Evidence map›Paper›PMID 24627632›Full record

ArticleInternational journal of nanomedicine2014

Chemotherapeutic potential of curcumin-bearing microcells against hepatocellular carcinoma in model animals.

Mohammad Farazuddin, Bhavyata Dua, Qamar Zia, Aijaz Ahmad Khan, Beenu Joshi, Mohammad Owais

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Immunotherapy for Bone and Soft Tissue Sarcomas.BioMed research international · 2015
    Review
  9. Article
  10. Article
  11. 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

6 authors at 1 institution in 1 country.

Mohammad FarazuddinInterdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, India.
Bhavyata DuaImmunology Division, National JALMA Institute for Leprosy and Other Mycobacterial Diseases (NJIL), Agra, India.
Qamar ZiaInterdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, India.
Aijaz Ahmad KhanDepartment of Anatomy, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, India.
Beenu JoshiImmunology Division, National JALMA Institute for Leprosy and Other Mycobacterial Diseases (NJIL), Agra, India.
Mohammad OwaisInterdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, India.
Aligarh Muslim University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Curcumin (diferuloylmethane) is found in large quantities in the roots of Curcuma longa. It possesses strong antioxidant and anti-inflammatory properties, and inhibits chemically-induced carcinogenesis in the skin, forestomach, colon, and liver. Unfortunately, the poor bioavailability and hydrophobicity of curcumin pose a major hurdle to its use as a potent anticancer agent. To circumvent some of these problems, we developed a novel, dual-core microcell formulation of curcumin. The encapsulation of curcumin in microcells increases its solubility and bioavailability, and facilitates slow release kinetics over extended periods. Besides being safe, these formulations do not bear any toxicity constraints, as revealed by in vitro and in vivo studies. Histopathological analysis revealed that curcumin-bearing microcells helped in regression of hepatocellular carcinoma and the maintenance of cellular architecture in liver tissue. Free curcumin had a very mild effect on cancer suppression. Empty (sham) microcells and microparticles failed to inhibit cancer cells. The novel curcumin formulation was found to suppress hepatocellular carcinoma efficiently in Swiss albino mice.

Indexed as

Drug Delivery SystemsPhytotherapyAnimalsAntineoplastic Agents, PhytogenicBiological AvailabilityCell SurvivalCurcuminDrug CompoundingFemaleHepatocytesHep G2 CellsHumansLactic AcidLiver Neoplasms, ExperimentalMiceNanomedicineAntineoplastic Agents, PhytogenicCurcuminLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerTumor Necrosis Factor-alphacancercarcinogenesisCurcuma longadiferuloylmethanemicroparticlenanocells

Identifiers

PMID24627632
PMCPMC3945993
OpenAlexW2019629634

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.