Efficacy analysis of targeted nanodrug for non-small cell lung cancer therapy

被引:2
作者
Li, Tongtong [1 ]
Zhou, Tong [2 ]
Liu, Ying [1 ]
Wang, Jingyue [3 ]
Yu, Zhenxiang [1 ]
机构
[1] First Hosp Jilin Univ, Dept Resp Med, Changchun, Peoples R China
[2] First Hosp Jilin Univ, Dept Endocrinol & Metab, Changchun, Peoples R China
[3] First Hosp Jilin Univ, Dept Cardiol, Changchun, Peoples R China
关键词
non-small cell lung cancer; antitumor efficacy; nanoparticles; RGD peptide; vincristine; IN-VITRO; DELIVERY; PEPTIDE; VIVO;
D O I
10.3389/fbioe.2022.1068699
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
Biological macromolecules have been widely used as biomedical carriers in treating non-small cell lung cancer (NSCLC) due to their biocompatibility, targeting, biodegradability, and antitumor efficacy. Nanotechnology has been used in clinics to treat many diseases, including cancer. Nanoparticles (NPs) can accumulate drugs into tumors because of their enhanced permeability and retention (EPR) effects. However, the lack of active targeting ligands affects NPs drug delivery. Arginine-glycine-aspartic (RGD), as a targeting ligand, has distinct advantages in targeting and safety. In the present study, an RGD peptide-modified nanogel called RGD-polyethylene glycol-poly (L-phenylalanine-co-L-cystine) (RGD-PEG-P (LP-co-LC-P (LP-co-LC) was investigated to deliver vincristine (VCR) as NSCLC therapy. The VCR-loaded targeted nanoparticle (RGD-NP/VCR) demonstrated excellent antitumor efficacy compared to the free drug (VCR) and untargeted nanoparticle (NP/VCR) without any significant side effects. RGD-NP/VCR has better tumor inhibition and fewer side effects, indicating its potential benefit in NSCLC treatment.
引用
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页数:10
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