Beta-cyclodextrin-capped self-assembled zein nanoparticles for stable quercetin delivery

被引:0
作者
Hassan, Nourhan Khaled [1 ]
Haider, Mohamed [2 ,3 ]
Jagal, Jayalakshmi [2 ]
El-Labbad, Eman [1 ,4 ]
Elsayed, Ibrahim [1 ,5 ]
Taha, Maie S. [5 ]
机构
[1] Gulf Med Univ, Coll Pharm, Dept Pharmaceut Sci, Ajman, U Arab Emirates
[2] Univ Sharjah, Res Inst Med & Hlth Sci, Sharjah 27272, U Arab Emirates
[3] Univ Sharjah, Coll Pharm, Dept Pharmaceut & Pharmaceut Technol, Sharjah 27272, U Arab Emirates
[4] Ain Shams Univ, Fac Pharm, Dept Med Chem, Cairo, Egypt
[5] Cairo Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo 11562, Egypt
关键词
Macromolecular nanoparticle; Quercetin; Beta cyclodextrin; Zein nanoparticles; Colorectal cancer; Capping agent; DRUG-DELIVERY; CANCER CELLS; RELEASE; EXPRESSION; APOPTOSIS; PROTEIN;
D O I
10.1016/j.jddst.2025.107174
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Quercetin (QR) holds a lot of promise for colorectal cancer therapy; however, its clinical efficacy is challenged by its limited solubility and chemical instability. To harness the anticancer potential of QR we have developed a macromolecular-based nanoparticle formulation, QRNP, encapsulating QR at high capacity. QRNP is composed of the natural plant-derived protein, zein, which self-assembles into a spherical structure via the nano-precipitation technique. Beta-cyclodextrin (beta-CD) was used as a capping agent to stabilize the nanoparticle surface and it served to enhance QR loading as well. Physicochemical characterization revealed QRNP's spherical morphology and confirmed its core-shell structure. QRNP exhibited a sustained biphasic release profile, enhanced colloidal stability, and enhanced metabolic stability. Encapsulation of QR in QRNP significantly reduced its IC50 in HCT-116 and HT-29 colorectal carcinoma cells. QRNP triggered significant late-stage apoptosis as determined by flow cytometric analysis. These results support QRNP as an effective therapeutic against colorectal cancer.
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页数:11
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