Arnold Matthew M, Gorman Eric M, Schieber Loren J, Munson Eric J, Berkland Cory
Department of Chemical and Petroleum Engineering, The University of Kansas, Lawrence, KS 66047, United States.
J Control Release. 2007 Aug 16;121(1-2):100-9. doi: 10.1016/j.jconrel.2007.05.039. Epub 2007 Jun 13.
Pulmonary drug delivery of controlled release formulations may provide an effective adjunct approach to orally delivered antibiotics for clearing persistent lung infections. Dry powder formulations for this indication should possess characteristics including; effective deposition to infected lung compartments, persistence at the infection site, and steady release of antibiotic. Large porous particles ( approximately 10-15 microm) have demonstrated effective lung deposition and enhanced lung residence as a result of their large diameter and reduced clearance by macrophages in comparison to small microparticles ( approximately 1-5 microm). In this report, Precision Particle Fabrication technology was used to create monodisperse large porous particles of poly(d,l-lactic-co-glycolic acid) (PLGA) utilizing oils as extractable porogens. After extraction, the resulting large porous PLGA particles exhibited a low density and a web-like or hollow interior depending on porogen concentration and type, respectively. Ciprofloxacin nanoparticles (nanoCipro) created by homogenization in dichloromethane, possessed a polymorph with a decreased melting temperature. Encapsulating nanoCipro in large porous PLGA particles resulted in a steady release of ciprofloxacin that was extended for larger particle diameters and for the solid particle morphology in comparison to large porous particles. The encapsulation efficiency of nanoCipro was quite low and factors impacting the entrapment of nanoparticles during particle formation were elucidated. A dry powder formulation with the potential to control particle deposition and sustain release to the lung was developed and insight to improve nanoparticle encapsulation is discussed.
控释制剂的肺部给药可能为口服抗生素清除持续性肺部感染提供一种有效的辅助方法。用于该适应症的干粉制剂应具备以下特性:有效沉积到受感染的肺部区域、在感染部位持续存在以及抗生素的稳定释放。与小粒径微粒(约1-5微米)相比,大粒径多孔微粒(约10-15微米)由于其较大的直径和巨噬细胞清除率降低,已显示出有效的肺部沉积和延长的肺部滞留时间。在本报告中,采用精密颗粒制造技术,以油作为可萃取致孔剂,制备聚(d,l-乳酸-共-乙醇酸)(PLGA)的单分散大粒径多孔微粒。萃取后,所得的大粒径多孔PLGA微粒分别根据致孔剂浓度和类型呈现低密度以及类似网状或中空的内部结构。通过在二氯甲烷中匀化制备的环丙沙星纳米颗粒(纳米环丙沙星)具有熔点降低的多晶型物。将纳米环丙沙星封装在大粒径多孔PLGA微粒中,导致环丙沙星的稳定释放,与大粒径多孔微粒相比,对于更大的粒径和固体颗粒形态,释放时间延长。纳米环丙沙星的包封效率相当低,并阐明了在颗粒形成过程中影响纳米颗粒包封的因素。开发了一种有可能控制颗粒沉积并持续释放到肺部的干粉制剂,并讨论了改善纳米颗粒包封的见解。