Evidence map›Paper›PMID 34211728›Full record

ArticleRegenerative biomaterials2021

Development of a modular, biocompatible thiolated gelatin microparticle platform for drug delivery and tissue engineering applications.

Hannah A Pearce, Yu Seon Kim, Emma Watson, Kiana Bahrami, Mollie M Smoak, Emily Y Jiang, Michael Elder, Tate Shannon, Antonios G Mikos

Open access · goldAbstract read
In one paragraph

Article in Regenerative biomaterials, 2021. 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
0.9field-weighted citation impact, top 31% 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, 15 citations in OpenAlex.

  1. Article
  2. Shaping the mechanical properties of a gelatin hydrogel interface via amination.Journal of the mechanical behavior of biomedical materials · 2026
    Article
  3. Article
  4. Recent advances in regenerative biomaterials.Regenerative biomaterials · 2022
    Review
  5. 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

9 authors at 1 institution in 1 country.

Hannah A PearceDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Yu Seon KimDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Emma WatsonDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Kiana BahramiDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Mollie M SmoakDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Emily Y JiangDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Michael ElderDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Tate ShannonDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.ORCID https://orcid.org/0000-0002-3528-7166
Antonios G MikosDepartment of Bioengineering, Rice University, 6500 Main Street, Houston, TX 77030, USA.
Rice University · US

Funding

Training and Dissemination CoreP41EB023833 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI FISHER, JOHN P · 2017 to 2021
$6.2M
In Situ Hardening Cell-Laden Constructs for Osteochondral Tissue EngineeringR01AR068073 · NIAMS · RICE UNIVERSITY · PI MIKOS, ANTONIOS G. · 2015 to 2019
$1.7M
"A Two-Stage High-Fidelity, Anti-Infective Approach to Craniofacial Repair in Novel Ovine Model"F31DE027586 · NIDCR · RICE UNIVERSITY · PI WATSON, EMMA · 2017 to 2019
$134k
NIAMS NIH HHS R01 AR068073NIBIB NIH HHS P41 EB023833NIDCR NIH HHS F31 DE027586
6 · The paper itself

Abstract

The field of biomaterials has advanced significantly in the past decade. With the growing need for high-throughput manufacturing and screening, the need for modular materials that enable streamlined fabrication and analysis of tissue engineering and drug delivery schema has emerged. Microparticles are a powerful platform that have demonstrated promise in enabling these technologies without the need to modify a bulk scaffold. This building block paradigm of using microparticles within larger scaffolds to control cell ratios, growth factors and drug release holds promise. Gelatin microparticles (GMPs) are a well-established platform for cell, drug and growth factor delivery. One of the challenges in using GMPs though is the limited ability to modify the gelatin post-fabrication. In the present work, we hypothesized that by thiolating gelatin before microparticle formation, a versatile platform would be created that preserves the cytocompatibility of gelatin, while enabling post-fabrication modification. The thiols were not found to significantly impact the physicochemical properties of the microparticles. Moreover, the thiolated GMPs were demonstrated to be a biocompatible and robust platform for mesenchymal stem cell attachment. Additionally, the thiolated particles were able to be covalently modified with a maleimide-bearing fluorescent dye and a peptide, demonstrating their promise as a modular platform for tissue engineering and drug delivery applications.

Indexed as

biomaterialscell deliveryclick chemistrydrug deliverygelatin microparticlesthiolated gelatin microparticlestissue engineering

Identifiers

PMID34211728
PMCPMC8240604
OpenAlexW3135059319

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.