Evidence map›Paper›PMID 27297021›Full record

ArticleJournal of nanobiotechnology2016

In vitro and in vivo uptake studies of PAMAM G4.5 dendrimers in breast cancer.

Natalia Oddone, Nicole Lecot, Marcelo Fernández, Alejandra Rodriguez-Haralambides, Pablo Cabral, Hugo Cerecetto, Juan Claudio Benech

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2016. 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
2.3field-weighted citation impact, top 13% 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, 55 citations in OpenAlex.

  1. Article
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  5. Mannosylated PAMAM G2 dendrimers mediated rate programmed delivery of efavirenz target HIV viral latency at reservoirs.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
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  11. Development ofJournal of cancer research and clinical oncology · 2023
    Article
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  14. Optimization of the Hemolysis Assay for the Assessment of Cytotoxicity.International journal of molecular sciences · 2023
    Article
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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

7 authors at 1 institution in 1 country.

Natalia OddoneLaboratorio de Señalización Celular y Nanobiología, Instituto de Investigaciones Biológicas Clemente Estable, Av. Italia 3318, CP 11600, Montevideo, Uruguay.
Nicole LecotÁrea de Radiofarmacia, Centro de Investigaciones Nucleares, UdelaR, Mataojo 2055, CP 11400, Montevideo, Uruguay.
Marcelo FernándezLaboratorio de Experimentación Animal, Centro de Investigaciones Nucleares, UdelaR, Mataojo 2055, CP 11400, Montevideo, Uruguay.
Alejandra Rodriguez-HaralambidesQuímica Bioanalítica, Instituto Polo Tecnológico de Pando, Facultad de Química, UdelaR, By Pass de Pando y Ruta 8, CP 91000, Pando, Canelones, Uruguay.
Pablo CabralÁrea de Radiofarmacia, Centro de Investigaciones Nucleares, UdelaR, Mataojo 2055, CP 11400, Montevideo, Uruguay.
Hugo CerecettoÁrea de Radiofarmacia, Centro de Investigaciones Nucleares, UdelaR, Mataojo 2055, CP 11400, Montevideo, Uruguay.
Juan Claudio BenechLaboratorio de Señalización Celular y Nanobiología, Instituto de Investigaciones Biológicas Clemente Estable, Av. Italia 3318, CP 11600, Montevideo, Uruguay. jbenech@iibce.edu.uy.
Instituto de Investigaciones Biológicas Clemente Estable · UY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer is the second leading cause of cancer death worldwide. Nanotechnology approaches can overcome the side effects of chemotherapy as well as improve the efficacy of drugs. Dendrimers are nanometric size polymers which are suitable as drug delivery systems. To the best of our knowledge, studies on the application of PAMAM G4.5 (polyamidoamine half generation 4) dendrimers as potential drug delivery systems in breast cancer have not been reported. In this work we developed a PAMAM G4.5 dendrimer containing FITC (fluorescein isothiocyanate) dye to study their uptake by murine breast cancer cells and BALB/c mice breast tumors.

resultsWe performed a reaction between FITC and PAMAM G4.5 dendrimers which were previously derivatized with piperazine (linker molecule), characterized them by (1)H NMR (proton nuclear magnetic resonance) spectroscopy and MALDI-TOF (matrix-assisted laser desorption/ionization- time-of-flight) mass spectrometry. The experimental data indicated that 2 FITC molecules could be bound covalently at the PAMAM G4.5 dendrimer surface, with 17 FITC molecules probably occluded in PAMAM dendrimers cavity. PAMAM-FITC dendrimer (PAMAM G4.5-piperazinyl-FITC dendrimer) size distribution was evaluated by DLS (dynamic light scattering) and TEM (transmission electron microscopy). The nanoparticle hydrodynamic size was 96.3 ± 1.4 nm with a PdI (polydispersion index) of 0.0296 ± 0.0171, and the size distribution measured by TEM was 44.2 ± 9.2 nm. PAMAM-FITC dendrimers were neither cytotoxic in 4T1 cells nor hemolytic up to 24 h of incubation. In addition, they were uptaken in vitro by 4T1 cells and in vivo by BALB/c mice breast tumors. PAMAM G4.5-piperazinyl-FITC dendrimer intracellular distribution was observed through histologic analysis of the tumor by laser confocal microscopy.

conclusionThese results indicate that PAMAM G4.5 dendrimers enter tumor tissue cells, being good candidates to be used as antitumor drug delivery systems for breast cancer treatment and diagnosis.

Indexed as

AnimalsAntineoplastic AgentsBreastBreast NeoplasmsCell Line, TumorDendrimersDrug CarriersFemaleFluorescein-5-isothiocyanateFluorescent DyesMiceMice, Inbred BALB CNylonsAntineoplastic AgentsDendrimersDrug CarriersFluorescein-5-isothiocyanateFluorescent DyesNylonsPAMAM-G4Antitumor drug delivery systemsBreast cancer treatment or diagnosisPAMAM G4.5 dendrimers

Identifiers

PMID27297021
PMCPMC4906583
OpenAlexW2423043747

What OpenQuestion holds

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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.