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Fig 1.

Alginate cross-linking.

Ionic cross-linking of sodium alginate sol in contact with calcium ions.

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Fig 1 Expand

Fig 2.

Internal gelation process.

Schematic workflow of alginate beads production by internal gelation. Using emulsification and an internal initiated gelation to produce beads in a mean size of 200–500 μm.

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Fig 2 Expand

Fig 3.

200–400 μm sized alginate beads.

Light optical microscope picture of 200–400 μm sized alginate beads produced by internal gelation.

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Fig 3 Expand

Fig 4.

Ultrasonic spray technique.

Schematic workflow of alginate beads production by ultrasonic activation.

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Fig 4 Expand

Fig 5.

50 μm sized alginate beads.

Light optical microscope picture of 50 μm sized alginate particles produced by ultrasonic activation.

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Fig 5 Expand

Table 1.

Content of artificial saliva.

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Table 1 Expand

Table 2.

Calibration standards of HPLC.

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Table 2 Expand

Table 3.

Samples for initial screening.

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Table 3 Expand

Table 4.

Sample definition of alginate and PLGA beads.

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Table 5.

Influence of different CHX-concentrations.

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Table 5 Expand

Table 6.

Influence of different loading times.

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Table 6 Expand

Table 7.

Combinations of different particle sizes.

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Table 7 Expand

Fig 6.

CHX release profiles of different sized alginate beads.

Cumulative CHX release of initial screening measurements (HPLC) over 120 h (n = 1 samples each). CHX release was determined from different sized alginate based particles.

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Fig 6 Expand

Fig 7.

CHX release profiles of different biodegradable materials.

Cumulative CHX release of 50 μm sized PLGA and 50 μm sized alginate particles over 630 h (mean ± SD, n = 5 samples each).

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Fig 7 Expand

Fig 8.

CHX release profiles of different CHX concentrations.

Cumulative CHX release of over 630 h (n = 5 samples each). Loading 50 μm sized alginate based particles for 24h in 10% and 20% concentrated CHX. (mean ± SD, n = 5 samples each).

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Fig 8 Expand

Fig 9.

Initial CHX release profiles of different CHX concentrations.

Cumulative CHX release of initial screening measurements (HPLC) over 20 h. Detailed view on the initial releasing profile of different loaded (10% and 20% CHX) particles. (mean ± SD, n = 5 samples each). (Compare Fig 8).

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Fig 9 Expand

Fig 10.

Initial CHX release profiles of different loading times.

Cumulative CHX release over 35 h from 200–400 μm sized alginate beads loaded for 1 min, 30 min, 6 h and 24 h and compared with Periochip and Chlosite (mean ± SD, n = 5 samples each).

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Fig 10 Expand

Fig 11.

CHX release profiles of different loading times.

Cumulative CHX release over 400 h from 200–400 μm sized alginate beads loaded for 1 min, 30 min, 6 h and 24 h and compared with Periochip and Chlosite (mean ± SD, n = 5 samples each).

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Fig 11 Expand

Fig 12.

Normed CHX release profiles of different loading times.

Normed cumulative CHX release over 400 h and 20 h from 200–400 μm sized alginate beads loaded for 1 min, 30 min, 6 h and 24 h and compared with Periochip and Chlosite (n = 5 samples each).(mean ± SD, n = 5 samples each).

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Fig 12 Expand

Fig 13.

CHX release profiles of bead combinations.

Cumulative CHX release over 400 h from alginate bead combinations, sized 50 μm and 200–400 μm in ratio 30/70 w/w and 50/50 w/w compared with Periochip (mean ± SD, n = 5 samples each).

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Fig 13 Expand

Fig 14.

Initial CHX release profiles of bead combinations.

Cumulative CHX release over 20 h from alginate bead combinations, sized 50 μm and 200–400 μm in ratio 30/70 w/w and 50/50 w/w compared with Periochip (mean ± SD, n = 5 samples each).

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Fig 14 Expand