Evidence map›Paper›PMID 41068828›Full record

ArticleBMC oral health2025

In vivo biocompatibility of elderberry-enriched carboxymethyl chitosan in soft tissue and calvaria bone defects.

Bilge Cansu Uzun Saylan, Gizem Baysan, Osman Yılmaz, Candan Efeoglu, Serap Cilaker Micili, Nevin Ersoy, Mustafa Mahmut Baris, Kaan Orhan, Hasan Havitcioglu

Abstract read
In one paragraph

Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Bilge Cansu Uzun SaylanFaculty of Dentistry, Department of Periodontology, Dokuz Eylül University, Izmir, Turkey. bilgecansu.uzunsaylan@deu.edu.tr.
Gizem BaysanInstitute of Health Science, Department of Biomechanics, Dokuz Eylül University, Izmir, Turkey.
Osman YılmazFaculty of Medicine Experimental Animals Laboratory, Dokuz Eylül University, Izmir, Turkey.
Candan EfeogluFaculty of Dentistry, Department of Oral and Maxillofacial Surgery, Dokuz Eylül University, Izmir, Turkey.
Serap Cilaker MiciliFaculty of Medicine, Department of Histology and Embryology, Dokuz Eylül University, Izmir, Turkey.
Nevin ErsoyFaculty of Medicine, Department of Histology and Embryology, İzmir Tınaztepe University, Izmir, Turkey.
Mustafa Mahmut BarisFaculty of Medicine, Department of Radiology, Dokuz Eylül University, Izmir, Turkey.
Kaan OrhanFaculty of Dentistry, Department of Oral and Maxillofacial Radiology, Ankara University, Izmir, Turkey.
Hasan HavitciogluInstitute of Health Science, Department of Biomechanics, Dokuz Eylül University, Izmir, Turkey.

Funding

Dokuz Eylul University 3274
6 · The paper itself

Abstract

backgroundRegeneration of soft and hard tissues remains a major challenge in periodontal and craniofacial applications, necessitating the development of multifunctional and biocompatible scaffolds. This study investigates the in vivo biocompatibility and regenerative potential of elderberry-enriched, polyethylene glycol diglycidyl ether (PEGDE)-crosslinked carboxymethyl chitosan (CMCht-E) in a rat model.

methodsTwenty-six eight-week-old female Wistar rats were randomly assigned to three experimental groups (subcutaneous, intramuscular, and calvarial; n = 7 per group). In each rat, symmetrical 5 mm defects were created, with the biomaterial implanted on one side and the contralateral side serving as the control. A sham group (n = 5) was included to account for surgical and imaging-related effects. Tissue responses were evaluated using ultrasonography, computed tomography (CT), micro-computed tomography (micro-CT), histomorphometry, and immunohistochemistry (CD68/CD163).

resultsSoft tissue healing, confirmed by both ultrasonography and histological analysis, revealed similar characteristics between the biomaterial and control sites, suggesting a regenerative response closely resembling native tissue architecture. In the calvarial group, histomorphometric assessment and micro-CT analysis demonstrated a statistically significant increase in new bone formation in the CMCht-E group compared to controls (p < 0.05). There were no significant differences in CD68 and CD163 expression between biomaterial and control groups (p > 0.05).

conclusionThis first in vivo study demonstrates that CMCht-E is biocompatible and supports bone and soft tissue regeneration through controlled biodegradation. These findings highlight its promise as a naturally derived biomaterial for future use in periodontal and tissue engineering applications.

Indexed as

Biocompatible MaterialsBone RegenerationChitosanSkullAnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 MoleculeFemaleOsteogenesisPolyethylene GlycolsRandom AllocationRatsRats, WistarReceptors, Cell SurfaceSubcutaneous TissueAntigens, CDAntigens, Differentiation, MyelomonocyticBiocompatible Materialscarboxymethyl-chitosanCD68 antigen, humanCD68 MoleculeCD68 protein, ratChitosanPolyethylene GlycolsReceptors, Cell SurfaceBiocompatibilityBiomaterialBone regenerationCarboxymethyl chitosanElderberryMicrocomputed tomographySoft tissueUltrasonography

Identifiers

PMID41068828
PMCPMC12512586

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LicenceCC BY-NC-ND
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Registered trials

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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.