Evidence map›Paper›PMID 35607417›Full record

ArticleMaterials today. Bio2022

Drug-loaded oleic-acid grafted mesoporous silica nanoparticles conjugated with α-lactalbumin resembling BAMLET-like anticancer agent with improved biocompatibility and therapeutic efficacy.

Wei Pei, Ling Cai, Xing Gong, Li Zhang, Jiarong Zhang, Ping Zhu, Huijun Jiang, Chao Wang, Shoulin Wang, Jin Chen

Abstract read
In one paragraph

Article in Materials today. Bio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Enteral Route Nanomedicine for Cancer Therapy.International journal of nanomedicine · 2024
    Review
  8. Review
  9. 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

10 authors.

Wei PeiCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Ling CaiSchool of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, China.
Xing GongCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Li ZhangCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Jiarong ZhangCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Ping ZhuCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Huijun JiangSchool of Pharmacy, Nanjing Medical University, 211166, Nanjing, China.
Chao WangCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Shoulin WangCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.
Jin ChenCenter for Global Health, School of Public Health, Nanjing Medical University, 211166, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite its prominent therapeutic efficacy, chemotherapy has raised serious concerns due to the severe adverse effects and multidrug resistance evoked, which propels the search for safe and green therapeutic agents. BAMLET (bovine α-lactalbumin made lethal against tumor cell) is a well-known protein-based anticancer agent of selective tumoricidal activity. Here, we prepared oleic acid-modified mesoporous silica nanoparticles (OA-MSNs) conjugated with bovine α-lactalbumin, a lipoprotein complex resembling BAMLET formed on the surface of MSNs (MSN-BAMLET) to load the anticancer drug of docetaxel (DTX). Compared to that of OA-MSNs/DTX, the obtained MSN-BAMLET/DTX with a sustained and pH-responsive drug release behaviors exhibited good biocompatibility and enhanced cytotoxic effect against cancer cells. Moreover, the presence of lipoprotein complex in MSN-BAMLET contributed to the improved dispersion of the composite in solution and the inhibitory effect on the migration of cancer cells. Furthermore, the adsorption profiles of protein corona on the obtained nanoparticles were analyzed. It was found that the marked low amount and abundance of plasma proteins were adsorbed on the α-lactalbumin coated siliceous composite demonstrated its long circulation property. Finally,

Indexed as

BAMLETDrug deliveryMesoporous silica nanoparticleProtein coronaα-lactalbumin

Identifiers

PMID35607417
PMCPMC9123267

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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.