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Destabilization Mechanism of Ionic Surfactant on Curcumin Nanocrystal against Electrolytes

机译:姜黄素纳米晶上离子表面活性剂对电解质的去稳定机理

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摘要

We have successfully developed curcumin nanosuspension intended for oral delivery. The main purpose is to improve bioavailability through enhancing its solubility. The nanoparticles were stabilized using various stabilizers, including polyvinyl pyrrolidone (PVP), polyvinyl alcohol (PVA), sodium carboxymethylcellulose (Na-CMC), d-α-tocopheryl polyethylene glycol 1000 succinate (TPGS), and sodium dodecyl sulfate (SDS). The average diameter of particles, microscopic appearance, and sedimentation of each preparation was observed and compared. Each stabilizer demonstrated a different degree of inhibition of particle aggregation under electrolyte-containing simulated gastrointestinal (GIT) fluid. Non-ionic stabilizers (PVA, PVP, and TPGS) were shown to preserve the nanosuspension stability against electrolytes. In contrast, strong ionic surfactants such as SDS were found to be very sensitive to electrolytes. The results can provide useful information for the formulators to choose the most suitable stabilizers by considering the nature of stabilizers and physiological characteristics of the target site of the drug.
机译:我们已经成功开发了用于口服的姜黄素纳米悬浮液。主要目的是通过提高其溶解度来提高生物利用度。使用各种稳定剂来稳定纳米颗粒,包括聚乙烯吡咯烷酮(PVP),聚乙烯醇(PVA),羧甲基纤维素钠(Na-CMC),d-α-生育酚聚乙二醇1000琥珀酸酯(TPGS)和十二烷基硫酸钠(SDS)。观察并比较了每种制剂的颗粒平均直径,微观外观和沉降。每种稳定剂在含电解质的模拟胃肠道(GIT)液中均表现出不同程度的颗粒聚集抑制作用。已显示非离子稳定剂(PVA,PVP和TPGS)可以保持纳米悬浮液对电解质的稳定性。相反,发现强离子表面活性剂如SDS对电解质非常敏感。通过考虑稳定剂的性质和药物靶位点的生理特性,该结果可为配制者选择最合适的稳定剂提供有用的信息。

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