Production and characterization of biocompatible nanofibrous scaffolds made of β-sitosterol loaded polyvinyl alcohol/tragacanth gum composites

2021 ◽  
Author(s):  
Salim Albukhaty ◽  
Hassan Al-Karagoly ◽  
alireza allafchian ◽  
Seyed Amir Hossein Jalali ◽  
Thair Alkelabi ◽  
...  

Abstract Electrospun polyvinyl alcohol and Tragacanth Gum were used to develop nanofibrous scaffolds containing poorly water-soluble beta-sitosterol. Different Concentration and Ratio of Polymeric composite: (10%) of β-S concentration in (PVA) 8 %, (TG) 0.5%, and 1% respectively were added, prepared and electrospun. The methods have included four parameters (Solution concentration, feeding rate, voltage, and distance of the collector to the tip of the needle) for designing and compared the nanofibers' average diameters. The nanofibers collected were identified via SEM, FTIR, and XRD measurements. A contact angle measurement described the hydrophilicity of the scaffold. MTT test was assessed for obtained nanofibers by using L929 normal fibroblast cells. The %age of mechanical strength, porosity, and deterioration of the scaffolds was well discussed. The average nanofibre ranged from 63 ± 20 nm to 97 ± 46 nm in diameters. The nanofibers loaded with β-S were freely soluble in water and displayed a short release lag time. The dissolution was related to an immediate dissolution, submicron-level recrystallization of β-S with sufficient conditions for nanofibers for L929 cell culture that could be used in biomedical applications. It concluded that electrospinning is a promising technique for poorly water-soluble β-S formulations that could be used in biomedical applications.

2015 ◽  
Vol 17 (1) ◽  
pp. 167-179 ◽  
Author(s):  
Chris Brough ◽  
Dave A. Miller ◽  
Justin M. Keen ◽  
Shawn A. Kucera ◽  
Dieter Lubda ◽  
...  

2016 ◽  
Vol 17 (1) ◽  
pp. 180-190 ◽  
Author(s):  
Chris Brough ◽  
Dave A. Miller ◽  
Daniel Ellenberger ◽  
Dieter Lubda ◽  
Robert O. Williams

INDIAN DRUGS ◽  
2021 ◽  
Vol 58 (02) ◽  
pp. 7-17
Author(s):  
Smita T. Kumbhar ◽  
◽  
Shitalkumar S. Patil ◽  
Manish S. Bhatia ◽  
Yogesh S. Thorata ◽  
...  

Polysaccharides demonstrate a wide diversity in their structural features as well as physicochemical properties owing to a variety of functional groups, chemical structure and a broad array of molecular mass. The most important feature of modified polysaccharides is their amphiphilic character which allows the application of these conjugates as an emulsifier, modifiers of surface in liposomes and micro/ nanoparticles, viscosity modifiers and drug delivery vehicles. Recently, the lipophilic modification of polysaccharides, which serve as a nano-container for water-insoluble or poorly water-soluble drugs, has gained attention in the biomedical applications due to their ability to form self-assembled nanoparticles. The natural polysaccharides are readily available, stable, biodegradable, economical, safe and biocompatible. It is difficult to synthesize compounds with such diversity in characteristics. In recent decades, many researchers have taken interest in polysaccharides and their derivatives for use in nanoparticulate systems. This review focuses on the chemical modification of mono and polysaccharides and the mechanisms involved in the formation of polysaccharide-based nanoparticles


2020 ◽  
Vol 55 ◽  
pp. 101401 ◽  
Author(s):  
Yoshiaki Umemoto ◽  
Shinya Uchida ◽  
Takatsune Yoshida ◽  
Ken Shimada ◽  
Hiroyuki Kojima ◽  
...  

2012 ◽  
pp. 31-35
Author(s):  
Truong Dinh Thao Tran ◽  
Ha Lien Phuong Tran ◽  
Nghia Khanh Tran ◽  
Van Toi Vo

Purposes: Aims of this study are dissolution enhancement of a poorly water-soluble drug by nano-sized solid dispersion and investigation of machenism of drug release from the solid dispersion. A drug for osteoporosis treatment was used as the model drug in the study. Methods: melting method was used to prepare the solid dispersion. Drug dissolution rate was investigated at pH 1.2 and pH 6.8. Drug crystallinity was studied using differential scanning calorimetric and powder X-ray diffraction. In addition, droplet size and contact angle of drug were determined to elucidate mechanism of drug release. Results: Drug dissolution from the solid dispersion was significantly increased at pH 1.2 and pH 6.8 as compared to pure drug. Drug crystallinity was changed to partially amorphous. Also dissolution enhancement of drug was due to the improved wettability. The droplet size of drug was in the scale of nano-size when solid dispersion was dispersed in dissolution media. Conclusions: nano-sized solid dispersion in this research was a successful preparation to enhance bioavailability of a poorly water-soluble drug by mechanisms of crystal changes, particle size reduction and increase of wet property.


Author(s):  
Meka Lingam ◽  
Vobalaboina Venkateswarlu

The low aqueous solubility of celecoxib (CB) and thus its low bioavailability is a problem.    Thus, it is suggested to improve the solubility using cosolvency and solid dispersions techniques. Pure CB has solubility of 6.26±0.23µg/ml in water but increased solubility of CB was observed with increasing concentration of cosolvents like PEG 400, ethanol and propylene glycol. Highest solubility (791.06±15.57mg/ml) was observed with cosolvency technique containing the mixture of composition 10:80:10%v/v of water: PEG 400: ethanol. SDs with different polymers like PVP, PEG were prepared and subjected to physicochemical characterization using Fourier-transform infrared (FTIR) spectroscopy, X-ray diffractometry (XRD), differential scanning calorimetry (DSC), solubility and dissolution studies. These studies reveals that CB exists mainly in amorphous form in prepared solid dispersions of PVP, PEG4000 and PEG6000 further it can also be confirmed by solubility and dissolution rate studies. Solid dispersions of PV5 and PV9 have shown highest saturation solubility and dissolution rate


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