Evidence map›Paper›PMID 36793351›Full record

ArticleNanotheranostics2023

Drug Encapsulated Lipid-Polymeric Nanohybrid as a Chemo-therapeutic Platform of Cancer.

Rahul Kumar, Vinish Ranjan Srivastava, Supratim Mahapatra, Daphika S Dkhar, Rohini Kumari, Kumari Prerna, Vikash Kumar Dubey, Pranjal Chandra

Open access · goldAbstract read
In one paragraph

Article in Nanotheranostics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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 2 institutions in 1 country.

Rahul KumarSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Vinish Ranjan SrivastavaSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Supratim MahapatraSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Daphika S DkharSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Rohini KumariSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Kumari PrernaSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Vikash Kumar DubeySchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Pranjal ChandraSchool of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi- 221005, Uttar Pradesh, India.
Indian Institute of Technology BHU · INBanaras Hindu University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The focus of this research is to design a bioengineered drug delivery vehicle that is efficient in anti-cancer drug delivery in a controlled manner. The experimental work focuses on constructing a methotrexate-loaded nano lipid polymer system (MTX-NLPHS) that can transport methotrexate (MTX) in MCF-7 cell lines in a controlled manner through endocytosis via phosphatidylcholine. In this experiment, MTX is embedded with polylactic-co-glycolic acid (PLGA) in phosphatidylcholine, which acts as a liposomal framework for regulated drug delivery. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and dynamic light scattering (DLS) were utilized to characterize the developed nanohybrid system. The particle size and encapsulation efficiency of the MTX-NLPHS were found to be 198 ± 8.44 nm and 86.48 ± 0.31 %, respectively, which is suitable for biological applications. The polydispersity index (PDI) and zeta potential of the final system were found to be 0.134 ± 0.048 and -28 ± 3.50 mV, respectively. The lower value of PDI showed the homogenous nature of the particle size, whereas higher negative zeta potential prevented the system from agglomeration. An

Indexed as

MethotrexateNeoplasmsHumansPharmaceutical PreparationsPhosphatidylcholinesPolymersReactive Oxygen SpeciesMethotrexatePharmaceutical PreparationsPhosphatidylcholinesPolymersReactive Oxygen Speciesdrug deliverylipidMCF-7 cellsmethotrexatenanohybrid systemtheranostics

Identifiers

PMID36793351
PMCPMC9925353
OpenAlexW4320489217

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.