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Extraction and Analysis of Taiwanese Green Propolis
Published on: January 7, 2019
Propolis-Loaded Niosomes for Dermopharmaceutic and Cosmetic Applications: Development, Stability, Safety, and In
Maria Beatriz Pinto1, Patrícia C Pires1,2,3, Mafalda Correia1,2
1Department of Pharmaceutical Technology, Faculty of Pharmacy of the University of Coimbra, University of Coimbra, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.
Researchers developed propolis-loaded niosomes for topical delivery. These novel nanocarriers show promising stability, controlled release, and anti-inflammatory effects, suitable for therapeutic and cosmetic uses.
Area of Science:
- * Pharmaceutical Nanotechnology
- * Materials Science
- * Cosmetic Science
Background:
- * Propolis, a bee-derived substance, contains phenolic compounds with diverse therapeutic properties (analgesic, anti-inflammatory, antioxidant, antibacterial).
- * Niosomes are advanced vesicular nanosystems for topical drug delivery, offering controlled release, enhanced stability, and good biocompatibility.
- * There is a growing interest in utilizing propolis for therapeutic and cosmetic applications, necessitating effective delivery systems.
Purpose of the Study:
- * To formulate and characterize novel propolis-loaded niosomes for topical application.
- * To achieve small, homogeneous particle size, high encapsulation efficiency, and controlled release kinetics.
- * To evaluate the safety and bioactivity (anti-inflammatory potential) of the developed niosomal formulations.
Main Methods:
- * Formulation of niosomes using Tween 20, Kolliphor RH 40, cetyl alcohol, and/or cholesterol via thin-film hydration and extrusion.
- * Characterization of particle size, polydispersity index (PDI), and zeta potential (ζ-potential).
- * Assessment of encapsulation efficiency, in vitro release profile, in vitro safety (keratinocytes, fibroblasts), HET-CAM irritation test, and in vitro anti-inflammatory activity.
Main Results:
- * Niosomes exhibited small particle size (100-200 nm), homogeneous distribution (PDI < 0.2), and favorable ζ-potential (~ -38 mV).
- * High encapsulation efficiency (78.8–87.4%) and controlled release profiles were achieved, ensuring prolonged bioactivity.
- * Formulations demonstrated adequate in vitro safety and significant anti-inflammatory potential (IC50: 14.90–17.89 ng/mL), with some showing low irritative potential.
Conclusions:
- * Novel propolis-loaded niosomes were successfully developed, meeting quality by design (QbD) criteria for topical applications.
- * The nanoplatforms offer enhanced stability, controlled release, and demonstrated safety and anti-inflammatory efficacy.
- * These versatile niosomal formulations hold potential for both pharmaceutical and cosmetic industries.
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