Evidence map›Paper›PMID 35335924›Full record

ArticlePharmaceutics2022

Mineralizing Gelatin Microparticles as Cell Carrier and Drug Delivery System for siRNA for Bone Tissue Engineering.

Sandra Hinkelmann, Alexandra H Springwald, Sabine Schulze, Ute Hempel, Franziska Mitrach, Christian Wölk, Michael C Hacker, Michaela Schulz-Siegmund

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Acta pharmaceutica Sinica. B · 2024
    Review
  3. Article
  4. Article
  5. Review
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 3 institutions in 1 country.

Sandra HinkelmannPharmaceutical Technology, Faculty of Medicine, Institute of Pharmacy, University of Leipzig, Eilenburger Straße 15A, 04317 Leipzig, Germany.ORCID 0000-0001-9184-1339
Alexandra H SpringwaldPharmaceutical Technology, Faculty of Medicine, Institute of Pharmacy, University of Leipzig, Eilenburger Straße 15A, 04317 Leipzig, Germany.
Sabine SchulzeJoint and Soft Tissue Research, Centre for Translational Bone, Faculty of Medicine, TU Dresden, Fiedlerstraße 34, 01307 Dresden, Germany.
Ute HempelInstitute of Physiological Chemistry, TU Dresden, Fiedlerstraße 42, 01307 Dresden, Germany.
Franziska MitrachPharmaceutical Technology, Faculty of Medicine, Institute of Pharmacy, University of Leipzig, Eilenburger Straße 15A, 04317 Leipzig, Germany.ORCID 0000-0003-4518-8054
Christian WölkPharmaceutical Technology, Faculty of Medicine, Institute of Pharmacy, University of Leipzig, Eilenburger Straße 15A, 04317 Leipzig, Germany.ORCID 0000-0002-8067-7307
Michael C HackerPharmaceutical Technology, Faculty of Medicine, Institute of Pharmacy, University of Leipzig, Eilenburger Straße 15A, 04317 Leipzig, Germany.ORCID 0000-0002-4776-2294
Michaela Schulz-SiegmundPharmaceutical Technology, Faculty of Medicine, Institute of Pharmacy, University of Leipzig, Eilenburger Straße 15A, 04317 Leipzig, Germany.ORCID 0000-0003-1340-1850
Leipzig University · DETechnische Universität Dresden · DEHeinrich Heine University Düsseldorf · DE

Funding

Deutsche Forschungsgemeinschaft 59307082-TRR67 (subproject A1)Leipzig University Open Access PublishingSaxon State Ministry for Science and the Arts 22157026
6 · The paper itself

Abstract

The local release of complexed siRNA from biomaterials opens precisely targeted therapeutic options. In this study, complexed siRNA was loaded to gelatin microparticles cross-linked (cGM) with an anhydride-containing oligomer (oPNMA). We aggregated these siRNA-loaded cGM with human mesenchymal stem cells (hMSC) to microtissues and stimulated them with osteogenic supplements. An efficient knockdown of chordin, a BMP-2 antagonist, caused a remarkably increased alkaline phosphatase (ALP) activity in the microtissues. cGM, as a component of microtissues, mineralized in a differentiation medium within 8-9 days, both in the presence and in the absence of cells. In order to investigate the effects of our pre-differentiated and chordin-silenced microtissues on bone homeostasis, we simulated in vivo conditions in an unstimulated co-culture system of hMSC and human peripheral blood mononuclear cells (hPBMC). We found enhanced ALP activity and osteoprotegerin (OPG) secretion in the model system compared to control microtissues. Our results suggest osteoanabolic effects of pre-differentiated and chordin-silenced microtissues.

Indexed as

chordin silencingco-culturegelatin microparticleshuman mesenchymal stem cells (hMSC)human peripheral blood mononuclear cells (hPBMC)osteogenic differentiation

Identifiers

PMID35335924
PMCPMC8949427
OpenAlexW4214733416

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.