical Sciences and Research, Balawala, Dehradun-248 161, India.

出版信息

Indian J Pharm Sci. 2009 May;71(3):276-84. doi: 10.4103/0250-474X.56028.

DOI:10.4103/0250-474X.56028
PMID:20490294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2865786/
Abstract

Natural resources in general and plant materials in particular are receiving more attention due to their safety as pharmaceutical excipients. Present work assessed the potential of a natural polysaccharide, pectin to mask the bitter taste of ambroxol hydrochloride, by microencapsulation technique, and its possibility to formulate as a fast disintegrating dosage form. Taste masking is an important developmental challenge in fast dissolving drug delivery system since it dissolves or disintegrates in the patient's mouth in close proximity to the taste buds. The prepared microspheres by emulsion solvent evaporation technique possessed good sphericity, smooth surface morphology, uniform and narrow size distribution (10-90 mum), when analyzed by scanning electron microscopy, laser diffraction and optical microscopy. Method of preparation has influenced the particle size and drug loading efficiency. Drug-polymer compatibility was confirmed by Fourier transform infrared spectroscopy and thin layer chromatography. DSC and X-ray diffraction studies revealed that the drug was dispersed inside the microspheres in the form of an insoluble matrix. The formation of microspheres was affected by glass transition temperature of the polymer, surfactant, type of plasticizers, volume of internal phase, stirrer speed etc. Fast dissolving tablets were prepared by the modification of melt granulation technique. The resulting granules were found to melt fast at body temperature, have smooth mouth feel and good physical stability. This study demonstrated that pectin could be a right choice in developing patient favored formulations for bitter drugs and can be utilized in fast disintegrating dosage forms as well.

摘要

一般来说,自然资源尤其是植物材料,因其作为药物辅料的安全性而受到越来越多的关注。目前的工作评估了一种天然多糖——果胶,通过微囊化技术掩盖盐酸氨溴索苦味的潜力,以及将其制成快速崩解剂型的可能性。在快速溶解给药系统中,掩味是一个重要的开发挑战,因为它在患者口腔中靠近味蕾的位置溶解或崩解。通过扫描电子显微镜、激光衍射和光学显微镜分析,采用乳液溶剂蒸发技术制备的微球具有良好的球形度、光滑的表面形态、均匀且狭窄的粒径分布(10 - 90μm)。制备方法影响了粒径和载药效率。通过傅里叶变换红外光谱和薄层色谱法证实了药物与聚合物的相容性。差示扫描量热法和X射线衍射研究表明,药物以不溶性基质的形式分散在微球内部。微球的形成受聚合物的玻璃化转变温度、表面活性剂、增塑剂类型、内相体积、搅拌速度等影响。通过改进熔融制粒技术制备了快速溶解片。发现所得颗粒在体温下快速熔融,口感顺滑且具有良好的物理稳定性。这项研究表明,果胶可能是开发受患者青睐的苦味药物制剂的正确选择,并且也可用于快速崩解剂型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/d141433ce22d/IJPhS-71-276-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/cc6d545627b9/IJPhS-71-276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/b452eab94d17/IJPhS-71-276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/d141433ce22d/IJPhS-71-276-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/cc6d545627b9/IJPhS-71-276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/b452eab94d17/IJPhS-71-276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd46/2865786/d141433ce22d/IJPhS-71-276-g003.jpg

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