Evidence map›Paper›PMID 25121577›Full record

ArticleBioconjugate chemistry2014

Reduction-sensitive dual functional nanomicelles for improved delivery of paclitaxel.

Xiaolan Zhang, Ke Liu, Yixian Huang, Jieni Xu, Jiang Li, Xiaochao Ma, Song Li

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. RSC advances · 2019
    Article
  4. Review
  5. Article
  6. Doxorubicin delivered by a redox-responsive dasatinib-containing polymeric prodrug carrier for combination therapy.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  7. Article
  8. Prodrug Strategies for Paclitaxel.International journal of molecular sciences · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

7 authors at 1 institution in 1 country.

Xiaolan ZhangCenter for Pharmacogenetics, ‡Department of Pharmaceutical Sciences, School of Pharmacy; §University of Pittsburgh Cancer Institute, University of Pittsburgh , Pittsburgh, Pennsylvania 15261, United States.
Ke Liu
Yixian Huang
Jieni Xu
Jiang Li
Xiaochao Ma
Song Li
UPMC Hillman Cancer Center · US

Funding

Targeted Combination Therapy for Breast CancerR01CA174305 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LI, SONG · 2014 to 2018
$1.6M
Rational Design of Lipidic Vectors for Mitochondria-Targeted AntioxidantsR01GM102989 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LI, SONG · 2013 to 2016
$1.1M
Nanomicellar Formulation for Synergistic Targeting of Prostate CancerR21CA173887 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LI, SONG · 2013 to 2014
$361k
NCI NIH HHS R01 CA174305NCI NIH HHS R01CA174305NCI NIH HHS R21 CA173887NCI NIH HHS R21CA173887NIGMS NIH HHS R01 GM102989NIGMS NIH HHS R01GM102989
6 · The paper itself

Abstract

We have developed a dual-functional nanocarrier composed of a hydrophilic polyethylene glycol (PEG) and a hydrophobic farnesylthiosalicylate (FTS, a nontoxic Ras antagonist), which is effective in delivery of hydrophobic anticancer drug, paclitaxel (PTX). To facilitate the retention of the therapeutic activity of the carrier, FTS was coupled to PEG via a reduction-sensitive disulfide linkage (PEG5k-S-S-FTS2). PEG5k-S-S-FTS2 conjugate formed uniform micelles with very small size (∼30 nm) and the hydrophobic drug PTX could be readily incorporated into the micelles. Interestingly, inclusion of a disulfide linkage into the PEG5k-FTS2 micellar system resulted in a 4-fold decrease in the critical micelle concentration (CMC). In addition, the PTX loading capacity and colloidal stability of PTX-loaded micelles were improved. HPLC-MS showed that parent FTS could be more effectively released from PEG5k-S-S-FTS2 conjugate in tumor cells/tissues compared to PEG5k-FTS2 conjugate in vitro and in vivo. PEG5k-S-S-FTS2 exhibited a higher level of cytotoxicity toward tumor cells than PEG5k-FTS2 without a disulfide linkage. Furthermore, PTX-loaded PEG5k-S-S-FTS2 micelles were more effective in inhibiting the proliferation of cultured tumor cells compared to Taxol and PTX loaded in PEG5k-FTS2 micelles. More importantly, PTX-loaded PEG5k-S-S-FTS2 micelles demonstrated superior antitumor activity compared to Taxol and PTX formulated in PEG5k-FTS2 micelles in an aggressive murine breast cancer model (4T1.2).

Indexed as

MicellesAnimalsAntineoplastic AgentsCell Line, TumorDrug CarriersFarnesolFemaleHumansHydrophobic and Hydrophilic InteractionsMammary Neoplasms, ExperimentalMiceNanostructuresOxidation-ReductionPaclitaxelPolyethylene GlycolsSalicylatesAntineoplastic AgentsDrug CarriersFarnesolfarnesylthiosalicylic acidMicellesPaclitaxelPolyethylene GlycolsSalicylates

Identifiers

PMID25121577
PMCPMC4166038
OpenAlexW2313877841

What OpenQuestion holds

Textmetadata
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.