pH sensitive or pH responsive polymers are materials which will respond to the changes in the pH of the surrounding medium by varying their dimensions. Materials may swell, collapse, or change depending on the pH of their environment. This behavior is exhibited due to the presence of certain functional groups in the polymer chain. pH-sensitive materials can be either acidic or basic, responding to either basic or acidic pH values. These polymers can be designed with many different architectures for different applications. Key uses of pH sensitive polymers are controlled drug delivery systems, biomimetics, micromechanical systems, separation processes, and surface functionalization. [1]
pH sensitive polymers can be broken into two categories: those with acidic groups (such as -COOH and -SO3H) and those with basic groups (-NH2). The mechanism of response is the same for both, only the stimulus varies. The general form of the polymer is a backbone with functional "pendant groups" that hang off of it. When these functional groups become ionized in certain pH levels, they acquire a charge (+/-). Repulsions between like charges cause the polymers to change shape. [1] [2]
Polyacids, also known as anionic polymers, are polymers that have acidic groups. [2] Examples of acidic functional groups include carboxylic acids (-COOH), sulfonic acids (-SO3H), phosphonic acids, and boronic acids. Polyacids accept protons at low pH values. At higher pH values, they deprotonate and become negatively charged. [1] The negative charges create a repulsion that causes the polymer to swell. This swelling behavior is observed when the pH is greater than the pKa of the polymer. [2] Examples include polymethyl methacrylate polymers (pharmacologyonline 1 (2011)152-164) and cellulose acetate phthalate.
Polybases are the basic equivalent of polyacids and are also known as cationic polymers. They accept protons at low pH like polyacids do, but they then become positively charged. In contrast, at higher pH values they are neutral. Swelling behavior is seen when the pH is less than the pKa of the polymer. [1]
Although many sources talk about synthetic pH sensitive polymers, natural polymers can also display pH-responsive behavior. Examples include chitosan, hyaluronic acid, alginic acid and dextran. [1] Chitosan, a frequently used example, is cationic. Since DNA is negatively charged, DNA could be attached to chitosan as a way to deliver genes to cells. [3] Alginic acid, on the other hand, is anionic. It is often evaluated as a calcium-salt for drug delivery applications(International journal of biological macromolecules 75 (2015) 409-17) . Natural polymers have appeal because they display good biocompatibility, which makes them useful for biomedical applications. However, a disadvantage to natural polymers is that researchers can have more control over the structure of synthetic polymers and so can design those polymers for specific applications. [2]
Polymers can be designed to respond to more than one external stimulus, such as pH and temperature. Often, these polymers are structured as a copolymer where each polymer displays one type of response. [1]
pH sensitive polymers have been created with linear block copolymer, star, branched, dendrimer, brush, and comb architectures. Polymers of different architectures will self-assemble into different structures. This self-assembly can occur due to the nature of the polymer and the solvent, or due to a change in pH. pH changes can also cause the larger structure to swell or deswell. For example, block copolymers often form micelles, as will star polymers and branched polymers. However, star and branched polymers can form rod or worm-shaped micelles rather than the typical spheres. Brush polymers are usually used for modifying surfaces since their structure doesn’t allow them to form a larger structure like a micelle. [1]
Often, the response to different pH values is swelling or deswelling. For example, polyacids release protons to become negatively charged at high pH. Since polymer chains are often in close proximity to other parts of the same chain or to other chains, like-charged parts of the polymer repel each other. This repulsion leads to a swelling of the polymer.[ citation needed ]
Polymers can also form micelles (spheres) in response to a change in pH. This behavior can occur with linear block copolymers. If the different blocks of the copolymer have different properties, they can form micelles with one type of block on the inside and one type on the outside. For example, in water the hydrophobic blocks of a copolymer could end up on the inside of a micelle, with hydrophilic blocks on the outside. [4] Additionally, a change in pH could cause micelles to swap their inner and outer molecules depending on the properties of the polymers involved. [1]
Responses other than simply swelling and deswelling with a change in pH are possible as well. Researchers have created polymers that undergo a sol-gel transition (from a solution to a gel) with a change in pH, but which also change from being a stiff gel to a soft gel for certain pH values. [5]
pH sensitive polymers can be synthesized using several common polymerization methods. Functional groups may need to be protected so that they do not react depending on the type of polymerization. The masking can be removed after polymerization so that they regain their pH-sensitive functionality. Living polymerization is often used for making pH sensitive polymers because molecular weight distribution of the final polymers can be controlled. Examples include group transfer polymerization (GTP), atom transfer radical polymerization (ATRP), and reversible addition-fragmentation chain transfer (RAFT). [1] Graft copolymers are a popular type to synthesize because their structure is a backbone with branches. The composition of the branches can be changed to achieve different properties. [2] Hydrogels can be produced using emulsion polymerization. [1]
Several methods can be used to measure the contact angle of a water drop on the surface of a polymer. The contact angle value is used to quantify wettability or hydrophobicity of the polymer. [2]
Equal to (swollen weight-deswelled weight)/deswelled weight *100% and determined by massing polymers before and after swelling. This indicates how much the polymer swelled upon a change in pH. [2]
The pH at which a significant structural change in how the molecules are arranged is observed. This structural change does not involve breaking bonds, but rather a change in conformation. For example, a swelling/deswelling transition would constitute a reversible conformational change. The value of the pH critical point can be determined by examining swelling percentage as a function of pH. Researchers aim to design molecules that transition at a pH that matters for the given application. [2]
Confocal microscopy, scanning electron microscopy, Raman spectroscopy, and atomic force microscopy are all used to determine how the surface of a polymer changes in response to pH. [2]
pH sensitive polymers have been considered for use in membranes. A change in pH could change the ability of the polymer to let ions through, allowing it to act as a filter. [1]
pH sensitive polymers have been used to modify the surfaces of materials. For example, they can be used to change the wettability of a surface. [1]
pH sensitive polymers have been used for drug delivery. For example, they can be used to release insulin in specific quantities. [6]
A gel is a semi-solid that can have properties ranging from soft and weak to hard and tough. Gels are defined as a substantially dilute cross-linked system, which exhibits no flow when in the steady-state, although the liquid phase may still diffuse through this system. A gel has been defined phenomenologically as a soft, solid or solid-like material consisting of two or more components, one of which is a liquid, present in substantial quantity.
In polymer chemistry, a copolymer is a polymer derived from more than one species of monomer. The polymerization of monomers into copolymers is called copolymerization. Copolymers obtained from the copolymerization of two monomer species are sometimes called bipolymers. Those obtained from three and four monomers are called terpolymers and quaterpolymers, respectively. Copolymers can be characterized by a variety of techniques such as NMR spectroscopy and size-exclusion chromatography to determine the molecular size, weight, properties, and composition of the material.
A hydrogel is a biphasic material, a mixture of porous, permeable solids and at least 10% by weight or volume of interstitial fluid composed completely or mainly by water. In hydrogels the porous permeable solid is a water insoluble three dimensional network of natural or synthetic polymers and a fluid, having absorbed a large amount of water or biological fluids. These properties underpin several applications, especially in the biomedical area. Many hydrogels are synthetic, but some are derived from nature. The term 'hydrogel' was coined in 1894.
Sodium polyacrylate (ACR, ASAP, or PAAS), also known as waterlock, is a sodium salt of polyacrylic acid with the chemical formula [−CH2−CH(CO2Na)−]n and has broad applications in consumer products. This super-absorbent polymer (SAP) has the ability to absorb 100 to 1000 times its mass in water. Sodium polyacrylate is an anionic polyelectrolyte with negatively charged carboxylic groups in the main chain. It is a chemical polymer made up of chains of acrylate compounds. It contains sodium, which gives it the ability to absorb large amounts of water. When dissolved in water, it forms a thick and transparent solution due to the ionic interactions of the molecules. Sodium polyacrylate has many favorable mechanical properties. Some of these advantages include good mechanical stability, high heat resistance, and strong hydration. It has been used as an additive for food products including bread, juice, and ice cream.
A superabsorbent polymer (SAP) (also called slush powder) is a water-absorbing hydrophilic homopolymers or copolymers that can absorb and retain extremely large amounts of a liquid relative to its own mass.
Poloxamers are nonionic triblock copolymers composed of a central hydrophobic chain of polyoxypropylene flanked by two hydrophilic chains of polyoxyethylene. The word poloxamer was coined by BASF inventor, Irving Schmolka, who received the patent for these materials in 1973. Poloxamers are also known by the trade names Pluronic, Kolliphor, and Synperonic.
A nerve guidance conduit is an artificial means of guiding axonal regrowth to facilitate nerve regeneration and is one of several clinical treatments for nerve injuries. When direct suturing of the two stumps of a severed nerve cannot be accomplished without tension, the standard clinical treatment for peripheral nerve injuries is autologous nerve grafting. Due to the limited availability of donor tissue and functional recovery in autologous nerve grafting, neural tissue engineering research has focused on the development of bioartificial nerve guidance conduits as an alternative treatment, especially for large defects. Similar techniques are also being explored for nerve repair in the spinal cord but nerve regeneration in the central nervous system poses a greater challenge because its axons do not regenerate appreciably in their native environment.
Thiolated polymers – designated thiomers – are functional polymers used in biotechnology product development with the intention to prolong mucosal drug residence time and to enhance absorption of drugs. The name thiomer was coined by Andreas Bernkop-Schnürch in 2000. Thiomers have thiol bearing side chains. Sulfhydryl ligands of low molecular mass are covalently bound to a polymeric backbone consisting of mainly biodegradable polymers, such as chitosan, hyaluronic acid, cellulose derivatives, pullulan, starch, gelatin, polyacrylates, cyclodextrins, or silicones.
Poly(acrylic acid) (PAA; trade name Carbomer) is a polymer with the formula (CH2-CHCO2H)n. It is a derivative of acrylic acid (CH2=CHCO2H). In addition to the homopolymers, a variety of copolymers and crosslinked polymers, and partially deprotonated derivatives thereof are known and of commercial value. In a water solution at neutral pH, PAA is an anionic polymer, i.e., many of the side chains of PAA lose their protons and acquire a negative charge. Partially or wholly deprotonated PAAs are polyelectrolytes, with the ability to absorb and retain water and swell to many times their original volume. These properties – acid-base and water-attracting – are the bases of many applications.
Poly(N-isopropylacrylamide) (variously abbreviated PNIPA, PNIPAM, PNIPAAm, NIPA, PNIPAA or PNIPAm) is a temperature-responsive polymer that was first synthesized in the 1950s. It can be synthesized from N-isopropylacrylamide which is commercially available. It is synthesized via free-radical polymerization and is readily functionalized making it useful in a variety of applications.
Temperature-responsive polymers or thermoresponsive polymers are polymers that exhibit drastic and discontinuous changes in their physical properties with temperature. The term is commonly used when the property concerned is solubility in a given solvent, but it may also be used when other properties are affected. Thermoresponsive polymers belong to the class of stimuli-responsive materials, in contrast to temperature-sensitive materials, which change their properties continuously with environmental conditions. In a stricter sense, thermoresponsive polymers display a miscibility gap in their temperature-composition diagram. Depending on whether the miscibility gap is found at high or low temperatures, either an upper critical solution temperature (UCST) or a lower critical solution temperature (LCST) exists.
A nanogel is a polymer-based, crosslinked hydrogel particle on the sub-micron scale. These complex networks of polymers present a unique opportunity in the field of drug delivery at the intersection of nanoparticles and hydrogel synthesis. Nanogels can be natural, synthetic, or a combination of the two and have a high degree of tunability in terms of their size, shape, surface functionalization, and degradation mechanisms. Given these inherent characteristics in addition to their biocompatibility and capacity to encapsulate small drugs and molecules, nanogels are a promising strategy to treat disease and dysfunction by serving as delivery vehicles capable of navigating across challenging physiological barriers within the body.
2-Acrylamido-2-methylpropane sulfonic acid (AMPS) was a Trademark name by The Lubrizol Corporation. It is a reactive, hydrophilic, sulfonic acid acrylic monomer used to alter the chemical properties of wide variety of anionic polymers. In the 1970s, the earliest patents using this monomer were filed for acrylic fiber manufacturing. Today, there are over several thousands patents and publications involving use of AMPS in many areas including water treatment, oil field, construction chemicals, hydrogels for medical applications, personal care products, emulsion coatings, adhesives, and rheology modifiers.
Smart polymers, stimuli-responsive polymers or functional polymers are high-performance polymers that change according to the environment they are in. Such materials can be sensitive to a number of factors, such as temperature, humidity, pH, chemical compounds, the wavelength or intensity of light or an electrical or magnetic field and can respond in various ways, like altering color or transparency, becoming conductive or permeable to water or changing shape. Usually, slight changes in the environment are sufficient to induce large changes in the polymer's properties.
Self-healing hydrogels are a specialized type of polymer hydrogel. A hydrogel is a macromolecular polymer gel constructed of a network of crosslinked polymer chains. Hydrogels are synthesized from hydrophilic monomers by either chain or step growth, along with a functional crosslinker to promote network formation. A net-like structure along with void imperfections enhance the hydrogel's ability to absorb large amounts of water via hydrogen bonding. As a result, hydrogels, self-healing alike, develop characteristic firm yet elastic mechanical properties. Self-healing refers to the spontaneous formation of new bonds when old bonds are broken within a material. The structure of the hydrogel along with electrostatic attraction forces drive new bond formation through reconstructive covalent dangling side chain or non-covalent hydrogen bonding. These flesh-like properties have motivated the research and development of self-healing hydrogels in fields such as reconstructive tissue engineering as scaffolding, as well as use in passive and preventive applications.
Nanocomposite hydrogels are nanomaterial-filled, hydrated, polymeric networks that exhibit higher elasticity and strength relative to traditionally made hydrogels. A range of natural and synthetic polymers are used to design nanocomposite network. By controlling the interactions between nanoparticles and polymer chains, a range of physical, chemical, and biological properties can be engineered. The combination of organic (polymer) and inorganic (clay) structure gives these hydrogels improved physical, chemical, electrical, biological, and swelling/de-swelling properties that cannot be achieved by either material alone. Inspired by flexible biological tissues, researchers incorporate carbon-based, polymeric, ceramic and/or metallic nanomaterials to give these hydrogels superior characteristics like optical properties and stimulus-sensitivity which can potentially be very helpful to medical and mechanical fields.
Hydrogels are three-dimensional networks consisting of chemically or physically cross-linked hydrophilic polymers. The insoluble hydrophilic structures absorb polar wound exudates and allow oxygen diffusion at the wound bed to accelerate healing. Hydrogel dressings can be designed to prevent bacterial infection, retain moisture, promote optimum adhesion to tissues, and satisfy the basic requirements of biocompatibility. Hydrogel dressings can also be designed to respond to changes in the microenvironment at the wound bed. Hydrogel dressings should promote an appropriate microenvironment for angiogenesis, recruitment of fibroblasts, and cellular proliferation.
Dextran drug delivery systems involve the use of the natural glucose polymer dextran in applications as a prodrug, nanoparticle, microsphere, micelle, and hydrogel drug carrier in the field of targeted and controlled drug delivery. According to several in vitro and animal research studies, dextran carriers reduce off-site toxicity and improve local drug concentration at the target tissue site. This technology has significant implications as a potential strategy for delivering therapeutics to treat cancer, cardiovascular diseases, pulmonary diseases, bone diseases, liver diseases, colonic diseases, infections, and HIV.
Conventional drug delivery is limited by the inability to control dosing, target specific sites, and achieve targeted permeability. Traditional methods of delivering therapeutics to the body experience challenges in achieving and maintaining maximum therapeutic effect while avoiding the effects of drug toxicity. Many drugs that are delivered orally or parenterally do not include mechanisms for sustained release, and as a result they require higher and more frequent dosing to achieve any therapeutic effect for the patient. As a result, the field of drug delivery systems developed into a large focus area for pharmaceutical research to address these limitations and improve quality of care for patients. Within the broad field of drug delivery, the development of stimuli-responsive drug delivery systems has created the ability to tune drug delivery systems to achieve more controlled dosing and targeted specificity based on material response to exogenous and endogenous stimuli.
Pullulan bioconjugates are systems that use pullulan as a scaffold to attach biological materials to, such as drugs. These systems can be used to enhance the delivery of drugs to specific environments or the mechanism of delivery. These systems can be used in order to deliver drugs in response to stimuli, create a more controlled and sustained release, and provide a more targeted delivery of certain drugs.