scholarly journals State of the Art on Biomaterials for Soft Tissue Augmentation in the Oral Cavity. Part II: Synthetic Polymers-Based Biomaterials

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1845
Author(s):  
Manuel Toledano ◽  
Manuel Toledano-Osorio ◽  
Álvaro Carrasco-Carmona ◽  
Cristina Vallecillo ◽  
Raquel Toledano ◽  
...  

Most of the polymers used as biomaterials for scaffolds are naturally occurring, synthetic biodegradable, and synthetic non-biodegradable polymers. Since synthetic polymers can be adapted for obtaining singular desired characteristics by applying various fabrication techniques, their use has increased in the biomedical field, in dentistry in particular. The manufacturing methods of these new structures include many processes, such as electrospinning, 3D printing, or the use of computer-aided design/computer-aided manufacturing (CAD/CAM). Synthetic polymers show several drawbacks that can limit their use in clinical applications, such as the lack of cellular recognition, biodegradability, and biocompatibility. Moreover, concerning biodegradable polymers, the time for matrix resorption is not predictable, and non-resorbable matrices are preferred for soft tissue augmentation in the oral cavity. This review aimed to determine a new biomaterial to offset the present shortcomings in the oral environment. Researchers have recently proposed a novel non-resorbable composite membrane manufactured via electrospinning that has allowed obtaining remarkable in vivo outcomes concerning angiogenesis and immunomodulation throughout the polarization of macrophages. A prototype of the protocol for in vitro and in vivo experimentation with hydrogels is explained in order to encourage innovation into the development of promising biomaterials for soft tissue augmentation in the near future.

2008 ◽  
Vol 69 (1) ◽  
pp. 148-156 ◽  
Author(s):  
James L. Cook ◽  
Derek B. Fox ◽  
Keiichi Kuroki ◽  
Manuel Jayo ◽  
Patrick G. De Deyne

2009 ◽  
Vol 80 (11) ◽  
pp. 1852-1858 ◽  
Author(s):  
Olivier Etienne ◽  
Aurore Schneider ◽  
Jonathan A. Kluge ◽  
Claire Bellemin-Laponnaz ◽  
Camille Polidori ◽  
...  

2016 ◽  
Vol 25 (3) ◽  
pp. 427-434 ◽  
Author(s):  
Jan Wolff ◽  
Elisabet Farré-Guasch ◽  
George K. Sándor ◽  
Susan Gibbs ◽  
Derk Jan Jager ◽  
...  

2019 ◽  
Author(s):  
Frederico Chaves Carvalho ◽  
Paulo Eduardo Ambrósio

The use of whole-cell models in research has the potential to be a powerful tool for scientific discovery, allowing researchers to test hypotheses faster than using in-vitro or in vivo methods. Such models can be considered the equivalent of Computer Aided Design for Biology. However, given their complexity, it is still difficult to employ them as an instrument in investigations. In order to solve this problem, we are developing a framework with the purpose to guide and help scientists through the process of creating whole-cell models faster, enabling them to use these tools as part of their research. This paper brings details of the early stages of the framework’s development process


2011 ◽  
Vol 37 (6) ◽  
pp. 760-767
Author(s):  
SEONG-HO JEONG ◽  
SEUNG-KYU HAN ◽  
WOO-KYUNG KIM

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2633
Author(s):  
Cristina Vallecillo ◽  
Manuel Toledano-Osorio ◽  
Marta Vallecillo-Rivas ◽  
Manuel Toledano ◽  
Raquel Osorio

Collagen matrices have become a great alternative to the use of connective tissue grafts for soft tissue augmentation procedures. One of the main problems with these matrices is their volume instability and rapid degradation. This study has been designed with the objective of examining the degradation of three matrices over time. For this purpose, pieces of 10 × 10 mm2 of Fibro-Gide, Mucograft and Mucoderm were submitted to three different degradation tests—(1) hydrolytic degradation in phosphate buffer solution (PBS); (2) enzyme resistance, using a 0.25% porcine trypsin solution; and (3) bacterial collagenase resistance (Clostridium histolyticum)—over different immersion periods of up to 50 days. Weight measurements were performed with an analytic microbalance. Thickness was measured with a digital caliper. A stereomicroscope was used to obtain the matrices’ images. ANOVA and Student–Newman–Keuls tests were used for mean comparisons (p < 0.05), except when analyzing differences between time-points within the same matrix and solution, where pair-wise comparisons were applied (p < 0.001). Fibro-Gide attained the highest resistance to all degradation challenges. The bacterial collagenase solution was shown to constitute the most aggressive test as all matrices presented 100% degradation before 14 days of storage.


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