Suppr超能文献

磷酸钙包被的载阿霉素脂质纳米粒作为人和犬骨肉瘤治疗的潜在工具

Doxorubicin-Loaded Lipid Nanoparticles Coated with Calcium Phosphate as a Potential Tool in Human and Canine Osteosarcoma Therapy.

作者信息

Chirio Daniela, Sapino Simona, Chindamo Giulia, Peira Elena, Vercelli Cristina, Riganti Chiara, Manzoli Maela, Gambino Graziana, Re Giovanni, Gallarate Marina

机构信息

Department of Drug Science and Technology, Turin University, Via P. Giuria 9, 10125 Torino, Italy.

Dipartimento di Scienze Veterinarie, Turin University, Largo P. Braccini, 2, 10095 Grugliasco, Italy.

出版信息

Pharmaceutics. 2022 Jun 27;14(7):1362. doi: 10.3390/pharmaceutics14071362.

Abstract

Osteosarcoma (OSA) is the most frequently diagnosed primary malignant bone tumor in humans and dogs. In both species, standard chemotherapy can be limited by multidrug resistance of neoplastic cells, which prevents intracellular accumulation of cytotoxic drugs, resulting in chemotherapy failure. In this study, a lipophilic ester of doxorubicin (C12DOXO) was loaded into nanoparticles (NPs) using the "cold microemulsion dilution" method. The resulting NPs were then coated with calcium phosphate (CaP) in two different ways to have calcium or phosphate ions externally exposed on the surface. These systems were characterized by determining mean diameter, zeta potential, and drug entrapment efficiency; afterward, they were tested on human and canine OSA cells to study the role that the coating might play in increasing both drug uptake into tumor cells and cytotoxicity. Mean diameter of the developed NPs was in the 200-300 nm range, zeta potential depended on the coating type, and C12DOXO entrapment efficiency was in the 60-75% range. Results of studies on human and canine OSA cells were very similar and showed an increase in drug uptake and cytotoxicity for CaP-coated NPs, especially when calcium ions were externally exposed. Therefore, applications in both human and veterinary medicine can be planned in the near future.

摘要

骨肉瘤(OSA)是人类和犬类中最常被诊断出的原发性恶性骨肿瘤。在这两个物种中,标准化疗可能会受到肿瘤细胞多药耐药性的限制,这会阻止细胞毒性药物在细胞内的积累,从而导致化疗失败。在本研究中,使用“冷微乳液稀释”方法将阿霉素的亲脂性酯(C12DOXO)载入纳米颗粒(NPs)中。然后,以两种不同的方式用磷酸钙(CaP)包覆所得的纳米颗粒,以使钙离子或磷酸根离子在表面外暴露。通过测定平均直径、zeta电位和药物包封效率对这些系统进行表征;之后,在人源和犬源OSA细胞上对它们进行测试,以研究这种包覆在增加药物进入肿瘤细胞的摄取量和细胞毒性方面可能发挥的作用。所制备的纳米颗粒的平均直径在200 - 300nm范围内,zeta电位取决于包覆类型,C12DOXO的包封效率在60 - 75%范围内。对人源和犬源OSA细胞的研究结果非常相似,并且表明对于CaP包覆的纳米颗粒,药物摄取量和细胞毒性有所增加,尤其是当钙离子在表面外暴露时。因此,在不久的将来可以规划在人类医学和兽医学中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ace/9322757/bccccd9528ea/pharmaceutics-14-01362-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验