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Development of an Oral Compound Pickering Emulsion Composed of Nanocrystals of Poorly Soluble Ingredient and Volatile Oils from Traditional Chinese Medicine

机译:难溶成分和挥发油纳米晶体组成的中药复方口服匹克乳剂的研制

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摘要

In this study, an oral drug nanocrystals self-stabilized Pickering emulsion (NSSPE), which used nanocrystals of a poorly soluble ingredient from Puerariae Radix called puerarin as solid particle stabilizers and Ligusticum chuanxiong essential oil since the main oil phase had been developed to improve the oral bioavailability of puerarin. The appearance of emulsions, size and zeta potential of droplets, and content of puerarin in emulsified layer during a storage of six months at 4, 25, and 40 °C were investigated. The centrifugation stability at 4000× g was also studied. The micro-structure of emulsion droplets was characterized by a scanning electron micrograph (SEM), confocal laser scanning microscopy (CLSM), a fluorescence microscope (FM), and differential scanning calorimetry (DSC). The in vivo oral bioavailability of puerarin NSSPE was investigated in rats. Results showed that appearances of puerarin NSSPE kept stable after centrifugation at 4000× g for 15 min or storage for six months at 4, 25, and 40 °C. SEM, CLSM, FM, and DSC showed that the puerarin NSSPE had a stable core-shell structure of emulsion droplets formed by the adsorption of puerarin nanocrystals on the surface of oil droplets of mixed oil of Ligusticum chuanxiong essential oil and Labrafil M 1944 CS (9:1, v/v). The relative bioavailability of puerarin NSSPE to puerarin coarse powder suspension, nanocrystal suspension, and surfactant emulsion were 262.43%, 155.92%, and 223.65%, respectively. All these results indicated that puerarin nanocrystals could stabilize Pickering emulsion of Ligusticum chuanxiong essential oil without any other stabilizers and Pickering emulsion could improve the oral bioavailability of puerarin, which suggests that the drug nanocrystal self-stabilized Pickering emulsion as a promising oral drug delivery system for Traditional Chinese Medicine containing poorly soluble ingredients and volatile oils.
机译:在这项研究中,口服药物纳米晶体自稳定Pickering乳液(NSSPE)使用了来自葛根的难溶成分的纳米晶体puerarin作为固体颗粒稳定剂和川Li(Ligusticum chuanxiong)精油,因为已经开发了主要油相来改善葛根素的口服生物利用度。研究了在4、25和40°C下储存六个月的乳化液外观,液滴大小和zeta电位以及乳化层中的葛根素含量。还研究了在4000×g下的离心稳定性。乳剂液滴的微观结构通过扫描电子显微镜(SEM),共聚焦激光扫描显微镜(CLSM),荧光显微镜(FM)和差示扫描量热法(DSC)进行表征。在大鼠中研究了葛根素NSSPE的体内口服生物利用度。结果表明,葛根素NSSPE的外观在4000x g离心15分钟或在4、25和40°C储存六个月后保持稳定。 SEM,CLSM,FM和DSC结果表明,葛根素NSSPE具有稳定的乳液液滴核壳结构,该液滴是由葛根素纳米晶体在川gust精油和Labrafil M 1944 CS( 9:1,v / v)。葛根素NSSPE对葛根素粗粉悬浮液,纳米晶体悬浮液和表面活性剂乳液的相对生物利用度分别为262.43%,155.92%和223.65%。所有这些结果表明葛根素纳米晶体可以稳定川gust精油的Pickering乳液而无需任何其他稳定剂,而Pickering乳液可以提高葛根素的口服生物利用度,这表明该药物纳米晶体自稳定Pickering乳液作为一种有前景的口服药物递送系统中药含有难溶成分和挥发油。

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