A. B. Adzhieva
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
A. B. Adzhieva has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- H. M. Nalchajyan
RUDN University
2 shared publications - Sergey Sergeevich Ivanov
RUDN University
2 shared publications - Elizaveta A Nenasheva
Peoples’ Friendship University of Russia named after Patrice Lumumba
1 shared publication - Igor. A. Voronov
Peoples’ Friendship University of Russia
1 shared publication - Zurab S. Khabadze
Peoples’ Friendship University of Russia named after Patrice Lumumba (RUDN University)
1 shared publication
Latest Publications
- Open Access
- 14 October 2022
- Published by Khabadze ZS in Эндодонтия Today
- Vol. 20 (3) , 251-254
Results of PCR diagnostics after gingiva soft tissue augmentation
Aim. To demonstrate the results of polymerase chain reaction in real time.Materials and methods. The gum fragment was placed in 1 ml of RNA-leiter ("QIAGEN", Germany), incubated for a day at +4C, samples were stored at -70 °C.To obtain cDNA from the RNA matrix, a ready-made set of reagents MMLV RT Kit ("Eurogen", Russia) was used, the reaction was carried out according to the attached instructions. 2 µl of random decanucleotide primer (Random dN) and 1 µl of sterile RNase-free water were added to 6 µl of RNA, heated at +70C in a “Termit” thermostat (“DNA-Technology”, Russia) for 2 min to melt secondary RNA structures, then stored on ice (+4C). 4 ml of 5X buffer was added to the reaction mixture for the synthesis of the first chain (280 mM Tris-HCl, 375 mM KCl, 30 mM MgCl2, pH 8,7), 2 ml of dNTP mixture, 2 ml of DTT and 2 ml of sterile water free of RNase. Immediately before the reaction, 1 ml of MMLV revertase (reverse transcriptase of mouse leukemia virus) was added to the mixture and added to the RNA. The test tubes were heated in the Gnome thermostat (“DNA- Technology”, Russia) at +39C for 60 minutes, then at +70C for 10 minutes in the “Termit” thermostat (“DNA-Technology”, Russia).Results. The expression of IL-4, IL-10, IL-6, IL-12b, IL-1ß, MMP9 mRNA was not detected in the studied samples. The results of the polymerase chain reaction in real time showed that the expression levels of the proinflammatory cytokine TNFa and TIMP1 genes did not differ in both the autograft group and the collagen membrane group. The expression of MMP 2 and TIMP 2 was higher in the group using a collagen membrane, which is probably associated with tissue regeneration processes.Conclusions. Fibro-guide collagen matrix shows no less effective clinical results in comparison with autografts
- 14 October 2022
- Published by Khabadze ZS in Эндодонтия Today
- Vol. 20 (3) , 251-254
Open AccessResults of PCR diagnostics after gingiva soft tissue augmentation
Aim. To demonstrate the results of polymerase chain reaction in real time.Materials and methods. The gum fragment was placed in 1 ml of RNA-leiter ("QIAGEN", Germany), incubated for a day at +4C, samples were stored at -70 °C.To obtain cDNA from the RNA matrix, a ready-made set of reagents MMLV RT Kit ("Eurogen", Russia) was used, the reaction was carried out according to the attached instructions. 2 µl of random decanucleotide primer (Random dN) and 1 µl of sterile RNase-free water were added to 6 µl of RNA, heated at +70C in a “Termit” thermostat (“DNA-Technology”, Russia) for 2 min to melt secondary RNA structures, then stored on ice (+4C). 4 ml of 5X buffer was added to the reaction mixture for the synthesis of the first chain (280 mM Tris-HCl, 375 mM KCl, 30 mM MgCl2, pH 8,7), 2 ml of dNTP mixture, 2 ml of DTT and 2 ml of sterile water free of RNase. Immediately before the reaction, 1 ml of MMLV revertase (reverse transcriptase of mouse leukemia virus) was added to the mixture and added to the RNA. The test tubes were heated in the Gnome thermostat (“DNA- Technology”, Russia) at +39C for 60 minutes, then at +70C for 10 minutes in the “Termit” thermostat (“DNA-Technology”, Russia).Results. The expression of IL-4, IL-10, IL-6, IL-12b, IL-1ß, MMP9 mRNA was not detected in the studied samples. The results of the polymerase chain reaction in real time showed that the expression levels of the proinflammatory cytokine TNFa and TIMP1 genes did not differ in both the autograft group and the collagen membrane group. The expression of MMP 2 and TIMP 2 was higher in the group using a collagen membrane, which is probably associated with tissue regeneration processes.Conclusions. Fibro-guide collagen matrix shows no less effective clinical results in comparison with autografts
- Open Access
- 23 December 2021
- Published by Khabadze ZS in Эндодонтия Today
- Vol. 19 (4) , 317-319-319
Optiminization of regeneration at the stages of soft tissue augmentation using a collagen matrix
Lack of adequate width and thickness of periodontal or peri-implant soft tissues can compromise the aesthetics, function or survival of teeth and dental implants. Biomaterials are widely used in dentistry to overcome the disadvantages of autogenous tissue transplantation. The advantage of using biomaterials is that there is no need for re-surgery and that they are available in large quantities. The most widely used biomaterial for soft tissue augmentation is collagen, as it is believed to best mimic the natural cellular environment of the extracellular matrix, although other biomaterials are also candidates for soft tissue regeneration. Collagen matrices differ in composition, three-dimensional structure, elasticity and mechanical stability. Aim. is to review the literature on the optimization of regeneration at the stages of soft tissue augmentation using a collagen matrix.
- 23 December 2021
- Published by Khabadze ZS in Эндодонтия Today
- Vol. 19 (4) , 317-319-319
Open AccessOptiminization of regeneration at the stages of soft tissue augmentation using a collagen matrix
Lack of adequate width and thickness of periodontal or peri-implant soft tissues can compromise the aesthetics, function or survival of teeth and dental implants. Biomaterials are widely used in dentistry to overcome the disadvantages of autogenous tissue transplantation. The advantage of using biomaterials is that there is no need for re-surgery and that they are available in large quantities. The most widely used biomaterial for soft tissue augmentation is collagen, as it is believed to best mimic the natural cellular environment of the extracellular matrix, although other biomaterials are also candidates for soft tissue regeneration. Collagen matrices differ in composition, three-dimensional structure, elasticity and mechanical stability. Aim. is to review the literature on the optimization of regeneration at the stages of soft tissue augmentation using a collagen matrix.