Semipermeable membrane

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Schematic of semipermeable membrane during hemodialysis, where blood is red, dialysing fluid is blue, and the membrane is yellow. Semipermeable membrane (svg).svg
Schematic of semipermeable membrane during hemodialysis, where blood is red, dialysing fluid is blue, and the membrane is yellow.

Semipermeable membrane is a type of synthetic or biologic, polymeric membrane that allows certain molecules or ions to pass through it by osmosis. The rate of passage depends on the pressure, concentration, and temperature of the molecules or solutes on either side, as well as the permeability of the membrane to each solute. Depending on the membrane and the solute, permeability may depend on solute size, solubility, properties, or chemistry. How the membrane is constructed to be selective in its permeability will determine the rate and the permeability. Many natural and synthetic materials which are rather thick are also semipermeable. One example of this is the thin film on the inside of an egg. [1]

Contents

Biological membranes are selectively permeable, [2] with the passage of molecules controlled by facilitated diffusion, passive transport or active transport regulated by proteins embedded in the membrane.

Biological membranes

Phospholipid bilayer

A phospholipid bilayer is an example of a biological semipermeable membrane. It consists of two parallel, opposite-facing layers of uniformly arranged phospholipids. Each phospholipid is made of one phosphate head and two fatty acid tails. [3] The plasma membrane that surrounds all biological cells is an example of a phospholipid bilayer. [2] The plasma membrane is very specific in its permeability, meaning it carefully controls which substances enter and leave the cell. Because they are attracted to the water content within and outside the cell (or hydrophillic), the phosphate heads assemble along the outer and inner surfaces of the plasma membrane, and the hydrophobic tails are the layer hidden in the inside of the membrane. Cholesterol molecules are also found throughout the plasma membrane and act as a buffer of membrane fluidity. [3] The phospholipid bilayer is most permeable to small, uncharged solutes. Protein channels are embedded in or through the phospholipids, [4] and, collectively, this model is known as the fluid mosaic model. Aquaporins are protein channel pores permeable to water.

Cellular communication

Information can also pass through the plasma membrane when signaling molecules bind to receptors in the cell membrane. The signaling molecules bind to the receptors, which alters the structure of these proteins. [5] A change in the protein structure initiates a signaling cascade. [5] G protein-coupled receptor signaling is an important subset of such signaling processes. [6]

Salt outside of the cell creates osmotic pressure that pushes water through the phospholipid bilayer Osmotic Pressure and a Semipermeable Membrane.png
Salt outside of the cell creates osmotic pressure that pushes water through the phospholipid bilayer

Osmotic stress

Because the lipid bilayer is semipermeable, it is subject to osmotic pressure. [7] When the solutes around a cell become more or less concentrated, osmotic pressure causes water to flow into or out of the cell to equilibrate. [8] This osmotic stress inhibits cellular functions that depend on the activity of water in the cell, such as the functioning of its DNA and protein systems and proper assembly of its plasma membrane. [9] This can lead to osmotic shock and cell death. Osmoregulation is the method by which cells counteract osmotic stress, and includes osmosensory transporters in the membrane that allow K+ [note 1] and other molecules to flow through the membrane. [8]

Artificial membranes

Artificial semipermeable membranes see wide usage in research and the medical field. Artificial lipid membranes can easily be manipulated and experimented upon to study biological phenomenon. [10] Other artificial membranes include those involved in drug delivery, dialysis, and bioseparations. [11]

Reverse osmosis

The bulk flow of water through a selectively permeable membrane because of an osmotic pressure difference is called osmosis. This allows only certain particles to go through including water and leaving behind the solutes including salt and other contaminants. In the process of reverse osmosis, water is purified by applying high pressure to a solution and thereby push water through a thin-film composite membrane (TFC or TFM). These are semipermeable membranes manufactured principally for use in water purification or desalination systems. They also have use in chemical applications such as batteries and fuel cells. In essence, a TFC material is a molecular sieve constructed in the form of a film from two or more layered materials. Sidney Loeb and Srinivasa Sourirajan invented the first practical synthetic semi-permeable membrane. [12] Membranes used in reverse osmosis are, in general, made out of polyamide, chosen primarily for its permeability to water and relative impermeability to various dissolved impurities including salt ions and other small molecules that cannot be filtered.

Regeneration of reverse osmosis membranes

Reverse osmosis membrane modules have a limited life cycle, several studies have endeavored to improve the performance of the process and extend the RO membranes lifespan. However, even with the appropriate pretreatment of the feed water, the membranes lifespan is generally limited to five to seven years.

Discarded RO membrane modules are currently classified worldwide as inert solid waste and are often disposed of in landfills, with limited reuse. Estimates indicated that the mass of membranes annually discarded worldwide reached 12,000 tons. At the current rate, the disposal of RO modules represents significant and growing adverse impacts on the environment, giving rise to the need to limit the direct discarding of these modules.

Discarded RO membranes from desalination operations could be recycled for other processes that do not require the intensive filtration criteria of desalination, they could be used in applications requiring nanofiltration (NF) membranes. [13]

Regeneration process steps:

1- Chemical Treatment

Chemical procedures aimed at removing fouling from the spent membrane; several chemicals agents are used; such as:

       - Sodium Hydroxide (alkaline)

      - Hydrochloric Acid (Acidic)

      - Chelating agents Such as Citric and Oxalic acids

There are three forms of membranes exposure to chemical agents; simple immersion, recirculating the cleaning agent, or immersion in an ultrasound bath.

2 - Oxidative treatment

It includes exposing the membrane to oxidant solutions in order to remove its dense aromatic polyamide active layer and subsequent conversion to a porous membrane. Oxidizing agents such as Sodium Hypochlorite NaClO (10–12%) and Potassium Permanganate KMnO₄ are used. [14] These agents remove organic and biological fouling from RO membranes, They also disinfect the membrane surface, preventing the growth of bacteria and other microorganisms.

Sodium Hypochlorite is the most efficient oxidizing agent in light of permeability and salt rejection solution.

Dialysis tubing allows waste molecules to be selectively removed from blood. Dialysis new.jpg
Dialysis tubing allows waste molecules to be selectively removed from blood.

Dialysis tubing

Dialysis tubing is used in hemodialysis to purify blood in the case of kidney failure. The tubing uses a semipermeable membrane to remove waste before returning the purified blood to the patient. [15] Differences in the semipermeable membrane, such as size of pores, change the rate and identity of removed molecules. Traditionally, cellulose membranes were used, but they could cause inflammatory responses in patients. Synthetic membranes have been developed that are more biocompatible and lead to fewer inflammatory responses. [16] However, despite the increased biocompatibility, synthetic membranes have not been linked to decreased mortality. [15]

Other types

Other types of semipermeable membranes are cation-exchange membranes (CEMs), anion-exchange membranes (AEMs), alkali anion-exchange membranes (AAEMs) and proton-exchange membranes (PEMs).

Notes

  1. K+ is the element potassium's positively charged ion (cation).

Related Research Articles

<span class="mw-page-title-main">Biological membrane</span> Enclosing or separating membrane in organisms acting as selective semi-permeable barrier

A biological membrane, biomembrane or cell membrane is a selectively permeable membrane that separates the interior of a cell from the external environment or creates intracellular compartments by serving as a boundary between one part of the cell and another. Biological membranes, in the form of eukaryotic cell membranes, consist of a phospholipid bilayer with embedded, integral and peripheral proteins used in communication and transportation of chemicals and ions. The bulk of lipids in a cell membrane provides a fluid matrix for proteins to rotate and laterally diffuse for physiological functioning. Proteins are adapted to high membrane fluidity environment of the lipid bilayer with the presence of an annular lipid shell, consisting of lipid molecules bound tightly to the surfac of integral membrane proteins. The cell membranes are different from the isolating tissues formed by layers of cells, such as mucous membranes, basement membranes, and serous membranes.

<span class="mw-page-title-main">Osmotic pressure</span> Measure of the tendency of a solution to take in pure solvent by osmosis

Osmotic pressure is the minimum pressure which needs to be applied to a solution to prevent the inward flow of its pure solvent across a semipermeable membrane. It is also defined as the measure of the tendency of a solution to take in its pure solvent by osmosis. Potential osmotic pressure is the maximum osmotic pressure that could develop in a solution if it were separated from its pure solvent by a semipermeable membrane.

<span class="mw-page-title-main">Vesicle (biology and chemistry)</span> Any small, fluid-filled, spherical organelle enclosed by a membrane

In cell biology, a vesicle is a structure within or outside a cell, consisting of liquid or cytoplasm enclosed by a lipid bilayer. Vesicles form naturally during the processes of secretion (exocytosis), uptake (endocytosis), and the transport of materials within the plasma membrane. Alternatively, they may be prepared artificially, in which case they are called liposomes. If there is only one phospholipid bilayer, the vesicles are called unilamellar liposomes; otherwise they are called multilamellar liposomes. The membrane enclosing the vesicle is also a lamellar phase, similar to that of the plasma membrane, and intracellular vesicles can fuse with the plasma membrane to release their contents outside the cell. Vesicles can also fuse with other organelles within the cell. A vesicle released from the cell is known as an extracellular vesicle.

<span class="mw-page-title-main">Cell theory</span> Biology of cells

In biology, cell theory is a scientific theory first formulated in the mid-nineteenth century, that living organisms are made up of cells, that they are the basic structural/organizational unit of all organisms, and that all cells come from pre-existing cells. Cells are the basic unit of structure in all living organisms and also the basic unit of reproduction.

<span class="mw-page-title-main">Lipid bilayer</span> Biological membrane structure

The lipid bilayer is a thin polar membrane made of two layers of lipid molecules. These membranes are flat sheets that form a continuous barrier around all cells. The cell membranes of almost all organisms and many viruses are made of a lipid bilayer, as are the nuclear membrane surrounding the cell nucleus, and membranes of the membrane-bound organelles in the cell. The lipid bilayer is the barrier that keeps ions, proteins and other molecules where they are needed and prevents them from diffusing into areas where they should not be. Lipid bilayers are ideally suited to this role, even though they are only a few nanometers in width, because they are impermeable to most water-soluble (hydrophilic) molecules. Bilayers are particularly impermeable to ions, which allows cells to regulate salt concentrations and pH by transporting ions across their membranes using proteins called ion pumps.

<span class="mw-page-title-main">Aquaporin</span> Water channel protein in cell membranes

Aquaporins, also called water channels, are channel proteins from a larger family of major intrinsic proteins that form pores in the membrane of biological cells, mainly facilitating transport of water between cells. The cell membranes of a variety of different bacteria, fungi, animal and plant cells contain aquaporins through which water can flow more rapidly into and out of the cell than by diffusing through the phospholipid bilayer. Aquaporins have six membrane-spanning alpha helical domains with both carboxylic and amino terminals on the cytoplasmic side. Two hydrophobic loops contain conserved asparagine–proline–alanine which form a barrel surrounding a central pore-like region that contains additional protein density. Because aquaporins are usually always open and are prevalent in just about every cell type, this leads to a misconception that water readily passes through the cell membrane down its concentration gradient. Water can pass through the cell membrane through simple diffusion because it is a small molecule, and through osmosis, in cases where the concentration of water outside of the cell is greater than that of the inside. However, because water is a polar molecule this process of simple diffusion is relatively slow, and in tissues with high water permeability the majority of water passes through aquaporin.

<span class="mw-page-title-main">Passive transport</span> Transport that does not require energy

Passive transport is a type of membrane transport that does not require energy to move substances across cell membranes. Instead of using cellular energy, like active transport, passive transport relies on the second law of thermodynamics to drive the movement of substances across cell membranes. Fundamentally, substances follow Fick's first law, and move from an area of high concentration to an area of low concentration because this movement increases the entropy of the overall system. The rate of passive transport depends on the permeability of the cell membrane, which, in turn, depends on the organization and characteristics of the membrane lipids and proteins. The four main kinds of passive transport are simple diffusion, facilitated diffusion, filtration, and/or osmosis.

A membrane transport protein is a membrane protein involved in the movement of ions, small molecules, and macromolecules, such as another protein, across a biological membrane. Transport proteins are integral transmembrane proteins; that is they exist permanently within and span the membrane across which they transport substances. The proteins may assist in the movement of substances by facilitated diffusion, active transport, osmosis, or reverse diffusion. The two main types of proteins involved in such transport are broadly categorized as either channels or carriers. Examples of channel/carrier proteins include the GLUT 1 uniporter, sodium channels, and potassium channels. The solute carriers and atypical SLCs are secondary active or facilitative transporters in humans. Collectively membrane transporters and channels are known as the transportome. Transportomes govern cellular influx and efflux of not only ions and nutrients but drugs as well.

In cellular biology, membrane transport refers to the collection of mechanisms that regulate the passage of solutes such as ions and small molecules through biological membranes, which are lipid bilayers that contain proteins embedded in them. The regulation of passage through the membrane is due to selective membrane permeability – a characteristic of biological membranes which allows them to separate substances of distinct chemical nature. In other words, they can be permeable to certain substances but not to others.

<span class="mw-page-title-main">Forward osmosis</span> Water purification process

Forward osmosis (FO) is an osmotic process that, like reverse osmosis (RO), uses a semi-permeable membrane to effect separation of water from dissolved solutes. The driving force for this separation is an osmotic pressure gradient, such that a "draw" solution of high concentration, is used to induce a net flow of water through the membrane into the draw solution, thus effectively separating the feed water from its solutes. In contrast, the reverse osmosis process uses hydraulic pressure as the driving force for separation, which serves to counteract the osmotic pressure gradient that would otherwise favor water flux from the permeate to the feed. Hence significantly more energy is required for reverse osmosis compared to forward osmosis.

The Starling principle holds that extracellular fluid movements between blood and tissues are determined by differences in hydrostatic pressure and colloid osmotic pressure between plasma inside microvessels and interstitial fluid outside them. The Starling equation, proposed many years after the death of Starling, describes that relationship in mathematical form and can be applied to many biological and non-biological semipermeable membranes. The classic Starling principle and the equation that describes it have in recent years been revised and extended.

Water potential is the potential energy of water per unit volume relative to pure water in reference conditions. Water potential quantifies the tendency of water to move from one area to another due to osmosis, gravity, mechanical pressure and matrix effects such as capillary action. The concept of water potential has proved useful in understanding and computing water movement within plants, animals, and soil. Water potential is typically expressed in potential energy per unit volume and very often is represented by the Greek letter ψ.

<span class="mw-page-title-main">Tonicity</span> Measure of water potential across a semi-permeable cell membrane

In chemical biology, tonicity is a measure of the effective osmotic pressure gradient; the water potential of two solutions separated by a partially-permeable cell membrane. Tonicity depends on the relative concentration of selective membrane-impermeable solutes across a cell membrane which determine the direction and extent of osmotic flux. It is commonly used when describing the swelling-versus-shrinking response of cells immersed in an external solution.

<span class="mw-page-title-main">Osmotic concentration</span> Molarity of osmotically active particles

Osmotic concentration, formerly known as osmolarity, is the measure of solute concentration, defined as the number of osmoles (Osm) of solute per litre (L) of solution. The osmolarity of a solution is usually expressed as Osm/L, in the same way that the molarity of a solution is expressed as "M". Whereas molarity measures the number of moles of solute per unit volume of solution, osmolarity measures the number of osmoles of solute particles per unit volume of solution. This value allows the measurement of the osmotic pressure of a solution and the determination of how the solvent will diffuse across a semipermeable membrane (osmosis) separating two solutions of different osmotic concentration.

<span class="mw-page-title-main">Osmotic shock</span> Shock caused by a sudden change in the solute concentration around a cell

Osmotic shock or osmotic stress is physiologic dysfunction caused by a sudden change in the solute concentration around a cell, which causes a rapid change in the movement of water across its cell membrane. Under hypertonic conditions - conditions of high concentrations of either salts, substrates or any solute in the supernatant - water is drawn out of the cells through osmosis. This also inhibits the transport of substrates and cofactors into the cell thus “shocking” the cell. Alternatively, under hypotonic conditions - when concentrations of solutes are low - water enters the cell in large amounts, causing it to swell and either burst or undergo apoptosis.

<span class="mw-page-title-main">Ultrafiltration (kidney)</span> Filtration by a semi-permeable membrane

In renal physiology, ultrafiltration occurs at the barrier between the blood and the filtrate in the glomerular capsule in the kidneys. As in nonbiological examples of ultrafiltration, pressure and concentration gradients lead to a separation through a semipermeable membrane. The Bowman's capsule contains a dense capillary network called the glomerulus. Blood flows into these capillaries through the afferent arterioles and leaves through the efferent arterioles.

Reverse osmosis (RO) is a water purification process that uses a semi-permeable membrane to separate water molecules from other substances. RO applies pressure to overcome osmotic pressure that favors even distributions. RO can remove dissolved or suspended chemical species as well as biological substances, and is used in industrial processes and the production of potable water. RO retains the solute on the pressurized side of the membrane and the purified solvent passes to the other side. The relative sizes of the various molecules determines what passes through. "Selective" membranes reject large molecules, while accepting smaller molecules.

<span class="mw-page-title-main">Osmosis</span> Migration of molecules to a region of lower solute concentration

Osmosis is the spontaneous net movement or diffusion of solvent molecules through a selectively-permeable membrane from a region of high water potential to a region of low water potential, in the direction that tends to equalize the solute concentrations on the two sides. It may also be used to describe a physical process in which any solvent moves across a selectively permeable membrane separating two solutions of different concentrations. Osmosis can be made to do work. Osmotic pressure is defined as the external pressure required to prevent net movement of solvent across the membrane. Osmotic pressure is a colligative property, meaning that the osmotic pressure depends on the molar concentration of the solute but not on its identity.

<span class="mw-page-title-main">History of cell membrane theory</span>

Cell theory has its origins in seventeenth century microscopy observations, but it was nearly two hundred years before a complete cell membrane theory was developed to explain what separates cells from the outside world. By the 19th century it was accepted that some form of semi-permeable barrier must exist around a cell. Studies of the action of anesthetic molecules led to the theory that this barrier might be made of some sort of fat (lipid), but the structure was still unknown. A series of pioneering experiments in 1925 indicated that this barrier membrane consisted of two molecular layers of lipids—a lipid bilayer. New tools over the next few decades confirmed this theory, but controversy remained regarding the role of proteins in the cell membrane. Eventually the fluid mosaic model was composed in which proteins “float” in a fluid lipid bilayer "sea". Although simplistic and incomplete, this model is still widely referenced today.

<span class="mw-page-title-main">Cell membrane</span> Biological membrane that separates the interior of a cell from its outside environment

The cell membrane is a biological membrane that separates and protects the interior of a cell from the outside environment. The cell membrane consists of a lipid bilayer, made up of two layers of phospholipids with cholesterols interspersed between them, maintaining appropriate membrane fluidity at various temperatures. The membrane also contains membrane proteins, including integral proteins that span the membrane and serve as membrane transporters, and peripheral proteins that loosely attach to the outer (peripheral) side of the cell membrane, acting as enzymes to facilitate interaction with the cell's environment. Glycolipids embedded in the outer lipid layer serve a similar purpose.

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Further reading