Evidence map›Paper›PMID 25725361›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2015

Poly(2-oxazoline) based micelles with high capacity for 3rd generation taxoids: preparation, in vitro and in vivo evaluation.

Zhijian He, Anita Schulz, Xiaomeng Wan, Joshua Seitz, Herdis Bludau, Daria Y Alakhova, David B Darr, Charles M Perou, Rainer Jordan, Iwao Ojima and 2 more

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.2field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 98 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Biological ActivityBiomacromolecules · 2023
    Article
  5. Article
  6. Review
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  8. Article
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  10. The Challenging Pharmacokinetics of Mitotane: An Old Drug in Need of New Packaging.European journal of drug metabolism and pharmacokinetics · 2021
    Review
  11. Article
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  17. Review
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  19. Article
  20. Novel poly(2-oxazoline) block copolymer with aromatic heterocyclic side chains as a drug delivery platform.Journal of controlled release : official journal of the Controlled Release Society · 2019
    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

12 authors at 4 institutions in 3 countries.

Zhijian He *Center for Nanotechnology in Drug Delivery and Division of Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill , NC 27599, USA.
Anita Schulz *Professur für Makromolekulare Chemie, Department Chemie, Technische Universität Dresden, Mommsenstr. 4, 01069 Dresden, Germany.
Xiaomeng WanCenter for Nanotechnology in Drug Delivery and Division of Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill , NC 27599, USA.
Joshua SeitzDepartment of Chemistry, Institute of Chemical Biology and Drug Discovery, State University of New York at Stony Brook, Stony Brook, NY 11794-3400, USA.
Herdis BludauProfessur für Makromolekulare Chemie, Department Chemie, Technische Universität Dresden, Mommsenstr. 4, 01069 Dresden, Germany.
Daria Y AlakhovaCenter for Nanotechnology in Drug Delivery and Division of Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill , NC 27599, USA.
David B DarrLineberger Comprehensive Cancer Center, The Animal Study Core, University of North Carolina at Chapel Hill, NC 27599, USA.
Charles M PerouLineberger Comprehensive Cancer Center, The Animal Study Core, University of North Carolina at Chapel Hill, NC 27599, USA.
Rainer JordanProfessur für Makromolekulare Chemie, Department Chemie, Technische Universität Dresden, Mommsenstr. 4, 01069 Dresden, Germany.
Iwao OjimaDepartment of Chemistry, Institute of Chemical Biology and Drug Discovery, State University of New York at Stony Brook, Stony Brook, NY 11794-3400, USA.
Alexander V KabanovCenter for Nanotechnology in Drug Delivery and Division of Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill , NC 27599, USA.
Robert LuxenhoferFunctional Polymer Materials, Chair for Chemical Technology of Materials Synthesis, Universität Würzburg, 97070 Würzburg, Germany.
University of North Carolina at Chapel Hill · USTechnische Universität Dresden · DEState University of New York · USUniversity of Würzburg · DE

Funding

Tumor -Targeting Chemotherapeutic AgentsR01CA103314 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI OJIMA, IWAO · 2003 to 2013
$3.1M
High Capacity Nanocarriers for Cancer ChemotherapeuticsU01CA151806 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KABANOV, ALEXANDER V · 2010 to 2014
$2.0M
Polymer Based Gene DeliveryR01CA116591 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KABANOV, ALEXANDER V · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA 103314NCI NIH HHS R01 CA103314NCI NIH HHS R01 CA116591NCI NIH HHS U01 CA116591NCI NIH HHS U01 CA151806
6 · The paper itself

Abstract

The clinically and commercially successful taxanes, paclitaxel and docetaxel suffer from two major drawbacks, namely their very low aqueous solubility and the risk of developing resistance. Here, we present a method that overcomes both drawbacks in a very simple manner. We formulated 3rd generation taxoids, able to avoid common drug resistance mechanisms with doubly amphiphilic poly(2-oxazoline)s (POx), a safe and highly efficient polymer for the formulation of extremely hydrophobic drugs. We found excellent solubilization of different 3rd generation taxoids irrespective of the drug's chemical structures with essentially quantitative drug loading and final drug to polymer ratios around unity. The small, highly loaded micelles with a hydrodynamic diameter of less than 100nm are excellently suited for parenteral administration. Moreover, a selected formulation with the taxoid SB-T-1214 is about one to two orders of magnitude more active in vitro than paclitaxel in the multidrug resistant breast cancer cell line LCC6-MDR. In contrast, in wild-type LCC6, no difference was observed. Using a q4d×4 dosing regimen, we also found that POx/SB-T-1214 significantly inhibits the growth of LCC6-MDR orthotropic tumors, outperforming commercial paclitaxel drug Taxol and Cremophor EL formulated SB-T-1214.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicBreast NeoplasmsCell Line, TumorCell SurvivalChemistry, PharmaceuticalDelayed-Action PreparationsFemaleHumansMiceMicellesMice, NudeOxazolesParticle SizeTaxoidsXenograft Model Antitumor AssaysAntineoplastic Agents, PhytogenicDelayed-Action PreparationsMicellesOxazolespoly(2-oxazoline)TaxoidsDrug deliveryIn vitroIn vivoLCC6Multi-drug resistanceNanomedicineOrthotopic tumor modelPaclitaxelPoly(2-oxazoline)Taxoids

Identifiers

PMID25725361
PMCPMC4479148
OpenAlexW1997789582

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.