Self hardening glass carbomer composition
A carbomer and self-hardening technology, applied in tissue regeneration, surgical adhesives, dental preparations, etc., can solve the problems of insufficient strength, wear sensitivity and poor aesthetics, and achieve low solubility, easy polishing, and short hardening the effect of time
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Embodiment 1
[0044] The following compositions were prepared using the following ingredients:
[0045] (a) polydimethylsiloxane with dynamic viscosity of 1000cSt, represented by S20;
[0046] (b) conventional fluorosilicate glass powder; and
[0047] (c) Aqueous solutions of conventional polyacrylates.
[0048] The fluorosilicate glass powder and polyacrylate aqueous solution used to prepare the compositions were from 3MESPE's A3 APLICAP capsules.
[0049] The amounts of the various ingredients are listed in Table 1, where 5% by weight of additional fluorosilicate glass powder corresponds to about 0.015 g of fluorosilicate glass powder and where 0.0015 g of S20 corresponds to about 1.6% of additional liquid, Add to conventional aqueous polyacrylate solution (ca. 0.0920 g).
[0050] product
Embodiment 2
[0052] The composition prepared in Example 1 was evaluated for in vitro wear using the ACTA-Abraser, a three-body wear system designed to simulate the wear that occurs in the oral cavity (see de Gee et al., 1994, 1996). Two reference materials (IFMC and KPFA; KPFA is KetacMolar from 3M ESPE ) as a comparative test. In the test, two wheels (the first wheel contains the sample to be tested, while the second wheel is the counter teeth) rotate in different directions, but there is a 15% difference in peripheral speed (called slip distance), and at the same time Close contact. The test sample is placed on the circumference of the first wheel. The force of the interaction of the two wheels is adjusted to be about 15N. Both wheels were placed in a slurry of rice flour and white rice husk sprayed in a buffer solution. In the abrasion test, food is squeezed between the wheels, creating scuff marks on the test sample, leaving an untouched area on either side of the control to test...
Embodiment 3
[0057] Solubility testing was performed in this example. The test was performed as follows. A hardened sample weight of about 0.4 to about 0.6 cm in diameter and about 1 to about 1.5 mm in thickness was determined as a reference. In the test, the samples were immersed in water of various pH values, where the pH was adjusted with citric acid. Tested at pH 2.5 as it is similar to the pH that exists between molars. The test runs for approximately 15 days. The weight of the test sample is determined at several time intervals, where a greater weight loss indicates a higher solubility of the material. Data are expressed as % solubility (calculated from original weight and weight loss at the indicated stages) and are shown in Table 3.
[0058] time (h)
[0059] As can be seen from the data in Table 3, the samples prepared according to the composition of the present invention have improved solubility properties compared with the commercially available material KPFA.
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