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基于顺铂-透明质酸配合物和 N-三甲基壳聚糖的新型纳米粒系统的制备、表征及初步抗肿瘤活性评价。

Preparation, characterisation and preliminary antitumour activity evaluation of a novel nanoparticulate system based on a cisplatin-hyaluronate complex and N-trimethyl chitosan.

机构信息

Dipartimento di Chimica e Tecnologie Farmaceutiche ed Alimentari, Via Brigata Salerno 13, 16147, Genoa, Italy.

出版信息

Invest New Drugs. 2011 Jun;29(3):443-55. doi: 10.1007/s10637-009-9373-y. Epub 2009 Dec 29.

Abstract

In this work, nanoparticles with a positive surface charge were prepared through the electrostatic interaction of a new cisplatin-hyaluronate complex with N-trimethyl chitosan (substitution degree of 85%). Mean particle diameter was approximately 195 nm. Drug loading of nanoparticles, which had a zeta potential of about 27 mV, was equal to 6% w/w. After 24 h, while the cisplatin-hyaluronate complex released approximately 60% w/w drug in phosphate buffered saline at pH 7.4, approximately 40% w/w of total cisplatin was released from nanoparticles. The same cumulative amounts of released drug were found after 48 h. These nanoparticles, as well as the starting cisplatin-hyaluronate complex, were active on all cell lines tested (P388, A2780, A549), with an antiproliferative activity similar to that of cisplatin. Apoptosis was markedly induced in A2780 cells by nanoparticles. In a preliminary in vivo experiment, the antitumour activity against a murine tumour (P388 cells) subcutaneously implanted in mice, resulted similar to that of cisplatin for nanoparticles whereas the starting complex showed a non-significant activity at the cisplatin dose tested. Body weight change of treated mice suggested a significantly better tolerance of the nanoparticles compared to cisplatin, after an initial brief period of acute toxicity higher than the parent drug. These results indicate that such a particulate system could be useful as a carrier for cisplatin delivery.

摘要

在这项工作中,通过新的顺铂-透明质酸盐复合物与 N-三甲基壳聚糖(取代度为 85%)的静电相互作用制备带正表面电荷的纳米颗粒。平均粒径约为 195nm。载药纳米颗粒的载药量为 6%(w/w),zeta 电位约为 27mV。在 pH7.4 的磷酸盐缓冲盐水中,顺铂-透明质酸盐复合物在 24 小时内释放约 60%(w/w)的药物,而纳米颗粒中约有 40%(w/w)的总顺铂被释放。48 小时后也发现了相同的累积释放药物量。这些纳米颗粒以及起始的顺铂-透明质酸盐复合物对所有测试的细胞系(P388、A2780、A549)均具有活性,其增殖抑制活性与顺铂相似。纳米颗粒明显诱导 A2780 细胞凋亡。在初步的体内实验中,顺铂-透明质酸纳米粒对皮下植入小鼠的 P388 肿瘤的抗肿瘤活性与顺铂相似,而起始复合物在测试的顺铂剂量下表现出非显著活性。与顺铂相比,经治疗的小鼠体重变化表明纳米粒具有更好的耐受性,尽管在初始短暂的急性毒性高于母体药物后。这些结果表明,这种颗粒系统可作为顺铂递送的载体。

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