Magnetic microspheres based on pectin coated by chitosan towards smart drug release

2021 ◽  
pp. 118013
Author(s):  
Thalia S.A. Lemos ◽  
Jaqueline F. de Souza ◽  
André R. Fajardo
2013 ◽  
Vol 13 (9) ◽  
pp. 1369-1380 ◽  
Author(s):  
Guangyan Qing ◽  
Minmin Li ◽  
Lijing Deng ◽  
Ziyu Lv ◽  
Peng Ding ◽  
...  

2013 ◽  
Vol 22 ◽  
pp. 31-40
Author(s):  
Jin Qiao Xu ◽  
Hai Xing Xu ◽  
Zubad Newaz ◽  
Ran Li ◽  
Yu Zhang ◽  
...  

A new method of reversible association of melphalan (MEL) to magnetic Fe3O4 nanoparticles preparing MEL magnetic microspheres was developed for magnetically targeted chemotherapy. The efficacy of this approach was evaluated in terms of encapsulation efficiency (EE), drug loading content (DLC), delivery properties and cytotoxicity in vitro. Magnetic Fe3O4 nanoparticles were synthesized by co-precipitation methods and characterized by X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and magnetization measurements. The MEL magnetic microspheres were obtained through emulsion cross-linking method and characterized by FTIR, magnetization measurements and scan electron microscopy (SEM). The EE and DLC were determined using a Spectro Vision DB-18805 spectrophotometer. The MEL magnetic microspheres showed good EE values, between 60.6% and 75.6%, as well as good DLC values, between 16.7% and 32.2%, and the magnetic properties were not significantly affected by incorporation of the drug. The in vitro drug release study was carried out in phosphate buffer solution (PBS), simulating physiologic body fluid conditions at 37o C with pH = 7.4. The release profiles showed an initial fast release rate, which decreased as time progressed; about 60% of the drug was released in the first 4 h, and about 78.23 % had been released after 24 h. The results indicated that the prepared magnetic microspheres may be useful for potential applications of MEL for magnetically targeted chemotherapy.


2016 ◽  
Vol 52 (74) ◽  
pp. 11151-11154 ◽  
Author(s):  
Liyang Shi ◽  
Yuanyuan Han ◽  
Jöns Hilborn ◽  
Dmitri Ossipov

A new self-healing hydrogel is developed using dynamic coordinate bonds between drug loaded MgSiO3 nanoparticles and bisphosphonate functionalized hyaluronic acid. The nanocomposite network is stable at neutral pH, but is disassembled in an acidic environment, providing “smart” drug release.


2019 ◽  
Vol 29 (31) ◽  
pp. 1901880 ◽  
Author(s):  
Lukáš Děkanovský ◽  
Roman Elashnikov ◽  
Markéta Kubiková ◽  
Barbora Vokatá ◽  
Václav Švorčík ◽  
...  

Nanoscale ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 5030-5037 ◽  
Author(s):  
Suyun He ◽  
Leixia Mei ◽  
Can Wu ◽  
Mingtao Tao ◽  
Ziran Zhai ◽  
...  

The integration of an anti-cancer drug bicalutamide with tissue-specific supramolecular self-assembly of peptide derivatives yielded in situ hydrogelation at prostate tissue for smart drug release.


Author(s):  
Akhilesh K. Singh ◽  
Thakur P. Yadav ◽  
Brijesh Pandey ◽  
Vinay Gupta ◽  
Satarudra P. Singh
Keyword(s):  

Biomolecules ◽  
2018 ◽  
Vol 8 (4) ◽  
pp. 103 ◽  
Author(s):  
Christian Tolle ◽  
Jan Riedel ◽  
Carina Mikolai ◽  
Andreas Winkel ◽  
Meike Stiesch ◽  
...  

Nanoparticles can be used as a smart drug delivery system, when they release the drug only upon degradation by specific enzymes. A method to create such responsive materials is the formation of hydrogel nanoparticles, which have enzymatically degradable crosslinkers. Such hydrogel nanoparticles were prepared by ionotropic gelation sodium alginate with lysine-rich peptide sequences—either α-poly-L-lysine (PLL) or the aggrecanase-labile sequence KKKK-GRD-ARGSV↓NITEGE-DRG-KKKK. The nanoparticle suspensions obtained were analyzed by means of dynamic light scattering and nanoparticle tracking analysis. Degradation experiments carried out with the nanoparticles in suspension revealed enzyme-induced lability. Drugs present in the polymer solution during the ionotropic gelation can be encapsulated in the nanoparticles. Drug loading was investigated for interferon- (IFN-) as a model, using a bioluminescence assay with MX2Luc2 cells. The encapsulation efficiency for IFN- was found to be approximately 25%. The nanoparticles suspension can be used to spray-coat titanium alloys (Ti-6Al-4V) as a common implant material. The coatings were proven by ellipsometry, reflection-absorption infrared spectroscopy, and X-ray photoelectron spectroscopy. An enzyme-responsive decrease in layer thickness is observed due to the degradation of the coatings. The Alg/peptide coatings were cytocompatible for human gingival fibroblasts (HGFIB), which was investigated by CellTiterBlue and lactate dehydrogenase (LDH) assay. However, HGFIBs showed poor adhesion and proliferation on the Alg/peptide coatings, but these could be improved by modification of the alginate with a RGD-peptide sequence. The smart drug release system presented can be further tailored to have the right release kinetics and cell adhesion properties.


Langmuir ◽  
2011 ◽  
Vol 27 (3) ◽  
pp. 1175-1180 ◽  
Author(s):  
Yujia Jing ◽  
Yihua Zhu ◽  
Xiaoling Yang ◽  
Jianhua Shen ◽  
Chunzhong Li

Author(s):  
Mingming Li ◽  
Xuyan Zhang ◽  
Shiping Zhan ◽  
Weimin Hou

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