Gated Drug Delivery Systems
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Gated Drug Delivery Systems
Gated drug delivery systems are a method of controlled drug delivery, drug release that center around the use of physical molecules that cover the pores of drug carriers until triggered for removal by an external stimulus. Gated drug delivery systems are a recent innovation in the field of drug delivery and pose as a promising candidate for future drug delivery systems that are effective at targeting certain sites without having leakages or off target effects in normal tissues. This new technology has the potential to be used in a variety of tissues over a wide range of disease states and has the added benefit of protecting healthy tissues and reducing systemic side effects. Uses Gated drug delivery systems are an emerging concept that have drawn a lot of attention for their wide variety of potential applications in the medical field. The abnormal physiological conditions found within the Tumor microenvironment, tumor environment provide a breadth of options that could be used f ...
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Ophthalmic Drug Administration
Ophthalmic drug administration is the administration of a drug to the eyes, most typically as an eye drop formulation. Topical formulations are used to combat a multitude of diseased states of the eye. These states may include bacterial infections, eye injury, glaucoma, and dry eye. However, there are many challenges associated with topical delivery of drugs to the cornea of the eye. Eye drop formulations Two of the largest challenges faced when using topicals to treat pathological states of the eye include Adherence (medicine), patient compliance and ineffective absorbance of drugs into the cornea due to short contact times, solution drainage, tears turnover, and dilution or lacrimation. In fact, researchers in this field of drug delivery agree that less than 7% of drugs delivered to the eye reach and penetrate the corneal barrier, therefore, increasing the frequency of dosing used for topicals. This is one of the fundamental problem associated with using topicals to deliver dr ...
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Deakin University
Deakin University is a public university in Victoria, Australia. Founded in 1974 with antecedent history since 1887, the university was named after Alfred Deakin, the second Prime Minister of Australia and a founding father of Australian Federation. Its main campuses are in Melbourne's Burwood suburb, Geelong Waurn Ponds, Geelong Waterfront, and Warrnambool. Deakin also has a learning centre in Werribee. Deakin University is ranked among the top 1% of universities in the world, is the 3rd-highest-ranked university in the world for Sport Science, is one of the top 29 universities in the world for Nursing, is one of the top 32 universities in the world for Education, and is among fewer than 5% of Business Schools worldwide with Association to Advance Collegiate Schools of Business accreditation. Deakin University consistently ranks highly in undergraduate student satisfaction; in the 2019 Student Experience Survey, Deakin had the fourth-highest student satisfaction rating ...
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Chemically Inert
In chemistry, the term chemically inert is used to describe a substance that is not chemically reactive. From a thermodynamic perspective, a substance is inert, or nonlabile, if it is thermodynamically unstable (negative standard Gibbs free energy of formation) yet decomposes at a slow, or negligible rate. Most of the noble gases, which appear in the last column of the periodic table, are classified as inert (or unreactive). These elements are stable in their naturally occurring form (gaseous form) and they are called inert gases. Noble gas The noble gases (helium, neon, argon, krypton, xenon and radon) were previously known as 'inert gases' because of their perceived lack of participation in any chemical reactions. The reason for this is that their outermost electron shells (valence shells) are completely filled, so that they have little tendency to gain or lose electrons. They are said to acquire a noble gas configuration, or a full electron configuration. It is now ...
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Biocompatibility
Biocompatibility is related to the behavior of biomaterials in various contexts. The term refers to the ability of a material to perform with an appropriate host response in a specific situation. The ambiguity of the term reflects the ongoing development of insights into how biomaterials interact with the human body and eventually how those interactions determine the clinical success of a medical device (such as pacemaker, hip replacement or stent). Modern medical devices and prostheses are often made of more than one material so it might not always be sufficient to talk about the biocompatibility of a specific material. Since the immune response and repair functions in the body are so complicated it is not adequate to describe the biocompatibility of a single material in relation to a single cell type or tissue. Sometimes one hears of biocompatibility testing that is a large battery of in vitro test that is used in accordance with ISO 10993 (or other similar standards) ...
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Mesoporous Silica
Mesoporous silica is a form of silica that is characterised by its mesoporous structure, that is, having pores that range from 2 nm to 50 nm in diameter. According to IUPAC's terminology, mesoporosity sits between microporous (50 nm). Mesoporous silica is a relatively recent development in nanotechnology. The most common types of mesoporous nanoparticles are MCM-41 and Santa Barbara Amorphous-15, SBA-15. Research continues on the particles, which have applications in catalysis, drug delivery and Medical imaging, imaging. Mesoporous ordered silica films have been also obtained with different pore topologies. A compound producing mesoporous silica was patented around 1970. It went almost unnoticed and was reproduced in 1997. Mesoporous silica nanoparticles (MSNs) were independently synthesized in 1990 by researchers in Japan. They were later produced also at Mobil Corporation laboratories and named Mobil Composition of Matter (or Mobil Crystalline Materials, MCM). S ...
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Nanoparticle Drug Delivery
Nanoparticle drug delivery systems are engineered technologies that use nanoparticles for the targeted delivery and controlled release of therapeutic agents. The modern form of a drug delivery system should minimize side-effects and reduce both dosage and dosage frequency. Recently, nanoparticles have aroused attention due to their potential application for effective drug delivery. Nanomaterials exhibit different chemical and physical properties or biological effects compared to larger-scale counterparts that can be beneficial for drug delivery systems. Some important advantages of nanoparticles are their high surface-area-to-volume ratio, chemical and geometric tunability, and their ability to interact with biomolecules to facilitate uptake across the cell membrane. The large surface area also has a large affinity for drugs and small molecules, like ligands or antibodies, for targeting and controlled release purposes. Nanoparticles refer to a large family of materials both orga ...
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Enhanced Permeation And Retention
''Enhanced'' is a 2019 Canadian-Japanese action film produced, written and directed by James Mark. The film premiered at the 2019 Toronto After Dark Film Festival. Plot A sinister government organization hunts down mutants, and one of such is a young woman with enhanced abilities. But when she encounters even stronger serial killer who emerges on the scene, agents and mutants are forced to question their allegiances. This is not an advertised sequel, but it is the continuation of the story from the 2017 movie "Kill Order". Cast * George Tchortov as George Shepherd * Alanna Bale as Anna * Adrian Holmes as Captain Williams * Chris Mark as David * Eric Hicks as Scott * Michael Joseph Delaney as Eli * Patrick Sabongui as Joseph * Elvis Stojko as Officer Reves * Stefano DiMatteo as Marco * Jeffrey R. Smith as Danny * Dorren Lee as Fanny * Eric Daniel as Mehran * Carl Bauer as Ritchie * Kevan Kase as Joey * Dylan Mask as Jim * Alain Moussi as Abel * Tyler James Williams as Ron * Mustafa ...
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PEGylation
PEGylation (or pegylation) is the process of both covalent and non-covalent attachment or amalgamation of polyethylene glycol (PEG, in pharmacy called macrogol) polymer chains to molecules and macrostructures, such as a drug, therapeutic protein or vesicle, which is then described as PEGylated. PEGylation affects the resulting derivatives or aggregates interactions, which typically slows down their coalescence and degradation as well as elimination in vivo. PEGylation is routinely achieved by the incubation of a reactive derivative of PEG with the target molecule. The covalent attachment of PEG to a drug or therapeutic protein can "mask" the agent from the host's immune system (reducing immunogenicity and antigenicity), and increase its hydrodynamic size (size in solution), which prolongs its circulatory time by reducing renal clearance. PEGylation can also provide water solubility to hydrophobic drugs and proteins. Having proven its pharmacological advantages and acceptability, ...
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Nanotherapeutics
Nanomedicine is the medical application of nanotechnology, translating historic nanoscience insights and inventions into practical application. Nanomedicine ranges from the medical applications of nanomaterials and biological devices, to nanoelectronic biosensors, and even possible future applications of molecular nanotechnology such as biological machines. Current problems for nanomedicine involve understanding the issues related to toxicity and environmental impact of nanoscale materials (materials whose structure is on the scale of nanometers, i.e. billionths of a meter). Functionalities can be added to nanomaterials by interfacing them with biological molecules or structures. The size of nanomaterials is similar to that of most biological molecules and structures; therefore, nanomaterials can be useful for both in vivo and in vitro biomedical research and applications. Thus far, the integration of nanomaterials with biology has led to the development of diagnostic devi ...
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Microparticle
Microparticles are particles between 0.1 and 100 μm in size. Commercially available microparticles are available in a wide variety of materials, including ceramics, glass, polymers, and metals. Microparticles encountered in daily life include pollen, sand, dust, flour, and powdered sugar. The study of microparticles has been called micromeritics, although this term is not very common. Microparticles have a much larger surface-to-volume ratio than at the macroscale, and thus their behavior can be quite different. For example, metal microparticles can be explosive in air. Microspheres are spherical microparticles, and are used where consistent and predictable particle surface area is important. In biological systems, a microparticle is synonymous with a microvesicle, a type of extracellular vesicle (EV). Applications Home pregnancy tests make use of gold microparticles. Many applications are also listed in the microsphere article. A recent study showed that infused, ...
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PLGA
PLGA, PLG, or poly(lactic-''co''-glycolic) acid (CAS Registry Number, CAS: ) is a copolymer which is used in a host of Food and Drug Administration (FDA) approved therapeutic devices, owing to its biodegradation, biodegradability and biocompatibility. PLGA is synthesized by means of ring-opening co-polymerization of two different monomers: glycolide and lactide, the cyclic dimers (1,4-dioxane-2,5-diones) of glycolic acid and lactic acid, respectively. Polymers can be synthesized as either random or block copolymers thereby imparting additional polymer properties. Common catalysts used in the preparation of this polymer include tin(II) 2-ethylhexanoate, tin(II) alkoxides, or aluminum isopropoxide. During polymerization, successive monomeric units of glycolic or lactic acid are linked together in PLGA by ester linkages, thus yielding a linear, polyester as a product. Copolymer Depending on the ratio of lactide to glycolide used for the polymerization, different forms of PLGA can be ...
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