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Spinning disc processing technology: potential for large-scale manufacture of chitosan nanoparticles.

机译:旋转盘加工技术:壳聚糖纳米粒子大规模生产的潜力。

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摘要

Mass production of nanoparticles using a reliable cost-effective approach is a challenge in the pharmaceutical industry. In this study, the spinning disc processing (SDP) technology was used to fabricate chitosan nanoparticles, with a view to commercially produce chitosan nanoparticle-based drug delivery platforms. Chitosan solution (0.25%, w/v, in dilute acid, 27.5 mL, 1.5 mL/s) was intensely mixed with sodium tripolyphosphate solution (0.10%, w/v, in water, 20 mL, 1.1 mL/s) on the spinning disc (1000 rpm). Transmission electron microscopy and dynamic light scattering data confirmed that the nanoparticles (20 +/- 3 nm) were comparable in size and shape to those synthesised using a beaker and magnetic stirrer (31 +/- 13 nm). Larger nanoparticles (131 +/- 5 nm) were produced by increasing the chitosan and TPP feed concentrations to 0.5% and 0.125%, respectively. Drug loading further increased the size of the nanoparticles, with N-acetyl cysteine (NAC) having a greater effect (403 +/- 4 nm) than paracetamol (165 +/- 4 nm). Co-loading of both drugs increased the size of the particles to the micron range. In conclusion, the SDP is a robust technology capable of expanding the production of blank and drug-loaded chitosan nanoparticles for the biomedical and pharmaceutical industries.
机译:使用可靠的具有成本效益的方法大规模生产纳米颗粒是制药行业的挑战。在这项研究中,旋转盘处理(SDP)技术用于制造壳聚糖纳米颗粒,以商业化生产基于壳聚糖纳米颗粒的药物递送平台。将壳聚糖溶液(0.25%,w / v,在稀酸中,27.5 mL,1.5 mL / s)与三聚磷酸钠溶液(0.10%,w / v,在水中,20 mL,1.1 mL / s)剧烈混合。旋转盘(1000 rpm)。透射电子显微镜和动态光散射数据证实,纳米颗粒(20 +/- 3 nm)的大小和形状与使用烧杯和磁力搅拌器(31 +/- 13 nm)合成的纳米颗粒相当。通过将壳聚糖和TPP进料浓度分别提高到0.5%和0.125%,可以生产更大的纳米颗粒(131 +/- 5 nm)。载药量进一步增加了纳米颗粒的尺寸,其中N-乙酰半胱氨酸(NAC)的作用(403 +/- 4 nm)比对乙酰氨基酚(165 +/- 4 nm)大。两种药物的共同装载将颗粒的尺寸增加到微米范围。总而言之,SDP是一项强大的技术,能够为生物医学和制药行业扩大空白和载有药物的壳聚糖纳米颗粒的生产。

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