Progress in Cytotoxicity of Biomaterials

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Biomedical Engineering and Materials".

Deadline for manuscript submissions: 31 August 2025 | Viewed by 581

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Guest Editor
Department of Mechanical Engineering, Yeungnam University, Gyeongsan si, Republic of Korea
Interests: bioactive glasses; bone tissue engineering; biocompatibility; anticancer

Special Issue Information

Dear Colleagues,

The cytotoxicity of biomaterials is a critical aspect of biomedical research, influencing the safety, efficacy, and long-term biocompatibility of materials used in medical implants, drug delivery systems, and tissue engineering. This Special Issue aims to highlight recent advances in the evaluation of biomaterial cytotoxicity, including in vitro and in vivo testing methodologies, mechanisms of cellular interactions, and strategies to enhance biocompatibility. Topics of interest for this Special Issue include the role of surface modifications, nanomaterials, and biodegradable polymers in reducing cytotoxic effects, as well as emerging techniques for assessing cell viability, oxidative stress, and inflammatory responses. We invite contributions that provide insights into novel biomaterial designs, toxicity mitigation strategies, and regulatory considerations to ensure safe biomedical applications.

Dr. Lakkamraju Vijayalakshmi
Guest Editor

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Keywords

  • biomaterial cytotoxicity
  • biocompatibility assessment
  • in vitro and in vivo toxicity
  • surface modification
  • nanomaterials in medicine
  • oxidative stress and inflammation
  • tissue engineering materials
  • drug delivery systems
  • biodegradable polymers
  • regulatory perspectives on biomaterial safety

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Published Papers (1 paper)

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Research

19 pages, 9060 KiB  
Article
Targeting CDK4/6 in Cancer: Molecular Docking and Cytotoxic Evaluation of Thottea siliquosa Root Extract
by Maruthamuthu Rathinam Elakkiya, Mohandas Krishnasreya, Sureshkumar Tharani, Muthukrishnan Arun, L. Vijayalakshmi, Jiseok Lim, Ayman A. Ghfar and Balasundaramsaraswathy Chithradevi
Biomedicines 2025, 13(7), 1658; https://doi.org/10.3390/biomedicines13071658 - 7 Jul 2025
Viewed by 419
Abstract
Background: Cyclin-dependent kinases 4 and 6 (CDK4/6) are pivotal regulators of the cell cycle, whose dysregulation is closely linked to cancer progression. While synthetic CDK4/6 inhibitors such as Palbociclib and Ribociclib are clinically effective, their use is limited by significant adverse effects. [...] Read more.
Background: Cyclin-dependent kinases 4 and 6 (CDK4/6) are pivotal regulators of the cell cycle, whose dysregulation is closely linked to cancer progression. While synthetic CDK4/6 inhibitors such as Palbociclib and Ribociclib are clinically effective, their use is limited by significant adverse effects. Methods: In this study, the aqueous root extract of Thottea siliquosa, a traditionally used medicinal plant, was evaluated for its potential as a natural CDK4/6 inhibitor. Phytochemical profiling using GC-MS identified bioactive compounds, which were subsequently subjected to molecular docking, ADME prediction, and in vitro cell-based assays using HCT116 and L929 cells. Results: The docking results revealed that Isocorydine (−7.4 kcal/mol for CDK4 and −7.2 kcal/mol for CDK6) and Thunbergol (−6.5 kcal/mol for CDK4 and −7.0 kcal/mol for CDK6) exhibited promising binding affinities comparable to standard CDK inhibitors, Palbociclib (−7.2, −8.3 kcal/mol) and Ribociclib (−7.1, −8.1 kcal/mol). Among the other tested natural compounds, Squalene (−7.1 kcal/mol for CDK4) and 2-palmitoylglycerol (−5.2 kcal/mol for CDK4, −4.9 kcal/mol for CDK6) demonstrated moderate binding affinities. ADME analysis confirmed favorable drug-like properties with minimal toxicity alerts. The extract displayed dose-dependent cytotoxicity with an IC50 of 140 μg/mL and reduced cell migration in HCT116 cells, indicating potential anti-proliferative effects. These findings suggest that T. siliquosa root extract, through synergistic phytochemical interactions, holds promise as a multi-targeted, plant-based therapeutic candidate for CDK4/6-associated cancers, warranting further in vitro and in vivo validation. Full article
(This article belongs to the Special Issue Progress in Cytotoxicity of Biomaterials)
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