IgY-loaded calcium phosphate nanospheres: Preparation, sustained release and antibacterial activity

2015 ◽  
Vol 213 ◽  
pp. e115-e116 ◽  
Author(s):  
Xi Chen ◽  
Feng Chen ◽  
Xi-Ping Feng ◽  
Ying-Jie Zhu
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.


2014 ◽  
Vol 43 ◽  
pp. 92-96 ◽  
Author(s):  
Boren Lin ◽  
Huan Zhou ◽  
Douglas W. Leaman ◽  
Vijay K. Goel ◽  
Anand K. Agarwal ◽  
...  

RSC Advances ◽  
2018 ◽  
Vol 8 (52) ◽  
pp. 29526-29534 ◽  
Author(s):  
Dongqin Xiao ◽  
Fei Yang ◽  
Qiao Zhao ◽  
Shixiao Chen ◽  
Feng Shi ◽  
...  

A Cu/Zn co-incorporated BCP scaffold-derived GDF-5 sustained release system was successfully prepared and exhibited improved angiogenic and osteogenic capacities.


2014 ◽  
Vol 631 ◽  
pp. 326-331 ◽  
Author(s):  
Takeshi Yabutsuka ◽  
Kazuma Iwahashi ◽  
Hiroki Nakamura ◽  
Takeshi Yao

When either the pH or temperature of simulated body fluid (SBF) are raised, fine particles of calcium phosphate are precipitated. We found that these fine particles actively induce hydroxyapatite formation from body fluid or SBF and named the particles Apatite Nuclei. In this study, we fabricated hollow hydroxyapatite microcapsules by using Apatite Nuclei. We inserted vitamin B12 in the hollow microcapsule and examined thesustained-release properties.


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.


2016 ◽  
Vol 94 (7) ◽  
pp. 645-652 ◽  
Author(s):  
Amgad Hanna ◽  
Daniel L. Thompson ◽  
Daniel J. Hellenbrand ◽  
Jae-Sung Lee ◽  
Casey J. Madura ◽  
...  

Author(s):  
Ganesh Basarkar ◽  
Vijay Suryawanshi ◽  
Dinesh Hire

The objective of the present study was to control the release of freely water soluble Tramadol hydrochloride over a prolonged period of time by embedding the drug into novel wax matrix system. The matrix granules were prepared by melt granulation technique. The need for the administration two to four times a day when larger dose are required can decrease patient compliance. Sustained release formulation that would maintain plasma levels for 24 hrs for once daily dosing of Tramadol hydrochloride was prepared. The compatibility of the drug and wax examined using Differential Scanning Calorimetry (DSC) and Fourier Transform Infrared Spectrophotometer (FTIR). The effect of wax concentration (5 to 35%) and channeling agents (Avicel PH-101 and Di-calcium phosphate) on the in vitro drug release at 24 hrs. was studied.  Results of DSC confirmed drug-wax compatibility. Increasing the wax concentration resulted in a significant retardation of drug release. The drug release study revealed that the optimized formulation (F6) 30% novel wax sustained drug release for 24hrs. At the same wax concentration, drug release from tablets decreased with Di-calcium phosphate and increased with Avicel PH 101. Kinetic modeling of in vitro dissolution profiles revealed the drug release mechanism ranges from diffusion controlled or Fickian transport to anomalous type or non-Fickian transport. A hydrophobic matrix system is thus useful technique for prolonging the drug release of freely water soluble drugs such as Tramadol hydrochloride


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