Evidence map›Paper›PMID 39001820›Full record

ArticleBiomacromolecules2024

Development of an Injectable, ECM-Derivative Embolic for the Treatment of Cerebral Saccular Aneurysms.

Seungil Kim, Kamil W Nowicki, Keishi Kohyama, Aditya Mittal, Sangho Ye, Kai Wang, Taro Fujii, Shivbaskar Rajesh, Catherine Cao, Rohit Mantena and 5 more

Abstract read
In one paragraph

Article in Biomacromolecules, 2024. 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. Article
  2. Article
  3. 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

15 authors.

Seungil KimDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.ORCID 0000-0002-4231-3721
Kamil W NowickiDepartment of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Keishi KohyamaDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Aditya MittalDepartment of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Sangho YeDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Kai WangDiscovery Center for Musculoskeletal Recovery, Schoen Adams Research Institute at Spaulding, Charlestown, Massachusetts 02115, United States.ORCID 0000-0001-8447-6177
Taro FujiiDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Shivbaskar RajeshDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Catherine CaoDivision of Experimental Pathology, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, United States.
Rohit MantenaDepartment of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Marianna BarbutoDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Youngmee JungCenter for Biomaterials, Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul 130-650, Republic of Korea.ORCID 0000-0002-4778-4629
Bradley A GrossDepartment of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Robert M FriedlanderDepartment of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
William R WagnerDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.ORCID 0000-0003-0082-8089

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral aneurysms are a source of neurological morbidity and mortality, most often as a result of rupture. The most common approach for treating aneurysms involves endovascular embolization using nonbiodegradable medical devices, such as platinum coils. However, the need for retreatment due to the recanalization of coil-treated aneurysms highlights the importance of exploring alternative solutions. In this study, we propose an injectable extracellular matrix-derived embolic formed in situ by Michael addition of gelatin-thiol (Gel-SH) and hyaluronic acid vinyl sulfone (HA-VS) that may be delivered with a therapeutic agent (here, RADA-SP) to fill and remodel aneurysmal tissue without leaving behind permanent foreign bodies. The injectable embolic material demonstrated rapid gelation under physiological conditions, forming a highly porous structure and allowing for cellular infiltration. The injectable embolic exhibited thrombogenic behavior in vitro that was comparable to that of alginate injectables. Furthermore, in vivo studies in a murine carotid aneurysm model demonstrated the successful embolization of a saccular aneurysm and extensive cellular infiltration both with and without RADA-SP at 3 weeks, with some evidence of increased vascular or fibrosis markers with RADA-SP incorporation. The results indicate that the developed embolic has inherent potential for acutely filling cerebrovascular aneurysms and encouraging the cellular infiltration that would be necessary for stable, chronic remodeling.

Indexed as

Embolization, TherapeuticExtracellular MatrixIntracranial AneurysmAnimalsGelatinHumansHyaluronic AcidMaleMiceGelatinHyaluronic Acid

Identifiers

PMID39001820
PMCPMC11323012

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.