Evidence map›Paper›PMID 38694466›Full record

ArticleNanoscale advances2024

Anurag Kumar Singh, Snigdha Singh, Tarun Minocha, Sanjeev Kumar Yadav, Reema Narayan, Usha Yogendra Nayak, Santosh Kumar Singh, Rajendra Awasthi

Open access · goldAbstract read
In one paragraph

Article in Nanoscale advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

5 citing papers in PubMed, 21 citations in OpenAlex.

  1. Mesoporous Silica with Different Channel Widths for CsMaterials (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. 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 at 5 institutions in 2 countries.

Anurag Kumar SinghCentre of Experimental Medicine & Surgery, Institute of Medical Sciences, Banaras Hindu University Varanasi 221005 Uttar Pradesh India singhsk71@yahoo.com +91-9415389046.ORCID https://orcid.org/0000-0003-2125-810X
Snigdha SinghCentre of Experimental Medicine & Surgery, Institute of Medical Sciences, Banaras Hindu University Varanasi 221005 Uttar Pradesh India singhsk71@yahoo.com +91-9415389046.
Tarun MinochaDepartment of Zoology, Institute of Science, Banaras Hindu University Varanasi 221005 India.
Sanjeev Kumar YadavDepartment of Zoology, Institute of Science, Banaras Hindu University Varanasi 221005 India.
Reema NarayanDepartment of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education Manipal 576104 Karnataka India.
Usha Yogendra NayakDepartment of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education Manipal 576104 Karnataka India.
Santosh Kumar SinghCentre of Experimental Medicine & Surgery, Institute of Medical Sciences, Banaras Hindu University Varanasi 221005 Uttar Pradesh India singhsk71@yahoo.com +91-9415389046.
Rajendra AwasthiDepartment of Pharmaceutical Sciences, School of Health Sciences & Technology, UPES University Dehradun 248007 Uttarakhand India rajendra.awasthi@ddn.upes.ac.in awasthi02@gmail.com +91-9495234530.ORCID https://orcid.org/0000-0002-1286-1874
Institute of Medical Sciences · INManipal Academy of Higher Education · INBanaras Hindu University · INCentre of Experimental Medicine of the Slovak Academy of Sciences · SKUniversity of Petroleum and Energy Studies · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal loss in Alzheimer's disease has been reported to display features of apoptosis, pyroptosis (programmed necrosis), or necroptosis. This study thoroughly examines the production and characterization of MCM-41 based berberine (BBR)-loaded porous silica nanoparticles (MSNs) by a modified Stöber method, focusing on their possible role in inhibiting the apoptotic process. Particle size, polydispersity index, morphology, drug loading, zeta potential, entrapment efficiency, and drug release were examined. The formulation was analyzed using various spectroscopic techniques. The surface area was computed by the Brunauer-Emmett-Teller plot. Computational models were developed for molecular dynamics simulation studies. A small PDI value indicated an even distribution of particles at nanoscale sizes (80-100 nm). Results from XRD and SEAD experiments confirmed the amorphous nature of BBR in nanoparticles. Nanoparticles had high entrapment (75.21 ± 1.55%) and drug loading (28.16 ± 2.5%) efficiencies. A negative zeta potential value (-36.861.1 mV) indicates the presence of silanol groups on the surface of silica. AFM findings reveal bumps due to the surface drug that contributed to the improved roughness of the MSNs-BBR surface. Thermal gravimetric analysis confirmed the presence of BBR in MSNs. Drug release was controlled by simple diffusion or quasi-diffusion. Molecular dynamics simulations confirmed the existence of diffused drug molecules. Cellular studies using SH-SY-5Y cells revealed dose-dependent growth inhibition. Fragmented cell nuclei and nuclear apoptotic bodies in DAPI-stained cells exposed to nanoparticles showed an increase in apoptotic cells. Flow cytometry analysis demonstrated a lower red-to-green ratio in SH-SY-5Y cells treated with nanoparticles. This suggests improved mitochondrial health, cellular viability restoration, and prevention of the apoptotic process. This study provides essential data on the synthesis and potential of MSNs loaded with BBR, which may serve as a viable therapeutic intervention for conditions associated with apoptosis.

Identifiers

PMID38694466
PMCPMC11059486
OpenAlexW4393954912

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.