Evidence map›Paper›PMID 32947799›Full record

ArticleMolecules (Basel, Switzerland)2020

Poly-(Lactic-co-Glycolic) Acid Nanoparticles for Synergistic Delivery of Epirubicin and Paclitaxel to Human Lung Cancer Cells.

Nikita Sharma, R Mankamna Kumari, Nidhi Gupta, Asad Syed, Ali H Bahkali, Surendra Nimesh

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Formulation Development andCurrent drug delivery · 2026
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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

6 authors.

Nikita SharmaDepartment of Biotechnology, School of Life Sciences, Central University of Rajasthan, Ajmer 305817, India.
R Mankamna KumariDepartment of Biotechnology, School of Life Sciences, Central University of Rajasthan, Ajmer 305817, India.
Nidhi GuptaDepartment of Biotechnology, IIS (Deemed to be University), Jaipur Rajasthan 302020, India.
Asad SyedDepartment of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Ali H BahkaliDepartment of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Surendra NimeshDepartment of Biotechnology, School of Life Sciences, Central University of Rajasthan, Ajmer 305817, India.

Funding

Department of Biotechnology, Government of India, India 6242-P82/ RGCB/PMD/DBT/SNMH/2015
6 · The paper itself

Abstract

Combination therapy using chemically distinct drugs has appeared as one of the promising strategies to improve anticancer treatment efficiency. In the present investigation, poly-(lactic-co-glycolic) acid (PLGA) nanoparticles electrostatically conjugated with polyethylenimine (PEI)-based co-delivery system for epirubicin and paclitaxel (PLGA-PEI-EPI-PTX NPs) has been developed. The PLGA-PEI-EPI-PTX NPs exhibited a monodispersed size distribution with an average size of 240.93 ± 12.70 nm as measured through DLS and 70.8-145 nm using AFM. The zeta potential of 41.95 ± 0.65 mV from -17.45 ± 2.15 mV further confirmed the colloidal stability and PEI modification on PLGA nanoparticles. Encapsulation and loading efficiency along with in vitro release of drug for nanoparticles were done spectrophotometrically. The FTIR analysis of PLGA-PEI-EPI-PTX NPs revealed the involvement of amide moiety between polymer PLGA and PEI. The effect of nanoparticles on the cell migration was also corroborated through wound healing assay. The MTT assay demonstrated that PLGA-PEI-EPI-PTX NPs exhibited considerable anticancer potential as compared to the naïve drugs. Further, p53 protein expression analysed through western blot showed enhanced expression. This study suggests that combination therapy using PLGA-PEI-EPI-PTX NPs represent a potential approach and could offer clinical benefits in the future for lung cancer patients.

Indexed as

Antineoplastic AgentsCell Line, TumorCell MovementCell SurvivalDrug CarriersDrug LiberationEpirubicinHumansHydrogen-Ion ConcentrationKineticsLung NeoplasmsNanoparticlesPaclitaxelPolylactic Acid-Polyglycolic Acid CopolymerAntineoplastic AgentsDrug CarriersEpirubicinPaclitaxelPolylactic Acid-Polyglycolic Acid CopolymerepirubicinMTTp53paclitaxelPLGA nanoparticles

Identifiers

PMID32947799
PMCPMC7570462

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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.