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抗坏血酸稳定的金纳米粒子中来曲唑与黄连素的协同组合:乳腺癌的一种有前景的解决方案

Synergistic Combination of Letrozole and Berberine in Ascorbic Acid-Stabilized AuNPs: A Promising Solution for Breast Cancer.

作者信息

Foudah Ahmed I, Alam Aftab, Salkini Mohammad Ayman, Ross Samir A, Kumar Piyush, Aldawsari Mohammed F, Alqarni Mohammed H, Sweilam Sherouk Hussein

机构信息

Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia.

National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, Oxford, MS 38677, USA.

出版信息

Pharmaceuticals (Basel). 2023 Aug 3;16(8):1099. doi: 10.3390/ph16081099.

DOI:10.3390/ph16081099
PMID:37631014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10459502/
Abstract

Breast cancer is a deadly disease that affects countless women worldwide. The most conventional treatments for breast cancer, such as the administration of anticancer medications such as letrozole (LTZ), pose significant barriers due to the non-selective delivery and low bioavailability of cytotoxic drugs leading to serious adverse effects and multidrug resistance (MDR). Addressing these obstacles requires an innovative approach, and we propose a combined strategy that synergistically incorporates LTZ with berberine (BBR) into stabilised AuNPs coated with ascorbic acid (AA), known as LTZ-BBR@AA-AuNPs. The LTZ-BBR@AA-AuNPs, a novel combined drug delivery system, were carefully designed to maximise the entrapment of both LTZ and BBR. The resulting spherical nanoparticles exhibited remarkable efficiency in trapping these two compounds, with rates of 58% and 54%, respectively. In particular, the average hydrodynamic diameter of these nanoparticles was determined to be 81.23 ± 4.0 nm with a PDI value of only 0.286, indicating excellent uniformity between them. Furthermore, their zeta potential was observed to be -14.5 mV, suggesting high stability even under physiological conditions. The release profiles showed that after being incubated for about 24 h at pH levels ranging from acidic (pH = 5) to basic (pH = 7), the percentage released for both drugs ranged from 56-72%. This sustained and controlled drug release can reduce any negative side effects while improving therapeutic efficacy when administered directly to cancer. MDA-MB-231 cells treated with LTZ-BBR@AA-AuNPs for 48 h exhibited IC values of 2.04 ± 0.011 μg/mL, indicating potent cytotoxicity against cells. Furthermore, the nanoparticles demonstrated excellent stability throughout the duration of the treatment.

摘要

乳腺癌是一种致命疾病,影响着全球无数女性。乳腺癌最传统的治疗方法,如使用来曲唑(LTZ)等抗癌药物,由于细胞毒性药物的非选择性递送和低生物利用度,会导致严重的不良反应和多药耐药性(MDR),从而构成了重大障碍。解决这些障碍需要创新方法,我们提出了一种联合策略,即将LTZ与黄连素(BBR)协同整合到包覆有抗坏血酸(AA)的稳定金纳米颗粒中,即LTZ-BBR@AA-AuNPs。LTZ-BBR@AA-AuNPs是一种新型联合药物递送系统,经过精心设计以最大限度地包封LTZ和BBR。所得的球形纳米颗粒在捕获这两种化合物方面表现出显著效率,捕获率分别为58%和54%。特别是,这些纳米颗粒的平均流体动力学直径测定为81.23±4.0nm,PDI值仅为0.286,表明它们之间具有出色的均匀性。此外,观察到它们的zeta电位为-14.5mV,表明即使在生理条件下也具有高稳定性。释放曲线表明,在从酸性(pH = 5)到碱性(pH = 7)的pH水平下孵育约24小时后,两种药物的释放百分比范围为56 - 72%。这种持续且可控的药物释放可以减少任何负面副作用,同时在直接施用于癌症时提高治疗效果。用LTZ-BBR@AA-AuNPs处理48小时的MDA-MB-231细胞表现出的IC值为2.04±0.011μg/mL,表明对细胞具有强大的细胞毒性。此外,纳米颗粒在整个治疗过程中表现出出色的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/f694036786d9/pharmaceuticals-16-01099-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/f694036786d9/pharmaceuticals-16-01099-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/a7d87c26c3f7/pharmaceuticals-16-01099-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/fdaf08358788/pharmaceuticals-16-01099-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/47b876627a4b/pharmaceuticals-16-01099-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/fb1b682bfd7b/pharmaceuticals-16-01099-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f641/10459502/f694036786d9/pharmaceuticals-16-01099-g006.jpg

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