Evidence map›Paper›PMID 28713372›Full record

ArticleFrontiers in immunology2017

Nanoparticle-Formulated Curcumin Prevents Posttherapeutic Disease Reactivation and Reinfection with

Sultan Tousif, Dhiraj Kumar Singh, Sitabja Mukherjee, Shaheer Ahmad, Rakesh Arya, Ranjan Nanda, Anand Ranganathan, Maitree Bhattacharyya, Luc Van Kaer, Santosh K Kar and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2017. 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. Article
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  6. Article
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  9. Article
  10. Article
  11. Article
  12. Review
  13. Tuberculosis: The success tale of less explored dormantFrontiers in cellular and infection microbiology · 2022
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Effects of Curcumin and Its Analogues on Infectious Diseases.Advances in experimental medicine and biology · 2021
    Review
  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

11 authors.

Sultan TousifSpecial Centre for Molecular Medicine (SCMM), Jawaharlal Nehru University, New Delhi, India.
Dhiraj Kumar SinghSpecial Centre for Molecular Medicine (SCMM), Jawaharlal Nehru University, New Delhi, India.
Sitabja MukherjeeSchool of Biotechnology, KIIT University, Bhubaneswar, Odisha, India.
Shaheer AhmadSpecial Centre for Molecular Medicine (SCMM), Jawaharlal Nehru University, New Delhi, India.
Rakesh AryaInternational Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Ranjan NandaInternational Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Anand RanganathanSpecial Centre for Molecular Medicine (SCMM), Jawaharlal Nehru University, New Delhi, India.
Maitree BhattacharyyaDepartment of Biochemistry, University of Calcutta, Kolkata, India.
Luc Van KaerDepartment of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN, United States.
Santosh K KarSchool of Biotechnology, KIIT University, Bhubaneswar, Odisha, India.
Gobardhan DasSpecial Centre for Molecular Medicine (SCMM), Jawaharlal Nehru University, New Delhi, India.

Funding

LSM880-Airyscan Confocal Microscope for Large Shared ResourceS10OD021630 · OD · VANDERBILT UNIVERSITY · PI WELLS, K. SAM · 2016 to 2016
$560k
NIH HHS S10 OD021630
6 · The paper itself

Abstract

Curcumin, the bioactive component of turmeric also known as "Indian Yellow Gold," exhibits therapeutic efficacy against several chronic inflammatory and infectious diseases. Even though considered as a wonder drug pertaining to a myriad of reported benefits, the translational potential of curcumin is limited by its low systemic bioavailability due to its poor intestinal absorption, rapid metabolism, and rapid systemic elimination. Therefore, the translational potential of this compound is specifically challenged by bioavailability issues, and several laboratories are making efforts to improve its bioavailability. We developed a simple one-step process to generate curcumin nanoparticles of ~200 nm in size, which yielded a fivefold enhanced bioavailability in mice over regular curcumin. Curcumin nanoparticles drastically reduced hepatotoxicity induced by antitubercular antibiotics during treatment in mice. Most interestingly, co-treatment of nanoparticle-formulated curcumin along with antitubercular antibiotics dramatically reduced the risk for disease reactivation and reinfection, which is the major shortfall of current antibiotic treatment adopted by Directly Observed Treatment Short-course. Furthermore, nanoparticle-formulated curcumin significantly reduced the time needed for antibiotic therapy to obtain sterile immunity, thereby reducing the possibility of generating drug-resistant variants of the organisms. Therefore, adjunct therapy of nano-formulated curcumin with enhanced bioavailability may be beneficial to treatment of tuberculosis and possibly other diseases.

Indexed as

AICDdisease relapsehelper T cellshepatotoxicityimmunotherapytuberculosis

Identifiers

PMID28713372
PMCPMC5491555

What OpenQuestion holds

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LicenceCC BY
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.