Evidence map›Paper›PMID 25422796›Full record

ArticleDrug delivery and translational research2014

Co-delivery of natural metabolic inhibitors in a self-microemulsifying drug delivery system for improved oral bioavailability of curcumin.

Alex E Grill, Brenda Koniar, Jayanth Panyam

Abstract read
In one paragraph

Article in Drug delivery and translational research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Green Cancer Prevention and Beyond.Cancer prevention research (Philadelphia, Pa.) · 2024
    Review
  7. Review
  8. Article
  9. Oral Preparation of Hyaluronic Acid, Chondroitin Sulfate, Curcumin, and Quercetin (IalurilPathophysiology : the official journal of the International Society for Pathophysiology · 2022
    Article
  10. Article
  11. Article
  12. Enhancing Curcumin Oral Bioavailability Through Nanoformulations.European journal of drug metabolism and pharmacokinetics · 2019
    Review
  13. Chemopreventive efficacy of oral curcumin: a prodrug hypothesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Enhancement of Curcumin Bioavailability Via the Prodrug Approach: Challenges and Prospects.European journal of drug metabolism and pharmacokinetics · 2017
    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

3 authors.

Alex E GrillDepartment of Pharmaceutics, College of Pharmacy, University of Minnesota, Minneapolis, MN 55455 ; Masonic Cancer Research Center, University of Minnesota, Minneapolis, MN 55455.
Brenda KoniarResearch Animal Resources, University of Minnesota, Minneapolis, MN 55455.
Jayanth PanyamDepartment of Pharmaceutics, College of Pharmacy, University of Minnesota, Minneapolis, MN 55455 ; Masonic Cancer Research Center, University of Minnesota, Minneapolis, MN 55455.

Funding

Sustained Release Curcumin Microspheres for Breast Cancer ChemopreventionR03CA141996 · NCI · UNIVERSITY OF MINNESOTA · PI PANYAM, JAYANTH · 2009 to 2010
$151k
NCI NIH HHS R03 CA141996
6 · The paper itself

Abstract

In spite of its well-documented anticancer chemopreventive and therapeutic activity, the clinical development of curcumin has been limited by its poor oral bioavailability. Curcumin has low aqueous solubility and undergoes extensive first pass metabolism following oral dosing. We hypothesized that oral bioavailability of curcumin can be enhanced by increasing its absorption and decreasing its metabolic clearance simultaneously. To test this hypothesis, we formulated curcumin with naturally occurring UGT inhibitors (piperine, quercetin, tangeretin, and silibinin) in a self-microemulsifying drug delivery system (SMEDDS). Mouse liver microsome studies showed that silibinin and quercetin inhibited curcumin glucuronidation effectively. When dosed orally in mice, the SMEDDS containing curcumin alone increased curcumin glucuronide concentrations in plasma without significantly affecting parent drug concentration. Of the four inhibitors examined in vivo, silibinin significantly improved the Cmax (0.15 μM vs. 0.03 μM for curcumin SMEDDS) and the overall bioavailability (3.5-fold vs. curcumin SMEDDS) of curcumin. Previous studies have shown that silibinin has anticancer activity as well. Thus, co-delivery of silibinin with curcumin in SMEDDS represents a novel and promising approach to improve curcumin bioavailability.

Indexed as

absorptioncancer chemopreventionMetabolismmicroemulsionoral drug delivery

Identifiers

PMID25422796
PMCPMC4240011

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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.