Evidence map›Paper›PMID 30689348›Full record

ArticleACS applied materials & interfaces2019

Zoledronic Acid-containing Nanoparticles With Minimum Premature Release Show Enhanced Activity Against Extraskeletal Tumor.

Xu Li, Solange A Valdes, Riyad F Alzhrani, Stephanie Hufnagel, Stephen D Hursting, Zhengrong Cui

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.5field-weighted citation impact, top 9% 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, 41 citations in OpenAlex.

  1. Article
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  11. PLGA-based drug delivery systems in treating bone tumors.Frontiers in bioengineering and biotechnology · 2023
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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 3 institutions in 2 countries.

Xu LiCollege of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery , The University of Texas at Austin , Austin , Texas 78723 , United States.ORCID http://orcid.org/0000-0002-6168-2442
Solange A ValdesCollege of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery , The University of Texas at Austin , Austin , Texas 78723 , United States.
Riyad F AlzhraniCollege of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery , The University of Texas at Austin , Austin , Texas 78723 , United States.
Stephanie HufnagelCollege of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery , The University of Texas at Austin , Austin , Texas 78723 , United States.
Stephen D HurstingDepartment of Nutrition , University of North Carolina at Chapel Hill , Chapel Hill , North Carolina 27599 , United States.
Zhengrong CuiCollege of Pharmacy, Division of Molecular Pharmaceutics and Drug Delivery , The University of Texas at Austin , Austin , Texas 78723 , United States.ORCID http://orcid.org/0000-0002-1789-910X
The University of Texas at Austin · USNorthwest University · CNUniversity of North Carolina at Chapel Hill · US

Funding

Higher Dietary Carbohydrates Detrimentally Impact Obesity-Associated Breast Cancer ChemoresistanceR35CA197627 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HURSTING, STEPHEN D · 2015 to 2021
$6.0M
Overcoming pancreatic tumor resistance to gemcitabineR01CA135274 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI CUI, ZHENGRONG · 2008 to 2017
$2.8M
A Creative Integration of Omega-3 Fatty Acids into Pancreatic Cancer ChemotherapyR21CA179362 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI CUI, ZHENGRONG · 2015 to 2016
$371k
NCI NIH HHS R01 CA135274NCI NIH HHS R21 CA179362NCI NIH HHS R35 CA197627
6 · The paper itself

Abstract

Bisphosphonates are generally used to treat bone diseases, such as bone metastasis from cancer. There is evidence that, through the modification of the pharmacokinetics and biodistribution of bisphosphonates by formulating them into nanoparticles, they may be able to treat extraskeletal tumors. However, many previously reported bisphosphonate nanoparticle formulations show extensive premature release of bisphosphonates. Herein, using zoledronate (Zol), a third-generation bisphosphonate, we developed a new Zol nanoparticle formulation (denoted as Zol-NPs) by encapsulating anionic lipid-coated Zol-calcium nanocomplexes into poly(lactic- co-glycolic) acid nanoparticles emulsified with octadecanoic acid-hydrazone-polyethylene glycol (2000), an acid-sensitive cleavable emulsifying agent. The resultant Zol-NPs, about 180 nm in hydrodynamic diameter, show very limited premature release of Zol (i.e., <5% in 48 h in a simulated physiological condition) and enhanced cytotoxicity to both murine cancer cells and macrophages. In a mouse model with orthotopically transplanted mammary tumors, Zol-NPs significantly reduced the distribution of Zol in bones, but increased its distribution in tumors. Importantly, Zol-NPs also significantly inhibited tumor growth, whereas the equivalent dose of free Zol did not. This platform technology may be exploited to treat extraskeletal tumors with bisphosphonates.

Indexed as

Antineoplastic AgentsMammary Neoplasms, ExperimentalNanoparticlesZoledronic AcidAnimalsCell Line, TumorDelayed-Action PreparationsFemaleMiceMice, TransgenicTissue DistributionAntineoplastic AgentsDelayed-Action PreparationsZoledronic Acidbiodistributionbisphosphonate-metal complexextraskeletal tumorPEG-sheddingPLGA nanoparticlereverse microemulsiontreatmentzoledronic acid

Identifiers

PMID30689348
PMCPMC6582365
OpenAlexW2911255253

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.