Fabrication of Co-delivery of Bortezomib and Vincristine Loaded Chitosan Cross-linked Polymeric Nanoparticles: Evaluation of Anticancer Activity and Apoptosis Induction in Lung Cancer Cells

IF 5 3区 工程技术 Q2 ENGINEERING, ENVIRONMENTAL Journal of Polymers and the Environment Pub Date : 2024-11-18 DOI:10.1007/s10924-024-03451-x
Wenze Sun, Shoushuai Li
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Abstract

Targeting crucial pathways in cancer cells with combination drugs becomes vital as treatment resistance is reduced and the drug’s efficacy improves even at low doses. Bortezomib (BTZ) and vincristine (VCR) are chemotherapy drugs provided to individuals with solid tumors. This work suggests encapsulating BTZ and VCR in chitosan (CS) nanoparticles (CSNPs@BTZ-VCR) grafted polymers to combat cancer. To enhance the solubility of CSNPs further cross-linked with polyethylene glycol (PEG) (PEG/CSNPs@BTZ-VCR). Several methods were used to examine the NPs. SEM images showed nanoparticle fabrication, drug loading into CSNPs, and PEG cross-linking. The studies were developed to assess the synergic effects of the drugs in NPs against NCI-H661, NCI-H460, A549, H157, and H1299 lung cancer cells. The PEG/CSNPs@BTZ-VCR NPs were found to synergistically reduce the cell survival of the NCI-H661, NCI-H460, A549, H157, and H1299 cell lines, with a combined result of 0.313. The synergic effect of the BTZ and VCR was considerably more potent, with 0.22 of PEG/CSNPs@BTZ-VCR NPs. In addition, PEG/CSNPs@BTZ-VCR NPs have a higher DPPH scavenging activity (58.32%) than drug-alone. The synergistic efficiency of the PEG/CSNPs@BTZ-VCR NPs triggers apoptosis variations was detected using Calcein AM/Propidium Iodide (PI), DAPI, and PI biochemical staining techniques. Further, the apoptosis mechanism was confirmed by FITC/Annexin-V and PI staining methods. Outcomes showed that the co-delivery of bortezomib and vincristine-loaded chitosan cross-linked polymeric nanoparticles was much higher in lung cancer cells when related to free drugs.

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硼替佐米和长春新碱负载壳聚糖交联聚合物纳米颗粒共递送的制备:肺癌细胞抗癌活性和诱导凋亡的评价
利用联合药物靶向癌细胞的关键通路变得至关重要,因为治疗耐药性降低了,即使在低剂量下药物的疗效也有所提高。硼替佐米(BTZ)和长春新碱(VCR)是提供给实体瘤患者的化疗药物。这项工作建议将BTZ和VCR包封在壳聚糖(CS)纳米颗粒(CSNPs@BTZ-VCR)接枝聚合物中以对抗癌症。为了提高csnp与聚乙二醇(PEG)进一步交联的溶解度(PEG/CSNPs@BTZ-VCR)。我们使用了几种方法来检查NPs。扫描电镜图像显示了纳米颗粒的制备,药物装载到csnp中,以及PEG交联。这些研究旨在评估NPs中药物对NCI-H661、NCI-H460、A549、H157和H1299肺癌细胞的协同作用。PEG/CSNPs@BTZ-VCR NPs可协同降低NCI-H661、NCI-H460、A549、H157和H1299细胞系的细胞存活率,其综合结果为0.313。BTZ和VCR的协同效应更为显著,PEG/CSNPs@BTZ-VCR NPs为0.22。此外,PEG/CSNPs@BTZ-VCR NPs比单独用药具有更高的DPPH清除活性(58.32%)。采用钙黄素AM/碘化丙啶(PI)、DAPI和PI生化染色技术检测PEG/CSNPs@BTZ-VCR NPs触发凋亡变异的协同效率。FITC/Annexin-V和PI染色证实细胞凋亡机制。结果表明,当与游离药物相关时,硼替佐米和长春新碱负载的壳聚糖交联聚合物纳米颗粒在肺癌细胞中的共递送量要高得多。
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来源期刊
Journal of Polymers and the Environment
Journal of Polymers and the Environment 工程技术-高分子科学
CiteScore
9.50
自引率
7.50%
发文量
297
审稿时长
9 months
期刊介绍: The Journal of Polymers and the Environment fills the need for an international forum in this diverse and rapidly expanding field. The journal serves a crucial role for the publication of information from a wide range of disciplines and is a central outlet for the publication of high-quality peer-reviewed original papers, review articles and short communications. The journal is intentionally interdisciplinary in regard to contributions and covers the following subjects - polymers, environmentally degradable polymers, and degradation pathways: biological, photochemical, oxidative and hydrolytic; new environmental materials: derived by chemical and biosynthetic routes; environmental blends and composites; developments in processing and reactive processing of environmental polymers; characterization of environmental materials: mechanical, physical, thermal, rheological, morphological, and others; recyclable polymers and plastics recycling environmental testing: in-laboratory simulations, outdoor exposures, and standardization of methodologies; environmental fate: end products and intermediates of biodegradation; microbiology and enzymology of polymer biodegradation; solid-waste management and public legislation specific to environmental polymers; and other related topics.
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