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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Preparation of uniform poly(lactide) microspheres by employing the Shirasu Porous Glass (SPG) emulsification technique
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Preparation of uniform poly(lactide) microspheres by employing the Shirasu Porous Glass (SPG) emulsification technique

机译:利用Shirasu多孔玻璃(SPG)乳化技术制备均匀的丙交酯微球

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摘要

Relatively uniform biodegradable poly(lactide) (PLA) microspheres were prepared by employing a Shirasu Porous Glass (SPG) membrane emulsification technique. Poly(lactide) dissolved in co-surfactant (hydrophobic substance)/dichloromethane (DCM) was used as a dispersed phase (oil phase) and an aqueous phase containing poly(vinyl alcohol) (PVA) and sodium lauryl sulfate (SLS) was used as a continuous phase. The oil phase permeated through the uniform pores of the SPG membrane into the continuous phase by a pressure of nitrogen gas to form the droplets. Then, the solid polymer microspheres were obtained by simply evaporating DCM at room temperature for 24 h. The effects of the type and the amount of the co-surfactant, and PLA concentration on the size, size distribution, and the morphologies of the droplets and particles were investigated. A relatively uniform spherical PLA microsphere was obtained successfully by using lauryl alcohol (LOH) rather than hexadecane (HD) as a co-surfactant. PLA concentration was varied from 10 to 20 wt.%/vol, and the LOH/DCM ratio changed from 0.5:11.5 to 2:10 by volume. At the polymer concentration range used in this study (10-20 wt.%), variation of the droplet size was not so apparent when 2 ml of LOH was used, but the droplet size showed a minimum value at 15 wt.% when 0.5 or 1 ml of LOH was used. The variation of CV value (coefficient of variation) was smaller in the PLA concentration range of 10-15 wt.%, then the CV value became larger as the PLA concentration was incrased from 15 to 20 wt.%. Although there was a tendency that the droplet size and the CV value decrased as the LOH/DCM ratio inceased, the CV value of the particle after the evaporation of DCM showed the lowest value when the amount of LOH was 1 ml (LOH/DCM=1:11, by vol.). Therefore it was most adequate to use 1 ml of LOH to prepare the particles with a relatively narrow size distribution. Furthermore, it was clarified that the phase-separation between PLA and LOH was apparent and the surface of the particle obtained was wrinkled when the PLA concentration was lower after DCM was evaporated, while the particles with the smooth surface were obtained when the PLA concentration was higher. This method provides a unique technique to prepare uniform polymer microspheres composed of natural polymers. bio-degradable polymers, co-polymers or polymer blends, polyesters and those which can not be polymerized by the radical polymerization.
机译:通过使用Shirasu多孔玻璃(SPG)膜乳化技术制备相对均匀的可生物降解的聚丙交酯(PLA)微球。将溶解在辅助表面活性剂(疏水性物质)/二氯甲烷(DCM)中的聚(丙交酯)用作分散相(油相),并使用包含聚乙烯醇(PVA)和十二烷基硫酸钠(SLS)的水相作为一个连续的阶段。在氮气压力下,油相通过SPG膜的均匀孔渗透到连续相中,形成液滴。然后,通过简单地在室温下蒸发DCM 24小时获得固体聚合物微球。研究了助表面活性剂的类型和数量以及PLA浓度对液滴,颗粒的大小,大小分布以及形态的影响。通过使用月桂醇(LOH)而不是十六烷(HD)作为辅助表面活性剂,成功获得了相对均匀的球形PLA微球。 PLA的浓度从10到20 wt。%/体积变化,LOH / DCM的体积比从0.5:11.5变为2:10。在本研究中使用的聚合物浓度范围(10-20 wt。%)下,当使用2 ml的LOH时,液滴尺寸的变化并不明显,但是当0.5时,液滴尺寸在15 wt。%处显示最小值。或使用1毫升的LOH。在10-15 wt。%的PLA浓度范围内,CV值的变化(变化系数)较小,然后当PLA浓度从15至20 wt。%时,CV值变大。尽管随着LOH / DCM比的增加,液滴的大小和CV值有降低的趋势,但当LOH量为1 ml时,DCM蒸发后颗粒的CV值显示最低值(LOH / DCM =体积:1:11)。因此,使用1 ml LOH制备粒度分布相对较窄的颗粒最为合适。此外,澄清了当蒸发DCM后,当PLA浓度降低时,PLA与LOH之间的相分离是明显的,并且所获得的颗粒的表面起皱,而当当PLA浓度为0时,获得了具有光滑表面的颗粒。更高。该方法提供了独特的技术来制备由天然聚合物组成的均匀聚合物微球。可生物降解的聚合物,共聚物或聚合物共混物,聚酯以及不能通过自由基聚合反应聚合的聚酯。

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