Evidence map›Paper›PMID 39430311›Full record

ArticleInternational journal of nanomedicine2024

Bio-Inspired Nanodelivery Platform: Platelet Membrane-Cloaked Genistein Nanosystem for Targeted Lung Cancer Therapy.

Rui Gao, Peihong Lin, Wenjing Yang, Zhengyu Fang, Chunxiao Gao, Bin Cheng, Jie Fang, Wenying Yu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
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  5. Review
  6. Review
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.

Rui Gao *School of Pharmacy, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.
Peihong Lin *School of Pharmacy, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.
Wenjing Yang *School of Pharmacy, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.
Zhengyu FangSchool of Pharmacy, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.ORCID 0000-0002-1460-293X
Chunxiao GaoSchool of Pharmacy, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.
Bin ChengDepartment of Traditional Chinese Medicine, Zhejiang Pharmaceutical University, Ningbo, 315500, People's Republic of China.
Jie FangZhejiang Provincial Laboratory of Experimental Animal's & Nonclinical Laboratory Studies, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.
Wenying YuSchool of Pharmacy, Hangzhou Medical College, Hangzhou, 310013, People's Republic of China.ORCID 0000-0003-3168-9472

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Genistein (Gen), a natural polyphenolic compound, has emerged as a promising candidate for lung cancer treatment. However, the potential clinical application of Gen is limited due to its poor solubility, low bioavailability, and toxic side effects. To address these challenges, a biomimetic delivery platform with cell membranes derived from natural cells as carrier material was constructed. This innovative approach aims to facilitate targeted drug delivery and solve the problem of biocompatibility of synthetic materials. Methods: First, the liposomes (LPs) loaded with Gen (LPs@Gen) was prepared using the ethanol injection method. Subsequently, PLTM-LPs@Gen was obtained through co-extrusion after mixing platelet membrane (PLTM) and LPs@Gen. Additionally, the biological and physicochemical properties of PLTM-LPs@Gen were investigated. Finally, the targeting ability, therapeutic efficacy, and safety of PLTM-LPs@Gen for lung cancer were evaluated using both a cell model and a tumor-bearing nude mouse model. Results: The optimal preparation ratio for LPs@Gen was Gen: soybean lecithin: cholesterol: DSPE-PEG2000 (3:30:5:10, mass ratio), while the ideal fusion ratio of LPs@Gen and PLTM was 1:1. The particle size of PLTM-LPs@Gen was 108.33 ± 1.06 nm, and the encapsulation efficiency and drug loading were 94.29% and 3.09% respectively. Gen was released continuously and slowly from PLTM-LPs@Gen. Moreover, PLTM-LPs@Gen exhibited good stability within one week. The results of in vitro cellular uptake and in vivo distribution experiments indicated that the carrier material, PLTM-LPs, has the immune escape ability and tumor targeting ability. Consequently, it showed better therapeutic effects than free drugs and traditional LPs in vitro and in vivo tumor models. In addition, safety experiments demonstrated that PLTM-LPs@Gen possesses good biocompatibility. Conclusion: Biomimetic nanomedicine provides a new strategy for the precision treatment of lung cancer in clinical practice.

Indexed as

GenisteinLiposomesLung NeoplasmsMice, NudeA549 CellsAnimalsBlood PlateletsCell Line, TumorDrug Delivery SystemsHumansMiceMice, Inbred BALB CParticle SizeXenograft Model Antitumor AssaysGenisteinLiposomesbionic technologygenisteinliposomeslung cancerplatelet membranetargeted therapy

Identifiers

PMID39430311
PMCPMC11491070

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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.