Metal-based nanoplatforms for enhancing the biomedical applications of berberine: current progress and future directions

被引:1
作者
Baidoo, Isaac [1 ]
Sarbadhikary, Paromita [1 ]
Abrahamse, Heidi [1 ]
George, Blassan P. [1 ]
机构
[1] Univ Johannesburg, Fac Hlth Sci, Laser Res Ctr, POB 17011, ZA-2028 Johannesburg, South Africa
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
Berberine; drug delivery; drug targeting; metallic nanoparticles; nanomedicine; natural products; ENDOPLASMIC-RETICULUM STRESS; TYPE-2; DIABETES-MELLITUS; RAT MODEL; PHOTODYNAMIC THERAPY; DELIVERY-SYSTEM; PROTEIN-KINASE; IN-VITRO; NANOPARTICLES; CANCER; COMBINATION;
D O I
10.1080/17435889.2025.2480051
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
The isoquinoline alkaloid berberine, a bioactive compound derived from various plants, has demonstrated extensive therapeutic potential. However, its clinical application is hindered by poor water solubility, low bioavailability, rapid metabolism, and insufficient targeting. Metal-based nanoplatforms offer promising solutions, enhancing drug stability, controlled release, and targeted delivery. This review comprehensively explores the synthesis, physicochemical properties, and biomedical applications of metal-based nanocarriers, including gold, silver, iron oxide, zinc oxide, selenium, and magnetic nanoparticles, for berberine delivery to improve berberine's therapeutic efficacy. Recent advancements in metal-based nanocarrier systems have significantly improved berberine delivery by enhancing cellular uptake, extending circulation time, and enabling site-specific targeting. However, metal-based nanoplatforms encounter several limitations of potential toxicity, limited large-scale productions, and regulatory constraints. Addressing these limitations necessitates extensive studies on biocompatibility, long-term safety, and clinical translation. By summarizing the latest innovations and clinical perspectives, this review aims to guide future research toward optimizing berberine-based nanomedicine for improved therapeutic efficacy.
引用
收藏
页码:851 / 868
页数:18
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