2020
DOI: 10.1016/j.ijpharm.2020.119118
|View full text |Cite
|
Sign up to set email alerts
|

Gelatin nanoparticles for NSAID systemic administration: Quality by design and artificial neural networks implementation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
12
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
6
2
1

Relationship

1
8

Authors

Journals

citations
Cited by 23 publications
(12 citation statements)
references
References 47 publications
0
12
0
Order By: Relevance
“…When looking more closely at the obtained results, it is obvious that all NP formulations followed a biphasic release profile, with an initial fast release (burst effect) seen in the first 4–5 h, followed by a sustained release until the end (i.e., 15 days). The burst release observed initially can be attributed to the drug placed/absorbed on the surface of the NPs, while the following slow-release rate is probably due to the polyester’s glass–rubbery transition leading to variations in two moving release controlling fronts, i.e., swelling and erosion/degradation [ 52 ]. Nevertheless, results regarding the initial fast release presented in Figure 10 b showed that PTX’s burst effect was dependent on the type of polyester used, with PCL-XYL-based NPs showing the highest burst release, ~50% of the API was released in the first 5 h, followed by the PCL-PE and PCL-GLY with ~40% and ~20% of the API being released in the same timeframe.…”
Section: Resultsmentioning
confidence: 99%
“…When looking more closely at the obtained results, it is obvious that all NP formulations followed a biphasic release profile, with an initial fast release (burst effect) seen in the first 4–5 h, followed by a sustained release until the end (i.e., 15 days). The burst release observed initially can be attributed to the drug placed/absorbed on the surface of the NPs, while the following slow-release rate is probably due to the polyester’s glass–rubbery transition leading to variations in two moving release controlling fronts, i.e., swelling and erosion/degradation [ 52 ]. Nevertheless, results regarding the initial fast release presented in Figure 10 b showed that PTX’s burst effect was dependent on the type of polyester used, with PCL-XYL-based NPs showing the highest burst release, ~50% of the API was released in the first 5 h, followed by the PCL-PE and PCL-GLY with ~40% and ~20% of the API being released in the same timeframe.…”
Section: Resultsmentioning
confidence: 99%
“…The size of these nanoparticles can be modulated by adjusting the concentration of the gelatin solution, reaction time and temperature. 117 Lee et al studied the drug delivery of GNPs loaded three drugs (tizanidine hydrochloride, gatifloxacin, and fluconazole). 118 Particles were prepared via nanoprecipitation using distilled water and ethanol as solvents.…”
Section: Nanoprecipitationmentioning
confidence: 99%
“…When the collagen gel impregnated with polyester tetrahydrofuran solution contacts PBS, the water molecule will diffuse to the polymer chain in the hydrogel, so that it can form solid particle precipitation in the 3D dense collagen network. The size of these nanoparticles can be modulated by adjusting the concentration of the gelatin solution, reaction time and temperature . Lee et al.…”
Section: Preparation Of Gelatin Micro/nanostructuresmentioning
confidence: 99%
“…Koletti et al [119] compared two preparation methods (nanoprecipitation and two-step desolvation) of diclofenac sodium gelatin nanoparticles using two optimization techniques (multilinear regression and an ANN). It was proved by the experiment that the ANN with the standard BP algorithm showed a significantly improved ability for the prediction of particle size, ζ-potential and encapsulation efficiency (EE) compared to the multilinear regression.…”
Section: Selection and Optimization Of Formulationsmentioning
confidence: 99%