Orthogonal Optimization and Physicochemical Characterization of Water-Soluble Gelatin-Chitosan Nanoparticles with Encapsulated Alcohol-Soluble Eugenol

2020 ◽  
Vol 13 (6) ◽  
pp. 1024-1034
Author(s):  
Qian Wang ◽  
Li Zhang ◽  
Wu Ding ◽  
Dequan Zhang ◽  
Kevin Reed ◽  
...  
2019 ◽  
Vol 38 (2) ◽  
pp. 385 ◽  
Author(s):  
Marwa M. El-Naggar ◽  
Wael S. I. Abou-Elmagd ◽  
Ashraf Suloma ◽  
Hamza A. El-Shabaka ◽  
Magdy T. Khalil ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1140
Author(s):  
Silvana Alfei ◽  
Gabriella Piatti ◽  
Debora Caviglia ◽  
Anna Maria Schito

The growing resistance of bacteria to current chemotherapy is a global concern that urgently requires new and effective antimicrobial agents, aimed at curing untreatable infection, reducing unacceptable healthcare costs and human mortality. Cationic polymers, that mimic antimicrobial cationic peptides, represent promising broad-spectrum agents, being less susceptible to develop resistance than low molecular weight antibiotics. We, thus, designed, and herein report, the synthesis and physicochemical characterization of a water-soluble cationic copolymer (P5), obtained by copolymerizing the laboratory-made monomer 4-ammoniumbuthylstyrene hydrochloride with di-methyl-acrylamide as uncharged diluent. The antibacterial activity of P5 was assessed against several multi-drug-resistant clinical isolates of both Gram-positive and Gram-negative species. Except for strains characterized by modifications of the membrane charge, most of the tested isolates were sensible to the new molecule. P5 showed remarkable antibacterial activity against several isolates of genera Enterococcus, Staphylococcus, Pseudomonas, Klebsiella, and against Escherichia coli, Acinetobacter baumannii and Stenotrophomonas maltophilia, displaying a minimum MIC value of 3.15 µM. In time-killing and turbidimetric studies, P5 displayed a rapid non-lytic bactericidal activity. Due to its water-solubility and wide bactericidal spectrum, P5 could represent a promising novel agent capable of overcoming severe infections sustained by bacteria resistant the presently available antibiotics.


2005 ◽  
Vol 283 (2) ◽  
pp. 344-351 ◽  
Author(s):  
T. López-León ◽  
E.L.S. Carvalho ◽  
B. Seijo ◽  
J.L. Ortega-Vinuesa ◽  
D. Bastos-González

2017 ◽  
Vol 4 (1) ◽  
pp. 94-99
Author(s):  
Syamsul Falah ◽  
Sulistiyani Sulistiyani ◽  
Dimas Andrianto

Nanoparticles-based drug delivery has been recognized to improve the solubility of poorly water-soluble drugs, prolong the half-life of drug systematic circulation by reducing immunogenicity, and releases drugs at a sustain rate. The present study reports on the characterization of mahogany bark extract-loaded chitosan nanoparticles and their antioxidant activity.  Mahogany bark meal was extracted in boiled water for four hours.  Chitosan-sodium tripolyphosphate (STPP) nanospheres were sonicated with ultrasonicator to obtain chitosan-STTP nanocapsules for 30 and 60 min and then were dried with spray dryer. The chitosan-STPP nanocapsules loaded by mahogany extract were then analysed for surface morphology and physical state by scanning electron microscope (SEM) and X ray diffraction (XRD), respectively. Antioxidant activity of the nanoparticles was evaluated by scavenging the 1,1-diphenyl-2-picrylhydrazyl (DPPH) using free radical method. Based on SEM data, the nanoparticle shapes were viewed to adhere to spherical shape. Spherical chitosan-STTP nanoparticles loaded with mahogany bark extract were obtained in the size range of 480 ~ 2000 nm and 240 ~ 1000 nm for 30 and 60 min of ultrasonication time, respectively. The antioxidant activity of the nanoparticles was lower than that of the native mahogany bark extract. 


2009 ◽  
Vol 59 (4) ◽  
pp. 453-461 ◽  
Author(s):  
Vikrant Vyas ◽  
Pankajkumar Sancheti ◽  
Poonam Karekar ◽  
Manali Shah ◽  
Yogesh Pore

Physicochemical characterization of solid dispersion systems of tadalafil with poloxamer 407 Dissolution behaviour of a poorly water-soluble drug, tadalafil, from its solid dispersion systems with poloxamer 407 has been investigated. Solid dispersion systems of tadalafil were prepared with poloxamer 407 in 1:0.5, 1:1.5 and 1:2.5 ratios using the melting method. Characterization of binary systems with FTIR and XRPD studies demonstrated the presence of strong hydrogen bonding interactions, a significant decrease in crystallinity and the possibility of existence of amorphous entities of the drug. In the binary systems tested, 1:0.5 proportion of tadalafil/poloxamer 407 showed rapid dissolution of tadalafil (DE30 70.9 ± 3.6 %). In contrast, higher proportions of poloxamer 407 (1:1.5 and 1:2.5) offered no advantage towards dissolution enhancement of the drug, indicating altered rheological characteristics of the polymer at its higher concentration, which might have retarded the release rate of tadalafil.


2017 ◽  
Vol 21 (04-06) ◽  
pp. 334-344 ◽  
Author(s):  
Maria Pia Donzello ◽  
Fabio Gigante ◽  
Fabiola Sciscione ◽  
Elisa Viola ◽  
Karl M. Kadish

The synthesis and physicochemical characterization of a new class of low-symmetry water soluble heteropentanuclear porphyrazine complexes are described. The investigated compounds, represented as [{Pd(OAc)[Formula: see text]}[Formula: see text](PtCl[Formula: see text]LM] •xH[Formula: see text]O where L [Formula: see text] tetrakis-2,3-[5,6-di(2-pyridyl)pyrazino]porphyrazinato dianion, M [Formula: see text] Mg[Formula: see text](H[Formula: see text]O), Zn[Formula: see text] or Pd[Formula: see text] and [Formula: see text] 3–8, were prepared under mild experimental conditions from the previously described heterobimetallic compounds [(PtCl[Formula: see text]LM]. Peripheral binding of one PtCl[Formula: see text]and three Pd(OAc)[Formula: see text]units in the new series of compounds occurs at the vicinal pyridine N atoms of each dipyridinopyrazine fragment via a “py–py” coordination. The newly synthesized porphyrazines were characterized by IR measurements in the solid state and UV-visible absorption spectroscopy in the polar nonaqueous solvents pyridine, dimethyl sulfoxide (DMSO) and dimethylformamide (DMF) as well as in water, the enhanced solubility in this medium being due to the presence of the external Pd(OAc)[Formula: see text] moieties. Data on the photosensitizing activity of the compounds for the generation of singlet oxygen, [Formula: see text]O[Formula: see text] were also obtained in DMF and should be of interest to researchers in the area of photodynamic therapy.


2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Hong-liang Zhang ◽  
Si-hui Wu ◽  
Yi Tao ◽  
Lin-quan Zang ◽  
Zheng-quan Su

The objective of this study was to investigate the potential of water soluble chitosan as a carrier in the preparation of protein-loaded nanoparticles. Nanoparticles were prepared by ionotropic gelation of water-soluble chitosan (WSC) with sodium tripolyphosphate (TPP). Bovine serum albumin (BSA) was applied as a model drug. The size and morphology of the nanoparticles were investigated as a function of the preparation conditions. The particles were spherical in shape and had a smooth surface. The size range of the nanoparticles was between 100 and 400 nm. Result of the in vitro studies showed that the WSC nanoparticles enhance and prolong the intestinal absorption of BSA. These results also indicated that WSC nanoparticles were a potential protein delivery system.


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