Evidence map›Paper›PMID 33731994›Full record

ArticleInternational journal of nanomedicine2021

Cancer Cell-Membrane Biomimetic Boron Nitride Nanospheres for Targeted Cancer Therapy.

Shini Feng, Yajing Ren, Hui Li, Yunfei Tang, Jinyu Yan, Zeyuan Shen, Huijie Zhang, Fuxue Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  8. Stimuli-Responsive Boron-Based Materials in Drug Delivery.International journal of molecular sciences · 2023
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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 2 institutions in 1 country.

Shini FengSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Yajing RenSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Hui LiSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Yunfei TangSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Jinyu YanSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Zeyuan ShenSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Huijie ZhangSchool of Pharmaceutical Sciences, Jiangnan University, Wuxi, 214122, People's Republic of China.ORCID 0000-0001-9676-4264
Fuxue ChenSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.
Shanghai University · CNJiangnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeNanomaterial-based drug-delivery systems allowing for effective targeted delivery of smallmolecule chemodrugs to tumors have revolutionized cancer therapy. Recently, as novel nanomaterials with outstanding physicochemical properties, boron nitride nanospheres (BNs) have emerged as a promising candidate for drug delivery. However, poor dispersity and lack of tumor targeting severely limit further applications. In this study, cancer cell-membrane biomimetic BNs were designed for targeted anticancer drug delivery.

methodsCell membrane extracted from HeLa cells (HM) was used to encapsulate BNs by physical extrusion. Doxorubicin (Dox) was loaded onto HM-BNs as a model drug.

resultsThe cell-membrane coating endowed the BNs with excellent dispersibility and cytocompatibility. The drug-release profile showed that the Dox@HM-BNs responded to acid pH, resulting in rapid Dox release. Enhanced cellular uptake of Dox@HM-BNs by HeLa cells was revealed because of the homologous targeting of cancer-cell membranes. CCK8 and live/dead assays showed that Dox@HM-BNs had stronger cytotoxicity against HeLa cells, due to self-selective cellular uptake. Finally, antitumor investigation using the HeLa tumor model demonstrated that Dox@HM-BNs possessed much more efficient tumor inhibition than free Dox or Dox@BNs.

conclusionThese findings indicate that the newly developed HM-BNs are promising as an efficient tumor-selective drug-delivery vehicle for tumor therapy.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsBiomimetic MaterialsBody WeightBoron CompoundsCell Line, TumorCell MembraneCell SurvivalDoxorubicinDrug CarriersDrug LiberationEndocytosisFemaleHEK293 CellsHumansAntineoplastic AgentsBoron Compoundsboron nitrideDoxorubicinDrug Carriersbiomimeticboron nitride nanospherescancer-cell membranechemotherapytargeted drug delivery

Identifiers

PMID33731994
PMCPMC7959002
OpenAlexW3134224925

What OpenQuestion holds

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Registered trials

None linked

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.