88 research outputs found
Membrane emulsification: droplet size and uniformity in the absence of surface shear
A series of tests with membrane pore sizes between 7 and 60 μm and uniform spacing between the pores of 80 and 200 μm, conducted under conditions of zero surface shear at the membrane, show that an additional force to the buoyancy and capillary forces exists in membrane emulsification. A push-off force, derived by consideration of the geometry of the drops as they deform at the surface of the pores under high injection rates when most of the pores are passing liquid, is shown to model the size of the drops formed in the emulsification. In the tests, sunflower oil was injected into water and as the emulsification injection rate increased it was noticeable that there was a point at which the resulting drop distribution is at its narrowest. For the two pore spacings studied: 80 and 200 μm, the point at which the distribution was at its narrowest was at a Weber number of 1.5 × 10−2, where the Weber number is defined using the drop diameter rather than the pore diameter
PLGA particle production for water soluble drug encapsulation: degradation and release behaviour
Particles for subcutaneous depot use encapsulating a model water soluble
drug have been produced from poly(lactic-glycolic acid) (PLGA) using a
membrane emulsification – solvent evaporation technique. The release
behaviour, mainly the change in size and inner morphology are reported.
During release, the particles initially swelled in size, then reduced. A diffusion
based model, taking in to account the change in particle size, is presented.
Surface erosion is evident from the particle size and image evidence, and the
diffusion model provides a fit to the data even during the surface erosion
period, suggesting that the model drug diffuses before the particle degrades
A New World Average Value for the Neutron Lifetime
The analysis of the data on measurements of the neutron lifetime is
presented. A new most accurate result of the measurement of neutron lifetime
[Phys. Lett. B 605 (2005) 72] 878.5 +/- 0.8 s differs from the world average
value [Phys. Lett. B 667 (2008) 1] 885.7 +/- 0.8 s by 6.5 standard deviations.
In this connection the analysis and Monte Carlo simulation of experiments
[Phys. Lett. B 483 (2000) 15] and [Phys. Rev. Lett. 63 (1989) 593] is carried
out. Systematic errors of about -6 s are found in each of the experiments. The
summary table for the neutron lifetime measurements after corrections and
additions is given. A new world average value for the neutron lifetime 879.9
+/- 0.9 s is presented.Comment: 27 pages, 13 figures; Fig.13 update
Preparation and characterization of PLGA particles for subcutaneous controlled drug release by membrane emulsification
Uniformly sized microparticles of poly(DL, lactic-co-glycolic) (PLGA) acid, with controllable
median diameters within the size range 40 to 140 microns, were successfully prepared by
membrane emulsification of an oil phase injected into an aqueous phase, followed by solvent
removal. Initially, simple particles were produced as an oil-in-water emulsion, where
dichloromethane (DCM) and PLGA were the oil phase and water with stabiliser was the
continuous phase. The oil was injected into the aqueous phase through an array type
microporous membrane, which has very regular pores equally spaced apart, and two different
pore sizes were used: 20 and 40 microns in diameter. Shear was provided at the membrane
surface, causing the drops to detach, by a simple paddle stirrer rotating above the membrane.
Further tests involved the production of a primary water-in-oil emulsion, using a mechanical
homogeniser, which was then subsequently injected into a water phase through the
microporous membrane to form a water-in-oil-in-water emulsion. These tests used a water
soluble model drug (blue dextran) and encapsulation efficiencies of up to 100% were obtained
for concentrations of 15% PLGA dissolved in the DCM and injected through a 40 micron
membrane.
Solidification of the PLGA particles followed by removal of the DCM through the surrounding
aqueous continuous phase. Different PLGA concentrations, particle size and osmotic
pressures were considered in order to find their effect on encapsulation efficiency. Osmotic
pressure was varied by changing the salt concentration in the external aqueous phase whilst
maintaining a constant internal aqueous phase salt concentration. Osmotic pressure was
found to be a significant factor on the resulting particle structure, for the tests conducted at
lower PLGA concentrations (10 and 5% PLGA). The PLGA concentration and particle size
distribution influence the time to complete the solidification stage and a slow solidification,
formed by stirring gently overnight, provided the most monosized particles and highest
encapsulation efficiency
Low pressure microfilter design aspects and filtration performance
A microfilter should retain micron sized material yet provide minimal resistance to
liquid flow. A slotted pore surface microfilter was oscillated whilst filtering yeast cells
under constant rate. At shear rates over 7760 s-1, a pore blocking model fitted the
data. The operating pressure was very low (<1000 Pa), but particle retention was
limited by the 4 micron pore slot width. A sintered glass micro-bead coating improved
yeast rejection: 95% at 1.7 microns at a shear rate of 5000 s-1, with a 1.2 kPa
transmembrane pressure. Two models were validated to assist with the design of
future micro-bead coatings constructed from spherical particles
The passage of deforming drops through a slotted microfilter
In the flow of a deforming drop through a slotted pore, such as during the microfiltration of oil drops suspended in water, the mechanism for the convection of the oil drops is liquid drag caused by permeate flow through the filter. If the slot is designed to have a converging inlet section then it is possible to estimate the force on the drop from the liquid drag and determine where the drop comes to rest within the converging slot. This equilibrium position is established due to a balance of forces between the liquid drag and the force required to deform the drop to create a larger surface area as the drop becomes less spherical. Experimental measurements are presented for a bubble deforming within an aqueous flow field and a paraffin oil flow field, together with results for the motion of a paraffin oil drop within an aqueous flow field. The data is correlated using a ratio of drop to channel diameter (analogous to slot width) against superficial liquid velocity. Different curves are provided depending only on the physical properties of the fluids used. An analytical mathematical development predicts these curves to a good degree of reliability, which can then be used to predict the oil drop size that is 100% rejected during the filtration of oil drops on slotted microfiltration membranes. Experimental evidence is presented to support the prediction using the filtration of a crude oil on a slotted microfilter with a minimum pore width of 5 microns
Controlled production of oil-in-water emulsions containing unrefined pumpkin seed oil using stirred cell membrane emulsification
Membrane emulsification of unrefined pumpkin seed oil was performed using microengineered flat disc membranes on top of which a paddle blade stirrer was operated to induce surface shear. The membranes used were fabricated by galvanic deposition of nickel onto a photolithographic template and contained hexagonal arrays of uniform cylindrical pores with a diameter of 19 or 40 mu m and a pore spacing of 140 mu m. The uniformly sized pumpkin seed oil drops with span values less than 0.4 were obtained at oil fluxes up to 640 L m(-2) h(-1) using 2 wt.% Tween 20 (polyoxyethylene sorbitan monolaurate) or 2-10 wt.% Pluronic F-68 (polyoxyethylene-polyoxypropylen copolymer) as an aqueous surfactant solution. Pumpkin seed oil is rich in surface active ingredients that can be adsorbed on the membrane surface, such as free fatty acids, phospholipids, and chlorophyll. The adsorption of these components on the membrane surface gradually led to membrane wetting by the oil phase and the formation of uniform drops was achieved only for dispersed phase contents less than 10 vol.% At high oil fluxes, Pluronic F-68 molecules present at a concentration of 2 wt.% could not adsorb fast enough, on the newly formed oil drops, to stabilise the expanding inter-face. (c) 2008 Elsevier B.V. All rights reserved
Membrane emulsification using membranes of regular pore spacing: droplet size and uniformity in the presence of surface shear
During membrane emulsification it is shown that the size of the drops formed at the membrane surface may increase with increasing dispersed phase injection rate through the membrane, or it may decrease, depending on the prevailing conditions. This is illustrated using a paddle stirrer positioned above flat disc membranes with regular arrays of pores of 20 μm diameter and spacing between the pores of 80 and 200 μm. In the former case an additional mechanism for drop detachment is the push-off force, which is determined by the geometry of the drops as they deform at the membrane surface. When dispersing sunflower oil in to aqueous solutions containing Tween 20, drop sizes between 60 and 200 μm were produced, and in the case of the membrane when the push-off force was working the Coefficient of Variation of the drops formed was below 10%. The push-off force may be added to the shear-drag force to predict drop detachment. For the 200 μm pore spaced membrane this force is much less prominent than the 80 μm spaced membrane. The capillary-shear model has been modified to include this push-off force. The experimental study required the use of very low dispersed phase injection rates as well as very high rates. Hence, two different types of pumps were used to provide these: a peristaltic and syringe pumps. A small study comparing the drop size, and size distributions, showed that the pump type did not influence the drops produced by the membrane emulsification process
Stirred cell membrane emulsification and factors influencing dispersion drop size and uniformity
Water-in-oil (w/o) and oil-in-water (o/w) emulsions were generated using 30-μm pore diameter surface membranes to investigate the factors influencing drop size, and the degree of uniformity of drop size distribution, using a stirred cell employing a simple paddle mounted above a circular disc membrane. The importance of the transitional radius, which is the radius at which the vortex around the unbaffled paddle stirrer changes from a forced vortex to a free vortex and the shear stress at the membrane surface below the stirrer is at its greatest, is demonstrated. Monosized emulsions were produced, with drop size distribution coefficient of variation values of 10% for o/w emulsions and 13.5% for w/o emulsions. These tests demonstrated that a membrane of reduced annular operating area (ringed membrane) produced a more monosized o/w emulsion than a membrane where the full area was used to generate the emulsion, without affecting the mean drop size. The improved size distribution was achieved while the transitional radius was located within the ringed annular section of the membrane. The force balance model, applied to drops formed at the surface of the membrane during emulsification, predicted the droplet diameter provided further drop break up within the stirred cell did not occur. Drop break up occurred at Reynolds numbers below 300 for both oil-in-water and water-in-oil dispersions. Therefore, for Reynolds numbers greater than this, an annular radial ring membrane can be designed to produce monosized droplets using the stirred cell at known continuous phase viscosities with predictable mean droplet size. This knowledge can be used as a design tool to produce monosized droplets of a specified size for various applications using simple stirred cell emulsification
Liquid-liquid membrane dispersion in a stirred cell with and without controlled shear
Oil was passed through membranes into a continuous water phase containing a surfactant (Tween 20) to form oil dispersions with drop diameters between 40 and 400 μm. Two types of stirred equipment were used:  a Weissenberg rheometer (cone and plate geometry) providing constant shear stress at all radial positions which was modified to include a membrane instead of the plate and a simple stirred cell, with a paddle rotating above the membrane, providing variable shear with radial position. Experiments show that the simple paddle-stirred cell provided an oil drop dispersion that was as monosized as that produced by the controlled shear device, if not better. An analysis indicated that only the section of the membrane close to the radius of the highest shear under the paddle stirred membrane produced oil drops. The membranes used in the experiments contained a regular array of nontortuous pores uniformly spaced and provided oil injection rates up to 1000 L m-2 h-1, which is much higher than reported fluxes for the alternative tortuous pore channel membranes made by sintering
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