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首页> 外文期刊>Journal of Aerosol Science >Low-temperature aerosol flow reactor method for preparation of surface stabilized pharmaceutical nanocarriers
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Low-temperature aerosol flow reactor method for preparation of surface stabilized pharmaceutical nanocarriers

机译:用于制备表面稳定的药物纳米载体的低温气溶胶流动反应器方法

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Nanoparticles can be used to improve the delivery of many drugs, especially peptides and proteins. Although several methods are available for polymeric nanoparticle preparation, there are few single-stage processes that produce dry, solid nanoparticles that can be easily re-dispersed in pharmaceutical vehicles. The aerosol flow reactor method is a single-stage process that has been used for the preparation of multi-component, coated nanoparticles under uniform temperature and gas flow field. However, it is traditionally used with high synthesis temperatures. In the present study, the aerosol flow reactor method was further optimized for processing and surface stabilization of pharmaceutical nanoparticles containing temperature sensitive biomolecules. In the developed method, drug-loaded carrier nanoparticles consisting of a biodegradable polymer (Eudragit L100) and a drug (phenylephrine hydrochloride) were first produced by aerosol droplet drying and subsequently coated in the gas phase. The carrier particles were coated with L-leucine in order to inhibit agglomeration of the nanoparticles in solutions before administration. In the coating process, a side stream of L-leucine vapor was directed into the main aerosol flow containing the drug-loaded carriers. The mixing with the main flow at ambient temperature induced a super-saturation of L-leucine vapor and condensation on the carrier particles. The results demonstrate that solid, hydrodynamically stable drug-loaded polymeric nanoparticles can be produced with a thin L-leucine coating. The low process temperature enables the surface engineering of particles loaded with temperature sensitive drugs or bioactive materials to be utilized for drug delivery purposes.
机译:纳米颗粒可用于改善许多药物的输送,尤其是肽和蛋白质。尽管有几种方法可用于制备聚合物纳米颗粒,但很少有单阶段方法可以生产干燥的固体纳米颗粒,这些纳米颗粒可以轻松地重新分散在药物载体中。气溶胶流动反应器方法是一种单步工艺,已用于在均匀的温度和气流场下制备多组分涂层纳米颗粒。然而,传统上它在高合成温度下使用。在本研究中,进一步优化了气溶胶流动反应器方法,以用于处理和表面稳定含有温度敏感生物分子的药物纳米颗粒。在开发的方法中,首先通过气雾剂液滴干燥生产由可生物降解的聚合物(Eudragit L100)和药物(盐酸去氧肾上腺素)组成的载有药物的载体纳米颗粒,然后在气相中进行包衣。为了抑制给药前溶液中纳米颗粒的团聚,将载体颗粒涂有L-亮氨酸。在包衣过程中,L-亮氨酸蒸气的侧流被引导到含有载药载体的主气溶胶流中。在环境温度下与主流混合会导致L-亮氨酸蒸气过饱和,并在载体颗粒上凝结。结果表明,可以用薄的L-亮氨酸涂层生产固体,流体动力学稳定的载有药物的聚合物纳米颗粒。较低的处理温度使负载有温度敏感药物或生物活性物质的颗粒的表面工程化可用于药物输送目的。

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