Evidence map›Paper›PMID 33954285›Full record

ArticleACS applied bio materials2021

Targeted polymeric nanoparticles for drug delivery to hypoxic, triple-negative breast tumors.

Babak Mamnoon, Jagadish Loganathan, Matthew I Confeld, Nimesha De Fonseka, Li Feng, Jamie Froberg, Yongki Choi, Daniel M Tuvin, Venkatachalem Sathish, Sanku Mallik

Open access · greenAbstract read
In one paragraph

Article in ACS applied bio materials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 45 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Babak MamnoonDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
Jagadish LoganathanDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
Matthew I ConfeldDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
Nimesha De FonsekaDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
Li FengDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
Jamie FrobergDepartment of Physics, North Dakota State University, Fargo, North Dakota 58102, United States.
Yongki ChoiDepartment of Physics, North Dakota State University, Fargo, North Dakota 58102, United States.
Daniel M TuvinSanford Broadway Clinic, Fargo, North Dakota 58102, United States.
Venkatachalem SathishDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
Sanku MallikDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota 58102, United States.
North Dakota State University · USSanford Broadway Medical Center · US

Funding

Targeting CLEC-2/podoplanin as a therapeutic strategy for pancreatic cancerP20GM109024 · NIGMS · NORTH DAKOTA STATE UNIVERSITY · PI Sanku Mallik · 2016 to 2026
$20.5M
Tracking and Evaluation CoreU54GM128729 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI SCHWARTZ, GARY G · 2018 to 2022
$20.3M
Echogenic Polymersomes for Triggered Contents ReleaseR01GM114080 · NIGMS · NORTH DAKOTA STATE UNIVERSITY · PI MALLIK, SANKU, SARKAR, KAUSIK · 2015 to 2023
$2.6M
NIGMS NIH HHS P20 GM109024NIGMS NIH HHS R01 GM114080NIGMS NIH HHS U54 GM128729
6 · The paper itself

Abstract

High recurrence and metastasis to vital organs are the major characteristics of triple-negative breast cancer (TNBC). Low vascular oxygen tension promotes resistance to chemo- and radiation therapy. Neuropilin-1 (NRP-1) receptor is highly expressed on TNBC cells. The tumor-penetrating iRGD peptide interacts with the NRP-1 receptor, triggers endocytosis and transcytosis, and facilitates penetration. Herein, we synthesized a hypoxia-responsive diblock PLA-diazobenzene-PEG copolymer and prepared self-assembled hypoxia-responsive polymersomes (Ps) in an aqueous buffer. The iRGD peptide was incorporated into the polymersome structure to make hypoxia-responsive iRGD-conjugated polymersomes (iPs). Doxorubicin (DOX) was encapsulated in the polymersomes to prepare both targeted and non-targeted hypoxia-responsive polymersomes (DOX-iPs and DOX-Ps, respectively). The polymeric nanoparticles released less than 30% of their encapsulated DOX within 12 hours under normoxic conditions (21% oxygen), whereas under hypoxia (2% Oxygen), doxorubicin release remarkably increased to over 95%. The targeted polymersomes significantly decreased TNBC cells' viability in monolayer and spheroid cultures under hypoxia compared to normoxia. Animal studies displayed that targeted polymersomes significantly diminished tumor growth in xenograft nude mice. Overall, the targeted polymersomes exhibited potent anti-tumor activity in monolayer, spheroid, and animal models of TNBC. With further developments, the targeted nanocarriers discussed here might have the translational potential as drug carriers for the treatment of TNBC.

Indexed as

Drug Delivery SystemsAnimalsAntineoplastic AgentsCell Line, TumorCell SurvivalDoxorubicinDrug LiberationFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeMolecular StructureNanoparticlesNeuropilin-1OxygenAntineoplastic AgentsDoxorubicinNeuropilin-1NRP1 protein, humanOxygenPolymersHypoxiaNanoparticlesNanotechnologyPolymersomesTargeted Drug Delivery

Identifiers

PMID33954285
PMCPMC8096163
OpenAlexW3116581619

What OpenQuestion holds

Textmetadata
LicenceTDM
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.