Evidence map›Paper›PMID 30929529›Full record

ArticleDrug delivery2019

Surface-engineered polyethyleneimine-modified liposomes as novel carrier of siRNA and chemotherapeutics for combination treatment of drug-resistant cancers.

Livia P Mendes, Can Sarisozen, Ed Luther, Jiayi Pan, Vladimir P Torchilin

Open access · goldAbstract readComparative Study
In one paragraph

Article in Drug delivery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Liposomal delivery of gene therapy for ovarian cancer: a systematic review.Reproductive biology and endocrinology : RB&E · 2023
    Pooled it
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  12. Polymer-Based Nanosystems-A Versatile Delivery Approach.Materials (Basel, Switzerland) · 2021
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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

5 authors at 1 institution in 2 countries.

Livia P Mendesa Center for Pharmaceutical Biotechnology and Nanomedicine , Northeastern University , Boston , MA , USA.ORCID http://orcid.org/0000-0002-8240-1048
Can Sarisozena Center for Pharmaceutical Biotechnology and Nanomedicine , Northeastern University , Boston , MA , USA.ORCID http://orcid.org/0000-0002-3987-6283
Ed Lutherc Department of Pharmaceutical Sciences , Northeastern University , Boston , MA , USA.
Jiayi Pana Center for Pharmaceutical Biotechnology and Nanomedicine , Northeastern University , Boston , MA , USA.
Vladimir P Torchilina Center for Pharmaceutical Biotechnology and Nanomedicine , Northeastern University , Boston , MA , USA.
Northeastern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modification of nanoparticle surfaces with PEG has been widely considered the gold standard for many years. However, PEGylation presents controversial and serious challenges including lack of functionality, hindered cellular interaction, allergic reactions, and stimulation of IgM production after repetitive dosing that accelerates blood clearance of the nanoparticles. We report the development of novel liposomal formulations surface-modified with a low molecular weight, branched polyethyleneimine (bPEI)-lipid conjugate for use as an alternative to PEG. The formulations had very good stability characteristics in ion- and protein-rich mediums. Protein adsorption onto the liposomal surface did not interfere with the cellular interaction. bPEI-modified liposomes (PEIPOS) showed enhanced association with three different cell lines by up to 75 times compared to plain or PEGylated liposomes and were without carrier toxicity. They also penetrated the deeper layers of 3D spheroids. Encapsulating paclitaxel (PTX) into PEIPOS did not change its main mechanism of action. PEIPOS complexed and intracellularly delivered siRNAs and downregulated resistance-associated proteins. Finally, tumor growth inhibition was observed in a mouse ovarian xenograft tumor model, without signs of toxicity, in animals treated with the siRNA/PTX co-loaded formulation. These complex-in-nature but simple-in-design novel liposomal formulations constitute viable and promising alternatives with added functionality to their PEGylated counterparts.

Indexed as

NanoparticlesAnimalsAntineoplastic Agents, PhytogenicCell Line, TumorDrug CarriersDrug Resistance, NeoplasmFemaleHumansLipidsLiposomesMiceMice, NudeOvarian NeoplasmsPaclitaxelPolyethylene GlycolsPolyethyleneimineAntineoplastic Agents, PhytogenicDrug CarriersLipidsLiposomesPaclitaxelPolyethylene GlycolsPolyethyleneimineRNA, Small Interferingcombination cancer therapyDrug deliveryliposomesmultidrug resistancepolyethyleneiminesiRNA deliverysurface-modification

Identifiers

PMID30929529
PMCPMC6450504
OpenAlexW2931115389

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.