Gelsleichter Nicolly Espindola, de Souza Priscila Oliveira, Teixeira Fernanda Cardoso, Debom Gabriela Nogueira, Lenz Gabriela Spies, Roliano Gabriela Gonçalves, de Cássia Sant'ana Rita, Visioli Fernanda, Fachel Flávia Nathiely Silveira, Michels Luana Roberta, Azambuja Juliana Hofstätter, Teixeira Helder Ferreira, Braganhol Elizandra
Programa de Pós-Graduação em Biociências, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Sarmento Leite Street, 245, Centro Histórico, Porto Alegre, RS, 90050-170, Brazil.
Faculdade de Odontologia, Universidade Federal Do Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil.
Cell Mol Neurobiol. 2023 Aug;43(6):2939-2951. doi: 10.1007/s10571-023-01338-4. Epub 2023 Apr 13.
Melanoma is the most aggressive type of skin cancer. Brain metastasis is the worst scenario in metastatic melanoma and the treatment options for these patients are limited. Temozolomide (TMZ) is a chemotherapy agent used to treat primary central nervous system tumors. Our objective was to develop chitosan-coated nanoemulsion containing temozolomide (CNE-TMZ) for nasal route administration to melanoma brain metastasis treatment. A preclinical model of metastatic brain melanoma was standardized, and the efficiency of the developed formulation was further determined in vitro and in vivo. The nanoemulsion was done by spontaneous emulsification method and the formulation was characterized by size, pH, polydispersity index, and zeta potential. Culture assessments to determine cell viability were done in the A375 human melanoma cell line. To determine the safety of formulation, healthy C57/BL6 mice were treated with a nanoemulsion without TMZ. The model in vivo used B16-F10 cells implanted by stereotaxic surgery in C57/BL6 mice brains. The results demonstrate that the preclinical model used showed to be useful to analyze the efficiency of new candidate drugs to treat melanoma brain metastasis. The chitosan-coated nanoemulsions with TMZ showed the expected physicochemical characteristics and demonstrated safety and efficacy, reducing around 70% the tumor size compared to control mice, and presenting a tendency in mitotic index reduction, becoming an interesting approach to treat melanoma brain metastasis.
黑色素瘤是最具侵袭性的皮肤癌类型。脑转移是转移性黑色素瘤最糟糕的情况,这些患者的治疗选择有限。替莫唑胺(TMZ)是一种用于治疗原发性中枢神经系统肿瘤的化疗药物。我们的目标是开发一种含替莫唑胺的壳聚糖包被纳米乳剂(CNE-TMZ),用于经鼻给药治疗黑色素瘤脑转移。建立了转移性脑黑色素瘤的临床前模型,并在体外和体内进一步确定所开发制剂的有效性。纳米乳剂通过自发乳化法制备,制剂通过粒径、pH值、多分散指数和zeta电位进行表征。在A375人黑色素瘤细胞系中进行培养评估以确定细胞活力。为了确定制剂的安全性,用不含TMZ的纳米乳剂处理健康的C57/BL6小鼠。体内模型采用将B16-F10细胞立体定向手术植入C57/BL6小鼠脑内。结果表明,所使用的临床前模型对于分析治疗黑色素瘤脑转移的新候选药物的有效性是有用的。含TMZ的壳聚糖包被纳米乳剂具有预期的理化特性,并显示出安全性和有效性,与对照小鼠相比,肿瘤大小减少了约70%,且有降低有丝分裂指数的趋势,成为治疗黑色素瘤脑转移的一种有吸引力的方法。