Development of a Novel Zinc Oxide/Polyvinyl Chloride Nanocomposite Material for Medical Implant Applications

2014 ◽  
Vol 1626 ◽  
Author(s):  
Benjamin M. Geilich ◽  
Thomas J. Webster

ABSTRACTIn hospitals and clinics worldwide, medical device surfaces have become a rapidly growing source of nosocomial infections. Almost immediately after adhering to a device surface, bacteria can begin to form a biofilm, which makes the infection especially difficult to treat and often necessitates device removal. Adding to the severity of this problem is the spread of bacterial genetic tolerance to antibiotics, in part demonstrated by the recent and significant increase in the prevalence of methicillin-resistant Staphylococcus aureus (MRSA).Nanomaterials are beginning to be used for a wide variety of biomedical applications due to their unique surface properties which have the ability to control initial protein adsorption and subsequent cell behavior. This “nanoroughness” gives nanomaterials a greater functional surface area than conventional materials, which do not have significant features on the nanoscale. In addition, it is theorized that nanoparticles may also have general mechanisms of toxicity towards bacteria that do not cause problems for mammalian cells.The objective of the present in vitro study was to develop a nanocomposite material by embedding conventional polyvinyl chloride (PVC) with zinc oxide nanoparticles through a simple and inexpensive procedure. The effect of different nanoparticle sizes and %wts were investigated. Results demonstrated that this technique significantly decreased S. aureus density and biofilm formation without the incorporation of antibiotics or other pharmaceuticals, as well as increased the adhesion of human fibroblast cells. Thus, this material could have much promise for use in the manufacture of common implanted medical devices.

2021 ◽  
Vol 22 (13) ◽  
pp. 6785
Author(s):  
Valeria Sogos ◽  
Paola Caria ◽  
Clara Porcedda ◽  
Rafaela Mostallino ◽  
Franca Piras ◽  
...  

Novel psychoactive substances (NPS) are synthetic substances belonging to diverse groups, designed to mimic the effects of scheduled drugs, resulting in altered toxicity and potency. Up to now, information available on the pharmacology and toxicology of these new substances is very limited, posing a considerable challenge for prevention and treatment. The present in vitro study investigated the possible mechanisms of toxicity of two emerging NPS (i) 4′-methyl-alpha-pyrrolidinoexanophenone (3,4-MDPHP), a synthetic cathinone, and (ii) 2-chloro-4,5-methylenedioxymethamphetamine (2-Cl-4,5-MDMA), a phenethylamine. In addition, to apply our model to the class of synthetic opioids, we evaluated the toxicity of fentanyl, as a reference compound for this group of frequently abused substances. To this aim, the in vitro toxic effects of these three compounds were evaluated in dopaminergic-differentiated SH-SY5Y cells. Following 24 h of exposure, all compounds induced a loss of viability, and oxidative stress in a concentration-dependent manner. 2-Cl-4,5-MDMA activates apoptotic processes, while 3,4-MDPHP elicits cell death by necrosis. Fentanyl triggers cell death through both mechanisms. Increased expression levels of pro-apoptotic Bax and caspase 3 activity were observed following 2-Cl-4,5-MDMA and fentanyl, but not 3,4-MDPHP exposure, confirming the different modes of cell death.


Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1700
Author(s):  
Atsushi Kameyama ◽  
Aoi Saito ◽  
Akiko Haruyama ◽  
Tomoaki Komada ◽  
Setsuko Sugiyama ◽  
...  

This study aimed to examine the marginal seal between various commercial temporary restorative materials and exposed dentin/built-up composite. Sixty bovine incisors were cut above the cemento-enamel junction, and half of the dentin was removed to form a step, which was built up using flowable resin composite. The root canals were irrigated, filled with calcium hydroxide, and sealed using one of six temporary sealing materials (hydraulic temporary restorative material, temporary stopping material, zinc oxide eugenol cement, glass-ionomer cement, auto-cured resin-based temporary restorative material, and light-cured resin-based temporary restorative material) (n = 10 for each material). The samples were thermocycled 500 times and immersed in an aqueous solution of methylene blue. After 2 days, they were cut along the long axis of the tooth and the depth of dye penetration was measured at the dentin side and the built-up composite side. For the margins of the pre-endodontic resin composite build-up, the two resin-based temporary restorative materials showed excellent sealing. Hydraulic temporary restorative material had a moderate sealing effect, but the sealing effect of both zinc oxide eugenol cement and glass-ionomer cement was poorer.


2019 ◽  
Vol 8 (4) ◽  
pp. 244
Author(s):  
SaiSankar J. Avula ◽  
Senapathi Navaneet ◽  
Sridhar Muktineni ◽  
Pranitha Kakarla ◽  
HarishC Kommineni ◽  
...  

2018 ◽  
Vol 9 (5) ◽  
pp. 137
Author(s):  
AnujHarish Chandak ◽  
SaeeP Deshmukh ◽  
UshaM Radke ◽  
RajlakshmiS Banerjee ◽  
TusharK Mowade ◽  
...  

Materials ◽  
2017 ◽  
Vol 10 (12) ◽  
pp. 1427 ◽  
Author(s):  
Agmal Scherzad ◽  
Till Meyer ◽  
Norbert Kleinsasser ◽  
Stephan Hackenberg

Background: Zinc oxide nanoparticles (ZnO NPs) are among the most frequently applied nanomaterials in consumer products. Evidence exists regarding the cytotoxic effects of ZnO NPs in mammalian cells; however, knowledge about the potential genotoxicity of ZnO NPs is rare, and results presented in the current literature are inconsistent. Objectives: The aim of this review is to summarize the existing data regarding the DNA damage that ZnO NPs induce, and focus on the possible molecular mechanisms underlying genotoxic events. Methods: Electronic literature databases were systematically searched for studies that report on the genotoxicity of ZnO NPs. Results: Several methods and different endpoints demonstrate the genotoxic potential of ZnO NPs. Most publications describe in vitro assessments of the oxidative DNA damage triggered by dissoluted Zn2+ ions. Most genotoxicological investigations of ZnO NPs address acute exposure situations. Conclusion: Existing evidence indicates that ZnO NPs possibly have the potential to damage DNA. However, there is a lack of long-term exposure experiments that clarify the intracellular bioaccumulation of ZnO NPs and the possible mechanisms of DNA repair and cell survival.


2019 ◽  
Vol 14 ◽  
pp. 100179 ◽  
Author(s):  
Shahnaz Majeed ◽  
Mohammed Danish ◽  
Muhammad Hisyamuddin Bin Ismail ◽  
Mohmmed Tahir Ansari ◽  
Mohamad Nasir Mohamad Ibrahim

2020 ◽  
Vol 1 (6) ◽  
pp. 1963-1970
Author(s):  
Hongjie Chen ◽  
Géraldine Albérola ◽  
Dominique de Caro ◽  
Christophe Faulmann ◽  
Muriel Golzio ◽  
...  

Soluble functionalized TTF·TCNQ nanoparticles do not induce cell death at concentrations up to 50 μg mL−1, a promising feature for biomedical devices.


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