首页> 外文会议>223rd American Chemical Society (ACS) National Meeting on Supercritical Carbon Dioxide: Separations and Processes Apr 7-11, 2002 Orlando, Florida >Fine Particle Pharmaceutical Manufacturing Using Dense Carbon Dioxide Mixed with Aqueous or Alcoholic Solutions
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Fine Particle Pharmaceutical Manufacturing Using Dense Carbon Dioxide Mixed with Aqueous or Alcoholic Solutions

机译:使用浓二氧化碳与水溶液或酒精溶液混合的精细药物制造

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This paper describes a newly patented CAN-BD (Carbon dioxide Assisted Nebulization with a Bubble Dryer~(~R)) process, utilizing dense CO_2 to micronize solutes to fine particles in a diameter range of 0.6 to 5 μm. The potential applications of this process are in thin film deposition, fine powder generation, and drug delivery. The fine particles are generated by (a) intimately mixing dense CO_2 (at super- or sub-critical conditions) and a liquid solution (containing a dissolved solute of interest) in a small volume tee at about 83 bar and room temperature, (b) expanding this mixture through a 10 cm long capillary tube flow restrictor (with inner diameters of 50, 74 or 100 μ) into a drying chamber at atmospheric pressure to generate an aerosol, and (c) drying the aerosol plume with preheated air or nitrogen gas at temperatures between 10 and 65℃ to form dry powders. Fine dry powders of disaccharide sugars, proteins, water-soluble and alcohol-soluble drugs have been generated with a lab CAN-BD unit (using a glass drying chamber with a volume of one to two liters) at a liquid flow rate of 0.3 to 2 mL/min. In a scaled up prototype unit (utilizing a 170-liter drying chamber with a thin stainless steel wall), aqueous solutions with 10% solute have successfully been nebulized and dried at a liquid flow rate of 20 mL/min. This paper presents experimental results of nebulizing aqueous solutions of mannitol and myo-inositol utilizing a lab CAN-BD unit. The effect of certain operating parameters on particle characteristics has been investigated. The particle size (a) decreases with reduction in solute concentration, and (b) decreases with increase in the ratio of dense CO_2 to aqueous solution flow rates.
机译:本文介绍了一种新专利的CAN-BD(带气泡干燥器的二氧化碳辅助雾化)工艺,该工艺利用致密的CO_2将溶质微粉化成直径为0.6至5μm的细颗粒。该方法的潜在应用是薄膜沉积,细粉生成和药物输送。细颗粒是通过(a)在约83 bar和室温下在小体积的三通中紧密混合稠密的CO_2(在超临界或亚临界条件下)和液体溶液(含有溶解的感兴趣的溶质)而制成的(b )将该混合物通过10厘米长的毛细管限流器(内径分别为50、74或100μ)膨胀到大气压下的干燥室中以产生气溶胶,并且(c)用预热的空气或氮气干燥气溶胶羽流气体在10到65℃之间形成干粉。用实验室的CAN-BD装置(使用容积为1至2升的玻璃干燥室)以0.3至60的液体流速产生了二糖,蛋白质,水溶性和醇溶性药物的细干粉末。 2 mL / min。在按比例放大的原型单元中(使用带薄不锈钢壁的170升干燥室),已成功雾化了含有10%溶质的水溶液,并以20 mL / min的液体流速对其进行了干燥。本文介绍了使用实验室CAN-BD装置雾化甘露醇和肌醇水溶液的实验结果。已经研究了某些操作参数对颗粒特性的影响。颗粒尺寸(a)随着溶质浓度的降低而减小,并且(b)随着致密CO_2与水溶液流速的比率增加而减小。

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