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Preparation of rifampicin-loaded PLGA microspheres for lung delivery as aerosol by premix membrane homogenization
被引:41
作者:
Doan, T. V. P.
[1
,2
]
Olivier, J. C.
[1
,2
]
机构:
[1] Univ Poitiers, Fac Med Pharm, F-86000 Poitiers, France
[2] INSERM, ERI 23, F-86000 Poitiers, France
关键词:
PLGA;
Microspheres;
SPG membrane;
Premix membrane emulsification;
Rifampicin;
MULTIPLE EMULSIONS;
EMULSIFICATION;
TUBERCULOSIS;
ANTIBIOTICS;
FORMULATION;
INHALATION;
DROPLETS;
SIZE;
D O I:
10.1016/j.ijpharm.2009.08.008
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The water-in-oil solvent evaporation method with premix membrane homogenization was investigated to improve productivity of the preparation of narrowly size-distributed poly(lactide-co-glycolide) (PLGA) microspheres for rifampicin lung delivery as dry aerosols. Using ethyl acetate as organic solvent, a coarse oil-in-water emulsion (or premix) was prepared under magnetic stirring and homogenized by extrusion through a Shirasu porous glass (SPG) membrane (5.9 mu m porosity). Microspheres were obtained after dilution and solvent evaporation. Formulation parameters investigated were: PLGA concentration, transmembrane pressure and oil:water volume ratio. The optimal formulation parameters were then applied to prepare rifampicin-loaded microspheres. Loaded microspheres were 1.72 +/- 0.16 mu m in diameter with a span of 0.86 +/- 0.04 and a rifampicin content of 52 +/- 6 mu g/mg microspheres. Release studies in phosphate-buffered saline showed a linear release profile with 40% rifampicin release over 4.5 days. The MMAD of 2.63 mu m of freeze-dried microspheres should be suitable for aerosol administration and delivery into the rat lungs by intratracheal insufflation. (C) 2009 Elsevier B.V. All rights reserved.
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页码:61 / 66
页数:6
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