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将替莫唑胺和姜黄素共负载到基于杯[4]芳烃的纳米容器中用于潜在的联合化疗:结合特性、增强的药物溶解度及在水性介质中的稳定性

Co-Loading of Temozolomide and Curcumin into a Calix[4]arene-Based Nanocontainer for Potential Combined Chemotherapy: Binding Features, Enhanced Drug Solubility and Stability in Aqueous Medium.

作者信息

Migliore Rossella, D'Antona Nicola, Sgarlata Carmelo, Consoli Grazia M L

机构信息

Istituto di Chimica Biomolecolare, Consiglio Nazionale delle Ricerche, Via Paolo Gaifami 18, 95126 Catania, Italy.

Dipartimento di Scienze Chimiche, Università degli Studi di Catania, Viale Andrea Doria 6, 95125 Catania, Italy.

出版信息

Nanomaterials (Basel). 2021 Nov 2;11(11):2930. doi: 10.3390/nano11112930.

Abstract

The co-delivery of anticancer drugs into tumor cells by a nanocarrier may provide a new paradigm in chemotherapy. Temozolomide and curcumin are anticancer drugs with a synergistic effect in the treatment of multiform glioblastoma. In this study, the entrapment and co-entrapment of temozolomide and curcumin in a -sulfonato-calix[4]arene nanoparticle was investigated by NMR spectroscopy, UV-vis spectrophotometry, isothermal titration calorimetry, and dynamic light scattering. Critical micellar concentration, nanoparticle size, zeta potential, drug loading percentage, and thermodynamic parameters were all consistent with a drug delivery system. Our data showed that temozolomide is hosted in the cavity of the calix[4]arene building blocks while curcumin is entrapped within the nanoparticle. Isothermal titration calorimetry evidenced that drug complexation and entrapment are entropy driven processes. The loading in the calixarene-based nanocontainer enhanced the solubility and half-life of both drugs, whose medicinal efficacy is affected by low solubility and rapid degradation. The calixarene-based nanocontainer appears to be a promising new candidate for nanocarrier-based drug combination therapy for glioblastoma.

摘要

通过纳米载体将抗癌药物共同递送至肿瘤细胞可能为化疗提供一种新的模式。替莫唑胺和姜黄素是在多形性胶质母细胞瘤治疗中具有协同作用的抗癌药物。在本研究中,通过核磁共振光谱、紫外可见分光光度法、等温滴定量热法和动态光散射研究了替莫唑胺和姜黄素在磺化杯[4]芳烃纳米颗粒中的包封和共包封情况。临界胶束浓度、纳米颗粒尺寸、zeta电位、药物负载百分比和热力学参数均与药物递送系统一致。我们的数据表明,替莫唑胺存在于杯[4]芳烃结构单元的空腔中,而姜黄素则被包封在纳米颗粒内。等温滴定量热法证明药物络合和包封是熵驱动的过程。基于杯芳烃的纳米容器中的负载提高了两种药物的溶解度和半衰期,这两种药物的药用功效受到低溶解度和快速降解的影响。基于杯芳烃的纳米容器似乎是用于胶质母细胞瘤基于纳米载体的联合药物治疗的一种有前景的新候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e754/8623626/325ef4cb237b/nanomaterials-11-02930-g001.jpg

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