Characterization and in vitro cytotoxicity evaluation of fish scale and seashell derived nano-hydroxyapatite high-density polyethylene composite

2020 ◽  
pp. 096739112098155
Author(s):  
C Balaji Ayyanar ◽  
K Marimuthu ◽  
B Gayathri ◽  
Sankarrajan
Keyword(s):  
High Density Polyethylene ◽  
Mg63 Cell ◽  
In Vitro Cytotoxicity ◽  
High Density ◽  
Fish Scale ◽  
Scanning Calorimetry ◽  
Chemical Route ◽  
Polyethylene Composite ◽  
Cytotoxicity Studies

Hydroxyapatite (HAp) is the major inorganic component of natural bone which exhibits better biocompatibility with various kinds of cells and tissues, making it an ideal candidate for dental and orthopedic applications. The naturally extracted HAp (Ca10(PO4)6(OH)2) from fish scale and seashell is exactly matched with the chemical composition of bone minerals. Nowadays, soft chemistry is used for the synthesis of bioceramics such as HAp. This is a chemical route that yields more homogeneous solid-state materials. In this study, the extracted powder from fish scale and seashell was heated in the furnace and maintained at 700°C for 3 hours and the powder was naturally cooled. The derived CaO was used for preparing HAp by the microwave irradiation techniques. The HAp was filled with High-Density Polyethylene (HDPE) in the ratio of 10:3 (Matrix 100 g: Filler 30 g) and composite was fabricated by the injection molding. The functional groups present in the HAp-HDPE specimen was identified using Fourier Transform Infrared (FTIR) spectroscopy analysis. The thermal stability of 30 wt. % HAp-HDPE composite was analyzed using Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA). In vitro cytotoxicity studies were carried out using MG63 cell line. In these studies, five different volumes of liquid extracts of the prepared HAp-HDPE specimen having different concentrations (10, 20, 30, 40, and 50 μl) were allowed to interact with fresh cell culture medium for 24 hours. The cell morphology, cell viability, and the levels of cytotoxicity of the composite specimen were studied as per 10993:12, and ISO 10993:5 test standards.

Investigation on the morphology, thermal properties, and in vitro cytotoxicity of the fish scale particulates filled high-density polyethylene composite

2019 ◽  
Vol 28 (4) ◽  
pp. 285-296
Author(s):  
C Balaji Ayyanar ◽  
K Marimuthu
Keyword(s):  
High Density Polyethylene ◽  
Natural Fiber ◽  
Polymeric Materials ◽  
In Vitro Cytotoxicity ◽  
High Density ◽  
Thermoplastic Composites ◽  
Fish Scale ◽  
Scanning Calorimetry ◽  
Polyethylene Composite

The high-density polyethylene (HDPE) and fish scale particulates are in the ratio of 10:3 (matrix 100 g:filler 30 g) which is filled and blended with thermoplastic composites and are then fabricated by the injection molding machine. In this work, the thermal energy absorption is obtained as 103.9 J g−1 that melts onset temperature at 121.75°C and melts peak temperature at 129.98°C of the specimen using differential scanning calorimetry instrument. A gradual mass degradation and decomposition of the prepared samples were analyzed from the thermogravimetric analysis. Evaluation of microstructure, surface morphology, and elemental analysis was carried out using field emission scanning electron microscope. The presence of functional groups in the polymeric materials was identified using Fourier transform infrared spectroscopy. The cytotoxicity testing of composites has been carried out using MG 63 cell line. In these studies, five different volumes of liquid extract of the prepared specimen having different concentrations (10, 20, 30, 40, and 50 μL) were allowed to interact with fresh cell culture medium for 24 h. The cell viability, cell morphology, and the levels of cytotoxicity of the composite specimen were studied as per ISO 10993:12 and ISO 10993:5 test standards. It was found that the natural fiber filled composite showed none to slight cytotoxic reactivity to MG-63 cells after 24 h contact. The cytotoxicity level of fish scale particulate filled HDPE composite material was compared with standard reactivity level and it was confirmed to have low toxic level (none to slight).

scholarly journals in vitro Cytotoxicity examination of the seashell and fish scale substances embedded with high degree of compactness in polyethylene composite

2021 ◽  
Author(s):  
A Anandha Moorthy ◽  
◽  
Natarajan Nanjappan ◽  
C. Balaji Ayyanar ◽  
Dinesh D ◽  
...  
Keyword(s):  
Cell Viability ◽  
Polymer Matrix Composites ◽  
In Vitro Cytotoxicity ◽  
Filler Materials ◽  
Fish Scale ◽  
Matrix Composites ◽  
Polyethylene Composite ◽  
Test Standards ◽  
High Degree

The organic response of polymer composites is facilitated by adding natural filler materials. Several new composite formulations claim to reduce the environmental impact. The present study assessed the cytotoxic responses of seashell and fish scale filled composite materials. The Polyethylene high-density (PEHD), 30 wt. % of the seashell and 30 wt. % of a seashell and fish scale combinations blended with the polymer matrix composites with 10:3 proportion (PEHD 100 g:Reinforcements 30 g), and are then fabricated by the plastic injection molding machine. To better imitator the microstructure and the mineral component of natural bone, novel hydroxyapatite / polymer composite scaffolds are allowed to interact 10, 20, 30, 40 and 50 μl of standard fresh cell culture medium for 24 hours. Morphology of cell, cell viability, and the effect of Cytotoxicity on polyethylene based composite samples were examined through ISO 10993:5, and 10993:12 test standards. The percentage of cell viability and the level of toxicity were compared.

scholarly journals Quality by Design Optimization of Cold Sonochemical Synthesis of Zidovudine-Lamivudine Nanosuspensions

Pharmaceutics ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 367 ◽  
Author(s):  
Bwalya A. Witika ◽  
Vincent J. Smith ◽  
Roderick B. Walker
Keyword(s):  
Particle Size ◽  
Zeta Potential ◽  
Sodium Dodecyl ◽  
In Vitro Cytotoxicity ◽  
Polydispersity Index ◽  
Glycol Succinate ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Cytotoxicity Studies

Lamivudine (3TC) and zidovudine (AZT) are antiviral agents used to manage HIV/AIDS infection. The compounds require frequent dosing, exhibit unpredictable bioavailability and a side effect profile that includes hepato- and haema-toxicity. A novel pseudo one-solvent bottom-up approach and Design of Experiments using sodium dodecyl sulphate (SDS) and α-tocopheryl polyethylene glycol succinate 1000 (TPGS 1000) to electrosterically stablize the nano co-crystals was used to develop, produce and optimize 3TC and AZT nano co-crystals. Equimolar solutions of 3TC in surfactant dissolved in de-ionised water and AZT in methanol were rapidly injected into a vessel and sonicated at 4 °C. The resultant suspensions were characterized using a Zetasizer and the particle size, polydispersity index and Zeta potential determined. Optimization of the nanosuspensions was conducted using a Central Composite Design to produce nano co-crystals with specific identified and desirable Critical Quality Attributes including particle size (PS) < 1000 nm, polydispersity index (PDI) < 0.500 and Zeta potential (ZP) < −30mV. Further characterization was undertaken using Fourier Transform infrared spectroscopy, energy dispersive X-ray spectroscopy, differential scanning calorimetry, powder X-ray diffraction and transmission electron microscopy. In vitro cytotoxicity studies revealed that the optimized nano co-crystals reduced the toxicity of AZT and 3TC to HeLa cells.

scholarly journals Physical and Mechanical Properties of Tilapia Scale Hydroxyapatite-Filled High-Density Polyethylene Composites

Polymers ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 251
Author(s):  
C. N. Aiza Jaafar ◽  
I. Zainol ◽  
M. I. Izyan Khairani ◽  
T. T. Dele-Afolabi
Keyword(s):  
High Density Polyethylene ◽  
Mechanical Performance ◽  
Chemical Interaction ◽  
Biomedical Application ◽  
Flexural Modulus ◽  
Physical And Mechanical Properties ◽  
Filler Loading ◽  
In Vitro Cytotoxicity ◽  
High Density

The effects of filler loading and silane coupling agent on the properties of hydroxyapatite (HAp)-filled high density polyethylene (HDPE) composites have been studied. The (HAp) powder was successfully produced from tilapia scales using the spray drying process utilized to prepare the HDPE/HAp composites. The FTIR peaks for the untreated HDPE/30HAp composite corresponded to the functional groups of HDPE (C-CH3) and –CH2 and HAp (PO4−3 and O-H). The FTIR spectrum for the silane-treated composite showed that the C=O and silanol groups were eliminated, which strongly confirms the chemical interaction between the HAp fillers and the HDPE matrix. The developed composites demonstrated enhanced mechanical performance, and in particular the treated HDPE/30HAp-S composite exhibited superior tensile strength, Young’s modulus and flexural modulus of 28.26 MPa, 1272 MPa and 796 MPa, respectively. In vitro cytotoxicity analysis showed that the developed composites were non-toxic and have great potential to be used for biomedical application.

Mannose Conjugated Starch Nanoparticles for Preferential Targeting of Liver Cancer

2020 ◽  
Vol 17 ◽  
Author(s):  
Akhlesh Kumar Jain ◽  
Hitesh Sahu ◽  
Keerti Mishra ◽  
Suresh Thareja
Keyword(s):  
Side Effects ◽  
Liver Cancer ◽  
Entrapment Efficiency ◽  
Xrd Analysis ◽  
In Vitro Cytotoxicity ◽  
Physical Interaction ◽  
Scanning Calorimetry ◽  
Starch Nanoparticles

Aim: To design D-Mannose conjugated 5-Fluorouracil (5-FU) loaded Jackfruit seed starch nanoparticles (JFSSNPs) for site specific delivery. Background: Liver cancer is the third leading cause of death in world and fifth most often diagnosed cancer is the major global threat to public health. Treatment of liver cancer with conventional method bears several side effects, thus to undertake these side effects as a formulation challenge, it is necessary to develop novel target specific drug delivery system for the effective and better localization of drug into the proximity of target with restricting the movement of drug in normal tissues. Objective: To optimize and characterize the developed D-Mannose conjugated 5-Fluorouracil (5-FU) loaded Jackfruit seed starch nanoparticles (JFSSNPs) for effective treatment of liver cancer. Materials and methods: 5-FU loaded JFSSNPs were prepared and optimized formulation had higher encapsulation efficiency were conjugated with D-Mannose. These formulations were characterized for size, morphology, zeta potential, X-Ray Diffraction, and Differential Scanning Calorimetry. Potential of NPs were studied using in vitro cytotoxicity assay, in vivo kinetic studies and bio-distribution studies. Result and discussion: 5-Fluorouracil loaded NPs had particle size between 336 to 802nm with drug entrapment efficiency was between 64.2 to 82.3%. In XRD analysis, 5-FU peak was diminished in the diffractogram, which could be attributed to the successful incorporation of drug in amorphous form. DSC study suggests there was no physical interaction between 5- FU and Polymer. NPs showed sustained in vitro 5-FU release up to 2 hours. In vivo, mannose conjugated NPs prolonged the plasma level of 5-FU and assist selective accumulation of 5-FU in the liver (vs other organs spleen, kidney, lungs and heart) compared to unconjugated one and plain drug. Conclusion: In vivo, bio-distribution and plasma profile studies resulted in significantly higher concentration of 5- Fluorouracil liver suggesting that these carriers are efficient, viable, and targeted carrier of 5-FU treatment of liver cancer.

The Effect of Phase Transition Temperature on Therapeutic Efficacy of Liposomal Bortezomib

2020 ◽  
Vol 20 (6) ◽  
pp. 700-708
Author(s):  
Mitra Korani ◽  
Sara Nikoofal-Sahlabadi ◽  
Amin R. Nikpoor ◽  
Solmaz Ghaffari ◽  
Hossein Attar ◽  
...  
Keyword(s):  
Side Effects ◽  
Cell Line ◽  
Therapeutic Efficacy ◽  
Drug Loading ◽  
Particle Diameter ◽  
In Vitro Cytotoxicity ◽  
Liposomal Formulations ◽  
Cytotoxicity Studies ◽  
Anti Tumor Activity

Aims: Here, three liposomal formulations of DPPC/DPPG/Chol/DSPE-mPEG2000 (F1), DPPC/DPPG/Chol (F2) and HSPC/DPPG/Chol/DSPE-mPEG2000 (F3) encapsulating BTZ were prepared and characterized in terms of their size, surface charge, drug loading, and release profile. Mannitol was used as a trapping agent to entrap the BTZ inside the liposomal core. The cytotoxicity and anti-tumor activity of formulations were investigated in vitro and in vivo in mice bearing tumor. Background: Bortezomib (BTZ) is an FDA approved proteasome inhibitor for the treatment of mantle cell lymphoma and multiple myeloma. The low solubility of BTZ has been responsible for the several side effects and low therapeutic efficacy of the drug. Encapsulating BTZ in a nano drug delivery system; helps overcome such issues. Among NDDSs, liposomes are promising diagnostic and therapeutic delivery vehicles in cancer treatment. Objective: Evaluating anti-tumor activity of bortezomib liposomal formulations. Methods: Data prompted us to design and develop three different liposomal formulations of BTZ based on Tm parameter, which determines liposomal stiffness. DPPC (Tm 41°C) and HSPC (Tm 55°C) lipids were chosen as variables associated with liposome rigidity. In vitro cytotoxicity assay was then carried out for the three designed liposomal formulations on C26 and B16F0, which are the colon and melanoma cancer mouse-cell lines, respectively. NIH 3T3 mouse embryonic fibroblast cell line was also used as a normal cell line. The therapeutic efficacy of these formulations was further assessed in mice tumor models. Result: MBTZ were successfully encapsulated into all the three liposomal formulations with a high entrapment efficacy of 60, 64, and 84% for F1, F2, and F3, respectively. The findings showed that liposomes mean particle diameter ranged from 103.4 to 146.8nm. In vitro cytotoxicity studies showed that liposomal-BTZ formulations had higher IC50 value in comparison to free BTZ. F2-liposomes with DPPC, having lower Tm of 41°C, showed much higher anti-tumor efficacy in mice models of C26 and B16F0 tumors compared to F3-HSPC liposomes with a Tm of 55°C. F2 formulation also enhanced mice survival compared with untreated groups, either in BALB/c or in C57BL/6 mice. Conclusion: Our findings indicated that F2-DPPC-liposomal formulations prepared with Tm close to body temperature seem to be effective in reducing the side effects and increasing the therapeutic efficacy of BTZ and merits further investigation.

Recent Advances in Curcumin Nanocarriers for the Treatment of Different Types of Cancer with Special Emphasis on In Vitro Cytotoxicity and Cellular Uptake Studies

2020 ◽  
Vol 10 (5) ◽  
pp. 577-590
Author(s):  
Jai B. Sharma ◽  
Shailendra Bhatt ◽  
Asmita Sharma ◽  
Manish Kumar
Keyword(s):  
Cancer Cells ◽  
Cellular Uptake ◽  
Anticancer Agents ◽  
Targeted Delivery ◽  
In Vitro Cytotoxicity ◽  
Curcumin Nanoparticles ◽  
Cytotoxicity Studies ◽  
Delivery Technique ◽  
Different Types

Background: The potential use of nanocarriers is being explored rapidly for the targeted delivery of anticancer agents. Curcumin is a natural polyphenolic compound obtained from rhizomes of turmeric, belongs to family Zingiberaceae. It possesses chemopreventive and chemotherapeutic activity with low toxicity in almost all types of cancer. The low solubility and bioavailability of curcumin make it unable to use for the clinical purpose. The necessity of an effective strategy to overcome the limitations of curcumin is responsible for the development of its nanocarriers. Objective: This study is aimed to review the role of curcumin nanocarriers for the treatment of cancer with special emphasis on cellular uptake and in vitro cytotoxicity studies. In addition to this, the effect of various ligand conjugated curcumin nanoparticles on different types of cancer was also studied. Methods: A systematic review was conducted by extensively surfing the PubMed, science direct and other portals to get the latest update on recent development in nanocarriers of curcumin. Results: The current data from recent studies showed that nanocarriers of curcumin resulted in the targeted delivery, higher efficacy, enhanced bioavailability and lower toxicity. The curcumin nanoparticles showed significant inhibitory effects on cancer cells as compared to free curcumin. Conclusion: It can be concluded that bioavailability of curcumin and its cytotoxic effect to cancer cells can be enhanced by the development of curcumin based nanocarriers and it was found to be a potential drug delivery technique for the treatment of cancer.

Chitosan nanoparticles for tamoxifen delivery and cytotoxicity to MCF-7 and Vero cells

2011 ◽  
Vol 83 (11) ◽  
pp. 2027-2040 ◽  
Author(s):  
Neralakere Ramanna Ravikumara ◽  
Basavaraj Madhusudhan
Keyword(s):  
Particle Size ◽  
Chitosan Nanoparticles ◽  
Vero Cells ◽  
In Vitro Cytotoxicity ◽  
Correlation Spectroscopy ◽  
Scanning Calorimetry ◽  
Ζ Potential ◽  
Human Red Blood Cells ◽  
Tamoxifen Citrate

In this study, tamoxifen citrate-loaded chitosan nanoparticles (tamoxcL-ChtNPs) and tamoxifen citrate-free chitosan nanoparticles (tamoxcF-ChtNPs) were prepared by an ionic gelation (IG) method. The physicochemical properties of the nanoparticles were analyzed for particle size, zeta (ζ) potential, and other characteristics using photon correlation spectroscopy (PCS), zeta phase analysis light scattering (PALS), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), and differential scanning calorimetry (DSC). The variation in particle size was assessed by changing the concentration of chitosan, pentasodium tripolyphosphate (TPP), and the pH of the solution. The optimized tamoxcL-ChtNPs showed mean diameter of 187 nm, polydispersity of 0.125, and ζ-potential of +19.1 mV. The encapsulation efficiency (EE) of tamoxifen citrate (tamoxc) increased at higher concentrations, and release of tamoxc from the chitosan matrix displayed controlled biphasic behavior. Those tamoxcL-ChtNPs tested for chemosensitivity showed dose- and time-dependent antiproliferative activity of tamoxc. Further, tamoxcL-ChtNPs were found to be hemocompatible with human red blood cells (RBCs) and safe by in vitro cytotoxicity tests, suggesting that they offer promise as drug delivery systems in therapy.

An efficient l-proline catalyzed synthesis of pyrazolo[3,4-e][1,4]thiazepine derivatives and their in vitro cytotoxicity studies

2014 ◽  
Vol 24 (2) ◽  
pp. 553-562 ◽  
Author(s):  
A. Srikanth ◽  
S. Sarveswari ◽  
V. Vijayakumar ◽  
P. Gridharan ◽  
S. Karthikeyan
Keyword(s):  
In Vitro Cytotoxicity ◽  
Cytotoxicity Studies
Sign in / Sign up

Export Citation Format

Share Document