scholarly journals Encapsulation of Metronidazole in Biocompatible Macrocycles and Structural Characterization of Its Nano Spray-Dried Nanostructured Composite

Molecules ◽  
2021 ◽  
Vol 26 (23) ◽  
pp. 7335
Author(s):  
Mirella Mirankó ◽  
Mónika Megyesi ◽  
Zsombor Miskolczy ◽  
Judit Tóth ◽  
Tivadar Feczkó ◽  
...  

Due to the great potential of biocompatible cucurbit[7]uril (CB7) and 4-sulfonatocalix[4]arene (SCX4) macrocycles in drug delivery, the confinement of the pharmaceutically important metronidazole as an ionizable model drug has been systematically studied in these cavitands. Absorption and fluorescence spectroscopic measurements gave 1.9 × 105 M−1 and 1.0 × 104 M−1 as the association constants of the protonated metronidazole inclusion in CB7 and SCX4, whereas the unprotonated guests had values more than one order of magnitude lower, respectively. The preferential binding of the protonated metronidazole resulted in 1.91 pH unit pKa diminution upon encapsulation in CB7, but the complexation with SCX4 led to a pKa decrease of only 0.82 pH unit. The produced protonated metronidazole–SCX4 complex induced nanoparticle formation with protonated chitosan by supramolecular crosslinking of the polysaccharide chains. The properties of the aqueous nanoparticle solutions and the micron-sized solid composite produced therefrom by nano spray drying were unraveled. The results of the present work may find application in the rational design of tailor-made self-assembled drug carrier systems.

2002 ◽  
Vol 7 (2) ◽  
pp. 147-153 ◽  
Author(s):  
Ami Teague Deaton ◽  
LaTarsha D. Jones ◽  
Craig A. Dunbar ◽  
Anthony J. Hickey ◽  
Dennis M. Williams

2016 ◽  
Vol 66 (1) ◽  
pp. 147-153 ◽  
Author(s):  
Jarosław Ciekot ◽  
Tomasz Marek Goszczyński ◽  
Janusz Boratyński

AbstractPemetrexed (PMX) is an antifolate drug utilized in the treatment of non-small cell lung cancer. For studies of potential macromolecular carriers for PMX, fast and precise methods were developed to determine the bound and free drug contained in investigated conjugate preparations. The analysis of the total amount of PMX in conjugates was based on absorption spectrophotometry. The linearity was found in the range of 4.697–46.97 μmol L−1PMX. The limit of quantitation was 1.070 μmol L−1. The method for the analysis of unbound PMX was based on size-exclusion chromatography and detection at 225 nm. This method shows linear range of 2.230–223.0 μmol L−1.LOQwas 0.539 μmol L−1. The proposed methods can be used both for the characterization of the polysaccharide based conjugates of PMX and for the determination of conjugate drug release profiles.


2012 ◽  
Vol 188 ◽  
pp. 1-14 ◽  
Author(s):  
Chau Chun Beh ◽  
Raffaella Mammucari ◽  
Neil R. Foster

Author(s):  
Abraham Domb ◽  
Neeraj Kumar ◽  
Tzviel Sheskin ◽  
Alfonso Bentolila ◽  
Joram Slager ◽  
...  

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