Journals / Turkish Journal of Biology / 2022 / Cilt: 46 - Sayı: 3

Design and in vitro, in vivo evaluation of antioxidant bioadhesive gels for burn treatment

Pages
251–262
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In conclusion, bio-adhesive CP 940 (2%) gel containing 50 mM taurine could be promising in the treatment of burns by balancing oxidative stress.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Burn wounds are frequently encountered health problems, which need a new treatment approach especially in terms of good patient compliance.
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Key Findings & Data:Antioxidant taurine containing bio-adhesive gels were prepared by using carbopol (CP) 940 and 934.
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Conclusion & Impact:In conclusion, bio-adhesive CP 940 (2%) gel containing 50 mM taurine could be promising in the treatment of burns by balancing oxidative stress.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Burn wounds are frequently encountered health problems, which need a new treatment approach especially in terms of good patient compliance. Availability of use of antioxidant agents and bio-adhesive gels in tissue healing can be an alternative as a new approach for wound healing. Antioxidant taurine containing bio-adhesive gels were prepared by using carbopol (CP) 940 and 934. Rheological and texture analyses were carried out on bio-adhesive gels for in vitro characterization. Wound model on Wistar rats was used to evaluate the in vivo evaluation of gels. Rheological and texture analyses showed that a carbopol bioadhesive gel has acceptable topically use dosage characteristics and in combination with Taurine it presented a successful wound healing effect via antioxidant parameters. In conclusion, bio-adhesive CP 940 (2%) gel containing 50 mM taurine could be promising in the treatment of burns by balancing oxidative stress.

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Cite This Article

PEKÇETİN, Ç., YAPAR, E. A., GÖKÇE, G., BAĞRIYANIK, A., KARAVANA, S. Y., TURAL, G. A., GÖKÇE, E. H. (2022). Design and in vitro, in vivo evaluation of antioxidant bioadhesive gels for burn treatment. Turkish Journal of Biology, Cilt: 46 - Sayı: 3, 251–262. https://ajindex.com/articles/600090

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References (10)

  1. Abdullahi A, Amini-Nik S, Jeschke MG (2014). Animal models in burn research. Cellular and Molecular Life Sciences 71 (17): 3241-55.
  2. Ashkani-Esfahani S, Zarifi F, Asgari Q, Samadnejad AZ, Rafiee S et al. (2014). Taurine improves the wound healing process in cutaneous leishmaniasis in mice model, based on stereological parameters. Advanced Biomedical Research 3: 204. Bonacucina G, Cespi M, Misici-Falzi M, Palmieri GF (2006). Rheological, adhesive and release characterization of semisolid Carbopol/tetraglycol systems. International Journal of Pharmaceutics 307: 129-140.
  3. Bradford MM (1976). A Rapid and Sensitive Method for the Quantition of Microgram Quantities of Protein Utilizing the Princible of Protein-Dye Binding. Analytical Biochemistry 72: 248-251.
  4. Çetinkalp Ş, Gökçe EH, Şimşir I, Tuncay Tanrıverdi S, Doğan F et al. (2021). Comparative Evaluation of Clinical Efficacy and Safety of Collagen Laminin-Based Dermal Matrix Combined with Resveratrol Microparticles (Dermalix) and Standard Wound Care for Diabetic Foot Ulcers. The International Journal of Lower Extremity Wounds 20 (3): 217-226. D’Avignon LC, Hogan BK, Murray CK, Loo FL, Hospenthal DR et al. (2010). Contribution of bacterial and viral infections to attributable mortality in patients with severe burns: an autopsy series. Burns 36 (6): 773–779.
  5. Deasy PB, Quigley KJ (1991). Rheological evaluation of deacetylated gellan gum (Gelrite) for pharmaceutical use. International Journal of Pharmaceutics 73: 117-123.
  6. Değim Z, Celebi N, Sayan H, Babül A, Erdoğan D et al. (2002). An investigation on skin wound healing in mice with a taurinechitosan gel formulation. Amino Acids 22 (2): 187-198.
  7. Dunnill C, Patton T, Brennan J, Barrett J, Dryden M et al. (2017). Reactive oxygen species (ROS) and wound healing: the functional role of ROS and emerging ROS-modulating technologies for augmentation of the healing process. International Wound Journal 14 (1): 89-96.
  8. Fitzmaurice SD, Sivamani RK, Isseroff RR (2011). Antioxidant therapies for wound healing: a clinical guide to currently commercially available products. Skin Pharmacology and Physiology 24 (3): 113–126.
  9. Gaikwad VL, Yadav VD, Dhavale RP, Choudhari PB, Jadhav SD (2012). Effect of Carbopol 934 and 940 on Fluconazole Release from Topical Gel Formulation: A Factorial Approach. Current Pharma Research 2 (2): 487-493.
  10. Hoyos M, Guerrero JM, Perez-Cano R, Olivan J, Fabiani F et al. (2000). Serum cholesterol and lipid peroxidation are decreased by melatonin in diet-indu