Enhanced curcumin solubility and antibacterial activity by encapsulation in PLGA oily core nanocapsules

2020 ◽  
Vol 11 (1) ◽  
pp. 448-455 ◽  
Author(s):  
Mengqian Gao ◽  
Xue Long ◽  
Jing Du ◽  
Mengting Teng ◽  
Weichen Zhang ◽  
...  

PLGA oily core CUR NCs show higher solubility, sustained release and enhanced antibacterial activity.

Author(s):  
Nanjunda Reddy B H ◽  
Prdadipta Ranjan Rauta ◽  
Venkatalakshimi V ◽  
Swamy Sreenivasa

 Objective: The main objective of this work was to formulate and evaluate Closite-30B/nanoAg filled hydrogel composites which are further intentended to be used for the study of drug delivery,antibacterial, and anticancer activityMethods: In this study, Cloisite-30B (C-30B) clay dispersed biopolymer sodium alginate (SA)-grafted-poly (acrylamide [AAm]-co-lignosulfonic acid) hydrogel composites were synthesized by free radical in situ polymerization reaction technique using SA, AAm, and lignosulfonic acid biopolymers in different proportions in combination. which are subjected to invitro drug delivery and Minimum inhibitory concentration(MIC) method for antibacterial activity study by using Streptococcus faecalis (S.faecalis) and Escherichia coli (E. coli)bacteria. The biocompatibility of the prepared gels were determined by standard protocol HaCaT-cells and MCF-7 cell lines further the prepared hydrogel composites were characterized for particle size,encapsulation efficiency,swelling properties,compatibility studies by FTIR etc.Results: The formulated hydrogels were characterized by X-ray diffraction (XRD) to analyze the particles size and crystallinity. The presence of functional groups and their chemical interaction with the drug, C-30B, and silver nanoparticles (AgNPs) were confirmed by the FTIR spectroscopy. Furthermore, the presence of AgNPs in the matrix was confirmed by ultraviolet/visible spectroscopy. Thermogravimetric analysis was performed to find out the thermal degradation, thermal stability, and the percentage of weight loss at various temperatures. Swelling studies revealed that C-30B and AgNPs induced composites exhibited higher swelling ratio than pure hydrogels. The hydrogels with C-30B/AgNPs displayed excellent antibacterial activity against both Gram-positive and Gram-negative bacteria. Further, these hydrogel composites were loaded with the drug paclitaxel (PT), and drug release study showed that the sustained release of the drug from C-30B/Ag hydrogel matrix compared to rest of other samples. Hydrogel composites were cytocompatible in nature (with HaCaT cells) and the cell viability decreased (with MCF-7cells) with the presence of lignosulfonic acid as well as C-30B and AgNPs in the samples as evaluated through 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide to its insoluble formazan assay.Conclusion: The synthesized hydrogel composites were successfully characterized and eavaluated for sustained release of paclitaxel drug delivery at different pHs and temperatures and it is found that C30B/Ag filled composites exhibits contolled release of drug with higher rate, especially at lower pH (pH2) and higher temperature (37oC) and the same formulations which exhibits better anitbcterial and anticancer activity compared to the virgin samples So the prepared C30B/AgNPs hydrogels composites used in drug dlivery for the effective treatment of cancer and used against bacterias and cancerous cells.


2019 ◽  
Vol 69 (6) ◽  
pp. 398-405 ◽  
Author(s):  
Ping Wu ◽  
Shi Hu ◽  
Qin Liang ◽  
Wang Guo ◽  
Yang Xia ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (97) ◽  
pp. 79820-79828 ◽  
Author(s):  
Ningning Xu ◽  
Derun Ding

A chitosan based material with a polyvinylpyrrolidone membrane was prepared and used to adsorb iodine. The resultant material exhibited the sustained-release of iodine, and significant antibacterial activity against E. coli and S. aureus.


RSC Advances ◽  
2015 ◽  
Vol 5 (122) ◽  
pp. 100682-100688 ◽  
Author(s):  
Feng Chen ◽  
Bin Yang ◽  
Chao Qi ◽  
Tuan-Wei Sun ◽  
Ying-Ying Jiang ◽  
...  

Amorphous calcium phosphate nanospheres with/without La doping are prepared and used for IgY storing, sustained release and antibacterial study.


2020 ◽  
Vol 26 (1) ◽  
pp. 84-98
Author(s):  
Yasutaka Shimotori ◽  
Masayuki Hoshi ◽  
Narihito Ogawa ◽  
Tetsuo Miyakoshi ◽  
Taisei Kanamoto

Abstract5-Acetoxy- and 5-hydroxyalkanethioamide analogues showed high antibacterial activity against Staphylococcus aureus. Antibacterial thioamides were prepared from 5-alkyl-δ-lactones by amidation, thionation, and subsequent deacetylation. Optically active thioamides with 99% diastereomeric excesses were prepared by diastereomeric resolution using Cbz-L-proline as the resolving agent. Antibacterial thioamides were slowly lactonized by a lipase catalyst. Therefore, these thioamides are potential sustained-release perfume compounds having antibacterial properties.


2013 ◽  
Vol 5 (10) ◽  
pp. 1400-1409 ◽  
Author(s):  
Dong Ma ◽  
Ting Wu ◽  
Jinglin Zhang ◽  
Minsong Lin ◽  
Wenjie Mai ◽  
...  

Author(s):  
Hakim Bangun

Objective: The aim of this study was to formulate floating gastroretentive of amoxicillin  using hard alginate capsules shell and to evaluate antibacterial activities of floating gastroretentive of amoxicillin.Methods: Alginate capsules shell were made by using sodium alginate 80-120 cP. Amoxicillin was prepared in solid dispersion to obtain sustained release requirement for 12 hours. Solid dispersion was prepared by solvent method using polyvinylpyrrolidone (PVP) K30. The solid dispersion was characterized by  X-ray diffraction and FTIR analysis.  The drug release test was carried out by using USP paddle method in simulated gastric fluid. Concentrations of amoxicillin were determined by using spectrophotometer UV at 272 nm. The antibacterial activity of  aliquots  dissolution were assessed by using agar plate diffusion method against Staphylococcus aureus and Escherichia coli as bacterial model.Results: The alginate capsules shell were made from sodium alginate 80-120 cP with size 0.  The dissolution test results showed that amoxicillin in the form of solid dispersions with weight  ratio amoxicillin with PVP K30 was 1:1 provided sustained release of amoxicillin during 12 hours, while the release of amoxicillin without solid dispersion was too slow.   The floating lag time was 0 minute and floating time was more than 12 hours. The X-ray diffraction pattern of amoxicillin solid dispersion had amorphous shape. Antibacterial activity test showed that the dissolution aliquots of amoxicillin solid dispersion were effective against  Staphylococcus aureus and Escherichia coli.Conclusions: Based on the results of this study, it is concluded that the alginate capsules shell can be used for preparation of floating gastroretentive of amoxicillin using amoxicillin solid dispersion and the dissolution aliqouts give antibacterial effect.Keywords: Floating; gastroretentive; alginate capsule; amoxicillin; solid dispersion; release; antibacterial  


2014 ◽  
Vol 131 (13) ◽  
pp. n/a-n/a ◽  
Author(s):  
Tao Liu ◽  
Ting Wu ◽  
Hongxi Liu ◽  
Bo Ke ◽  
Hongxing Huang ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-15
Author(s):  
Dexiong Li ◽  
Yubei Qiu ◽  
Sihui Zhang ◽  
Mi Zhang ◽  
Zexi Chen ◽  
...  

Treatments for infectious bone defects such as periodontitis require antibacterial and osteogenic differentiation capabilities. Nanotechnology has prompted the development of multifunctional material. In this research, we aim to synthesize a nanoparticle that can eliminate periodontal pathogenic microorganisms and simultaneously stimulate new bone tissue regeneration and mineralization. QAS-modified core-shell mesoporous silica containing Ag nanoparticles (Ag@QHMS) was successfully synthesized through the classic hydrothermal method and surface quaternary ammonium salt functionalization. The Ag@QHMS in vitro antibacterial activity was explored via coculture with Staphylococcus aureus, Escherichia coli, and Porphyromonas gingivalis biofilms. Bone mesenchymal stem cells (BMSCs) were selected for observing cytotoxicity, apoptosis, and osteogenic differentiation. Ag@QHMS showed a good sustained release profile of Ag+ and a QAS-grafted mesoporous structure. Compared with the single-contact antibacterial activity of QHMS, Ag@QHMS exhibited a more efficient and stable concentration-dependent antimicrobial efficacy; the minimum inhibitory concentration was within 100 μg/ml, which was below the BMSC biocompatibility concentration (200 μg/ml). Thus, apoptosis would not occur while promoting the increased expression of osteogenic-associated factors, such as runt-related transcription factor 2 (RUNX2), alkaline phosphatase (ALP), osteopontin (OPN), osteocalcin (OCN), bone sialoprotein (BSP), and collagen type 1 (COL-1). A safe concentration of particles can stimulate cell alkaline phosphatase and matrix calcium salt deposition. The dual antibacterial effect from the direct contact killing of QAS and the sustained release of Ag nanoparticles, along with the Ag-promoted osteogenic differentiation, had been verified and utilized in Ag@QHMS. This system demonstrates the potential for utilizing pluripotent biomaterials to treat complex lesions.


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