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布地奈德和茶碱吸入固体制剂的设计用于肺部联合治疗。

Design of Inhalable Solid Dosage Forms of Budesonide and Theophylline for Pulmonary Combination Therapy.

机构信息

Department of Pharmacy, Faculty of Health and Medical Science, University of Copenhagen, Universitetsparken 2, DK-2100, Copenhagen, Denmark.

Department of Pharmacy, University of Oslo, P.O. Box 1068, Blindern, N-0316, Oslo, Norway.

出版信息

AAPS PharmSciTech. 2019 Mar 7;20(3):137. doi: 10.1208/s12249-019-1344-9.

Abstract

Corticosteroid resistance poses a major challenge to effective treatment of chronic obstructive pulmonary diseases. However, corticosteroid resistance can be overcome by co-administration of theophylline. The aim of this study was to formulate the corticosteroid budesonide with theophylline into inhalable dry powders intended for pulmonary combination therapy. Four types of spray-dried powders were prepared: (i) budesonide and theophylline co-dissolved and processed using a 2-fluid nozzle spray drier, (ii) budesonide nanocrystals and dissolved theophylline co-dispersed and processed using a 2-fluid nozzle spray drier, (iii) dissolved budesonide and dissolved theophylline processed using a 3-fluid nozzle spray drier, and (iv) budesonide nanocrystals and dissolved theophylline processed using a 3-fluid nozzle spray drier. Spray drying from the solutions resulted in co-amorphous (i) and partially amorphous powders (iii), whereas spray drying of the nanosuspensions resulted in crystalline products (ii and iv). Even though budesonide was amorphous in (i) and (iii), it failed to exhibit any dissolution advantage over the unprocessed budesonide. In contrast, the dissolution of budesonide from its nanocrystalline formulations, i.e., (ii) and (iv), was significantly higher compared to a physical mixture or unprocessed budesonide. Furthermore, the spray-dried powders obtained from the 2-fluid nozzle spray drier, i.e., (i) and (ii), exhibited co-deposition of budesonide and theophylline at the same weight ratio in the aerodynamic assessment using the New Generation Impactor. In contrast, the depositions of budesonide and theophylline deviated from the starting weight ratio in the aerodynamic assessment of spray-dried powders obtained from the 3-fluid nozzle spray drier, i.e., (iii) and (iv). Based on these results, the powders spray-dried from the suspension by using the 2-fluid nozzle spray drier, i.e., (ii), offered the best formulation properties given the physically stable crystalline solid-state properties and the co-deposition profile.

摘要

皮质类固醇耐药性是慢性阻塞性肺疾病有效治疗的主要挑战。然而,通过联合使用茶碱可以克服皮质类固醇耐药性。本研究的目的是将皮质类固醇布地奈德与茶碱制成可吸入干粉,用于肺部联合治疗。制备了四种喷雾干燥粉末:(i)布地奈德和茶碱共溶解并使用双流体喷嘴喷雾干燥器处理,(ii)布地奈德纳米晶体和溶解的茶碱共分散并使用双流体喷嘴喷雾干燥器处理,(iii)溶解的布地奈德和溶解的茶碱使用三流体喷嘴喷雾干燥器处理,(iv)布地奈德纳米晶体和溶解的茶碱使用三流体喷嘴喷雾干燥器处理。从溶液中喷雾干燥导致共无定形(i)和部分无定形粉末(iii),而纳米混悬液的喷雾干燥导致结晶产物(ii 和 iv)。尽管(i)和(iii)中的布地奈德是无定形的,但与未处理的布地奈德相比,它未能表现出任何溶解优势。相比之下,布地奈德从其纳米结晶制剂(ii 和 iv)中的溶解明显高于物理混合物或未处理的布地奈德。此外,使用新一代撞击器进行空气动力学评估时,从双流体喷嘴喷雾干燥器获得的喷雾干燥粉末(i)和(ii)显示出布地奈德和茶碱以相同的重量比共同沉积。相比之下,从三流体喷嘴喷雾干燥器获得的喷雾干燥粉末(iii)和(iv)的空气动力学评估中,布地奈德和茶碱的沉积偏离了起始重量比。基于这些结果,从悬浮液中使用双流体喷嘴喷雾干燥器喷雾干燥的粉末(ii),由于其物理稳定的结晶固态性质和共同沉积特性,提供了最佳的制剂性质。

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