Novel drug delivery systems targeting oxidative stress in chronic obstructive pulmonary disease: a review

被引:64
|
作者
Xu, You [1 ,2 ]
Liu, Hongmei [1 ]
Song, Lei [1 ]
机构
[1] First Hosp Jilin Univ, Dept Resp Med, Key Lab Organ Regeneration & Transplantat, Minist Educ, Changchun 130061, Peoples R China
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Pharm, DK-2100 Copenhagen, Denmark
关键词
Oxidative stress; Chronic obstructive pulmonary disease; Drug delivery; Nanoparticles; Microparticles; Nanocomposite microparticles; AIRWAY EPITHELIAL-CELLS; BRONCHOALVEOLAR LAVAGE FLUID; NF-KAPPA-B; IN-VITRO; LUNG INFLAMMATION; NITRIC-OXIDE; ANTIOXIDANT ENZYMES; GOLD NANOPARTICLES; LIPID-PEROXIDATION; HYDROGEN-PEROXIDE;
D O I
10.1186/s12951-020-00703-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Oxidative stress is significantly involved in the pathogenesis and progression of chronic obstructive pulmonary disease (COPD). Combining antioxidant drugs or nutrients results in a noteworthy therapeutic value in animal models of COPD. However, the benefits have not been reproduced in clinical applications, this may be attributed to the limited absorption, concentration, and half-life of exogenous antioxidants. Therefore, novel drug delivery systems to combat oxidative stress in COPD are needed. This review presents a brief insight into the current knowledge on the role of oxidative stress and highlights the recent trends in novel drug delivery carriers that could aid in combating oxidative stress in COPD. The introduction of nanotechnology has enabled researchers to overcome several problems and improve the pharmacokinetics and bioavailability of drugs. Large porous microparticles, and porous nanoparticle-encapsulated microparticles are the most promising carriers for achieving effective pulmonary deposition of inhaled medication and obtaining controlled drug release. However, translating drug delivery systems for administration in pulmonary clinical settings is still in its initial phases.
引用
收藏
页数:25
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