Evidence map›Paper›PMID 25102172›Full record

ArticlePLoS neglected tropical diseases2014

Viper and cobra venom neutralization by alginate coated multicomponent polyvalent antivenom administered by the oral route.

Sourav Bhattacharya, Mousumi Chakraborty, Piyasi Mukhopadhyay, P P Kundu, Roshnara Mishra

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

5 authors at 1 institution in 1 country.

Sourav BhattacharyaDepartment of Physiology, University of Calcutta, Kolkata, India; Centre for Research in Nanoscience and Nanotechnology, University of Calcutta, Kolkata, India.
Mousumi ChakrabortyDepartment of Physiology, University of Calcutta, Kolkata, India.
Piyasi MukhopadhyayDepartment of Polymer Science and Technology, University of Calcutta, Kolkata, India.
P P KunduDepartment of Polymer Science and Technology, University of Calcutta, Kolkata, India.
Roshnara MishraDepartment of Physiology, University of Calcutta, Kolkata, India; Centre for Research in Nanoscience and Nanotechnology, University of Calcutta, Kolkata, India.
University of Calcutta · IN

Funding

RAPID TRANSMISSION OF EEE VIRUS BY CULISETA MELANURAR01AI022119 · NIAID · UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS · PI SCOTT, THOMAS WALLACE · 1986 to 2003
$1.2M
NIAID NIH HHS R01 AI022119
6 · The paper itself

Abstract

backgroundSnake bite causes greater mortality than most of the other neglected tropical diseases. Snake antivenom, although effective in minimizing mortality in developed countries, is not equally so in developing countries due to its poor availability in remote snake infested areas as, and when, required. An alternative approach in this direction could be taken by making orally deliverable polyvalent antivenom formulation, preferably under a globally integrated strategy, for using it as a first aid during transit time from remote trauma sites to hospitals. METHODOLOGY/PRINCIPAL

findingsTo address this problem, multiple components of polyvalent antivenom were entrapped in alginate. Structural analysis, scanning electron microscopy, entrapment efficiency, loading capacity, swelling study, in vitro pH sensitive release, acid digestion, mucoadhesive property and venom neutralization were studied in in vitro and in vivo models. Results showed that alginate retained its mucoadhesive, acid protective and pH sensitive swelling property after entrapping antivenom. After pH dependent release from alginate beads, antivenom (ASVS) significantly neutralized phospholipaseA2 activity, hemolysis, lactate dehydrogenase activity and lethality of venom. In ex vivo mice intestinal preparation, ASVS was absorbed significantly through the intestine and it inhibited venom lethality which indicated that all the components of antivenom required for neutralization of venom lethality were retained despite absorption across the intestinal layer. Results from in vivo studies indicated that orally delivered ASVS can significantly neutralize venom effects, depicted by protection against lethality, decreased hemotoxicity and renal toxicity caused by russell viper venom. CONCLUSIONS/SIGNIFICANCE: Alginate was effective in entrapping all the structural components of ASVS, which on release and intestinal absorption effectively reconstituted the function of antivenom in neutralizing viper and cobra venom. Further research in this direction can strategize to counter such dilemma in snake bite management by promoting control release and oral antivenom rendered as a first aid.

Indexed as

Administration, OralAlginatesAnimalsAntiveninsElapid VenomsGlucuronic AcidHemolysisHexuronic AcidsHydrogen-Ion ConcentrationIntestinal AbsorptionMaleMiceMicroscopy, Electrochemical, ScanningMucinsViper VenomsAlginatesAntiveninsElapid VenomsGlucuronic AcidHexuronic AcidsMucinsViper Venoms

Identifiers

PMID25102172
PMCPMC4125299
OpenAlexW2001588096

What OpenQuestion holds

Textmetadata
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.