Oliveira Catiúscia P, Prado Willian A, Lavayen Vladimir, Büttenbender Sabrina L, Beckenkamp Aline, Martins Bruna S, Lüdtke Diogo S, Campo Leandra F, Rodembusch Fabiano S, Buffon Andréia, Pessoa Adalberto, Guterres Silvia S, Pohlmann Adriana R
Programa de Pós-Graduação em Ciências Farmacêuticas, Faculdade de Farmácia, Universidade Federal do Rio Grande do Sul, Av. Ipiranga, 2752, Porto Alegre, 90610-000, RS, Brazil.
Departamento de Química Orgânica, Instituto de Química, Universidade Federal do Rio Grande do Sul, Porto Alegre, 91501-970, RS, Brazil.
Pharm Res. 2017 Feb;34(2):438-452. doi: 10.1007/s11095-016-2074-2. Epub 2016 Dec 15.
This study was conducted a promising approach to surface functionalization developed for lipid-core nanocapsules and the merit to pursue new strategies to treat solid tumors.
Bromelain-functionalized multiple-wall lipid-core nanocapsules (Bro-MLNC-Zn) were produced by self-assembling following three steps of interfacial reactions. Physicochemical and structural characteristics, in vitro proteolytic activity (casein substrate) and antiproliferative activity (breast cancer cells, MCF-7) were determined.
Bro-MLNC-Zn had z-average diameter of 135 nm and zeta potential of +23 mV. The complex is formed by a Zn-N chemical bond and a chelate with hydroxyl and carboxyl groups. Bromelain complexed at the nanocapsule surface maintained its proteolytic activity and showed anti-proliferative effect against human breast cancer cells (MCF-7) (72.6 ± 1.2% at 1.250 μg mL and 65.5 ± 5.5% at 0.625 μg mL). Comparing Bro-MLNC-Zn and bromelain solution, the former needed a dose 160-folds lower than the latter for a similar effect. Tripan blue dye assay corroborated the results.
The surface functionalization approach produced an innovative formulation having a much higher anti-proliferative effect than the bromelain solution, even though both in vitro proteolytic activity were similar, opening up a great opportunity for further studies in nanomedicine.
本研究针对脂质核纳米胶囊开发了一种有前景的表面功能化方法,并探讨了采用新策略治疗实体瘤的价值。
通过界面反应的三个步骤自组装制备菠萝蛋白酶功能化的多壁脂质核纳米胶囊(Bro-MLNC-Zn)。测定其物理化学和结构特征、体外蛋白水解活性(酪蛋白底物)和抗增殖活性(乳腺癌细胞,MCF-7)。
Bro-MLNC-Zn的z平均直径为135 nm,zeta电位为+23 mV。该复合物由Zn-N化学键以及与羟基和羧基形成的螯合物构成。在纳米胶囊表面复合的菠萝蛋白酶保持其蛋白水解活性,并对人乳腺癌细胞(MCF-7)显示出抗增殖作用(在1.250 μg/mL时为72.6±1.2%,在0.625 μg/mL时为65.5±5.5%)。与菠萝蛋白酶溶液相比,前者达到相似效果所需剂量比后者低160倍。台盼蓝染料试验证实了该结果。
表面功能化方法产生了一种创新制剂,其抗增殖作用比菠萝蛋白酶溶液高得多,尽管两者的体外蛋白水解活性相似,为纳米医学的进一步研究开辟了巨大机遇。