BioNanoScience, Journal Year: 2025, Volume and Issue: 15(2)
Published: March 20, 2025
Language: Английский
BioNanoScience, Journal Year: 2025, Volume and Issue: 15(2)
Published: March 20, 2025
Language: Английский
Drug Delivery and Translational Research, Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 10, 2024
Language: Английский
Citations
6Expert Opinion on Drug Delivery, Journal Year: 2024, Volume and Issue: 21(10), P. 1479 - 1490
Published: Oct. 2, 2024
Nanoparticles (NPs) are widely used in the pharmaceutical field to treat various human disorders. Among these, lipid-based NPs (LNPs), including solid lipid nanoparticles (SLN) and nanostructured carriers (NLC), favored for drug/bioactive delivery due their high stability, biocompatibility, encapsulation efficiency, sustained/controlled release. These properties make them particularly suitable as of compounds derived from plant sources.
Language: Английский
Citations
6International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 272, P. 132888 - 132888
Published: June 1, 2024
Language: Английский
Citations
5International Journal of Pharmaceutics, Journal Year: 2024, Volume and Issue: 667, P. 124919 - 124919
Published: Nov. 7, 2024
Language: Английский
Citations
5BioNanoScience, Journal Year: 2024, Volume and Issue: 14(3), P. 3496 - 3521
Published: Aug. 13, 2024
Language: Английский
Citations
4International Journal of Applied Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 82 - 91
Published: Jan. 7, 2025
Objective: Rosuvastatin calcium, a BCS class II drug with low solubility, was optimized using central composite design to improve its bioavailability. Methods: The study utilized Kolliphor RH 40 as an emulsifier and glyceryl monostearate solid lipid in preparing nanoparticle dispersion, optimizing formulations based on mean dissolution time entrapment efficiency. Results: analyzed the efficiency of prepared nanoparticles. range found 7.1+0.5 8.9+0.6 h. highest be 90.28%, standard deviation 0.2. linear model chosen data precision trend, while quadratic selected for time. 3D view graph indicated model/equation followed by formulations. formulation had particle size 16.16+10 nm distribution index 0.729+002, indicating high homogeneity. Transmission electron microscopy images dynamic light scattering were correlation. XRD, DSC used analyze drug's transformation into amorphous form. profile different plotted, Korsmeyer-Peppas model. FTIR showed peaks, no interaction. Conclusion: suggested that bioavailability rosuvastatin calcium can enhanced through preparation nanoparticles smaller sustained release rosuvastatin.
Language: Английский
Citations
0International Journal of Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 125203 - 125203
Published: Jan. 1, 2025
Language: Английский
Citations
0Journal of Drug Delivery Science and Technology, Journal Year: 2025, Volume and Issue: 105, P. 106612 - 106612
Published: Jan. 9, 2025
Language: Английский
Citations
0Journal of Pharmaceutical Sciences, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
0Therapeutic Delivery, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 11
Published: Jan. 28, 2025
Aim The study aimed to formulate solid lipid nanoparticles (SLNs) for the transdermal delivery of PPL improve skin retention and efficacy.
Language: Английский
Citations
0