Effect of nanoemulsion-loaded hybrid biopolymeric hydrogel beads on the release kinetics, antioxidant potential and antibacterial activity of encapsulated curcumin

2021 ◽  
pp. 131925
Author(s):  
Pawandeep Kour ◽  
Saima Afzal ◽  
Adil Gani ◽  
Mohammed Iqbal Zargar ◽  
Umar Nabi Tak ◽  
...  
2020 ◽  
Vol 145 ◽  
pp. 466-475 ◽  
Author(s):  
Abdelkrim Soumia ◽  
Mokhtar Adel ◽  
Sardi Amina ◽  
Boukoussa Bouhadjar ◽  
Djelad Amal ◽  
...  

Author(s):  
SHUSHIL BHUSAL ◽  
KHAGA RAJ SHARMA

Objectives: The present study was designed to investigate the phytochemical analysis, antioxidant potential, and antibacterial activities of the traditionally used medicinal plant Glycyrrhiza glabra. Methods: The plant secondary metabolites were extracted through cold percolation using methanol (MeOH) as a solvent. The MeOH extract was further fractionated in different solvents in increasing order of polarity. The antioxidant activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl assay. The antibacterial activity was studied by agar well diffusion method. Results: The antioxidant potential IC50 was found 43.13, 104.83, and 200.11 μg/ml for ethyl acetate (EtOAc), MeOH, and chloroform (CHCl3) extracts, respectively. The EtOAc fraction showed the potent antioxidant with IC50 43.13 μg/ml compared to the standard ascorbic acid 58.76 μg/ml. The antimicrobial activity exhibited by MeOH extract against Bacillus subtilis (ATCC 6051) and Staphylococcus aureus (ATCC 6538P) zone of inhibition was 18 mm and 17 mm, for chloroform extracts 15 mm and 13 mm, and for EtOAc fraction 11 mm against Bacillus subtilis. The highest dilution that yielded no single bacteria colony on the nutrient agar plates for Bacillus subtilis and S. aureus of MeOH extract was found 0.39 mg/ml and 6.25 mg/ml, for chloroform extract 3.125 mg/ml and 6.25 mg/ml and EtOAc fraction against Bacillus subtilis was 12.50 mg/ml as minimum bactericidal concentration. Conclusion: The plant extracts showed potent antioxidant and antibacterial activity. The results support for using the G. glabra in bacterial infection which provides partial scientific validation for using the plant against bacterial infections.


2021 ◽  
Vol 1225 ◽  
pp. 129095
Author(s):  
Samira Alinavaz ◽  
Gholam Reza Mahdavinia ◽  
Hessam Jafari ◽  
Maryam Hazrati ◽  
Ali Akbari

2020 ◽  
Vol 109 ◽  
pp. 106104
Author(s):  
Dariusz Kowalczyk ◽  
Monika Pytka ◽  
Urszula Szymanowska ◽  
Tomasz Skrzypek ◽  
Katarzyna Łupina ◽  
...  

Molecules ◽  
2016 ◽  
Vol 21 (8) ◽  
pp. 1008 ◽  
Author(s):  
Gianmaria Ferrazzano ◽  
Tiziana Cantile ◽  
Marco Coda ◽  
Brunella Alcidi ◽  
Giancarla Sangianantoni ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
pp. 38-45 ◽  
Author(s):  
Santoshi Naik ◽  
Prasiddhi Raikar ◽  
Mohammed Gulzar Ahmed

In the present study an attempt has been made to formulate and evaluate a sustained release periodontal film of Sparfloxacin with biodegradable, cost effective polymer Chitosan. The objective of the study was to formulate intra-pocket periodontal films, which could be easily placed into the periodontal pocket, and thus be capable of delivering therapeutic concentrations of drug. Sparfloxacin is an antibiotic, showing wide spectrum antibacterial activity against a number of periodontal pathogens. Hence Sparfloxacin is selected as model for site specific delivery, i.e., into periodontal pocket for the treatment of periodontitis. In the present investigation Chitosan films containing Sparfloxacin were prepared by solution casting method using acetic acid. The copolymers HPMC K4M, Sodium CMC and Eudragit RL 100 in the concentrations of 10%, 20% and 30% w/w of Chitosan were added into the polymeric solution. Propylene glycol was used as plasticizer. FT-IR and UV spectroscopic methods revealed no interaction between Sparfloxacin and polymers. The drug loaded films were evaluated for their thickness, weight variation, content uniformity, tensile strength, percent elongation, percentage moisture loss, surface pH, folding endurance, in- vitro drug release studies, in - vitro antibacterial activity and stability studies. Periodontal films showed initial burst release of drug on 1st day and then the release was sustained for a period of 8 days. In – vitro antibacterial activity was carried out on staphylococcus aureus and the antibacterial activity was retained for 96 hours. In - vitro release from periodontal films was fit to kinetic models to reveal drug release kinetics. Keywords: Periodontitis, Sparfloxacin, Bio-adhesive polymers.


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