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Wyświetlanie 1-8 z 8
Tytuł:
Black Orlon as promising material for bone tissue engineering
Autorzy:
Parizek, M.
Vetrik, M.
Hruby, M.
Lisa, V.
Bacakova, L.
Powiązania:
https://bibliotekanauki.pl/articles/284127.pdf
Data publikacji:
2014
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
Orlon
polyacrylonitrile
tissue engineering
porous 3D scaffolds
cell adhesion
cell growth
osteoblasts
Źródło:
Engineering of Biomaterials; 2014, 17, no. 128-129; 4-6
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Modyfikacja powierzchni kopolimeru glikolidu z L-laktydem dla zastosowania w inżynierii tkankowej kości
Surface modification of poly(glycolide-co-L-lactide) for bone tissue engineering
Autorzy:
Kaczmarczyk, M.
Pamuła, E.
Bacakova, L.
Parizek, M.
Dobrzyński, P.
Powiązania:
https://bibliotekanauki.pl/articles/284335.pdf
Data publikacji:
2007
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
kopolimery
inżynieria tkankowa
copolymers
tissue engineering
Opis:
Praca dotyczy modyfikacji powierzchni kopolimeru glikolidu z L-laktydem w 0,1M NaOH przez różne okresy czasu tj. od 2 do 24 h. W pracy scharakteryzowano topografię i budowę chemiczną powierzchni folii polimerowych w funkcji czasu modyfikacji. Zbadano też wpływ zmodyfikowanej powierzchni na jej własności biologiczne in vitro w kontakcie z osteoblastami. Badania wykazały, że zastosowana metoda modyfikacji powoduje zmiany w topografii i wzrost chropowatości powierzchni, ale nie wpływa na skład chemiczny, zwilżalność wodą i masę cząsteczkową polimeru. Najlepszy wzrost osteoblastów obserwowano na folii modyfikowanej przez 6h w 0,1M NaOH (o chropowatości ok. 60nm), natomiast na foliach o chropowatości niższej i wyższej adhezja i zdolność do proliferacji komórek były istotnie niższe.
The study was focused on surface modifications of poly(glycolide-co-L-lactide) films (PGLA) after their exposure to 0.1 M NaOH for 2 to 24 h. Topography and surface chemical structure of the films were characterized. The influence of the modified surface on biological properties in contact with human osteoblast-like cells in vitro was evaluated. The results showed that the modification in NaOH caused topographical changes, such as the increase in surface roughness, without affecting the surface chemical composition, wettability and molecular mass. The best growth of osteoblast-like cells was observed on PGLA films modified in 0.1M NaOH for 6 h (average surface roughness of about 60 nm), whereas on the films with lower or higher roughness, the cell adhesion and proliferation activity were lower.
Źródło:
Engineering of Biomaterials; 2007, 10, 62; 12-17
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Application of cellulose-based biomaterials in vascular tissue engineering - a review and our experience
Autorzy:
Bacakova, L.
Novotna, K.
Parizek, M.
Havelka, P.
Sopuch, T.
Powiązania:
https://bibliotekanauki.pl/articles/284148.pdf
Data publikacji:
2012
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
biomaterials
tissue engineering
vascular
Opis:
Artificial vascular replacements used in current clinical practice are fabricated from polyethylene terephthalate (PET, e.g. Dacron) orpolyterafluoroethylene (PTFE, e.g. Teflon). Older materials used earlier for constructing vascular prostheses are polyamide (Nylon), polyvinyl alcohol (Ivalon) and polyacrylonitrile (Orlon). New promising materials include polyurethane and a wide range of biodegradable synthetic or nature-derived polymers, which are usually designed as temporary scaffolds for vascular cells forming a new regenerated blood vessel wall (for a review, see [1]). One of the nature-derived polymers is cellulose and its derivatives and composites with other materials. Cellulose is the most abundant biopolymer on Earth. It is a polysaccharide consisting of a linear chain of several hundred to over ten thousand ß(1\to 4) linked D-glucose units [2,3]. Cellulose is the structural component of the primary cell wall of green plants, many forms of algae and the oomycetes. In plant cells, cellulose microfibrils are synthesized at the plasma membrane by hexameric protein complexes, also known as cellulose synthase complexes [4]. Some species of bacteria secrete cellulose to form biofilms. For industrial use, cellulose is mainly obtained from wood pulp and cotton. For tissue engineering applications, bacterial cellulose has been predominantly used, mainly that synthesized by Acetobacterxylinum. Bacterial cellulose is identical to plant cellulose in chemical structure, but it can be produced without contaminant molecules, such as lignin and hemicelluloses, and does not require intensive purification processes. In addition, it is remarkable for its mechanical strength, its ability to be engineered structurally and chemically at nano-, micro-, and macroscales, its biocompatibility and chemical and morphologic controllability [5]. Bacterial cellulose has been used for experimental engineering of bone tissue [6], cartilage [7], skin [8], heart valve [9], and also for urinary reconstruction and diversion [10]. One of the first attempts at vascular tissue engineering was made with cellulose fibers, which were used for constructing three-dimensional vascularized tissue in vitro. These fibers were immobilized with fibronectin in order to improve cell adhesion, and were seeded with bovine coronary artery smooth muscle cells. These cells proliferated on the scaffolds and, after they formed multilayers on the fibers, the fibers were removed by enzymatic digestion using cellulase. The remaining smooth muscle cell aggregates maintained lumens after this procedure, and thus mimicked newly-formed blood vessels [11]. Similarly, three-dimensional nanofibrous scaffolds with micropores made of bacterial cellulose allowed attachment and proliferation of human saphenous vein smooth muscle cells on the surface and also in the inside of the scaffolds [12]. In addition, the mechanical properties of nanofibrous bacterial cellulose scaffolds, evaluated by the shape of the stress-strain response, were reminiscent of the properties of the carotid artery, most probably due to the similarity in architecture of the nanofibril network [13]. The adhesion and growth of vascular endothelial cells was also supported by cellulose-based scaffolds, namely by nanofibrous bacterial cellulose or cellulose acetate scaffolds, especially if these scaffolds were functionalized with RGD-containing oligopeptides, i.e. ligands for integrin adhesion receptors on cells [14, 15], or if they were combined with chitosan [16]. The angiogenic response to bacterial cellulose was also observed under in vivo conditions, i.e. after implantation of these scaffolds in the form of dorsal skinfold chambers into Syrian golden hamsters [17]. Cellulose has also been used for creating tubular structures designed for replacing small-caliber vessels. Hollow-shaped segments of bacterial cellulose were created with a length of 10 mm, an inner diameter of 3.0-3.7 mm and a wall thickness of 0.6 -1.0 mm. These grafts were used to replace the carotid arteries of eight pigs. After a follow-up period of 3 months, seven grafts (87.5%) remained patent, whereas one graft was found to be occluded. All patent grafts developed a single inner layer of endothelium with a basement membrane and a thin layer of collagen, followed by a concentric medial layer containing smooth muscle cells and cellulose, and an outer layer of fibrous cells [18]. Similarly, bacterial cellulose grafts 4 cm in length and 4 mm in internal diameter were implanted bilaterally in the carotid arteries of eight sheep. Although 50% of the grafts occluded within 2 weeks, all patent grafts developed a confluent inner layer of endothelial- like cells [19]. In addition, the mechanical properties of tubular structures created from bacterial cellulose seemed to be advantageous for vascular tissue engineering. For example, these structures exhibited a compliance response similar to that of human saphenous vein [20]. In our experiments, we have concentrated on cellulose-based materials modified with oxidation and/or functionalization with biomolecules. We have prepared fibrous scaffolds made of non-oxidized viscose, dialdehyde cellulose and 6-carboxycellulose with 2.1 wt.% or 6.6 wt.% of -COOH groups. In addition, all these material types were functionalized with arginine, i.e. an amino acid with a basic side chain, or with chitosan, in order to balance (compensate) the relatively acid character of oxidized cellulose molecules. Two groups of samples with and without functionalization were then seeded with vascular smooth muscle cells (VSMC) derived from the rat thoracic aorta by an explantation method [21]. We found that the oxidized cellulose with 2.1 wt.% of-COOH groups was the most appropriate of all the tested materials for colonization with VSMC. The cells on this material achieved an elongated shape, while they were spherical in shape on the other materials. In addition, the numbers of cells obtained in one week after seeding and the concentration of alpha-actin and SM1 and SM2 myosins, measured per mg of protein, were significantly higher on oxidized cellulose with 2.1 wt.% of -COOH groups. Functionalization with arginine and chitosan improved the cell adhesion, but usually only slightly. The most apparent increase in cell number after functionalization was observed on oxidized cellulose with 2.1 wt.% of -COOH groups functionalized with chitosan, and on viscose functionalized with chitosan or arginin. However, the cells on all samples proliferated slowly and with a non-significant increase in cell population densities from day 1 to 7 after seeding. This suggests that cellulose-based materials can be used in applications where high proliferation activity of vascular smooth muscle cells is not desirable. They can therefore be used on vascular prostheses, where excessive VSMC proliferation can lead to the restenosis of the graft. Alternatively, cell proliferation might be enhanced by some other more efficient modification. This would require further research.
Źródło:
Engineering of Biomaterials; 2012, 15, no. 116-117 spec. iss.; 128-130
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The adhesion and growth of vascular smooth muscle cells in cultures on carboranethiol-modified gold films
Autorzy:
Parizek, M.
Base, T.
Londesborough, M. G. S.
Lisa, V.
Bacakova, L.
Powiązania:
https://bibliotekanauki.pl/articles/286249.pdf
Data publikacji:
2008
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
implanty chirurgiczne
biomateriały
powłoki metalowe
inżynieria materiałowa
metal coatings
gold film
carboranethiol
cell adhesion
cell spreading
cell proliferation
biomaterials
tissue engineering
surgical implants
Opis:
Metal surfaces have become important over the last decade for potential surgical implants, and within this context we present here a study of the cell growth on modified gold surfaces. Gold films, deposited on glass plates and annealed with a hydrogen flame, were modified with four different carboranethiol derivatives: 1-(HS)-1,2-C2 B10H11(A), 1,2-(HS)2-1,2-C2B10H10(B), 9,12-(HS)2-1,2-C2B10H10(C) and 1,12-(HS)2-1,12- C2B10H10(D). The materials engendered from these modifications were used to investigate the adhesion and growth of rat aortic smooth muscle cells cultured on these surfaces in a DMEM medium with 10% of fetal bovine serum. One day after seeding, the highest number of initially adhered cells was found on the surface of a bare gold film. However, three days after seeding, the number of cells on carboranethiol-modified gold samples B, C and D was significantly higher than the number on a bare gold film. After seven days, the number of cells on a bare gold film and on gold films modified with derivatives A, B and D was very similar, but the surface of a gold film modified with derivative C exhibited a significantly smaller number of cells. This may be explained by the exposure of the CH vertices of the carborane cluster, which are more acidic than the BH vertices exposed toward the cells in either A or B.
Źródło:
Engineering of Biomaterials; 2008, 11, 75; 6-8
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Vascular smooth muscle cells in cultures on low density polyethylene modified with plasma discharge and biofunctionalization
Autorzy:
Parizek, M.
Kasalkova, N.
Bacakova, L.
Kolarova, K.
Lisa, V.
Svorcik, V.
Powiązania:
https://bibliotekanauki.pl/articles/285087.pdf
Data publikacji:
2009
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
Ar plasma discharge
biomaterials
low-density polyethylene
cell adhesion
cell proliferation
grafting
tissue engineering
vascular smooth muscle cells
Opis:
Low density polyethylene (LDPE) was modified by an Ar plasma discharge and then grafted with glycine (Gly), bovine serum albumin (BSA) or polyethylene glykol (PEG). Some plasma-treated samples and samples grafted with BSA were exposed to a suspension of colloidal carbon particles (C, BSA+C). Pristine LDPE and tissue culture polystyrene dishes (PSC) were used as control samples. The materials were seeded with rat aortic smooth muscle cells and incubated in a medium DMEM with 10% of fetal bovine serum. On day 1 after seeding, the cells on LDPE modified with plasma only, Gly, BSA and BSA+C adhered in similar numbers as on PSC, while the values on non-modified and PEG-modified samples were significantly lower. On day 5, the highest cell numbers were found again on LDPE with Gly, BSA and BSA+C. On day 7, the highest number of cells was found on LDPE modified only with plasma. The latter cells also dis-played the largest cell spreading area. The increased cell colonization was probably due to the formation of oxygen-containing chemical functional groups after plasma irradiation, and also due to positive effects of grafted Gly, BSA and BSA in combination with colloidal C particles.
Źródło:
Engineering of Biomaterials; 2009, 12, no. 89-91; 25-28
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The adhesion and growth of vascular smooth muscle cells in cultures on carboranethiol-modified gold films
Autorzy:
Parizek, M.
Base, T.
Londesborough, M. G. S.
Lisa, V.
Bacakova, L.
Powiązania:
https://bibliotekanauki.pl/articles/285409.pdf
Data publikacji:
2008
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
metal coating
gold film
carboranethiol
cell adhesion
cell spreading
cell proliferation
biomaterials
tissue engineering
surgical implants
Opis:
Metal surfaces have become important over the last decade for potential surgical implants, and within this context we present here a study of the cell growth on modified gold surfaces. Gold films, deposited on glass plates and annealed with a hydrogen flame, were modified with four different carboranethiol derivatives: 1-(HS)-1,2-C2B10H11 (A), 1,2-(HS)2-1,2-C2B10H10 (B), 9,12-(HS)2-1,2-C2B10H10 (C) and 1,12-(HS)2-1,12- C2B10H10 (D). The materials engendered from these modifications were used to investigate the adhesion and growth of rat aortic smooth muscle cells cultured on these surfaces in a DMEM medium with 10% of fetal bovine serum. One day after seeding, the highest number of initially adhered cells was found on the surface of a bare gold film. However, three days after seeding, the number of cells on carboranethiol-modified gold samples B, C and D was significantly higher than the number on a bare gold film. After seven days, the number of cells on a bare gold film and on gold films modified with derivatives A, B and D was very similar, but the surface of a gold film modified with derivative C exhibited a significantly smaller number of cells. This may be explained by the exposure of the CH vertices of the carborane cluster, which are more acidic than the BH vertices exposed toward the cells in either A or B.
Źródło:
Engineering of Biomaterials; 2008, 11, no. 81-84; 117-119
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Improved adhesion and growth of vascular smooth muscle cells in cultures on polyethylene modified by plasma discharge
Autorzy:
Parizek, M.
Kasalkova, N.
Bacakova, L.
Kolarova, K.
Lisa, V.
Svorcik, V.
Powiązania:
https://bibliotekanauki.pl/articles/284295.pdf
Data publikacji:
2007
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
biomateriały
inżynieria tkankowa
Ar plasma discharge
high density and low density polyethylene
cell adhesion
cell proliferation
vascular smooth muscle cells
biomaterials
tissue engineering
Opis:
The attractiveness of synthetic polymers for cell colonization can be affected by physical and chemical modification of the polymer surface. In this study, high density polyethylene (HDPE, m.w. 0.952g/cm3) and low density polyethylene (LDPE, m.w. 0.922g/cm3) were modified by an Ar plasma discharge using Balzers SCD 050 device (exposure time 10, 50, 150 and 400 seconds, discharge power 1.7W). The material was then seeded with rat aortic smooth muscle cells (RASMC; passages 8 to 9, 17 000 cells/cm3) and incubated in a DMEM medium with 10% of fetal calf serum. On day 1 after seeding, the number of initially adhered cells was significantly higher on all modified HDPE and LDPE samples. On day 2, this difference persisted in HDPE, whereas in LDPE only the values on the samples modified by 150 and 400 seconds were significantly higher. On the 5th and 7th day, there were no significant differences in cell number among all LDPE samples. However, on the HDPE foils, significant differences were still apparent on the samples modified for 400 seconds. The cell spreading areas measured on day 1 after seeding were significantly larger on all modified LDPE samples, and, on day 2, on the HDPE samples exposed for 150s. The increased cell colonization was probably due to the formation of oxygen-containing chemical functional groups in the polymer. These results suggest that the responsiveness of the cell to the changes in physiochemical surface properties was more pronounced in HDPE than in LDPE. On both types of polyethylene, the most appropriate exposure time for the enhancement of cell adhesion and growth seemed to be 150 and 400 seconds.
Źródło:
Engineering of Biomaterials; 2007, 10, no. 67-68; 1-4
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Włókniste podłoża dla inżynierii tkankowej kości: hodowle komórek MG 63 w warunkach statycznych i dynamicznych
Fibrous scaffolds for bone tissue engineering: static and dynamic in vitro studies with MG 63 cells
Autorzy:
Buczyńska, J.
Pamuła, E.
Błażewicz, S.
Bacakova, L.
Parizek, M.
Chlupac, J.
Mikołajczyk, T.
Boguń, M.
Dobrzyński, P.
Powiązania:
https://bibliotekanauki.pl/articles/285121.pdf
Data publikacji:
2007
Wydawca:
Akademia Górniczo-Hutnicza im. Stanisława Staszica w Krakowie. Polskie Towarzystwo Biominerałów
Tematy:
inżynieria tkankowa
tissue engineering
Opis:
Resorbowalne włókna z kopolimeru L-laktydu z glikolidem (PLG) i PLG z hydroksyapatytem rozprowadzonym w ich objętości (PLG-HAP) zostały otrzymane metodą formowania z roztworu. Włókna zostały przetworzone w trójwymiarowe podłoża za pomocą metody łączenia włókien. Mikrostrukturę otrzymanych podłoży scharakteryzowano za pomocą mikroskopu stereoskopowego. Wykazano, że podłoża miały różną porowatość, wielkość i orientację pojedynczych włókien. Oddziaływanie włóknistych podłoży z komórkami kostnymi MG 63 było badane in vitro w warunkach statycznych i dynamicznych. Liczba komórek i ich morfologia były oceniane po 3 i 7 dniach od założenia hodowli. Badania wykazały że liczba komórek na materiałach włóknistych rosła wraz z czasem prowadzenia hodowli, chociaż była znacznie niższa niż na płaskiej powierzchni kontrolnej (polistyren do celów kultur komórkowych). W dynamicznych warunkach hodowli obserwowano różną proliferację komórek w zależności od rodzaju użytego podłoża: na PLG występował spadek, zaś na PLG-HAP istotny wzrost liczby komórek. Wyniki sugerują, że obecność cząstek hydroksyapatytu rozprowadzonych w objętości włókien polimerowych poprawia adhezje i proliferacje osteoblastów.
Resorbable poly(L-lactide-co-glycolide) fibres (PLG) and poly(L-lactide-co-glycolide) fibres containing hydroxyapatite nanoparticles in volume of PLG fibres (PLG-HAP) were manufactured by solution spinning process. The resultant fibres were processed into three-dimensional scaffolds using fibre bounding method. The microstructure of resorbable scaffolds was characterized by stereomicroscope. The results show that the scaffolds have different fibrous architecture including porosity, size and arrangement of individual fibres. The interaction of fibrous scaffolds with osteoblast-like MG 63 cells was tested in vitro in static and dynamic cell culture conditions. The number of adhering cells and their morphology were evaluated on days 3 and 7 after seeding. It was found that cell number increased with the cultivation time, although it was significantly lower than on control polystyrene dish (TCPS). During dynamic cultivation the number of cells decreased on PLG scaffolds, whereas on PLG-HAP scaffolds it increased. These results suggest that presence of hydroxyapatite distributed within the whole volume of resorbable polymer fibres promoted adhesion and proliferation of osteoblasts.
Źródło:
Engineering of Biomaterials; 2007, 10, no. 65-66; 1-6
1429-7248
Pojawia się w:
Engineering of Biomaterials
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-8 z 8

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