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使用基于计算机的研究来增强 Hemimycale sp. 总粗提物细胞毒性的脂质体作为一种很有前途的方法。

Niosomes as promising approach for enhancing the cytotoxicity of Hemimycale sp. total crude extract supported with in-silico studies.

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, Minia University, Minia, 61519, Egypt.

Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Deraya University, Minya, Egypt.

出版信息

Sci Rep. 2024 Jan 31;14(1):2546. doi: 10.1038/s41598-024-52918-3.

Abstract

The crude extract of Hemimycale sp. marine sponge was evaluated as a cytotoxic drug against different cell lines; whereas it exhibited promising selective activity toward the breast cancer cell line only with IC value 199.6 ± 0.00512 µg/ml. Moreover, its cytotoxic activity against the breast cancer cell line was reevaluated upon forming total extract-loaded niosomes. This revealed an IC value of 44.35 ± 0.011128 µg/ml, indicating the potential contribution of niosomes in boosting cell penetration and activity as a result. Owing to highlight the bioactive constituents responsible for the cytotoxic activity, metabolomics profiling of Hemimycale sp. was performed using liquid chromatography coupled with high-resolution electrospray ionization mass spectrometry (LC-HR-ESI-MS) revealing tentative identification of phytoconstituents clusters like as, diterpenes, sesterterpenes and sterols. Additionally, the cytotoxic activity of the crude extract was explained on the molecular level, whereas the dereplicated compounds were evaluated in silico against the Epidermal Growth Factor Receptor tyrosine kinase (EGFR). The sesterterpenoid derivatives phorbaketal A acetate (12) and secoepoxy ansellone A (13) together with mycalol-522 (17) showed the best binding energy.

摘要

海绵 Hemimycale sp. 的粗提取物被评估为具有细胞毒性的药物,对不同的细胞系具有潜在的选择性活性,对乳腺癌细胞系的 IC 值为 199.6 ± 0.00512μg/ml。此外,其对乳腺癌细胞系的细胞毒性活性在形成总提取物负载的非离子型脂质体后重新进行评估。结果表明,IC 值为 44.35 ± 0.011128μg/ml,表明非离子型脂质体在提高细胞通透性和活性方面具有潜在的贡献。为了突出对细胞毒性活性有贡献的生物活性成分,采用液相色谱-高分辨电喷雾电离质谱联用技术(LC-HR-ESI-MS)对海绵 Hemimycale sp. 进行代谢组学分析,推测鉴定出了植物化学成分群,如二萜、倍半萜、甾体和固醇。此外,从分子水平上解释了粗提取物的细胞毒性活性,对非冗余化合物进行了计算机筛选,评估其对表皮生长因子受体酪氨酸激酶(EGFR)的抑制活性。甾体倍半萜衍生物 phorbaketal A 醋酸盐(12)和 secoepoxy ansellone A(13)以及 mycalol-522(17)表现出最佳的结合能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d48e/10827731/590c5c1ffffc/41598_2024_52918_Fig1_HTML.jpg

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