Herein, we present an elegant and simple method for significant improvement of eugenol water solubility using the polymers Soluplus and Lutrol F 127 as carriers and spray drying as an encapsulation method. The formulations were optimized by adding -inositol-a sweetening agent-and Aerosil 200 (colloidal, fumed silica)-an anticaking agent. The highest encapsulation efficiency of 97.9-98.2% was found for the samples containing 5% eugenol with respect to the mass of Soluplus. The encapsulation efficiencies of the spray-dried samples with 15% eugenol are around 90%. Although lowering the yield, the addition of Lutrol F 127 results in a more regular particle shape and enhanced powder flowability. The presence of Aerosil 200 and -inositol also improves the rheological powder properties. The obtained formulations can be used in various dosage forms like powders, granules, capsules, creams, and gels.
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http://dx.doi.org/10.3390/ph17091156 | DOI Listing |
Pharmaceuticals (Basel)
August 2024
Faculty of Chemistry and Pharmacy, Sofia University "St. Kliment Ohridski", 1 J. Bourchier Blvd., 1164 Sofia, Bulgaria.
Herein, we present an elegant and simple method for significant improvement of eugenol water solubility using the polymers Soluplus and Lutrol F 127 as carriers and spray drying as an encapsulation method. The formulations were optimized by adding -inositol-a sweetening agent-and Aerosil 200 (colloidal, fumed silica)-an anticaking agent. The highest encapsulation efficiency of 97.
View Article and Find Full Text PDFBiomed Phys Eng Express
March 2020
ARC Centre of Excellence for Electromaterials Science, Intelligent Polymer Research Institute, University of Wollongong, Wollongong, NSW 2522, Australia.
As scaffolds approach dimensions that are of clinical relevance, mechanical integrity and distribution becomes an important factor to the overall success of the implant. Hydrogels often lack the structural integrity and mechanical properties for use in vivo or handling. The inclusion of a structural support during the printing process, referred to as hybrid printing, allows the implant to retain structure and protect cells during maturation without needing to compromise its biological performance.
View Article and Find Full Text PDFDrug Dev Ind Pharm
November 2018
a School of Pharmacy , Ningxia Medical University, Yinchuan , PR China.
Objective: The objective of this study was to design and prepare a novel solid dispersion using spray congealing to achieve fast and synchronous dissolution of bufalin, cinobufagin, and resibufogenin, three therapeutically complementary drugs.
Methods: The solid dispersion was characterized with dissolution, X-ray diffractometry, and fourier transform infrared spectroscopy after preparation and storage for four weeks at different temperatures and relative humidity.
Results: It was found that all drugs were molecularly dispersed within matrix and had a significant enhancement (∼4-fold higher) of dissolution rate.
Drug Dev Ind Pharm
February 2018
a Department of Pharmaceutical Technology, School of Pharmacy, Faculty of Health Sciences , Aristotle University of Thessaloniki, Thessaloniki , Greece.
Unlabelled: Objective/significance: To elucidate the role of plasticizers in different mini matrices and correlate mechanical properties with drug release.
Methods: Cylindrical pellets were prepared by hot-melt extrusion (HME) and mini tablets by hot (HC) and ambient compression (AC). Venlafaxine HCl was the model drug, Eudragit RSPO the matrix former and citric acid or Lutrol F127 the plasticizers.
Drug Dev Ind Pharm
October 2017
a Department of Pharmaceutics , Sinhgad College of Pharmacy, Vadgaon , Pune, Maharashtra , India.
The aim of this study was to enhance the delivery of resveratrol to the brain through the transnasal route by cubosomes. Cubosomes were prepared using glycerol monooleate and Lutrol F127 by probe sonication method. A 3 full factorial design was used for optimization of cubosomes and batch containing 4% w/v glycerol monooleate and 1.
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