Evidence map›Paper›PMID 25072100›Full record

ArticleMolecular pharmaceutics2014

Targeted nanogel conjugate for improved stability and cellular permeability of curcumin: synthesis, pharmacokinetics, and tumor growth inhibition.

Xin Wei, Thulani H Senanayake, Anna Bohling, Serguei V Vinogradov

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Recent advances in drug delivery and targeting for the treatment of pancreatic cancer.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
  7. Review
  8. Review
  9. Review
  10. 3-Polymers · 2022
    Article
  11. Review
  12. Drug delivery carriers with therapeutic functions.Advanced drug delivery reviews · 2021
    Review
  13. Recent Advances and Disputes About Curcumin in Retinal Diseases.Clinical ophthalmology (Auckland, N.Z.) · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Xin WeiDepartment of Pharmaceutical Sciences and Center for Drug Delivery and Nanomedicine, College of Pharmacy, University of Nebraska Medical Center , Omaha, Nebraska 68198, United States.
Thulani H Senanayake
Anna Bohling
Serguei V Vinogradov
University of Nebraska Medical Center · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Overcoming Drug Resistance to Nucleoside Analogs by Tumor-Targeted Active NanoforR01CA136921 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI VINOGRADOV, SERGUEI V · 2009 to 2013
$1.1M
NCI NIH HHS P30 CA036727NCI NIH HHS R01 CA136921NCI NIH HHS R01CA136921
6 · The paper itself

Abstract

Curcumin (CUR) is a unique natural compound with promising anticancer and anti-inflammatory activities. However, the therapeutic efficacy of curcumin was challenged in clinical trials, mostly due to its low bioavailability, rapid metabolism, and elimination. We designed a nanodrug form of curcumin, which makes it stable and substantially enhances cellular permeability and anticancer activity at standard oral administration. Curcumin was conjugated as an ester to cholesteryl-hyaluronic acid (CHA) nanogel that is capable of targeted delivery to CD44-expressing drug-resistant cancer cells. CHA-CUR nanogels demonstrated excellent solubility and sustained drug release in physiological conditions. It induced apoptosis in cancer cells, suppressing the expression of NF-κB, TNF-α, and COX-2 cellular targets similar to free curcumin. Pharmacokinetic/pharmacodynamic (PK/PD) studies also revealed improved circulation parameters of CHA-CUR at oral, i.p. and i.v. administration routes. CHA-CUR showed targeted tumor accumulation and effective tumor growth inhibition in human pancreatic adenocarcinoma MiaPaCa-2 and aggressive orthotropic murine mammary carcinoma 4T1 animal models. CHA-CUR treatment was well-tolerated and resulted in up to 13-fold tumor suppression, making this nanodrug a potential candidate for cancer prevention and therapeutic treatment.

Indexed as

AdenomaAdministration, OralAnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCurcuminCyclooxygenase 2Delayed-Action PreparationsDrug Delivery SystemsDrug Resistance, NeoplasmDrug Screening Assays, AntitumorEstersFemaleHumansAntineoplastic AgentsCurcuminCyclooxygenase 2Delayed-Action PreparationsEstersHyaluronan ReceptorsHyaluronic AcidNanogelsNF-kappa Bpolyethylene glycol polyethyleneimine nanogelPolyethylene GlycolsPolyethyleneiminePTGS2 protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID25072100
PMCPMC4151794
OpenAlexW1974854083

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.