Evidence map›Paper›PMID 31426507›Full record

ArticleMolecules (Basel, Switzerland)2019

Crude Heparin Preparations Unveil the Presence of Structurally Diverse Oversulfated Contaminants.

Aline Mendes, Maria C Z Meneghetti, Marcelly Valle Palladino, Giselle Zenker Justo, Guilherme L Sassaki, Jawed Fareed, Marcelo A Lima, Helena B Nader

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 3 countries.

Aline MendesDepartamento de Bioquímica, Instituto de Farmacologia e Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - São Paulo, SP 04044-020, Brazil.
Maria C Z MeneghettiDepartamento de Bioquímica, Instituto de Farmacologia e Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - São Paulo, SP 04044-020, Brazil.
Marcelly Valle PalladinoDepartamento de Bioquímica, Instituto de Farmacologia e Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - São Paulo, SP 04044-020, Brazil.
Giselle Zenker JustoDepartamento de Bioquímica, Instituto de Farmacologia e Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - São Paulo, SP 04044-020, Brazil.
Guilherme L SassakiDepartamento de Bioquímica, Setor de Ciências Biológicas, Centro Politécnico, Universidade Federal do Paraná, Avenida Coronel Francisco H. dos Santos, 100, Caixa Postal 19031, Curitiba, PR 81531-980, Brazil.
Jawed FareedDepartment of Molecular Pharmacology & Therapeutics, Hemostasis & Thrombosis Research Laboratories, Loyola University Medical Center, 2160 S. First Avenue Maywood, IL 60153, USA.
Marcelo A LimaDepartamento de Bioquímica, Instituto de Farmacologia e Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - São Paulo, SP 04044-020, Brazil.
Helena B NaderDepartamento de Bioquímica, Instituto de Farmacologia e Biologia Molecular, Escola Paulista de Medicina, Universidade Federal de São Paulo, Rua Três de Maio, 100 - São Paulo, SP 04044-020, Brazil. hbnader@unifesp.br.ORCID 0000-0002-7569-2166
Universidade Federal de São Paulo · BRKeele University · GBLoyola University Medical Center · USUniversidade Federal do Paraná · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303362/2016-2; 140985/2015-8; 442357/2014-1Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 0599/2018Financiadora de Estudos e Projetos 01/2013 - 736/13Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/03964-6; 2017/14179-3
6 · The paper itself

Abstract

Nowadays, pharmaceutical heparin is purified from porcine and bovine intestinal mucosa. In the past decade there has been an ongoing concern about the safety of heparin, since in 2008, adverse effects associated with the presence of an oversulfated chondroitin sulfate (OSCS) were observed in preparations of pharmaceutical porcine heparin, which led to the death of patients, causing a global public health crisis. However, it has not been clarified whether OSCS has been added to the purified heparin preparation, or whether it has already been introduced during the production of the raw heparin. Using a combination of different analytical methods, we investigate both crude and final heparin products and we are able to demonstrate that the sulfated contaminants are intentionally introduced in the initial steps of heparin preparation. Furthermore, the results show that the oversulfated compounds are not structurally homogeneous. In addition, we show that these contaminants are able to bind to cells in using well known heparin binding sites. Together, the data highlights the importance of heparin quality control even at the initial stages of its production.

Indexed as

Drug ContaminationAnimalsAnticoagulantsCattleChondroitin SulfatesHeparinHeparin LyaseHumansHydrolysisIntestinal MucosaMagnetic Resonance SpectroscopyPolysaccharide-LyasesQuality ControlSwineAnticoagulantsChondroitin SulfatesHeparinHeparin Lyaseheparitinsulfate lyasePolysaccharide-Lyases1H NMR and COSYFACEheparin and oversulfated chondroitin sulfate anticoagulant activitiesheparinasesoversulfated chondroitin sulfate

Identifiers

PMID31426507
PMCPMC6721129
OpenAlexW2967716334

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.