Evidence map›Paper›PMID 20536174›Full record

ArticleBioconjugate chemistry2010

Well-defined, size-tunable, multifunctional micelles for efficient paclitaxel delivery for cancer treatment.

Juntao Luo, Kai Xiao, Yuanpei Li, Joyce S Lee, Lifang Shi, Yih-Horng Tan, Li Xing, R Holland Cheng, Gang-Yu Liu, Kit S Lam

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
–field-weighted citation impact
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

75 citing papers in PubMed.

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  17. Article
  18. Sub-100nm, long tumor retention SN-38-loaded photonic micelles for tri-modal cancer therapy.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  19. Cell-free production of a functional oligomeric form of aThe Journal of biological chemistry · 2017
    Article
  20. Article

15 more citing papers are in PubMed but not listed here.

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

10 authors.

Juntao LuoDivision of Hematology and Oncology, University of California, Davis Cancer Center, Sacramento, California 95817, USA.
Kai Xiao
Yuanpei Li
Joyce S Lee
Lifang Shi
Yih-Horng Tan
Li Xing
R Holland Cheng
Gang-Yu Liu
Kit S Lam

Funding

Therapeutic Targeting Agents for Ovarian CancerR01CA115483 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI LAM, KIT S · 2005 to 2019
$5.5M
Targeting Agents for Human and Canine LymphomaU19CA113298 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI LAM, KIT S · 2005 to 2009
$5.4M
Using Nanotechnology to Regulate Integrin Clustering and Tensin LocalizationR21GM077850 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LIU, GANG-YU · 2006 to 2008
$556k
High affinity ligand to deliver nanoparticle drugs to lymphoid cancersR21CA128501 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LAM, KIT S · 2007 to 2009
$456k
NCI NIH HHS R01 CA115483NCI NIH HHS R01CA115483NCI NIH HHS R21 CA128501NCI NIH HHS R21CA128501NCI NIH HHS U19 CA113298NCI NIH HHS U19CA113298NIGMS NIH HHS R21 GM077850NIGMS NIH HHS R21GM77850-01
6 · The paper itself

Abstract

We have developed a well-defined and biocompatible amphiphilic telodendrimer system (PEG-b-dendritic oligo-cholic acid) which can self-assemble into multifunctional micelles in aqueous solution for efficient delivery of hydrophobic drugs such as paclitaxel. In this telodendrimer system, cholic acid is essential for the formation of stable micelles with high drug loading capacity, owing to its facial amphiphilicity. A series of telodendrimers with variable length of PEG chain and number of cholic acid in the dendritic blocks were synthesized. The structure and molecular weight of each of these telodendrimers were characterized, and their critical micellization concentration (CMC), drug-loading properties, particle sizes, and cytotoxicity were examined and evaluated for further optimization for anticancer drug delivery. The sizes of the micelles, with and without paclitaxel loading, could be tuned from 11.5 to 21 nm and from 15 to 141 nm, respectively. Optical imaging studies in xenograft models demonstrated preferential uptake of the smaller paclitaxel-loaded micelles (17-60 nm) by the tumor and the larger micelles (150 nm) by the liver and lung. The toxicity and antitumor efficacy profiles of these paclitaxel-loaded micelles in xenograft models were found to be superior to those of Taxol and Abraxane.

Indexed as

Drug Delivery SystemsAnimalsAntineoplastic Agents, PhytogenicCell ProliferationCholic AcidsDendrimersDose-Response Relationship, DrugFemaleHumansLigandsMiceMicellesMice, NudeMolecular StructureNeoplasmsParticle SizeAntineoplastic Agents, PhytogenicCholic AcidsDendrimersLigandsMicellesPolyethylene Glycols

Identifiers

PMID20536174
PMCPMC2912451

What OpenQuestion holds

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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.