Hasil untuk "physics.app-ph"

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CrossRef Open Access 2025
pH-RESPONSIVE EUDRAGIT® S-100 COATED CHITOSAN NANOPARTICLES FOR TARGETED CURCUMIN DELIVERY IN ULCERATIVE COLITIS: FORMULATION AND OPTIMIZATION

NEELESH KUMAR SAHU, NARENDRA KUMAR LARIYA

Objective: This study aimed to develop and optimize pH-responsive Eudragit S-100 coated chitosan Nanoparticles (NPs) for targeted curcumin delivery in Ulcerative Colitis (UC). The objectives included enhancing curcumin's bioavailability, achieving colon-specific release through mucoadhesive, pH-sensitive nanocarriers, and evaluating their long-term stability. Methods: Curcumin-loaded chitosan NPs were prepared via ionotropic gelation using Sodium Tripolyphosphate (STPP) and coated with Eudragit S-100 via solvent evaporation. Nine formulations (F1–F9) were optimized by varying chitosan (250–750 mg) and STPP (500–1000 mg) concentrations. The NPs were characterized for particle size, zeta potential, Entrapment Efficiency (EE), morphology (SEM), and in vitro drug release in simulated gastrointestinal pH (1.2 → 7.5). Release kinetics were analyzed using Zero-Order, Higuchi, and Korsmeyer-Peppas models. Stability studies were conducted at 4 °C, 28 °C/65% RH, and 40 °C/75% RH for 90 days to assess particle size and drug retention. Results: The optimized formulation (F4: 500 mg chitosan, 500 mg STPP) exhibited a mean particle size of 355.5 nm, high EE (76.65%), and a zeta potential of −36.32 mV, confirming colloidal stability. Coated NPs demonstrated pH-dependent release: minimal in acidic pH (2.32% at pH 1.2) and sustained in colonic pH (98.33% at pH 7.5). Release kinetics followed the Korsmeyer-Peppas model (R² = 0.9892, n = 0.62), indicating anomalous transport. Stability studies revealed excellent retention of particle size (≤361.4 nm) and drug content (>99%) under varied storage conditions, confirming long-term stability. Conclusion: Eudragit S-100 coated chitosan NPs successfully addressed curcumin's solubility and bioavailability challenges while ensuring pH-responsive, targeted colonic delivery. The optimized formulation (F4) exhibited robust stability, making it a promising candidate for UC therapy. Future studies should focus on in vivo efficacy and clinical translation.

3 sitasi en
CrossRef Open Access 2021
Flocculation of <i>Chlorella vulgaris</i> with alum and pH adjustment

Farnaz Mohseni, Alireza Moosavi Zenooz

AbstractMicroalgae, a group of photosynthetic microorganisms, are a promising feedstock for biodiesel production, but their biomass retrieval is a challenging task. Flocculation is a feasible method for dewatering and harvesting microalgae biomass. In the current study, the effect of alum flocculation on Chlorella vulgaris biomass retrieval has been studied. Alum structural changes with pH were led to a full factorial design to address the effect of this chemical structure changes at different pH values. It is observed that the best flocculation efficiency could be achieved in the natural pH value of C. vulgaris growth medium (8.2) with less than 0.5 g/L flocculant addition, which would lead to the flocculation efficiency of more than 90%. An ensemble architecture of neural networks successfully employed for flocculation modeling.

8 sitasi en
CrossRef Open Access 2016
pH‐Sensitive pectin polymeric rafts for controlled‐release delivery of pantoprazole sodium sesquihydrate

Ghulam Abbas, Muhammad Hanif

ABSTRACTThe aim of the present work was to develop pectin raft‐forming tablets for controlled‐release delivery of pantoprazole sodium sesquihydrate (PSS). A Box–Behnken design was used to optimize 15 formulations with three independent and three dependent variables. The physical tests of all compressed formulations were within pharmacopoeial limits. The rafts were characterized by their strength, thickness, resilience, reflux resistance, acid‐neutralizing capacity, floating lag time, and total floating time. The raft strength, thickness, resilience, and reflux resistance through a 10‐mm orifice of optimized formulation PR9 were 7.43 ± 0.019 g, 5.8 ± 0.245 cm, greater than 480 min, and 2490 ± 0.004 g, respectively. The buffering and neutralizing capacity was 11.2 ± 1.01 meq and 6.5 ± 0.56 meq, respectively. Dissolution studies were performed by using simulated gastric fluid at pH 1.2, and the cumulative percentage release of PR9 was found to be 97%. First‐order release kinetics were followed, and non‐Fickian diffusion was observed as the value of n was greater than 0.45 in the Korsmeyer–Peppas model. The Fourier transform infrared spectra of the PSS, polymers, and optimized raft formulation PR9 showed peaks at 3223.09 cm−1, 1688.17 cm−1, 1586.67 cm−1, 1302.64 cm−1, and 1027.74 cm−1 that are due to OH stretching, ester carbonyl group (CO) stretching, the existence of water and carboxylic groups in the raft, CN stretching, and OH bending vibrations and showed no interaction between them. The developed raft was suitable for sustained‐release delivery of PSS. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 44442.

CrossRef Open Access 2004
pH‐reversible magnetic gel with a biodegradable polymer

Jhunu Chatterjee, Yousef Haik, Ching‐Jen Chen

AbstractPolymer gels that react to external stimuli, such as pH, temperature, and electromagnetic fields, are an important class of materials. Such materials have pharmaceutical, industrial, and biomedical applications. Our intention in this study was to synthesize a stimuli‐responsive polymer gel with a biodegradable polymer. However, the chemical crosslinker, divinyl sulfone, which is most widely used for the crosslinking of this type of material, is highly toxic in nature. To overcome this problem, a reversible magnetic gel was synthesized with hydroxy propyl cellulose (HPC) and maghemite at pH 13 without with a chemical crosslinker. With a decrease in pH from 13 to 9, the gel formed a homogeneous dispersion of HPC particles with maghemite in it. This process was a reversible physical gelation where the crosslinks of the network had a physical origin (in this case, hydrogen bonding) and, therefore, were sensitive to variations in pH. When this physically prepared gel was compared with the chemically crosslinked one, no significant differences in structural properties were noted. At higher pH values, the gel was formed due to weak intermolecular hydrogen bonding, as observed by the broadening of the IR band in both the magnetic and nonmagnetic gels. Transmission electron micrographs also showed no significant difference in the gel morphology. Differential scanning calorimetry showed an increase in melting temperature for the gel sample compared to that of pure HPC. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3337–3341, 2004

19 sitasi en
CrossRef Open Access 1972
Study of the pyrolysis of saturated chlorinated polyethylene fibers

N. Saglio, Ph. Berticat, G. Vallet

AbstractThe thermal degradation of saturated chlorinated polyethylene in powder and fiber form has been studied. Direct observations of fiber length variations have enabled us to prove the reactional mechanisms proposed. In the temperature range of 200°–300°C, the material exhibits some fluidity. Its degradation is explained by intrachain and interchain dehydrochlorination reactions, followed by an arrangement of conjugated double bonds obtained in the shape of polyacenic cycles. Between 300°C and 800°C, the polyacenic cycles react with each other to give a pregraphitic structure which is responsible for the increase in rigidity of the material. The fibers of saturated chlorinated polyethylene can be used as a precursor of carbon fiber.

CrossRef Open Access 1979
A study of PVC stabilization with epoxides using dynamic pH determinations

V. Gonzalez‐Gonzalez

AbstractThe activation energy (Ea) for the dehydrochlorination of PVC and PVC stabilized with an epoxide was determined by a method involving dynamic pH measurements. The Ea increase was 5 kcal/mole between unformulated PVC (Ea = 22.6 kcal/mole) and any of the other formulations (Ea = 27.7–28.6 kcal/mole). On the basis of this and data contained in the literature, research alternatives for the stabilization mechanism are proposed using model compounds.

CrossRef 2021
Effect of space charge on vacuum pre-breakdown voltage and electron emission current

B. Seznec, Ph. Dessante, Ph. Teste et al.

The recent developments in nanosecond pulsed power supplies facilitate the emission of high density electron bursts but their safe operation demands avoiding breakdowns. Using the theoretical and numerical modeling of the electron emission phenomena from a tip (micro-protrusion), the breakdown threshold (pre-breakdown) is analyzed considering it as the highest value of the voltage preserving the system out of the thermo-emission instability regime. However, the space charge that builds up in front of the tip limits the performance of these electron sources by decreasing the local electric field and consequently the thermo-field emission as well as the temperature of the emissive surface. Hence, it is found that the system can safely hold higher voltages (without breakdown) in the presence of dense space charge. In direct current, for a titanium elliptic tip, the highest operation voltage increases by about 15%, whereas for a tungsten hyperbolic tip, it increases by 70%. Remarkably, the emitted current close to the pre-breakdown voltage stays unchanged with or without taking into account the space charge. Surprisingly, when very short pulses (3 ns) are applied to a tungsten hyperbolic tip, the pre-breakdown voltage additionally increases by 30%, and the Coulomb screening, very effective in front of the tip apex, enlarges the electron emission area by 60%, releasing about 1.3 times more electrons compared to vacuum emission (without the space charge). Moreover, the ring effect, experimentally discovered by Dyke and Trolan [Phys. Rev. 89, 799 (1953)] on the radial electron density distribution, can be microscopically observed and understood with your model.

7 sitasi en
CrossRef 1987
Adiabatic decomposition of mass-selected alkali clusters

C. Bréchignac, Ph. Cahuzac, J.-Ph. Roux et al.

The decomposition of metastable photoionized mass-selected alkali clusters is investigated using a tandem time-of-flight spectrometer. Na+n and K+n are found to decompose mainly by the evaporation of either a single neutral atom or a neutral dimer in a time scale of about 10 μs. The predominant fragmentation channels are found to follow the adiabatic dissociation channels associated with the lowest energies accordingly to our CI calculations. In the light of our experimental and theoretical results a comparison between the different calculations of the absolute atomization energies available in the literature is presented.

62 sitasi en
CrossRef 1992
Radiative instability in a diverted plasma

H. Capes, Ph. Ghendrih, A. Samain

Bifurcations between thermal equilibria are studied in a slab radiating plasma at constant pressure. The thermal stability is discussed in connection with the behavior of the equilibrium solutions when the input power flux in the radiating layer is varied. A general necessary and sufficient stability criterion is demonstrated. In the case of a constant impurity concentration it leads to a simple stability condition in terms of the edge temperature only.

35 sitasi en
CrossRef 1986
Performance of a hydrogen uranyl phosphate—carbon double-layer solid capacitor

M. Pham-Thi, Ph. Adet, G. Velasco et al.

A mixture of commercially available carbon black powders and hydrogen uranyl phosphate (HUP) precipitate can be used as the electrode material for miniaturized double-layer capacitors. A solid cell of C-HUP‖HUP‖C-HUP has a capacitance of 1 F which, given the device area and thickness of 0.8 cm2 and 0.2 cm respectively, corresponds to an energy density of more than 5 J/cm3. The charge×voltage factor is higher than 5×10−6 s and the working voltage is over 1.6 V. The leakage current is lower than 3 μA at room temperature. The electrolyte can be operated up to about 120 °C if the device is hermetically sealed.

14 sitasi en
CrossRef 2002
Real time probing of magnetization switching in magnetic nanostructures

Ph. Guittienne, L. Gravier, J.-E. Wegrowe et al.

Time-resolved anisotropic magnetoresistance (AMR) measurements of the irreversible switching of the magnetization were performed on isolated Ni nanowires. The magnetization reversal was triggered by injection of high current densities in a static magnetic field. The detection was achieved by means of a Wheatstone bridge with a 1 GHz bandwidth. Time-resolved switching was obtained in single shot measurements. Nanowires with diameter of about 100 nm that present a uniform rotation in the reversible regime detected in quasistatic AMR measurements are found to have switching in about 14 ns. This value can be accounted for in the framework of an uniform rotation model with value of the Gilbert damping coefficient of 0.005–0.01. Nanowires with larger diameters (typ. 200 nm) that manifest inhomogeneous magnetization in quasistatic AMR measurements have a switching time of about 37 ns.

10 sitasi en

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