Evidence map›Paper›PMID 24355163›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2014

Theranostic tumor homing nanocarriers for the treatment of lung cancer.

Apurva R Patel, Mahavir B Chougule, Ed Lim, Kevin P Francis, Stephen Safe, Mandip Singh

Abstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Role of Exosomes for Delivery of Chemotherapeutic Drugs.Critical reviews in therapeutic drug carrier systems · 2021
    Review
  6. Article
  7. Article
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 1 country.

Apurva R PatelCollege of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL, USA.
Mahavir B ChouguleDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Hawai'i at Hilo, Hilo, HI, USA.
Ed LimCalipers-Life Sciences & Technology, A Perkin Elmer Company, Alameda, CA, USA.
Kevin P FrancisCalipers-Life Sciences & Technology, A Perkin Elmer Company, Alameda, CA, USA.
Stephen SafeInstitute of Biosciences and Technology, Texas A&M University, Houston, TX, USA.
Mandip SinghCollege of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, FL, USA. Electronic address: mandip.sachdeva@famu.edu.
Florida Agricultural and Mechanical University · USTexas A&M University · USUniversity of Hawaii at Hilo · US

Funding

Targeted Nanocarriers for Treatment of Lung CancerSC1CA161676 · NCI · FLORIDA AGRICULTURAL AND MECHANICAL UNIV · PI SACHDEVA, MANDIP SINGH · 2011 to 2014
$1.1M
NCI NIH HHS SC1 CA161676NIGMS NIH HHS SC1 GM092779-01
6 · The paper itself

Abstract

The drugs/strategies to selectively inhibit tumor blood supply have generated interest in recent years for enhancement of cancer therapeutics. The objective of this study was to formulate tumor homing PEGylated CREKA peptide conjugated theranostic nanoparticles of DIM-C-pPhC6H5 (DIM-P) and investigate in vivo antitumor activity as well as evaluate the targeted efficiency to lung tumors using imaging techniques. DIM-P loaded Nanoparticles (NCs-D) were prepared using lipids, and DOGS-NTA-Ni and the surface of NCs-D were modified with PEGylated CREKA peptide (PCNCs-D). PCNCs-D showed 3 fold higher binding to clotted plasma proteins in tumor vasculature compared to NCs-D. PCNCs-D showed 26%±4% and 22%±5% increase in tumor reduction compared to NCs-D in metastatic and orthotopic models respectively. In-vivo imaging studies showed ~40 folds higher migration of PCNCs-Di in tumor vasculature than NCs-Di. Our studies demonstrate the role of PCNCs-D as theranostic tumor homing drug delivery and imaging systems for lung cancer diagnosis and treatment. FROM THE CLINICAL EDITOR: This study demonstrates a very efficient delivery system to address lung cancer growth through blood supply inhibition.

Indexed as

AnimalsAntineoplastic AgentsDrug Delivery SystemsFemaleHumansLung NeoplasmsMiceMice, NudeNanoparticlesOligopeptidesXenograft Model Antitumor AssaysAntineoplastic Agentscysteinyl-arginyl-glutamyl-lysyl-alanylOligopeptidesCancer treatmentIn-vivo imagingNanoparticlesTargeted deliveryTheranosticTumor homing

Identifiers

PMID24355163
PMCPMC4061286
OpenAlexW2042639165

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.