Evidence map›Paper›PMID 24124132›Full record

ArticleAdvanced healthcare materials2014

Osteotropic therapy via targeted layer-by-layer nanoparticles.

Stephen W Morton, Nisarg J Shah, Mohiuddin A Quadir, Zhou J Deng, Zhiyong Poon, Paula T Hammond

Open access · greenAbstract read
In one paragraph

Article in Advanced healthcare materials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.3field-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

30 citing papers in PubMed, 81 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

6 authors at 1 institution in 1 country.

Stephen W MortonThe David H. Koch Institute for Integrative Cancer Research, Department of Chemical Engineering Institute for Soldier Nanotechnologies 77 Massachusetts Avenue, Cambridge, MA, 02139.
Nisarg J Shah
Mohiuddin A Quadir
Zhou J Deng
Zhiyong Poon
Paula T Hammond
Institute for Soldier Nanotechnologies · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
The Development of Clinical Grade, Targeted Magnetic NanoparticlesU54CA151884 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL · 2010 to 2014
$11.3M
Perfused 3D Tissue Surrogates for Complex Cell-Cell Communication SystemsR01EB010246 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRIFFITH, LINDA G · 2009 to 2013
$3.3M
Nanoscale Electrostatic Assemblies for Multi-Agent Drug Delivery fromR01AG029601 · NIA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HAMMOND, PAULA T · 2007 to 2011
$1.9M
NCI NIH HHS 5 U54 CA151884-02NCI NIH HHS P30 CA014051NCI NIH HHS P30 CA14051NCI NIH HHS U54 CA151884NIA NIH HHS R01 AG029601NIBIB NIH HHS R01 EB010246
6 · The paper itself

Abstract

Current treatment options for debilitating bone diseases such as osteosarcoma, osteoporosis, and bone metastatic cancer are suboptimal and have low efficacy. New treatment options for these pathologies require targeted therapy that maximizes exposure to the diseased tissue and minimizes off-target side effects. This work investigates an approach for generating functional and targeted drug carriers specifically for treating primary osteosarcoma, a disease in which recurrence is common and the cure rate has remained around 20%. This approach utilizes the modularity of Layer-by-Layer (LbL) assembly to generate tissue-specific drug carriers for systemic administration. This is accomplished via surface modification of drug-loaded nanoparticles with an aqueous polyelectrolyte, poly(acrylic acid) (PAA), side-chain functionalized with alendronate, a potent clinically used bisphosphonate. Nanoparticles coated with PAA-alendronate are observed to bind and internalize rapidly in human osteosarcoma 143B cells. Encapsulation of doxorubicin, a front-line chemotherapeutic, in an LbL-targeted liposome demonstrates potent toxicity in vitro. Active targeting of 143B xenografts in NCR nude mice with the LbL-targeted doxorubicin liposomes promotes enhanced, prolonged tumor accumulation and significantly improved efficacy. This report represents a tunable approach towards the synthesis of drug carriers, in which LbL enables surface modification of nanoparticles for tissue-specific targeting and treatment.

Indexed as

Acrylic ResinsAlendronateAnimalsBone Density Conservation AgentsBone NeoplasmsCell Line, TumorDoxorubicinDrug CarriersHalf-LifeHumansLiposomesMiceMice, Inbred BALB CMice, NudeNanoparticlesOsteosarcomaAcrylic ResinsAlendronateBone Density Conservation Agentscarbopol 940DoxorubicinDrug Carriersliposomal doxorubicinLiposomesPolyethylene Glycolsbisphosphonatebonecancer therapylayer-by-layer

Identifiers

PMID24124132
PMCPMC4041853
OpenAlexW2155528429

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.