Preparation and in vitro release of albumin nanoparticles loaded with isoniazid and rifampicin
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Preparation and in vitro release of albumin nanoparticles loaded with isoniazid and rifampicin
Journal of Army Medical UniversityVol. 35, Issue 21, Pages: 2336-2339(2013)
作者机构:
宁夏医科大学:研究生院,药学院,总医院药剂科,总医院骨科
作者简介:
基金信息:
DOI:
CLC:R912;R944.9;R978.3
Published:2013,
Published Online:15 November 2013,
稿件说明:
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MA RONG, CHEN ZHEN, ZHANG HUIYONG, et al. Preparation and in vitro release of albumin nanoparticles loaded with isoniazid and rifampicin. [J]. Journal of army medical university, 2013, 35(21): 2336-2339.
DOI:
MA RONG, CHEN ZHEN, ZHANG HUIYONG, et al. Preparation and in vitro release of albumin nanoparticles loaded with isoniazid and rifampicin. [J]. Journal of army medical university, 2013, 35(21): 2336-2339.DOI:
Preparation and in vitro release of albumin nanoparticles loaded with isoniazid and rifampicin
Objective To prepare of bovine serum albumin nanoparticles loaded with isoniazid and rifampicin (INH-RFP-BSA-NPs)and investigate its
in vitro
release characteristics. Methods INH-RFP-BSA-NPs were prepared by modified self-emulsion solvent diffusion method. Albumin and polylactic acid was used as a carrier as well as skeleton structure. Transmission electron microscopy was used to observe the morphology of INH-RFP-BSA-NPs. The nanoparticle’s size and distribution of INH-RFP-BSA-NPs were performed by submicron particle size analyzer. High performance liquid ch
romatography (HPLC) was used to measure the drug loadings and the coating rate of INH-RFP-BSA-NPs. Dynamic membrane dialysis was used to study the
in vitro
release characteristics of INH-RFP-BSA-NPs. Results The INH-RFP-BSA-NPs were smooth
sphere-like
relatively uniform in size and good dispersion. The submicron particle size analyzer showed the diameter was 60.5±4.6 nm. The drug loading and entrapment efficiency of isoniazid were 19.8% and 87.8% respectively
and those of rifampicin were 20.1% and 98% respectively
INH cumulative release of 97.02% to 6 d
RFP to 5 d fully released. Conclusion INH-RFP-BSA-NPs can be prepared by drug-loading with albumin and polylactic acid
matrix modified self-emulsion solvent diffusion
with higher encapsulation efficiency
higher drug loading
and smaller particle size.
In vitro
drug release shows INH-RFP-BSA-NPs has good slow release effect.
关键词
白蛋白异烟肼利福平纳米粒体外释药
Keywords
albuminisoniazidrifampicinnanoparticlesin vitro drug release
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