Facile synthesis, microstructure, formation mechanism, in vitro biocompatibility, and drug delivery property of novel dendritic TiO2 nanofibers with ultrahigh surface area

2020 ◽  
Vol 115 ◽  
pp. 111100
Author(s):  
Song Chen ◽  
Lulu Shen ◽  
Di Huang ◽  
Juan Du ◽  
Xiaoxu Fan ◽  
...  
2021 ◽  
Vol 89 (2) ◽  
pp. 15
Author(s):  
M. R. Mozafari ◽  
E. Mazaheri ◽  
K. Dormiani

Introduction: Bioactive encapsulation and drug delivery systems have already found their way to the market as efficient therapeutics to combat infections, viral diseases and different types of cancer. The fields of food fortification, nutraceutical supplementation and cosmeceuticals have also been getting the benefit of encapsulation technologies. Aim: Successful formulation of such therapeutic and nutraceutical compounds requires thorough analysis and assessment of certain characteristics including particle number and surface area without the need to employ sophisticated analytical techniques. Solution: Here we present simple mathematical formulas and equations used in the research and development of drug delivery and controlled release systems employed for bioactive encapsulation and targeting the sites of infection and cancer in vitro and in vivo. Systems covered in this entry include lipidic vesicles, polymeric capsules, metallic particles as well as surfactant- and tocopherol-based micro- and nanocarriers.


Author(s):  
Manohar D Mullassery ◽  
Noeline B Fernandez ◽  
Surya R ◽  
Diana Thomas

Objective: The scope of the present study was the preparation and characterization of a novel composite acrylamide β-cyclodextrin grafted 3-aminopropyltriethoxysilane bentonite (AMCD-g-APSB), for the controlled delivery of curcumin (CUR).Methods: AMCD-g-APSB, was synthesized by solvent-free conditions using microwave irradiation. The structure and surface morphology of the composite was established using Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, thermal analysis, etc.Results: The swelling percentage of the composite depends on both time and pH of the medium. The maximum swelling of the composite occurred at a pH of 7.4. The maximum drug encapsulation was occurring at a pH 3. About 96.5% of drug was loaded at pH 3. In vitro biocompatibility study was performed, and the result showed good biocompatibility of the composite in the concentration range 2.5–50 μg/ml.Conclusions: Drug delivery study of the composite proved that CUR could be successfully released in a controlled manner in the colon without much loses of the drug in the stomach.


RSC Advances ◽  
2015 ◽  
Vol 5 (121) ◽  
pp. 100256-100267 ◽  
Author(s):  
Jue Hu ◽  
Molamma P. Prabhakaran ◽  
Lingling Tian ◽  
Xin Ding ◽  
Seeram Ramakrishna

Emulsion electrospun drug–PCL nanofibrous mats were demonstrated as better drug delivery substrates and tissue engineering scaffold compared to PHBV nanofibers.


2012 ◽  
Vol 55 ◽  
pp. 131-137 ◽  
Author(s):  
Inmaculada Salcedo ◽  
Carola Aguzzi ◽  
Giuseppina Sandri ◽  
Maria C. Bonferoni ◽  
Michela Mori ◽  
...  

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