Evidence map›Paper›PMID 21807409›Full record

ArticleBiomaterials2011

Accelerated healing of cutaneous leishmaniasis in non-healing BALB/c mice using water soluble amphotericin B-polymethacrylic acid.

Karina Corware, Debra Harris, Ian Teo, Matthew Rogers, Kikkeri Naresh, Ingrid Müller, Sunil Shaunak

Open access · bronzeAbstract read
In one paragraph

Article in Biomaterials, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Frontiers in chemistry · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Recent insights on nanomedicine for augmented infection control.International journal of nanomedicine · 2019
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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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

7 authors at 2 institutions in 1 country.

Karina CorwareDepartment of Medicine, Infectious Diseases & Immunity, Hammersmith Hospital, Faculty of Medicine, Imperial College London, London W12 0NN, UK.
Debra Harris
Ian Teo
Matthew Rogers
Kikkeri Naresh
Ingrid Müller
Sunil Shaunak
Imperial College London · GBHammersmith Hospital · GB

Funding

Dendrimer aminosaccharide drug to modulate inflammatory responses in shigellosisU01AI075351 · NIAID · IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE · PI SHAUNAK, SUNIL · 2007 to 2008
$663k
Biotechnology and Biological Sciences Research Council BB/H022406/1NIAID NIH HHS U01 AI075351PHS HHS 1U01A1075726Wellcome TrustWellcome Trust 078223MA
6 · The paper itself

Abstract

Cutaneous leishmaniasis (CL) is a neglected tropical disease that causes prominent skin scaring. No water soluble, non-toxic, short course and low cost treatment exists. We developed a new water soluble amphotericin B-polymethacrylic acid (AmB-PMA) using established and scalable chemistries. AmB-PMA was stable for 9 months during storage. In vitro, it was effective against Leishmania spp. promastigotes and amastigote infected macrophages. It was also less toxic and more effective than deoxycholate-AmB, and similar to liposomal AmB. Its in vivo activity was determined in both early and established CL lesion models of Leishmania major infection in genetically susceptible non-healing BALB/c mice. Intradermal AmB-PMA at a total dose of 18 mg of AmB/kg body weight led to rapid parasite killing and lesion healing. No toxicity was seen. No parasite relapse occurred after 80 days follow-up. Histological studies confirmed rapid parasite clearance from macrophages followed by accelerated fibroblast mediated tissue repair, regeneration and cure of the infection. Quantitative mRNA studies of the CL lesions showed that accelerated healing was associated with increased Tumour Necrosis Factor-α and Interferon-γ, and reduced Interleukin-10. These results suggest that a cost-effective AmB-PMA could be used to pharmacologically treat and immuno-therapeutically accelerate the healing of CL lesions.

Indexed as

Wound HealingAmphotericin BAnimalsCell LineChemokinesDisease Models, AnimalErythrocytesHumansHypersensitivity, DelayedImmunomodulationLeishmania majorLeishmaniasis, CutaneousMacrophagesMiceMice, Inbred BALB CParasite LoadAmphotericin BChemokinespolymethacrylic acidPolymethacrylic AcidsRNA, MessengerWater

Identifiers

PMID21807409
PMCPMC3168736
OpenAlexW2122684688

What OpenQuestion holds

Textmetadata
LicenceTDM
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.