Evidence map›Paper›PMID 32127636›Full record

ArticleCommunications biology2020

pH-responsive high stability polymeric nanoparticles for targeted delivery of anticancer therapeutics.

L Palanikumar, Sumaya Al-Hosani, Mona Kalmouni, Vanessa P Nguyen, Liaqat Ali, Renu Pasricha, Francisco N Barrera, Mazin Magzoub

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 1 pooled it
12.9field-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

116 citing papers in PubMed, 1 synthesis or guideline pooled it, 330 citations in OpenAlex.

  1. Pooled it
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  14. Tumor-Targeted Delivery Therapy Based on PLGA Nanoparticles.Journal of functional biomaterials · 2026
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56 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

L PalanikumarBiology Program, Division of Science, New York University Abu Dhabi, Abu Dhabi, UAE.
Sumaya Al-HosaniBiology Program, Division of Science, New York University Abu Dhabi, Abu Dhabi, UAE.
Mona KalmouniBiology Program, Division of Science, New York University Abu Dhabi, Abu Dhabi, UAE.
Vanessa P NguyenDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee at Knoxville, Knoxville, TN, USA.ORCID http://orcid.org/0000-0002-7650-0138
Liaqat AliCore Technology Platforms, New York University Abu Dhabi, Abu Dhabi, UAE.
Renu PasrichaCore Technology Platforms, New York University Abu Dhabi, Abu Dhabi, UAE.
Francisco N BarreraDepartment of Biochemistry & Cellular and Molecular Biology, University of Tennessee at Knoxville, Knoxville, TN, USA.ORCID http://orcid.org/0000-0002-5200-7891
Mazin MagzoubBiology Program, Division of Science, New York University Abu Dhabi, Abu Dhabi, UAE. mazin.magzoub@nyu.edu.ORCID http://orcid.org/0000-0003-3414-6617
New York University · USUniversity of Tennessee at Knoxville · USNew York University Abu Dhabi · AE

Funding

Transmembrane Peptides for Targeting Acidosis - Equipment SupplementR01GM120642 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI BARRERA, FRANCISCO NICOLAS · 2016 to 2020
$1.7M
NIGMS NIH HHS R01 GM120642
6 · The paper itself

Abstract

The practical application of nanoparticles (NPs) as chemotherapeutic drug delivery systems is often hampered by issues such as poor circulation stability and targeting inefficiency. Here, we have utilized a simple approach to prepare biocompatible and biodegradable pH-responsive hybrid NPs that overcome these issues. The NPs consist of a drug-loaded polylactic-co-glycolic acid (PLGA) core covalently 'wrapped' with a crosslinked bovine serum albumin (BSA) shell designed to minimize interactions with serum proteins and macrophages that inhibit target recognition. The shell is functionalized with the acidity-triggered rational membrane (ATRAM) peptide to facilitate internalization specifically into cancer cells within the acidic tumor microenvironment. Following uptake, the unique intracellular conditions of cancer cells degrade the NPs, thereby releasing the chemotherapeutic cargo. The drug-loaded NPs showed potent anticancer activity in vitro and in vivo while exhibiting no toxicity to healthy tissue. Our results demonstrate that the ATRAM-BSA-PLGA NPs are a promising targeted cancer drug delivery platform.

Indexed as

Drug CarriersAcidsAnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationDoxorubicinDrug CompoundingDrug Delivery SystemsDrug LiberationDrug StabilityFemaleHeLa CellsHumansHydrogen-Ion ConcentrationMCF-7 CellsAcidsAntineoplastic AgentsDoxorubicinDrug CarriersPeptide FragmentsPolylactic Acid-Polyglycolic Acid CopolymerSerum Albumin, Bovine

Identifiers

PMID32127636
PMCPMC7054360
OpenAlexW3009701618

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.