Rapid coating of Ti6Al4V at room temperature with a calcium phosphate solution similar to 10× simulated body fluid

2004 ◽  
Vol 19 (9) ◽  
pp. 2742-2749 ◽  
Author(s):  
A. Cuneyt Tas ◽  
Sarit B. Bhaduri
Keyword(s):  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Body Fluid ◽  
Room Temperature ◽  
Molar Ratio ◽  
Carbonate Content ◽  
Phosphate Solution ◽  
Phosphate Ions ◽  
Homogeneous Formation ◽  
Robust Process

In this paper, we report the utilization of high ionic strength (>1100 mM) calcium phosphate solutions in depositing 20–65-μm-thick, bonelike apatitic calcium phosphate on Ti6Al4V within 2–6 h, at room temperature. The super-strength solution used here multiplied the concentrations of calcium and phosphate ions in human plasma or simulated body fluid (SBF) by a factor of ten. The interesting features of the technique are given in the following. First, the solutions did not contain any buffering agents, such as Tris or Hepes. Second, during the process, homogeneous formation of calcium phosphate nano-clusters took place. However, their presence did not adversely affect the coating process. Third, other than simple surface treatments to begin with, no other additional intermediate steps were necessary. The only step needed after the preparation of the solution from reagents is the addition of proper amounts of NaHCO3 to raise the pH to 6.5 prior to the coating procedure. Fourth, there is no CO2 bubbling required, and hence, this is a robust process. Fifth, such a procedure led to a significant enhancement of coating rate enabling the formation in as little as 2–6 h. Coating proceeded with a linear rate. Sixth, the adhesion strength (12 ± 2 MPa) of the present coatings was comparable to coatings produced by soaking in 1.5× SBF solutions over a prolonged period of time, typically two to three weeks. Finally, the carbonate content (8 wt%) and Ca/P molar ratio (1.57) qualify the coating as bonelike.

scholarly journals Biphasic composite of calcium phosphate-based mesoporous silica as a novel bone drug delivery system

2019 ◽  
Vol 10 (2) ◽  
pp. 455-470 ◽  
Author(s):  
Magdalena Prokopowicz ◽  
Adrian Szewczyk ◽  
Adrianna Skwira ◽  
Rafał Sądej ◽  
Gavin Walker
Keyword(s):  
Drug Delivery ◽  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Mesoporous Silica ◽  
Drug Delivery System ◽  
Delivery System ◽  
Body Fluid ◽  
Molecular Surface ◽  
Molar Ratio ◽  
Mineralization Potential

AbstractWe reported the new biphasic composites of calcium phosphate and mesoporous silica material (CaP@MSi) in the form of powders and pellets as a potential bone drug delivery system for doxycycline hydrochloride (DOX). The CaP@MSi powders were synthesized by cationic surfactant-templating method. The effects of 10, 20, and 30% CaP content in the CaP@MSi powders on the molecular surface structure, the cytotoxicity against osteoblast cells in vitro, and the mineralization potential in simulated body fluid were investigated. The CaP@MSi characterized by the highest mineralization potential (30% CaP content) were used for DOX adsorption and pelletization process. The CaP which precipitated in the CaP@MSi composites was characterized as calcium-deficient with the Ca:P molar ratio between 1.0 and 1.2. The cytotoxicity assays demonstrated that the CaP content in MSi increases osteoblasts viability indicating the CaP@MSi (30% CaP content) as the most biocompatible. The combination of CaP and MSi was an effective strategy to improve the mineralization potential of parent material. Upon immersion in simulated body fluid, the CaP of composite converted into the bone-like apatite. The obtained pellets preserved the mineralization potential of CaP@MSi and provided the prolonged 5-day DOX release. The obtained biphasic CaP@MSi composites seem to have an application potential as bone-specific drug delivery system.

Effect of Other Oxides on Solubility and Bioactivity in Calcium Phosphate Glasses

2005 ◽  
Vol 284-286 ◽  
pp. 513-516 ◽  
Author(s):  
Min Chul Kim ◽  
Kyoung Nam Kim ◽  
Kwang Mahn Kim ◽  
Seong Ho Choi ◽  
Chong Kwan Kim ◽  
...  
Keyword(s):  
Weight Loss ◽  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Body Fluid ◽  
Potassium Acetate ◽  
Phosphate Glasses ◽  
Molar Ratio ◽  
Distilled Water ◽  
Ion Release ◽  
Buffer Solution

The development of phosphate glasses for use in orthopaedic implants has attracted much interest because their chemical and physical properties make them suitable for use as bone-bonding materials. We prepared various compositions of CaO-P2O5-MO or CaO-P2O5-M2O (M: K, Li, Na, Mg, Zn) glasses to measure ion release, solubility and bioactivity. The compositions with (Ca,M)/P molar ratio 0.6 were fixed P2O5 mol% content at 45.45 mol%, and varying MO or M2O mol% at 10, 20 and 30 mol%. Ca2+ ion release properties were investigated in 0.1M potassium acetate with pH 6 at 37oC by immersing 50 mg of powder into 100 ml of acidic buffer solution. The highest and lowest extent of released Ca2+ ion was observed for composition with 10 mol% of K2O and 30 mol% of MgO, respectively. The weight loss in distilled water at 37oC was measured. Solubility increased with decreasing CaO content, but decreased with increasing MgO content. Bioactivity in the simulated body fluid at 37oC was measured.

In vitro study of electron beam deposited calcium phosphate coating in simulated body fluid

2007 ◽  
Vol 22 (3) ◽  
pp. 621-626
Author(s):  
M. Hamdi ◽  
Ari Ide-Ektessabi ◽  
J.A. Toque
Keyword(s):  
Electron Beam ◽  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Body Fluid ◽  
In Vitro Study ◽  
Calcium Phosphate Coating ◽  
Carbonate Content ◽  
Apatite Formation ◽  
Calcium Phosphate Coatings

Calcium phosphate coatings prepared using the technique of electron beam deposition were immersed in a simulated body fluid for different periods of time to determine their response in vitro. The amorphous as-deposited coatings dissolved completely after a few days of immersion. After annealing in air at 700 °C, the dissolution of a small amount of amorphous phase in the crystalline coatings promotes the precipitation of bonelike apatite on the recessed regions by increasing the local supersaturation of calcium and phosphate ions. Formation of apatite was confirmed by the x-ray diffraction peaks at (200), (211), and (203) planes which grew after immersion in simulated body fluid. Fourier transform infrared results conformed to this with the increase in intensity of the absorption band at 1450 cm−1, signifying the increase in carbonate content. Scanning electron microscopy results showed spherical-shaped apatite nucleated on dissolved surface after 8 days of immersion. Sixteen days after immersion, almost 80% of the surface area was covered with apatite formation and grew to coalesce between neighboring particles forming an integrated platelike layer after 28 days. No obvious detachment between the grown layer and the underlying coating was observed.

IN-VITRO BEHAVIOUR OF BIPHASIC CALCIUM PHOSPHATE WITH DIFFERENT RATIO OF SILICA CONTENT IN SIMULATED BODY FLUID

2015 ◽  
Vol 23 (1) ◽  
pp. 1-14
Author(s):  
Sudirman Sahid ◽  
◽  
Nor Shahida Kader Bashah ◽  
Salina Sabudin ◽  
◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Body Fluid ◽  
Biphasic Calcium Phosphate ◽  
Silica Content

scholarly journals Pure hydroxyapatite synthesis originating from amorphous calcium carbonate

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Michika Sawada ◽  
Kandi Sridhar ◽  
Yasuharu Kanda ◽  
Shinya Yamanaka
Keyword(s):  
Calcium Carbonate ◽  
Calcium Phosphate ◽  
Room Temperature ◽  
Molar Ratio ◽  
Final Phase ◽  
Amorphous Calcium Carbonate ◽  
Phosphate Compound ◽  
Synthesis Strategy ◽  
Phosphorylation Reaction ◽  
Subsequent Calcination

AbstractWe report a synthesis strategy for pure hydroxyapatite (HAp) using an amorphous calcium carbonate (ACC) colloid as the starting source. Room-temperature phosphorylation and subsequent calcination produce pure HAp via intermediate amorphous calcium phosphate (ACP). The pre-calcined sample undergoes a competitive transformation from ACC to ACP and crystalline calcium carbonate. The water content, ACC concentration, Ca/P molar ratio, and pH during the phosphorylation reaction play crucial roles in the final phase of the crystalline phosphate compound. Pure HAp is formed after ACP is transformed from ACC at a low concentration (1 wt%) of ACC colloid (1.71 < Ca/P < 1.88), whereas Ca/P = 1.51 leads to pure β-tricalcium phosphate. The ACP phases are precursors for calcium phosphate compounds and may determine the final crystalline phase.

Effect of Electrical Polarization on the Behavior of Bioactive Glass Containing MgO and B2O3 in SBF

2006 ◽  
Vol 309-311 ◽  
pp. 333-336
Author(s):  
Emiko Amaoka ◽  
Erik Vedel ◽  
Satoshi Nakamura ◽  
Yusuke Moriyoshi ◽  
Jukka I. Salonen ◽  
...  
Keyword(s):  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Bioactive Glass ◽  
Body Fluid ◽  
Charged Surface ◽  
Depolarization Current ◽  
Electrical Polarization ◽  
Thermally Stimulated Depolarization Current ◽  
Thermally Stimulated Depolarization ◽  
Calcium Phosphate Precipitation

We investigated the electrical polarizability of MgO and B2O3 containing bioactive glass (MBG). The MBG material with good manufacturing properties but low bioactivity was electrically polarized at a high dc field. The electrical polarizability of MBG was evaluated by thermally stimulated depolarization current (TSDC) measurements and immersion in simulated body fluid (SBF). The early precipitation of calcium phosphate on the negatively charged surface of the treated MBG demonstrated the increased bioactivity of the material and confirmed its polarizability. It is suggested that the electrical interactions between the polarized MBG and ions in SBF promoted the formation of the calcium phosphate precipitation. Accordingly, the increased bioactivity of the MBG in SBF is suggested to demonstrate the conversion of MBG into electrovector ceramics by the polarization treatment.

Bioactivity Assessment of Apatite Nuclei-PVDF Composite Thin Films

2018 ◽  
Vol 782 ◽  
pp. 78-83
Author(s):  
Hasnat Zamin ◽  
Takeshi Yabutsuka ◽  
Shigeomi Takai
Keyword(s):  
Thin Films ◽  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Body Fluid ◽  
Polyvinylidene Fluoride ◽  
Solution Casting ◽  
Casting Technique ◽  
Doctor Blade ◽  
Solution Casting Technique ◽  
Hydroxyapatite Formation

Particles of calcium phosphate were precipitated by raising the temperature and the pH of simulated body fluid (SBF) named Apatite Nuclei (AN). AN and polyvinylidene fluoride (PVDF) composites thin films with different weight percentages of AN in PVDF were fabricated by solution casting technique, using doctor blade method. In order to assess the bioactivity, the thin films were soaked in simulated body fluid (SBF). It was found that the film containing 30 wt.% of AN in PVDF actively induced hydroxyapatite formation in 3 days soaking period in SBF.

Biodegradable Bone Cement Using Calcium Phosphate Glass

2006 ◽  
Vol 309-311 ◽  
pp. 861-864 ◽  
Author(s):  
Byung Hyun Lee ◽  
Min Chul Kim ◽  
Kyoung Nam Kim ◽  
Kwang Mahn Kim ◽  
Seong Ho Choi ◽  
...  
Keyword(s):  
Weight Loss ◽  
Compressive Strength ◽  
Calcium Phosphate ◽  
Simulated Body Fluid ◽  
Dissolution Rate ◽  
Phosphate Glass ◽  
Body Fluid ◽  
Setting Time ◽  
Ageing Test ◽  
Dynamic Assay

In preliminary ageing test, the cement using only calcium phosphate glass as power phase cracked with 1 day in simulated body fluid because of high dissolution rate of the cement. We added 30 wt% of either β-TCP or HA to 70 wt% calcium phosphate glass as powder phase to control the dissolution rate of the cement and performed in vitro ageing test in simulated body fluid by dynamic protocol as well as static protocol to confirm the possibility of controlling. Adding either β-TCP or HA to the cement increases the setting time and decreases the compressive strength. In dynamic assay, the pH of extract is maintained over 7. However, pH decreased to around 5 in static assay. Therefore, weight loss by static protocol continuously increased for 14 days, while weight loss by dynamic protocol almost saturated. In XRD patterns of ageing cements, CaO peaks appeared. CaO peak was maximized most lately in dynamic assay of the cement adding HA and within 7 days, the cement adding HA showed higher weight loss. It is indicated that CaO formed in surface of the cement hinder the dissolution of the cement. In addition, compressive strength increased when the CaO peak was maximized.

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