scholarly journals Soft Tissue Augmentation Using Silk Gels: An In Vitro and In Vivo Study

2009 ◽  
Vol 80 (11) ◽  
pp. 1852-1858 ◽  
Author(s):  
Olivier Etienne ◽  
Aurore Schneider ◽  
Jonathan A. Kluge ◽  
Claire Bellemin-Laponnaz ◽  
Camille Polidori ◽  
...  
2008 ◽  
Vol 69 (1) ◽  
pp. 148-156 ◽  
Author(s):  
James L. Cook ◽  
Derek B. Fox ◽  
Keiichi Kuroki ◽  
Manuel Jayo ◽  
Patrick G. De Deyne

2007 ◽  
Vol 342-343 ◽  
pp. 349-352 ◽  
Author(s):  
Jong Won Rhie ◽  
Jin Kyung Song ◽  
Paik Kwon Lee ◽  
Sang Tae Ahn

Alginate was a proven biocompatible biomatrice for cells but it was known not to provide a proper microenvironment needed for the proliferation of cells because of its anionic property, which caused its low affinity for cells. Water-soluble chitosan was well known as wound healing material and it also had cationic property which helped cell-to-matrix adhesion. The purpose of this study is to assess the ability of a chitosan/alginate mixed sponge as a scaffold for preadipocytes to serve as a biological implant for soft tissue augmentation. Chitosan/alginate and calcium alginate sponges were made by lyophilizing of alginate with water-soluble chitosan mixture and with calcium chloride mixture, respectively, and those were observed by SEM. Preadipocytes seeded in those sponges were cultured for 2 weeks. In vivo study was designed that chitosan/alginate sponges with and without preadipocytes were implanted subcutaneously into nude mouse. Chitosan/alginate and calcium alginate sponges which had highly porosity and 50-200㎛ pore size. In the chitosan/alginate sponge, the levels of DNA amount were significantly higher than those in calcium alginate sponge (P<0.05). In both groups, they increased progressively with time. On the in vivo study, it was observed that adipose tissue layer in the margin of chitosan/alginate sponge on the 2 weeks after implantation of nude mouse. On the 8 weeks after implantation, thick layer of adipose tissue and neovascularization were observed in the chitosan/alginate sponge. Consequently, chitosan/alginate sponge provided proper microenvironment to human preadipocyte, increased the cell proliferation and maintained the pore that offered neovascularization, so turned out to be effective form of fat transplantation for soft tissue augmentation and reconstruction.


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.


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.


2018 ◽  
Vol 4 (1) ◽  
pp. 237-241
Author(s):  
Leon Olde Damink ◽  
Ingo Heschel ◽  
Hans Leemhuis ◽  
Martina Tortorici ◽  
Bastian Wessing

AbstractIn this study, characteristic features of a new regenerative 3D collagen matrix with an orientated open pore structure are studied in-vitro and in-vivo. The noncrosslinked porcine-based resorbable collagen-elastin matrix is designed to provide support during coverage procedures of localized gingival recessions and for local soft tissue augmentation around teeth and implants and is designed to provide an off-the-shelf alternative to autogenous soft tissue grafts. The in-vitro studies show that the mechanical properties (e.g. suture retention, volume recovery after cyclic compression) and the observed active cell migration into the open porous structure of the matrix fulfil essential design requirements. The in-vivo pig animal study shows that the matrix is well integrated into the surrounding tissue and replaced by newly formed autogenous soft tissue without a significant loss in tissue volume. First clinical case series are being performed to further analyse the new 3D matrix in clinical settings.


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