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sp. 粗提物的细胞毒性潜力、代谢特征分析及脂质体研究——基于计算机分析

Cytotoxic Potential, Metabolic Profiling, and Liposomes of sp. Crude Extract Supported by in silico Analysis.

机构信息

Department of Pharmacognosy, College of Pharmacy, Jouf University, Sakaka, 72341, Saudi Arabia.

Department of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Cairo, 11371, Egypt.

出版信息

Int J Nanomedicine. 2021 Jun 4;16:3861-3874. doi: 10.2147/IJN.S310720. eCollection 2021.

DOI:10.2147/IJN.S310720
PMID:34113103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8187037/
Abstract

INTRODUCTION

Sponge- sp. (Family: Spongiidae) is a coastal sponge that possesses a broad variety of natural-products. However, the exact chemical constituents and cytotoxic activity of the extract are still undefinable.

METHODOLOGY

In the present study, the metabolomic profiling of sp. dereplicated 20 compounds, utilizing liquid chromatography coupled with high-resolution mass spectrometry (LC-HRESIMS). derived crude extract, before and after encapsulation within nanosized liposomes, was in vitro screened against hepatic, breast, and colorectal carcinoma human cell lines (HepG2, MCF-7, and Caco-2, respectively).

RESULTS

The identified metabolites were fit to diverse chemical classes, covering diterpenes, an indole alkaloid, sesterterpenoid, sterol, and methylherbipoline salt. Comprehensive in silico experiments predicted several compounds in the sponge-derived extract (eg, compounds -) to have an anticancer potential via targeting multiple targets. The crude extract showed moderate antiproliferative activities towards studied cell lines with IC values range from 10.7 to 12.4 µg/mL. The formulated extract-containing liposomes (size 141±12.3nm, PDI 0.222, zeta potential 20.8 ± 2.3), significantly enhanced the in vitro anticancer activity of the entrapped extract (IC values ranged from 1.7 to 4.1 µg/mL).

DISCUSSION

Encapsulation of both the hydrophilic and the lipophilic components of the extract within the lipid-based nanovesicles enhanced the cellular uptake and accessibility of the entrapped cargo. This study introduces liposomal nano-vesicles as a promising approach to improve the therapeutic potential of sponge-derived extracts.

摘要

简介

海绵- sp.(海绵科)是一种沿海海绵,具有广泛的天然产物。然而,提取物的确切化学成分和细胞毒性活性仍未确定。

方法

在本研究中,利用液相色谱-高分辨率质谱联用(LC-HRESIMS)对海绵 sp. 的代谢组学进行了剖析,分离出 20 种化合物。在纳米脂质体包封前后,对来源于海绵的粗提物进行了体外筛选,针对肝癌、乳腺癌和结直肠癌细胞系(HepG2、MCF-7 和 Caco-2)。

结果

鉴定出的代谢产物适合多种化学类,包括二萜、吲哚生物碱、甾体萜烯、固醇和甲基胡椒林盐。综合的计算机实验预测,海绵来源的提取物中的几种化合物(例如化合物 -)通过靶向多个靶点具有抗癌潜力。粗提物对研究的细胞系表现出中等的增殖抑制活性,IC 值范围为 10.7 至 12.4µg/mL。含有包封提取物的制剂脂质体(粒径 141±12.3nm,PDI 0.222,zeta 电位 20.8±2.3)显著增强了包封提取物的体外抗癌活性(IC 值范围为 1.7 至 4.1µg/mL)。

讨论

将提取物的亲水性和疏水性成分同时包封在脂质纳米囊泡中,提高了细胞内摄取和包裹货物的可及性。本研究介绍了脂质体纳米囊泡作为一种有前途的方法来提高海绵来源提取物的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/d2f3cb9d199f/IJN-16-3861-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/6ea62bc0b90f/IJN-16-3861-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/b8110126d267/IJN-16-3861-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/31a353e10515/IJN-16-3861-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/c7e5ea2aeb6c/IJN-16-3861-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/02c827542fa2/IJN-16-3861-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/aa4e4bdc1458/IJN-16-3861-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/da53e51fe31c/IJN-16-3861-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/b3c659b88b76/IJN-16-3861-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/a4f2033b6e93/IJN-16-3861-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/d2f3cb9d199f/IJN-16-3861-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/6ea62bc0b90f/IJN-16-3861-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/b8110126d267/IJN-16-3861-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/31a353e10515/IJN-16-3861-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/c7e5ea2aeb6c/IJN-16-3861-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/02c827542fa2/IJN-16-3861-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/aa4e4bdc1458/IJN-16-3861-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/da53e51fe31c/IJN-16-3861-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/b3c659b88b76/IJN-16-3861-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/a4f2033b6e93/IJN-16-3861-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dc8/8187037/d2f3cb9d199f/IJN-16-3861-g0010.jpg

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