Co-Encapsulation of Paclitaxel and Doxorubicin in Liposomes Layer by Layer

IF 2.5 Q3 CHEMISTRY, PHYSICAL
Isaac Izcoatl Mota Díaz, Janna Douda, Patricia García López, Sandra Edith Cabrera Becerra, Miguel Ángel Gómez Álvarez, Rebeca Jiménez Rodríguez, Rafael Jurado León, Pedro López Sánchez
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引用次数: 0

Abstract

The synergistic effect of antineoplastic drug co-encapsulation systems has made them highly regarded due to their improved pharmacological efficacy. Biopolymer-coated liposomes were evaluated for paclitaxel and doxorubicin co-encapsulation in MCF-7 and MDA-MB-231 breast cancer cell lines. These nanosystems are characterized by dynamic light scattering, transmission electron microscopy, and UV–VIS spectroscopy. The conventional and hybrid liposomal systems presented sizes of 150 to 230 nm and %EE greater than 80% for the encapsulated active ingredients. These drug-laden liposomal systems significantly decreased cell viability in both breast cancer cell lines compared with liposome-free drugs. The delivery of antineoplastic drugs in breast cancer therapy could potentially benefit from new hybrids for drug co-encapsulation.
紫杉醇和多柔比星在脂质体中逐层共包囊
抗肿瘤药物共包囊系统具有协同增效作用,可提高药效,因此备受关注。本研究评估了生物聚合物包被脂质体在 MCF-7 和 MDA-MB-231 乳腺癌细胞系中紫杉醇和多柔比星共包被的效果。这些纳米系统通过动态光散射、透射电子显微镜和紫外-可见光谱进行表征。传统脂质体系统和混合脂质体系统的尺寸为 150 至 230 nm,包裹活性成分的 %EE 超过 80%。与不含脂质体的药物相比,这些载药脂质体系统能显著降低两种乳腺癌细胞系的细胞活力。在乳腺癌治疗中输送抗肿瘤药物可能会受益于新的混合药物共包囊技术。
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来源期刊
Colloids and Interfaces
Colloids and Interfaces CHEMISTRY, PHYSICAL-
CiteScore
3.90
自引率
4.20%
发文量
64
审稿时长
10 weeks
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