Evidence map›Paper›PMID 32983445›Full record

ArticleAnnals of medicine and surgery (2012)2020

Collagen scaffold for mesencyhmal stem cell from stromal vascular fraction (biocompatibility and attachment study): Experimental paper.

Panji Sananta, I G M O Rahaditya, Mohamad I Imadudin, Marvin A Putera, Sri Andarini, Umi Kalsum, Edi Mustamsir, Respati S Dradjat

Abstract read
In one paragraph

Article in Annals of medicine and surgery (2012), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

8 authors.

Panji SanantaDoctoral Program of Medical Science, Faculty of Medicine, Universitas Brawijaya, Indonesia.
I G M O RahadityaOrthopaedic and Traumatology Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.
Mohamad I ImadudinOrthopaedic and Traumatology Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.
Marvin A PuteraOrthopaedic and Traumatology Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.
Sri AndariniPublic Health Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.
Umi KalsumPharmacology Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.
Edi MustamsirOrthopaedic and Traumatology Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.
Respati S DradjatOrthopaedic and Traumatology Department, Faculty of Medicine, Universitas Brawijaya, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOne of the most important part of tissue engineering (TE) is a matrix called scaffold. A good scaffold integrates with the host tissue and support the growth and differentiation of the cells. Collagen is the most abundant protein in the ECM and has been considered to be a group of proteins with a characteristic molecular structure-fibrillar structure, which contributes to the extracellular scaffolding.

objectiveIn this research we study the biocompatibility and attachment of collagen scaffold by measuring the level of availability of mesenchymal stem cell (MSC) cluster from stromal vascular fraction (SVF).

methodThis study was experimental invitro on MSC culture derived from SVF, with post-test control group design. Biocompatibility was measured by viability of MSC from SVF with marker Propidium Iodine through flowcytometry and electron microscope was used to assess the population density of MSC from SVF by measuring the number of cluster cells seen.

resultOxidize cellulose has the greatest value of MSC cluster with average number of 2003 cell cluster. This result was significant with p < 0.05 using One-Way Anova and Tukey Test.

conclusionCollagen scaffold is ideal for MSC from SVF because of its compatibility and attachment.

Indexed as

Collagen scaffoldMesenchymal stem cellStromal vascular fraction

Identifiers

PMID32983445
PMCPMC7498726

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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.