ABSTRACT
This study reports the preparation of microspheres of pectin and magnetite nanoparticles coated by chitosan to encapsulate and deliver drugs. Magnetic-pectin microspheres were obtained by ionotropic gelation followed by polyelectrolyte complexation with chitosan. Characterization data show that magnetite changes the physicochemical and morphological properties of the microspheres compared to the non-magnetic samples. Using metamizole (Mtz) as a drug model, the magnetic microspheres showed appreciable encapsulation efficiency (85 %). Release experiments performed in simulated gastric (pH 1.2) and intestinal (pH 6.8) fluids suggested that the release process is pH-dependent. At pH 6.8, the Mtz release is favored achieving 75 % after 12â¯h. The application of an external magnetic field increased the release to 91 % at pH 6.8, indicating that the release also is magnetic-dependent. The results suggest that the magnetic microspheres based on pectin/chitosan biopolymers show the potential to be used as a multi-responsive drug delivery system.
Subject(s)
Chitosan/chemistry , Dipyrone/chemistry , Drug Delivery Systems/methods , Magnetite Nanoparticles/chemistry , Microspheres , Pectins/chemistry , Animals , Biopolymers/chemistry , Citrus sinensis/chemistry , Drug Compounding/methods , Drug Liberation , Gastrointestinal Contents/chemistry , Gels/chemistry , Humans , Hydrogen-Ion Concentration , Magnetic Fields , Spectroscopy, Fourier Transform Infrared/methodsABSTRACT
Waste coffee-grounds (WCG), a poorly explored source of biocompounds, were combined with chitosan (Cs) and poly(vinyl alcohol) (PVA) in order to obtain composites. Overall, WCG showed a good interaction with the polymeric matrix and good dispersibility up to 10â¯wt-%. At 5â¯wt-% WCG, the composite exhibited a noticeable enhancement (from 10 to 44%) of the adsorption of pharmaceuticals (metamizol (MET), acetylsalicylic acid (ASA), acetaminophen (ACE), and caffeine (CAF)) as compared to the pristine sample. The highest removal efficiency was registered at pH 6 and the removal followed the order ASAâ¯>â¯CAFâ¯>â¯ACEâ¯>â¯MET. For all pharmaceuticals, the adsorption kinetics was found to follow the pseudo-second order model, while the adsorption mechanism was explained by the Freundlich isotherm. Reuse experiments indicated that the WCG-containing composite has an attractive cost-effectiveness since it presented a remarkable reusability in at least five consecutive adsorption/desorption cycles.
Subject(s)
Chitosan/chemistry , Coffee/chemistry , Water Purification/methods , Acetaminophen/chemistry , Adsorption , Aspirin/chemistry , Caffeine/chemistry , Dipyrone/chemistry , Kinetics , Pharmaceutical Preparations/chemistryABSTRACT
An acid-dye colormetric method was described for the determination of chlorpromazine hydrochloride in the compound preparation. The method was based on the reaction of chlorpromazine hydrochloride with methyl orange, to form a yellow complex, which then was extracted by chloroform and exhibited a maximum absorption at 424 nm. The optimal conditions for determination were selected by orthogonal design test. The linear range of this method was 20-120 micrograms/ml (r = 0.9997). The average recovery of the three sample solutions of different concentrations was 99.72% +/- 0.46% (n = 6). The other ingredients of preparation do not interfere with chlorpromazine determination. This method is more sensitive and accurate and can be used for quality control of this compound preparation.