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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Systematic studies of Pickering emulsions stabilized by uniform-sized PLGA particles: preparation and stabilization mechanism
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Systematic studies of Pickering emulsions stabilized by uniform-sized PLGA particles: preparation and stabilization mechanism

机译:均相PLGA颗粒稳定的Pickering乳液的系统研究:制备和稳定机理

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摘要

Pickering emulsions stabilized by solid particles have been widely studied in the past decades due to improved stability and reduced use of small molecular surfactants. Recently, the application of Pickering emulsions in pharmaceutics has been attracting increasing attention but very limited practical use has been demonstrated, because most of the investigated particles possess poor biodegradability, which is inappropriate in pharmaceutics. Some reported biodegradable particles were too hydrophilic to stabilize emulsions, which needs further particle modification or additional surfactants. Fortunately, biodegradable poly(D,L-!actic-co-glycolic acid) (PLGA) with tunable hydrophilicity makes itself a promising material to prepare Pickering emulsions. However, the mechanism of emulsion stabilization still remains unknown. Moreover, fabrication of large amounts of uniform-sized and size-controlled PLGA particles by traditional methods is very difficult, which further increases the difficulty to perform the research, in the present study, we applied Shirasu Porous Glass (SPG) premix membrane emulsification to solve this problem. The stabilization mechanism of Pickering emulsions stabilized by PLGA particles was systematically studied for the first time. The factors including oil type, particle properties, concentration, molecular weight (M_w) and oil-water volume ratio were analyzed through particle wettability and interfacial influence. We found that octanol was an appropriate oil type, and its small particle size, high particle concentration and high M_w were favorable for emulsion stability. By changing the oil-water volume ratio, stable emulsions were also readily achieved. These studies proved that Pickering emulsions stabilized by PLGA particles had wide potential applications in pharmaceutics and tissue engineering.
机译:在过去的几十年中,由于提高了稳定性并减少了小分子表面活性剂的使用,已广泛研究了由固体颗粒稳定的Pickering乳液。近来,Pickering乳液在药物中的应用已引起越来越多的关注,但是由于大多数被研究的颗粒具有差的生物降解性,因此已证明其实际用途非常有限,这在药物中是不合适的。一些报道的可生物降解的颗粒亲水性太强,无法稳定乳液,这需要进一步的颗粒改性或其他表面活性剂。幸运的是,具有可调节的亲水性的可生物降解的聚(D,L-乳酸-乙醇酸共聚物)(PLGA)使其本身成为制备Pickering乳液的有前途的材料。但是,乳液稳定的机理仍然未知。此外,通过传统方法制造大量均匀尺寸和尺寸可控的PLGA颗粒非常困难,这进一步增加了进行研究的难度。在本研究中,我们将Shirasu多孔玻璃(SPG)预混膜乳化用于解决这个问题。首次系统地研究了PLGA颗粒稳定的Pickering乳液的稳定机理。通过颗粒润湿性和界面影响,分析了油的类型,颗粒性质,浓度,分子量(M_w)和油水体积比等因素。我们发现辛醇是一种合适的油类型,其小粒径,高颗粒浓度和高M_w有利于乳液的稳定性。通过改变油水体积比,也容易获得稳定的乳液。这些研究证明,由PLGA颗粒稳定的Pickering乳液在制药和组织工程中具有广泛的潜在应用。

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