Development and characterization of a novel pH-Responsive nanocarrier for enhanced quercetin delivery and cytotoxicity in lung cancer

被引:0
|
作者
Abad, Fateme Rezaei Abbas [1 ]
Pourmadadi, Mehrab [2 ]
Abdouss, Majid [1 ]
机构
[1] Amirkabir Univ Technol, Dept Chem, Tehran, Iran
[2] Shahid Beheshti Univ, Prot Res Ctr, Tehran 1983963113, GC, Iran
关键词
Chitosan; Quercetin; Graphene quantum dots; Halloysite nanotubes; Targeted drug delivery; GRAPHENE QUANTUM DOTS; DRUG-DELIVERY; HALLOYSITE NANOTUBE; CHITOSAN; NANOPARTICLES; CURCUMIN; RELEASE; CHITIN; OXIDE;
D O I
10.1016/j.inoche.2024.113175
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Quercetin (QC) is a potent polyphenol with numerous health benefits, but its use is limited due to its low bioavailability and high toxicity. Accordingly, a pH-responsive nanocarrier was created using chitosan (CS), halloysite nanotubes (HNTs), and graphene quantum dots (GQDs). It was found that LE and EE values of the CS/ GQDs nanocomposites were 32.0% and 69.0%, respectively, increasing to 44.25% and 85.5% upon HNTs addition. The QC release study of pH-responsive CS/HNTs/GQDs nanocomposite in buffer environments showed that with the presence of GQDs in the CS/HNTs composite, the release rate increased from 73% and 54% at pH 5.4 and 7.4 to 97.5% and 67%. Examining the release data with kinetic models showed that the data corresponded to the first-order model, which indicates concentration-dependent drug release. In this study, the cytotoxicity of CS/HNT, CS/HNTs/GQDs, and CS/HNTs/GQDs@QC nanocomposites against L929 and A549 lung cell lines was investigated. The results showed that CS/HNTs/GQDs@QC had the highest cytotoxicity and had a more profound effect on A549 cells. The proportion of apoptotic cells in the CS/HNTs/GQDs@QC group was also higher than in the control group, with early and late apoptosis of 74.4% and 5.15%, respectively.
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页数:12
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