利用纳米沉淀技术制备和评估阿瑞匹坦纳米悬浮剂

H. B. Samal, Lipsa Samal, Annada Kar, Itishree Jogamaya Das, Bishal Sarkar, Arijit Mondal, Suddhasattya Dey
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引用次数: 0

摘要

药物开发过程中产生的新化学物质大多水溶性差或亲脂性差。对于制药行业来说,配制水溶性差的物质是一项艰巨的任务。本研究旨在研究纳米沉淀技术制备的纳米悬浮剂的粒径,并提高其有效性。对优化后的纳米悬浮液进行了进一步的溶解度、溶出度、表面形态、FT-IR、DSC 以及稳定性研究。药物开发过程中产生的大多数新化学物质都是水溶性差或亲脂性差的,配制水溶性差的物质是制药业的一项艰巨任务。人们普遍认为,在给药过程中使用纳米悬浮剂可以提高药物的溶解度、溶出度以及最终的生物利用度。本研究旨在考察纳米沉淀技术制备的纳米悬浮液的粒径,并提高其有效性。将吐温 80 和聚氧乙烯 188 结合起来作为稳定剂,制备出了优化的纳米悬浮液(F9),其粒径为 738 nm,多分散指数为 0.236,ZETA 电位为 -15.1 mV,与普通药物相比,溶解度和溶出曲线均有所改善。通过扫描电子显微镜、傅立叶变换红外光谱和 DSC 分析,阿瑞匹坦纳米悬浮剂的结晶度在纳米化后发生了变化。通过纳米沉淀技术制备了阿瑞匹坦纳米悬浮液,并测量了所制备纳米悬浮液的粒度、多分散指数和 zeta 电位。对优化后的纳米悬浮液进一步进行了溶解度、溶解度、表面形态、傅立叶变换红外光谱、电导率稳定分析以及稳定性研究。
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Formulation and Evaluation of Aprepitant Nanosuspension by Nano Precipitation Techniques
The majority of new chemical substances generated by the drug development process are poorly water-soluble or lipophilic. Formulation of a poorly water-soluble substance is a difficult task for the pharmaceutical industry. It is widely acknowledged that using nanosuspension in drug administration enhances the drug’s solubility, dissolution, and ultimately bioavailability. This study aimed to examine the particle sizes of nanosuspensions made by nanoprecipitation techniques and improve their effectiveness. Aprepitant’s nanosuspension has been produced by nanoprecipitation techniques. The particle size, polydispersity index, along zeta potential of the produced nanosuspensions were measured. The optimized nanosuspension has been investigated further for solubility, dissolution, surface morphology, FT-IR, DSC as well as stability studies. The majority of new chemical substances generated by the drug development process are poorly water soluble or lipophilic. Formulation of a poorly water-soluble substance is a difficult task for the pharmaceutical industry. It is widely acknowledged that using nanosuspension in drug administration enhances the drug’s solubility, dissolution, and ultimately bioavailability. This study aimed to examine the particle sizes of nanosuspensions made by nano precipitation techniques and improve its effectiveness. The combination of tween 80 and poloxamer 188 as stabilizer resulted in the preparation of an optimized nanosuspension (F9) with a particle size of 738 nm, polydispersity index 0.236, zeta potential -15.1 mV and an improved solubility and dissolution profile compared to pure drugs. Positive performance improvement was observed in the solubility and dissolution studies. The crystallinity changed upon nanosizing, as demonstrated by the SEM, FT-IR and DSC analysis. Aprepitant’s nanosuspension has been produced by nano precipitation techniques. The particle size, polydispersity index along with zeta potential of the produced nanosuspensions were measured. The optimized nanosuspension has been investigated further for solubility, dissolution, surface morphology, FT-IR, DSC as well as stability studies. The nanoprecipitation method was effective in producing a stable Aprepitant nanosuspension with improved solubility and dissolution rate.
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来源期刊
Current Nanomedicine
Current Nanomedicine Medicine-Medicine (miscellaneous)
CiteScore
2.00
自引率
0.00%
发文量
15
期刊最新文献
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