Evidence map›Paper›PMID 38305859›Full record

ArticleAnalytical and bioanalytical chemistry2024

Development of target-based cell membrane affinity ultrafiltration technology for a simplified approach to discovering potential bioactive compounds in natural products.

Xuan Chen, Jian-Liang Zhou, Jinhao Yu, Ningbo Chen, Wenda Chen, Huaqiu Lu, Gui-Zhong Xin, Yuanyuan Lin

Abstract read
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In one paragraph

Article in Analytical and bioanalytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Xuan Chen *School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Jian-Liang Zhou *School of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Jinhao YuSchool of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Ningbo ChenSchool of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Wenda ChenSchool of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Huaqiu LuSchool of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Gui-Zhong XinState Key Laboratory of Natural Medicines, Department of Chinese Medicines Analysis, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Yuanyuan LinSchool of Pharmacy, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China. Ylin2412@163.com.
Hangzhou Normal University · CNHangzhou Hospital of Traditional Chinese Medicine · CNChina Pharmaceutical University · CN

Funding

National Natural Science Foundation of China 82074270National Natural Science Foundation of China 82104544
6 · The paper itself

Abstract

Target-based drug discovery technology based on cell membrane targets has gained significant traction and has been steadily advancing. However, current methods still face certain limitations that need to be addressed. One of the challenges is the laborious preparation process of screening materials, which can be time-consuming and resource-intensive. Additionally, there is a potential issue of non-specific adsorption caused by carrier materials, which can result in false-positive results and compromise the accuracy of the screening process. To address these challenges, this paper proposes a target-based cell membrane affinity ultrafiltration technology for active ingredient discovery in natural products. In this technique, the cell membranes of human lung adenocarcinoma epithelial cells (A549) with a high expression of epidermal growth factor receptor (EGFR) were incubated with candidate drugs and then transferred to an ultrafiltration tube. Through centrifugation, components that interacted with EGFR were retained in the ultrafiltration tube as "EGFR-ligand" complex, while the components that did not interact with EGFR were separated. After thorough washing and eluting, the components interacting with EGFR were dissociated and further identified using LC-MS, enabling the discovery of bioactive compounds. Moreover, the target-based cell membrane affinity ultrafiltration technology exhibited commendable binding capacity and selectivity. Ultimately, this technology successfully screened and identified two major components from the Curcumae Rhizoma-Sparganii Rhizoma (CS) herb pair extracts, which were further validated for their potential anti-tumor activity through pharmacological experiments. By eliminating the need for laborious preparation of screening materials and the potential non-specific adsorption caused by carriers, the development of target-based cell membrane affinity ultrafiltration technology provides a simplified approach and method for bioactive compounds discovery in natural sources.

Indexed as

Biological ProductsUltrafiltrationCell MembraneErbB ReceptorsHumansTechnologyBiological ProductsErbB ReceptorsBioactive compoundsCell membrane affinity ultrafiltrationCurcumae Rhizoma-Sparganii Rhizoma herb pairNatural productsTarget-based drug discovery

Identifiers

PMID38305859
OpenAlexW4391479565

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.