Nano Drug Delivery Strategies for an Oral Bioenhanced Quercetin Formulation

被引:19
作者
Attar, Esha S. [1 ]
Chaudhari, Vanashree H. [1 ]
Deokar, Chaitanya G. [1 ]
Dyawanapelly, Sathish [1 ]
Devarajan, Padma V. [1 ]
机构
[1] Inst Chem Technol, Dept Pharmaceut Sci & Technol, Mumbai 400019, Maharashtra, India
关键词
IN-VIVO EVALUATION; CANCER CELL-LINE; SOLID LIPID NANOPARTICLES; LOADED MIXED MICELLES; BREAST-CANCER; POLYMERIC MICELLES; LIPOSOMAL QUERCETIN; MEDIATED APOPTOSIS; GOLD NANOPARTICLES; HYBRID NANOPARTICLES;
D O I
10.1007/s13318-023-00843-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Quercetin, a naturally occurring flavonoid, has been credited with a wide spectrum of therapeutic properties. However, the oral use of quercetin is limited due to its poor water solubility, low bioavailability, rapid metabolism, and rapid plasma clearance. Quercetin has been studied extensively when used with various nanodelivery systems for enhancing quercetin bioavailability. To enhance its oral bioavailability and efficacy, various quercetin-loaded nanosystems such as nanosuspensions, polymer nanoparticles, metal nanoparticles, emulsions, liposomes or phytosomes, micelles, solid lipid nanoparticles, and other lipid-based nanoparticles have been investigated in in-vitro cells, in-vivo animal models, and humans. Among the aforementioned nanosystems, quercetin phytosomes are attracting more interest and are available on the market. The present review covers insights into the possibilities of harnessing quercetin for several therapeutic applications and a special focus on anticancer applications and the clinical benefits of nanoquercetin formulations.
引用
收藏
页码:495 / 514
页数:20
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