Evidence map›Paper›PMID 23827653›Full record

ArticleInternational journal of pharmaceutics2013

Biodegradable multiblock poly(N-2-hydroxypropyl)methacrylamide gemcitabine and paclitaxel conjugates for ovarian cancer cell combination treatment.

Nate Larson, Jiyuan Yang, Abhijit Ray, Darwin L Cheney, Hamidreza Ghandehari, Jindřich Kopeček

Abstract readComparative Study
In one paragraph

Article in International journal of pharmaceutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Nanocarrier drug delivery systems for gynecological cancer therapeutics.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Polymer nanomedicines.Advanced drug delivery reviews · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Polymer conjugate of a microtubule destabilizer inhibits lung metastatic melanoma.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Article
  15. Design of smart HPMA copolymer-based nanomedicines.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  16. Article
  17. Article
  18. Review
  19. POLYMERIC BIOMATERIALS AND NANOMEDICINES.Journal of drug delivery science and technology · 2015
    Article
  20. Review
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.

Nate LarsonTheraTarget, Inc., Salt Lake City, UT 84108, USA.
Jiyuan Yang
Abhijit Ray
Darwin L Cheney
Hamidreza Ghandehari
Jindřich Kopeček

Funding

Backbone Degradable Polymer-drug Conjugates for the Treatment of Ovarian CancerR41CA156933 · NCI · THERATARGET · PI CHENEY, DARWIN LEROY, KOPECEK, JINDRICH H. · 2011 to 2011
$148k
NCI NIH HHS R41 CA156933
6 · The paper itself

Abstract

The synthesis, characterization, and in vitro evaluation of a combination delivery of multiblock poly(N-2-hydroxypropyl)methacrylamide (HPMA), gemcitabine (GEM) and paclitaxel (PTX) conjugates is described in this study. Multiblock copolymer conjugates of a large molecular weight (Mw>200 kDa) were studied and compared to traditional, small molecular weight (Mw<45 kDa) conjugates. Stability of the conjugates in different pH was assessed, and their cytotoxicity in combination toward A2780 human ovarian cancer cells was evaluated by combination index analysis. Treatment duration (4 and 72 h) and sequence of addition were explored. In addition, an HPMA copolymer conjugate with both GEM and PTX in the side chains was evaluated in a similar manner and compared to a physical mixture of individual conjugates. Conjugates with narrow molecular weight distribution (Mw/Mn<1.1) were obtained via RAFT polymerization, and drug loadings of between 5.5 and 9.2 wt% were achieved. Conjugates demonstrated moderate stability with less than 65% release over 24h at pH 7.4, and near complete drug release in the presence of the lysosomal enzyme cathepsin B in 3h. In combination, the cytotoxic effects of a mixture of the conjugates were primarily additive. Synergistic effects were observed when A2780 human ovarian cancer cells were treated simultaneously for 4h with multiblock conjugates (CI<0.7). When both GEM and PTX were conjugated to the same copolymer backbone, moderate antagonism (CI 1.3-1.6) was observed. These results demonstrate that multiblock HPMA copolymer-GEM and -PTX conjugates, when delivered as a mixture of individual agents, are promising for the treatment of ovarian cancer.

Indexed as

Drug CarriersAntineoplastic Combined Chemotherapy ProtocolsCathepsin BCell Line, TumorCell SurvivalChemistry, PharmaceuticalDeoxycytidineDrug StabilityDrug SynergismFemaleGemcitabineHumansHydrogen-Ion ConcentrationHydrolysisKineticsMaleCathepsin BDeoxycytidineDrug CarriersDuxonGemcitabinePaclitaxelPolymethacrylic AcidsBiodegradable polymersCombination therapyGemcitabineHPMA copolymersOvarian cancerPaclitaxel

Identifiers

PMID23827653
PMCPMC3786603

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Registered trials

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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.