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Characterization of spray dried powders with nucleic acid-containing PEI nanoparticles

机译:用含核酸PEI纳米颗粒喷雾干燥粉末的表征

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摘要

Localized aerosol delivery of gene therapies is a promising treatment of severe pulmonary diseases including lung cancer, cystic fibrosis, COPD and asthma. The administration of drugs by inhalation features multiple benefits including an enhanced patient acceptability and compliance. The application of a spray dried powder formulation has advantages over solutions due to their increased stability and shelf life. Furthermore, optimal sizes of the powder can be obtained by spray drying to allow a deep lung deposition. The present study optimized the parameters involved with spray drying polyplexes formed by polyethylenimine (PEI) and nucleic acids in inert excipients to generate a nano-embedded microparticle (NEM) powder with appropriate aerodynamic diameter. Furthermore, the effects of the excipient matrix used to generate the NEM powder on the biological activity of the nucleic acid and the ability to recover the embedded nanoparticles was investigated. The study showed that bioactivity and nucleic acid integrity was preserved after spray drying, and that polyplexes could be reconstituted from the dry powders made with trehalose but not mannitol as a stabilizer. Scanning electron microscopy (SEM) showed trehalose formulations that formed fused, lightly corrugated spherical particles in the range between 1 and 5 mu m, while mannitol formulations had smooth surfaces and consisted of more defined particles. After redispersion of the microparticles in water, polyplex dispersions are obtained that are comparable to the initial formulations before spray drying. Cellular uptake and transfection studies conducted in lung adenocarcinoma cells show that redispersed trehalose particles performed similar to or better than polyplexes that were not spray dried. A method for quantifying polymer and nucleic acid loss following spray drying was developed in order to ensure that equal nucleic acid amounts were used in all in vitro experiments. The results confirm that spray dried NEM formulations containing nucleic acids can be prepared with characteristics known to be optimal for inhalation therapy.
机译:本地化气溶胶的基因疗法是对肺癌,囊性纤维化,COPD和哮喘等严重肺部疾病的有前途的治疗。吸入药物的给药具有多种益处,包括增强的患者可接受性和合规性。喷雾干燥的粉末配方的施加在稳定性和保质期增加的原因中具有优于溶液的优点。此外,通过喷雾干燥可以获得粉末的最佳尺寸以允许深肺沉积。本研究优化了由聚乙基菊氨酸(PEI)和惰性赋形剂中的核酸形成的喷雾干燥比分中涉及的参数,以产生具有适当的空气动力直径的纳米嵌入的微粒(NEM)粉末。此外,研究了用于在核酸的生物活性上产生NEM粉末的赋形剂基质的效果和回收嵌入纳米颗粒的能力。该研究表明,喷雾干燥后保存生物活性和核酸完整性,并且可以从用海藻糖制备的干粉中重构,但不是甘露醇作为稳定剂重构。扫描电子显微镜(SEM)显示了在1至5μm的范围内形成的熔化,轻质波纹球颗粒的海藻糖制剂,而甘露醇制剂具有光滑的表面并由更明确的颗粒组成。在水中重新分散在水中,获得与喷雾干燥前的初始配方相当的多分布分散体。在肺腺癌细胞中进行的细胞摄取和转染研究表明,再分散的海藻糖颗粒与未喷涂干燥的多单独进行或更好地进行。开发了一种用于量化喷雾干燥后的聚合物和核酸损失的方法,以确保在所有体外实验中使用等于核酸量。结果证实,含有核酸的喷雾干燥的NEM制剂可以用已知是对吸入治疗最佳的特征来制备。

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