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Topical delivery of urea encapsulated in biodegradable PLGA microparticles: O/W and W/O creams

机译:局部递送封装在可生物降解PLGA微粒中的尿素:O / W和W / O乳膏

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摘要

This study describes the formulation and characterization of O/W and W/O creams containing urea-loaded microparticles prepared with poly (d, L-lactic-co-glycolic acid) (PLGA) in order to encapsulate and stabilize urea. The solvent evaporation method was used for preparing PLGA microparticles containing urea. The microparticles size was evaluated by laser light diffractometry. The resulting microparticles were then incorporated in O/W and W/O creams and stability and the release pattern from the creams was evaluated by UV-spectrophotometry. The particle size of PLGA microparticles was in the range of 1-5 μm and most microparticles had a particle size smaller than 3 μm. The encapsulation efficiency was calculated as 40.5% ± 3.4. This study also examined release pattern of urea which varied among different formulations. The results showed that the release from O/W creams followed Higuchi kinetics while the release from W/O creams showed the zero order kinetics and the creams containing microparticulated urea had slower release than free urea creams.
机译:这项研究描述了O / W和W / O乳膏的配方和特性,这些乳膏包含用聚(d,L-乳酸-乙醇酸共聚物)(PLGA)制备的尿素负载微粒,以封装和稳定尿素。溶剂蒸发法用于制备含尿素的PLGA微粒。通过激光衍射法评估微粒尺寸。然后将所得的微粒掺入O / W和W / O乳膏中,并通过UV-分光光度法评价其稳定性和从乳膏中的释放方式。 PLGA微粒的粒径在1-5μm的范围内,大多数微粒的粒径小于3μm。包封效率经计算为40.5%±3.4。这项研究还检查了尿素的释放模式,这种释放模式在不同的配方中有所不同。结果表明,O / W乳膏的释放遵循Higuchi动力学,而W / O乳膏的释放则显示零级动力学,并且含有微粒化尿素的乳膏的释放比游离尿素乳膏的释放慢。

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